15-101933497-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101933497
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101933497
    reference: chr 15
allele count: 1
allele frequency: 8.37184381488179e-6
allele num: 119448
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000332052
  ensembl transcript: ENST00000331826
  gene symbol: PCSK6
  hgvsc: ENST00000331826.7:c.631T>C
  hgvsp: ENSP00000332052.7:p.Tyr211His
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000452997
  ensembl transcript: ENST00000559417
  gene symbol: PCSK6
  hgvsc: ENST00000559417.1:c.750T>C
  hgvsp: ENSP00000452997.1:p.Tyr251His
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560271
  gene symbol: PCSK6
  hgvsc: ENST00000560271.1:n.1154T>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000351193
  ensembl transcript: ENST00000358417
  gene symbol: PCSK6
  hgvsc: ENST00000358417.3:c.1126T>C
  hgvsp: ENSP00000351193.3:p.Tyr376His
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381243
  ensembl transcript: ENST00000398181
  gene symbol: PCSK6
  hgvsc: ENST00000398181.2:c.1126T>C
  hgvsp: ENSP00000381243.2:p.Tyr376His
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000558716
  gene symbol: PCSK6
  hgvsc: ENST00000558716.1:n.1154T>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381246
  ensembl transcript: ENST00000398185
  gene symbol: PCSK6
  hgvsc: ENST00000398185.2:c.835T>C
  hgvsp: ENSP00000381246.2:p.Tyr279His
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561109
  gene symbol: PCSK6
  hgvsc: ENST00000561109.1:n.1201T>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561444
  gene symbol: PCSK6
  hgvsc: ENST00000561444.1:n.1296T>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000344410
  ensembl transcript: ENST00000344273
  gene symbol: PCSK6
  hgvsc: ENST00000344273.2:c.1126T>C
  hgvsp: ENSP00000344410.2:p.Tyr376His
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000559678
  gene symbol: PCSK6
  hgvsc: ENST00000559678.1:n.1201T>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000305056
  ensembl transcript: ENST00000348070
  gene symbol: PCSK6
  hgvsc: ENST00000348070.1:c.1126T>C
  hgvsp: ENSP00000305056.4:p.Tyr376His
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000557794
  gene symbol: PCSK6
  hgvsc: ENST00000557794.1:n.124-79787T>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560921
  gene symbol: PCSK6
  hgvsc: ENST00000560921.1:n.1201T>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561177
  gene symbol: PCSK6
  hgvsc: ENST00000561177.1:n.1296T>C
  variant of: http://identifiers.org/hgnc/8569
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 939
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40383
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 872
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2898
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13625
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr376His
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD

15-101933498-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101933498
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101933498
    reference: chr 15
allele count: 1
allele frequency: 8.373105584861425e-6
allele num: 119430
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000557794
  gene symbol: PCSK6
  hgvsc: ENST00000557794.1:n.124-79788C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561444
  gene symbol: PCSK6
  hgvsc: ENST00000561444.1:n.1295C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560271
  gene symbol: PCSK6
  hgvsc: ENST00000560271.1:n.1153C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000305056
  ensembl transcript: ENST00000348070
  gene symbol: PCSK6
  hgvsc: ENST00000348070.1:c.1125C>T
  hgvsp: ENST00000348070.1:c.1125C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000559678
  gene symbol: PCSK6
  hgvsc: ENST00000559678.1:n.1200C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000344410
  ensembl transcript: ENST00000344273
  gene symbol: PCSK6
  hgvsc: ENST00000344273.2:c.1125C>T
  hgvsp: ENST00000344273.2:c.1125C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561109
  gene symbol: PCSK6
  hgvsc: ENST00000561109.1:n.1200C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561177
  gene symbol: PCSK6
  hgvsc: ENST00000561177.1:n.1295C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381243
  ensembl transcript: ENST00000398181
  gene symbol: PCSK6
  hgvsc: ENST00000398181.2:c.1125C>T
  hgvsp: ENST00000398181.2:c.1125C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000351193
  ensembl transcript: ENST00000358417
  gene symbol: PCSK6
  hgvsc: ENST00000358417.3:c.1125C>T
  hgvsp: ENST00000358417.3:c.1125C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000452997
  ensembl transcript: ENST00000559417
  gene symbol: PCSK6
  hgvsc: ENST00000559417.1:c.749C>T
  hgvsp: ENST00000559417.1:c.749C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381246
  ensembl transcript: ENST00000398185
  gene symbol: PCSK6
  hgvsc: ENST00000398185.2:c.834C>T
  hgvsp: ENST00000398185.2:c.834C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000332052
  ensembl transcript: ENST00000331826
  gene symbol: PCSK6
  hgvsc: ENST00000331826.7:c.630C>T
  hgvsp: ENST00000331826.7:c.630C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000558716
  gene symbol: PCSK6
  hgvsc: ENST00000558716.1:n.1153C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560921
  gene symbol: PCSK6
  hgvsc: ENST00000560921.1:n.1200C>T
  variant of: http://identifiers.org/hgnc/8569
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13636
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40314
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly375Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD

15-101933507-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101933507
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101933507
    reference: chr 15
allele count: 1
allele frequency: 8.363161944267889e-6
allele num: 119572
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000452997
  ensembl transcript: ENST00000559417
  gene symbol: PCSK6
  hgvsc: ENST00000559417.1:c.740C>T
  hgvsp: ENST00000559417.1:c.740C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381243
  ensembl transcript: ENST00000398181
  gene symbol: PCSK6
  hgvsc: ENST00000398181.2:c.1116C>T
  hgvsp: ENST00000398181.2:c.1116C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561109
  gene symbol: PCSK6
  hgvsc: ENST00000561109.1:n.1191C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000559678
  gene symbol: PCSK6
  hgvsc: ENST00000559678.1:n.1191C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381246
  ensembl transcript: ENST00000398185
  gene symbol: PCSK6
  hgvsc: ENST00000398185.2:c.825C>T
  hgvsp: ENST00000398185.2:c.825C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000344410
  ensembl transcript: ENST00000344273
  gene symbol: PCSK6
  hgvsc: ENST00000344273.2:c.1116C>T
  hgvsp: ENST00000344273.2:c.1116C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561444
  gene symbol: PCSK6
  hgvsc: ENST00000561444.1:n.1286C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000351193
  ensembl transcript: ENST00000358417
  gene symbol: PCSK6
  hgvsc: ENST00000358417.3:c.1116C>T
  hgvsp: ENST00000358417.3:c.1116C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560271
  gene symbol: PCSK6
  hgvsc: ENST00000560271.1:n.1144C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000332052
  ensembl transcript: ENST00000331826
  gene symbol: PCSK6
  hgvsc: ENST00000331826.7:c.621C>T
  hgvsp: ENST00000331826.7:c.621C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561177
  gene symbol: PCSK6
  hgvsc: ENST00000561177.1:n.1286C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000558716
  gene symbol: PCSK6
  hgvsc: ENST00000558716.1:n.1144C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000305056
  ensembl transcript: ENST00000348070
  gene symbol: PCSK6
  hgvsc: ENST00000348070.1:c.1116C>T
  hgvsp: ENST00000348070.1:c.1116C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560921
  gene symbol: PCSK6
  hgvsc: ENST00000560921.1:n.1191C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000557794
  gene symbol: PCSK6
  hgvsc: ENST00000557794.1:n.124-79797C>T
  variant of: http://identifiers.org/hgnc/8569
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13710
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2859
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40409
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr372Thr
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: DP

15-101933511-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101933511
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101933511
    reference: chr 15
allele count: 5
allele frequency: 4.179413878997609e-5
allele num: 119634
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561444
  gene symbol: PCSK6
  hgvsc: ENST00000561444.1:n.1282C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560271
  gene symbol: PCSK6
  hgvsc: ENST00000560271.1:n.1140C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000332052
  ensembl transcript: ENST00000331826
  gene symbol: PCSK6
  hgvsc: ENST00000331826.7:c.617C>T
  hgvsp: ENSP00000332052.7:p.Ala206Val
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000559678
  gene symbol: PCSK6
  hgvsc: ENST00000559678.1:n.1187C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000344410
  ensembl transcript: ENST00000344273
  gene symbol: PCSK6
  hgvsc: ENST00000344273.2:c.1112C>T
  hgvsp: ENSP00000344410.2:p.Ala371Val
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560921
  gene symbol: PCSK6
  hgvsc: ENST00000560921.1:n.1187C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000351193
  ensembl transcript: ENST00000358417
  gene symbol: PCSK6
  hgvsc: ENST00000358417.3:c.1112C>T
  hgvsp: ENSP00000351193.3:p.Ala371Val
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000452997
  ensembl transcript: ENST00000559417
  gene symbol: PCSK6
  hgvsc: ENST00000559417.1:c.736C>T
  hgvsp: ENSP00000452997.1:p.Ala246Val
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381243
  ensembl transcript: ENST00000398181
  gene symbol: PCSK6
  hgvsc: ENST00000398181.2:c.1112C>T
  hgvsp: ENSP00000381243.2:p.Ala371Val
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561177
  gene symbol: PCSK6
  hgvsc: ENST00000561177.1:n.1282C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381246
  ensembl transcript: ENST00000398185
  gene symbol: PCSK6
  hgvsc: ENST00000398185.2:c.821C>T
  hgvsp: ENSP00000381246.2:p.Ala274Val
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000305056
  ensembl transcript: ENST00000348070
  gene symbol: PCSK6
  hgvsc: ENST00000348070.1:c.1112C>T
  hgvsp: ENSP00000305056.4:p.Ala371Val
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000557794
  gene symbol: PCSK6
  hgvsc: ENST00000557794.1:n.124-79801C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000558716
  gene symbol: PCSK6
  hgvsc: ENST00000558716.1:n.1140C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561109
  gene symbol: PCSK6
  hgvsc: ENST00000561109.1:n.1187C>T
  variant of: http://identifiers.org/hgnc/8569
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1015
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40485
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala371Val
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: QD

15-101933512-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101933512
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101933512
    reference: chr 15
allele count: 6
allele frequency: 5.019996318669366e-5
allele num: 119522
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000557794
  gene symbol: PCSK6
  hgvsc: ENST00000557794.1:n.124-79802G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381246
  ensembl transcript: ENST00000398185
  gene symbol: PCSK6
  hgvsc: ENST00000398185.2:c.820G>A
  hgvsp: ENSP00000381246.2:p.Ala274Thr
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561444
  gene symbol: PCSK6
  hgvsc: ENST00000561444.1:n.1281G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000305056
  ensembl transcript: ENST00000348070
  gene symbol: PCSK6
  hgvsc: ENST00000348070.1:c.1111G>A
  hgvsp: ENSP00000305056.4:p.Ala371Thr
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560271
  gene symbol: PCSK6
  hgvsc: ENST00000560271.1:n.1139G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000344410
  ensembl transcript: ENST00000344273
  gene symbol: PCSK6
  hgvsc: ENST00000344273.2:c.1111G>A
  hgvsp: ENSP00000344410.2:p.Ala371Thr
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561177
  gene symbol: PCSK6
  hgvsc: ENST00000561177.1:n.1281G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000558716
  gene symbol: PCSK6
  hgvsc: ENST00000558716.1:n.1139G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000351193
  ensembl transcript: ENST00000358417
  gene symbol: PCSK6
  hgvsc: ENST00000358417.3:c.1111G>A
  hgvsp: ENSP00000351193.3:p.Ala371Thr
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000559678
  gene symbol: PCSK6
  hgvsc: ENST00000559678.1:n.1186G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381243
  ensembl transcript: ENST00000398181
  gene symbol: PCSK6
  hgvsc: ENST00000398181.2:c.1111G>A
  hgvsp: ENSP00000381243.2:p.Ala371Thr
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560921
  gene symbol: PCSK6
  hgvsc: ENST00000560921.1:n.1186G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000452997
  ensembl transcript: ENST00000559417
  gene symbol: PCSK6
  hgvsc: ENST00000559417.1:c.735G>A
  hgvsp: ENSP00000452997.1:p.Ala246Thr
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000332052
  ensembl transcript: ENST00000331826
  gene symbol: PCSK6
  hgvsc: ENST00000331826.7:c.616G>A
  hgvsp: ENSP00000332052.7:p.Ala206Thr
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561109
  gene symbol: PCSK6
  hgvsc: ENST00000561109.1:n.1186G>A
  variant of: http://identifiers.org/hgnc/8569
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2807
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13627
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40408
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala371Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: Other
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD

15-101933513-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101933513
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101933513
    reference: chr 15
allele count: 6
allele frequency: 5.019828321871392e-5
allele num: 119526
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000332052
  ensembl transcript: ENST00000331826
  gene symbol: PCSK6
  hgvsc: ENST00000331826.7:c.615C>T
  hgvsp: ENST00000331826.7:c.615C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000558716
  gene symbol: PCSK6
  hgvsc: ENST00000558716.1:n.1138C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000351193
  ensembl transcript: ENST00000358417
  gene symbol: PCSK6
  hgvsc: ENST00000358417.3:c.1110C>T
  hgvsp: ENST00000358417.3:c.1110C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000305056
  ensembl transcript: ENST00000348070
  gene symbol: PCSK6
  hgvsc: ENST00000348070.1:c.1110C>T
  hgvsp: ENST00000348070.1:c.1110C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000344410
  ensembl transcript: ENST00000344273
  gene symbol: PCSK6
  hgvsc: ENST00000344273.2:c.1110C>T
  hgvsp: ENST00000344273.2:c.1110C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000452997
  ensembl transcript: ENST00000559417
  gene symbol: PCSK6
  hgvsc: ENST00000559417.1:c.734C>T
  hgvsp: ENST00000559417.1:c.734C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000559678
  gene symbol: PCSK6
  hgvsc: ENST00000559678.1:n.1185C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561177
  gene symbol: PCSK6
  hgvsc: ENST00000561177.1:n.1280C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560271
  gene symbol: PCSK6
  hgvsc: ENST00000560271.1:n.1138C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560921
  gene symbol: PCSK6
  hgvsc: ENST00000560921.1:n.1185C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561109
  gene symbol: PCSK6
  hgvsc: ENST00000561109.1:n.1185C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381246
  ensembl transcript: ENST00000398185
  gene symbol: PCSK6
  hgvsc: ENST00000398185.2:c.819C>T
  hgvsp: ENST00000398185.2:c.819C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381243
  ensembl transcript: ENST00000398181
  gene symbol: PCSK6
  hgvsc: ENST00000398181.2:c.1110C>T
  hgvsp: ENST00000398181.2:c.1110C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561444
  gene symbol: PCSK6
  hgvsc: ENST00000561444.1:n.1280C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000557794
  gene symbol: PCSK6
  hgvsc: ENST00000557794.1:n.124-79803C>T
  variant of: http://identifiers.org/hgnc/8569
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13628
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2808
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser370Ser
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: Other
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

15-101933521-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101933521
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101933521
    reference: chr 15
allele count: 31
allele frequency: 2.591236604978518e-4
allele num: 119634
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000344410
  ensembl transcript: ENST00000344273
  gene symbol: PCSK6
  hgvsc: ENST00000344273.2:c.1102G>A
  hgvsp: ENSP00000344410.2:p.Val368Ile
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000558716
  gene symbol: PCSK6
  hgvsc: ENST00000558716.1:n.1130G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560921
  gene symbol: PCSK6
  hgvsc: ENST00000560921.1:n.1177G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000559678
  gene symbol: PCSK6
  hgvsc: ENST00000559678.1:n.1177G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560271
  gene symbol: PCSK6
  hgvsc: ENST00000560271.1:n.1130G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000332052
  ensembl transcript: ENST00000331826
  gene symbol: PCSK6
  hgvsc: ENST00000331826.7:c.607G>A
  hgvsp: ENSP00000332052.7:p.Val203Ile
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561109
  gene symbol: PCSK6
  hgvsc: ENST00000561109.1:n.1177G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000452997
  ensembl transcript: ENST00000559417
  gene symbol: PCSK6
  hgvsc: ENST00000559417.1:c.726G>A
  hgvsp: ENSP00000452997.1:p.Val243Ile
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381243
  ensembl transcript: ENST00000398181
  gene symbol: PCSK6
  hgvsc: ENST00000398181.2:c.1102G>A
  hgvsp: ENSP00000381243.2:p.Val368Ile
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561444
  gene symbol: PCSK6
  hgvsc: ENST00000561444.1:n.1272G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000351193
  ensembl transcript: ENST00000358417
  gene symbol: PCSK6
  hgvsc: ENST00000358417.3:c.1102G>A
  hgvsp: ENSP00000351193.3:p.Val368Ile
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561177
  gene symbol: PCSK6
  hgvsc: ENST00000561177.1:n.1272G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000305056
  ensembl transcript: ENST00000348070
  gene symbol: PCSK6
  hgvsc: ENST00000348070.1:c.1102G>A
  hgvsp: ENSP00000305056.4:p.Val368Ile
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000557794
  gene symbol: PCSK6
  hgvsc: ENST00000557794.1:n.124-79811G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381246
  ensembl transcript: ENST00000398185
  gene symbol: PCSK6
  hgvsc: ENST00000398185.2:c.811G>A
  hgvsp: ENSP00000381246.2:p.Val271Ile
  variant of: http://identifiers.org/hgnc/8569
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2733
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 3.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13722
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40620
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val368Ile
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ

15-101933524-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101933524
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101933524
    reference: chr 15
allele count: 1
allele frequency: 8.360784576024614e-6
allele num: 119606
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560921
  gene symbol: PCSK6
  hgvsc: ENST00000560921.1:n.1174T>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000452997
  ensembl transcript: ENST00000559417
  gene symbol: PCSK6
  hgvsc: ENST00000559417.1:c.723T>C
  hgvsp: ENSP00000452997.1:p.Ser242Pro
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000305056
  ensembl transcript: ENST00000348070
  gene symbol: PCSK6
  hgvsc: ENST00000348070.1:c.1099T>C
  hgvsp: ENSP00000305056.4:p.Ser367Pro
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560271
  gene symbol: PCSK6
  hgvsc: ENST00000560271.1:n.1127T>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381243
  ensembl transcript: ENST00000398181
  gene symbol: PCSK6
  hgvsc: ENST00000398181.2:c.1099T>C
  hgvsp: ENSP00000381243.2:p.Ser367Pro
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381246
  ensembl transcript: ENST00000398185
  gene symbol: PCSK6
  hgvsc: ENST00000398185.2:c.808T>C
  hgvsp: ENSP00000381246.2:p.Ser270Pro
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000559678
  gene symbol: PCSK6
  hgvsc: ENST00000559678.1:n.1174T>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000558716
  gene symbol: PCSK6
  hgvsc: ENST00000558716.1:n.1127T>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000332052
  ensembl transcript: ENST00000331826
  gene symbol: PCSK6
  hgvsc: ENST00000331826.7:c.604T>C
  hgvsp: ENSP00000332052.7:p.Ser202Pro
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561109
  gene symbol: PCSK6
  hgvsc: ENST00000561109.1:n.1174T>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561444
  gene symbol: PCSK6
  hgvsc: ENST00000561444.1:n.1269T>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000344410
  ensembl transcript: ENST00000344273
  gene symbol: PCSK6
  hgvsc: ENST00000344273.2:c.1099T>C
  hgvsp: ENSP00000344410.2:p.Ser367Pro
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000351193
  ensembl transcript: ENST00000358417
  gene symbol: PCSK6
  hgvsc: ENST00000358417.3:c.1099T>C
  hgvsp: ENSP00000351193.3:p.Ser367Pro
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000557794
  gene symbol: PCSK6
  hgvsc: ENST00000557794.1:n.124-79814T>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561177
  gene symbol: PCSK6
  hgvsc: ENST00000561177.1:n.1269T>C
  variant of: http://identifiers.org/hgnc/8569
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1179
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40514
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser367Pro
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP

15-101933531-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101933531
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101933531
    reference: chr 15
allele count: 1
allele frequency: 8.356592515835743e-6
allele num: 119666
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000452997
  ensembl transcript: ENST00000559417
  gene symbol: PCSK6
  hgvsc: ENST00000559417.1:c.716C>T
  hgvsp: ENST00000559417.1:c.716C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560921
  gene symbol: PCSK6
  hgvsc: ENST00000560921.1:n.1167C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561109
  gene symbol: PCSK6
  hgvsc: ENST00000561109.1:n.1167C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000344410
  ensembl transcript: ENST00000344273
  gene symbol: PCSK6
  hgvsc: ENST00000344273.2:c.1092C>T
  hgvsp: ENST00000344273.2:c.1092C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381246
  ensembl transcript: ENST00000398185
  gene symbol: PCSK6
  hgvsc: ENST00000398185.2:c.801C>T
  hgvsp: ENST00000398185.2:c.801C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000559678
  gene symbol: PCSK6
  hgvsc: ENST00000559678.1:n.1167C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000332052
  ensembl transcript: ENST00000331826
  gene symbol: PCSK6
  hgvsc: ENST00000331826.7:c.597C>T
  hgvsp: ENST00000331826.7:c.597C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000558716
  gene symbol: PCSK6
  hgvsc: ENST00000558716.1:n.1120C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561177
  gene symbol: PCSK6
  hgvsc: ENST00000561177.1:n.1262C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381243
  ensembl transcript: ENST00000398181
  gene symbol: PCSK6
  hgvsc: ENST00000398181.2:c.1092C>T
  hgvsp: ENST00000398181.2:c.1092C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000351193
  ensembl transcript: ENST00000358417
  gene symbol: PCSK6
  hgvsc: ENST00000358417.3:c.1092C>T
  hgvsp: ENST00000358417.3:c.1092C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561444
  gene symbol: PCSK6
  hgvsc: ENST00000561444.1:n.1262C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560271
  gene symbol: PCSK6
  hgvsc: ENST00000560271.1:n.1120C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000557794
  gene symbol: PCSK6
  hgvsc: ENST00000557794.1:n.124-79821C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000305056
  ensembl transcript: ENST00000348070
  gene symbol: PCSK6
  hgvsc: ENST00000348070.1:c.1092C>T
  hgvsp: ENST00000348070.1:c.1092C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13706
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40629
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2687
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr364Tyr
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: Other
population: European (Finnish)
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum

15-101933534-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101933534
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101933534
    reference: chr 15
allele count: 1
allele frequency: 8.358548287333457e-6
allele num: 119638
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381246
  ensembl transcript: ENST00000398185
  gene symbol: PCSK6
  hgvsc: ENST00000398185.2:c.798C>T
  hgvsp: ENST00000398185.2:c.798C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000559678
  gene symbol: PCSK6
  hgvsc: ENST00000559678.1:n.1164C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561444
  gene symbol: PCSK6
  hgvsc: ENST00000561444.1:n.1259C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000305056
  ensembl transcript: ENST00000348070
  gene symbol: PCSK6
  hgvsc: ENST00000348070.1:c.1089C>T
  hgvsp: ENST00000348070.1:c.1089C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560921
  gene symbol: PCSK6
  hgvsc: ENST00000560921.1:n.1164C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381243
  ensembl transcript: ENST00000398181
  gene symbol: PCSK6
  hgvsc: ENST00000398181.2:c.1089C>T
  hgvsp: ENST00000398181.2:c.1089C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000452997
  ensembl transcript: ENST00000559417
  gene symbol: PCSK6
  hgvsc: ENST00000559417.1:c.713C>T
  hgvsp: ENST00000559417.1:c.713C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000558716
  gene symbol: PCSK6
  hgvsc: ENST00000558716.1:n.1117C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000351193
  ensembl transcript: ENST00000358417
  gene symbol: PCSK6
  hgvsc: ENST00000358417.3:c.1089C>T
  hgvsp: ENST00000358417.3:c.1089C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560271
  gene symbol: PCSK6
  hgvsc: ENST00000560271.1:n.1117C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000344410
  ensembl transcript: ENST00000344273
  gene symbol: PCSK6
  hgvsc: ENST00000344273.2:c.1089C>T
  hgvsp: ENST00000344273.2:c.1089C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561177
  gene symbol: PCSK6
  hgvsc: ENST00000561177.1:n.1259C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561109
  gene symbol: PCSK6
  hgvsc: ENST00000561109.1:n.1164C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000557794
  gene symbol: PCSK6
  hgvsc: ENST00000557794.1:n.124-79824C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000332052
  ensembl transcript: ENST00000331826
  gene symbol: PCSK6
  hgvsc: ENST00000331826.7:c.594C>T
  hgvsp: ENST00000331826.7:c.594C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2686
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile363Ile
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum

15-101933546-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101933546
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101933546
    reference: chr 15
allele count: 1
allele frequency: 8.371423309391063e-6
allele num: 119454
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561444
  gene symbol: PCSK6
  hgvsc: ENST00000561444.1:n.1247C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000344410
  ensembl transcript: ENST00000344273
  gene symbol: PCSK6
  hgvsc: ENST00000344273.2:c.1077C>T
  hgvsp: ENST00000344273.2:c.1077C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000332052
  ensembl transcript: ENST00000331826
  gene symbol: PCSK6
  hgvsc: ENST00000331826.7:c.582C>T
  hgvsp: ENST00000331826.7:c.582C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000305056
  ensembl transcript: ENST00000348070
  gene symbol: PCSK6
  hgvsc: ENST00000348070.1:c.1077C>T
  hgvsp: ENST00000348070.1:c.1077C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381246
  ensembl transcript: ENST00000398185
  gene symbol: PCSK6
  hgvsc: ENST00000398185.2:c.786C>T
  hgvsp: ENST00000398185.2:c.786C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000557794
  gene symbol: PCSK6
  hgvsc: ENST00000557794.1:n.124-79836C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561177
  gene symbol: PCSK6
  hgvsc: ENST00000561177.1:n.1247C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561109
  gene symbol: PCSK6
  hgvsc: ENST00000561109.1:n.1152C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381243
  ensembl transcript: ENST00000398181
  gene symbol: PCSK6
  hgvsc: ENST00000398181.2:c.1077C>T
  hgvsp: ENST00000398181.2:c.1077C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560271
  gene symbol: PCSK6
  hgvsc: ENST00000560271.1:n.1105C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000558716
  gene symbol: PCSK6
  hgvsc: ENST00000558716.1:n.1105C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000452997
  ensembl transcript: ENST00000559417
  gene symbol: PCSK6
  hgvsc: ENST00000559417.1:c.701C>T
  hgvsp: ENST00000559417.1:c.701C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000351193
  ensembl transcript: ENST00000358417
  gene symbol: PCSK6
  hgvsc: ENST00000358417.3:c.1077C>T
  hgvsp: ENST00000358417.3:c.1077C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560921
  gene symbol: PCSK6
  hgvsc: ENST00000560921.1:n.1152C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000559678
  gene symbol: PCSK6
  hgvsc: ENST00000559678.1:n.1152C>T
  variant of: http://identifiers.org/hgnc/8569
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 40242
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1578
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr359Tyr
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

15-101933554-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101933554
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101933554
    reference: chr 15
allele count: 2
allele frequency: 1.678781875870868e-5
allele num: 119134
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000351193
  ensembl transcript: ENST00000358417
  gene symbol: PCSK6
  hgvsc: ENST00000358417.3:c.1069G>A
  hgvsp: ENSP00000351193.3:p.Asp357Asn
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381243
  ensembl transcript: ENST00000398181
  gene symbol: PCSK6
  hgvsc: ENST00000398181.2:c.1069G>A
  hgvsp: ENSP00000381243.2:p.Asp357Asn
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000332052
  ensembl transcript: ENST00000331826
  gene symbol: PCSK6
  hgvsc: ENST00000331826.7:c.574G>A
  hgvsp: ENSP00000332052.7:p.Asp192Asn
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000344410
  ensembl transcript: ENST00000344273
  gene symbol: PCSK6
  hgvsc: ENST00000344273.2:c.1069G>A
  hgvsp: ENSP00000344410.2:p.Asp357Asn
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560271
  gene symbol: PCSK6
  hgvsc: ENST00000560271.1:n.1097G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561444
  gene symbol: PCSK6
  hgvsc: ENST00000561444.1:n.1239G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000452997
  ensembl transcript: ENST00000559417
  gene symbol: PCSK6
  hgvsc: ENST00000559417.1:c.693G>A
  hgvsp: ENSP00000452997.1:p.Asp232Asn
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000559678
  gene symbol: PCSK6
  hgvsc: ENST00000559678.1:n.1144G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000305056
  ensembl transcript: ENST00000348070
  gene symbol: PCSK6
  hgvsc: ENST00000348070.1:c.1069G>A
  hgvsp: ENSP00000305056.4:p.Asp357Asn
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561177
  gene symbol: PCSK6
  hgvsc: ENST00000561177.1:n.1239G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561109
  gene symbol: PCSK6
  hgvsc: ENST00000561109.1:n.1144G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000557794
  gene symbol: PCSK6
  hgvsc: ENST00000557794.1:n.124-79844G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560921
  gene symbol: PCSK6
  hgvsc: ENST00000560921.1:n.1144G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381246
  ensembl transcript: ENST00000398185
  gene symbol: PCSK6
  hgvsc: ENST00000398185.2:c.778G>A
  hgvsp: ENSP00000381246.2:p.Asp260Asn
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000558716
  gene symbol: PCSK6
  hgvsc: ENST00000558716.1:n.1097G>A
  variant of: http://identifiers.org/hgnc/8569
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 995
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13389
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1783
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp357Asn
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: FS
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum

15-101933555-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101933555
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101933555
    reference: chr 15
allele count: 8
allele frequency: 6.718736877467037e-5
allele num: 119070
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560271
  gene symbol: PCSK6
  hgvsc: ENST00000560271.1:n.1096C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000344410
  ensembl transcript: ENST00000344273
  gene symbol: PCSK6
  hgvsc: ENST00000344273.2:c.1068C>T
  hgvsp: ENST00000344273.2:c.1068C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000452997
  ensembl transcript: ENST00000559417
  gene symbol: PCSK6
  hgvsc: ENST00000559417.1:c.692C>T
  hgvsp: ENST00000559417.1:c.692C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561444
  gene symbol: PCSK6
  hgvsc: ENST00000561444.1:n.1238C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561109
  gene symbol: PCSK6
  hgvsc: ENST00000561109.1:n.1143C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381246
  ensembl transcript: ENST00000398185
  gene symbol: PCSK6
  hgvsc: ENST00000398185.2:c.777C>T
  hgvsp: ENST00000398185.2:c.777C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000558716
  gene symbol: PCSK6
  hgvsc: ENST00000558716.1:n.1096C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000351193
  ensembl transcript: ENST00000358417
  gene symbol: PCSK6
  hgvsc: ENST00000358417.3:c.1068C>T
  hgvsp: ENST00000358417.3:c.1068C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000559678
  gene symbol: PCSK6
  hgvsc: ENST00000559678.1:n.1143C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381243
  ensembl transcript: ENST00000398181
  gene symbol: PCSK6
  hgvsc: ENST00000398181.2:c.1068C>T
  hgvsp: ENST00000398181.2:c.1068C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000332052
  ensembl transcript: ENST00000331826
  gene symbol: PCSK6
  hgvsc: ENST00000331826.7:c.573C>T
  hgvsp: ENST00000331826.7:c.573C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000305056
  ensembl transcript: ENST00000348070
  gene symbol: PCSK6
  hgvsc: ENST00000348070.1:c.1068C>T
  hgvsp: ENST00000348070.1:c.1068C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000557794
  gene symbol: PCSK6
  hgvsc: ENST00000557794.1:n.124-79845C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561177
  gene symbol: PCSK6
  hgvsc: ENST00000561177.1:n.1238C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560921
  gene symbol: PCSK6
  hgvsc: ENST00000560921.1:n.1143C>T
  variant of: http://identifiers.org/hgnc/8569
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1814
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2664
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys356Cys
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

15-101933558-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101933558
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101933558
    reference: chr 15
allele count: 32
allele frequency: 2.690115506834575e-4
allele num: 118954
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561109
  gene symbol: PCSK6
  hgvsc: ENST00000561109.1:n.1140G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000559678
  gene symbol: PCSK6
  hgvsc: ENST00000559678.1:n.1140G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561177
  gene symbol: PCSK6
  hgvsc: ENST00000561177.1:n.1235G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381243
  ensembl transcript: ENST00000398181
  gene symbol: PCSK6
  hgvsc: ENST00000398181.2:c.1065G>A
  hgvsp: ENST00000398181.2:c.1065G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000332052
  ensembl transcript: ENST00000331826
  gene symbol: PCSK6
  hgvsc: ENST00000331826.7:c.570G>A
  hgvsp: ENST00000331826.7:c.570G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561444
  gene symbol: PCSK6
  hgvsc: ENST00000561444.1:n.1235G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000558716
  gene symbol: PCSK6
  hgvsc: ENST00000558716.1:n.1093G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381246
  ensembl transcript: ENST00000398185
  gene symbol: PCSK6
  hgvsc: ENST00000398185.2:c.774G>A
  hgvsp: ENST00000398185.2:c.774G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000452997
  ensembl transcript: ENST00000559417
  gene symbol: PCSK6
  hgvsc: ENST00000559417.1:c.689G>A
  hgvsp: ENST00000559417.1:c.689G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000305056
  ensembl transcript: ENST00000348070
  gene symbol: PCSK6
  hgvsc: ENST00000348070.1:c.1065G>A
  hgvsp: ENST00000348070.1:c.1065G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000351193
  ensembl transcript: ENST00000358417
  gene symbol: PCSK6
  hgvsc: ENST00000358417.3:c.1065G>A
  hgvsp: ENST00000358417.3:c.1065G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000344410
  ensembl transcript: ENST00000344273
  gene symbol: PCSK6
  hgvsc: ENST00000344273.2:c.1065G>A
  hgvsp: ENST00000344273.2:c.1065G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560921
  gene symbol: PCSK6
  hgvsc: ENST00000560921.1:n.1140G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560271
  gene symbol: PCSK6
  hgvsc: ENST00000560271.1:n.1093G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000557794
  gene symbol: PCSK6
  hgvsc: ENST00000557794.1:n.124-79848G>A
  variant of: http://identifiers.org/hgnc/8569
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2656
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 13303
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser355Ser
num of homozygotes: 1
population: European (Finnish)
population: South Asian
population: African
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ

15-101933559-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101933559
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101933559
    reference: chr 15
allele count: 3
allele frequency: 2.521856086079354e-5
allele num: 118960
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560271
  gene symbol: PCSK6
  hgvsc: ENST00000560271.1:n.1092C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561109
  gene symbol: PCSK6
  hgvsc: ENST00000561109.1:n.1139C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000332052
  ensembl transcript: ENST00000331826
  gene symbol: PCSK6
  hgvsc: ENST00000331826.7:c.569C>T
  hgvsp: ENSP00000332052.7:p.Ser190Leu
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381246
  ensembl transcript: ENST00000398185
  gene symbol: PCSK6
  hgvsc: ENST00000398185.2:c.773C>T
  hgvsp: ENSP00000381246.2:p.Ser258Leu
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381243
  ensembl transcript: ENST00000398181
  gene symbol: PCSK6
  hgvsc: ENST00000398181.2:c.1064C>T
  hgvsp: ENSP00000381243.2:p.Ser355Leu
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000351193
  ensembl transcript: ENST00000358417
  gene symbol: PCSK6
  hgvsc: ENST00000358417.3:c.1064C>T
  hgvsp: ENSP00000351193.3:p.Ser355Leu
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000452997
  ensembl transcript: ENST00000559417
  gene symbol: PCSK6
  hgvsc: ENST00000559417.1:c.688C>T
  hgvsp: ENSP00000452997.1:p.Ser230Leu
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000344410
  ensembl transcript: ENST00000344273
  gene symbol: PCSK6
  hgvsc: ENST00000344273.2:c.1064C>T
  hgvsp: ENSP00000344410.2:p.Ser355Leu
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560921
  gene symbol: PCSK6
  hgvsc: ENST00000560921.1:n.1139C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561444
  gene symbol: PCSK6
  hgvsc: ENST00000561444.1:n.1234C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000557794
  gene symbol: PCSK6
  hgvsc: ENST00000557794.1:n.124-79849C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000305056
  ensembl transcript: ENST00000348070
  gene symbol: PCSK6
  hgvsc: ENST00000348070.1:c.1064C>T
  hgvsp: ENSP00000305056.4:p.Ser355Leu
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000559678
  gene symbol: PCSK6
  hgvsc: ENST00000559678.1:n.1139C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000558716
  gene symbol: PCSK6
  hgvsc: ENST00000558716.1:n.1092C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561177
  gene symbol: PCSK6
  hgvsc: ENST00000561177.1:n.1234C>T
  variant of: http://identifiers.org/hgnc/8569
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39804
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2655
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13300
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser355Leu
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: QD

15-101933570-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101933570
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101933570
    reference: chr 15
allele count: 1
allele frequency: 8.446516656530846e-6
allele num: 118392
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381243
  ensembl transcript: ENST00000398181
  gene symbol: PCSK6
  hgvsc: ENST00000398181.2:c.1053G>A
  hgvsp: ENST00000398181.2:c.1053G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000452997
  ensembl transcript: ENST00000559417
  gene symbol: PCSK6
  hgvsc: ENST00000559417.1:c.677G>A
  hgvsp: ENST00000559417.1:c.677G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000344410
  ensembl transcript: ENST00000344273
  gene symbol: PCSK6
  hgvsc: ENST00000344273.2:c.1053G>A
  hgvsp: ENST00000344273.2:c.1053G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561444
  gene symbol: PCSK6
  hgvsc: ENST00000561444.1:n.1223G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000558716
  gene symbol: PCSK6
  hgvsc: ENST00000558716.1:n.1081G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000557794
  gene symbol: PCSK6
  hgvsc: ENST00000557794.1:n.124-79860G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561177
  gene symbol: PCSK6
  hgvsc: ENST00000561177.1:n.1223G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000351193
  ensembl transcript: ENST00000358417
  gene symbol: PCSK6
  hgvsc: ENST00000358417.3:c.1053G>A
  hgvsp: ENST00000358417.3:c.1053G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000559678
  gene symbol: PCSK6
  hgvsc: ENST00000559678.1:n.1128G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000305056
  ensembl transcript: ENST00000348070
  gene symbol: PCSK6
  hgvsc: ENST00000348070.1:c.1053G>A
  hgvsp: ENST00000348070.1:c.1053G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560271
  gene symbol: PCSK6
  hgvsc: ENST00000560271.1:n.1081G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000332052
  ensembl transcript: ENST00000331826
  gene symbol: PCSK6
  hgvsc: ENST00000331826.7:c.558G>A
  hgvsp: ENST00000331826.7:c.558G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381246
  ensembl transcript: ENST00000398185
  gene symbol: PCSK6
  hgvsc: ENST00000398185.2:c.762G>A
  hgvsp: ENST00000398185.2:c.762G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560921
  gene symbol: PCSK6
  hgvsc: ENST00000560921.1:n.1128G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561109
  gene symbol: PCSK6
  hgvsc: ENST00000561109.1:n.1128G>A
  variant of: http://identifiers.org/hgnc/8569
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13060
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2593
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly351Gly
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

15-101933572-CCT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101933572
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101933570
    reference: chr 15
allele count: 3
allele frequency: 2.533484216393332e-5
allele num: 118414
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560271
  gene symbol: PCSK6
  hgvsc: ENST00000560271.1:n.1077_1078delAG
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000557794
  gene symbol: PCSK6
  hgvsc: ENST00000557794.1:n.124-79864_124-79863delAG
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000305056
  ensembl transcript: ENST00000348070
  gene symbol: PCSK6
  hgvsc: ENST00000348070.1:c.1049_1050delAG
  hgvsp: ENSP00000305056.4:p.Glu350GlyfsTer49
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000344410
  ensembl transcript: ENST00000344273
  gene symbol: PCSK6
  hgvsc: ENST00000344273.2:c.1049_1050delAG
  hgvsp: ENSP00000344410.2:p.Glu350GlyfsTer49
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000452997
  ensembl transcript: ENST00000559417
  gene symbol: PCSK6
  hgvsc: ENST00000559417.1:c.673_674delAG
  hgvsp: ENSP00000452997.1:p.Glu225GlyfsTer49
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000558716
  gene symbol: PCSK6
  hgvsc: ENST00000558716.1:n.1077_1078delAG
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561109
  gene symbol: PCSK6
  hgvsc: ENST00000561109.1:n.1124_1125delAG
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561177
  gene symbol: PCSK6
  hgvsc: ENST00000561177.1:n.1219_1220delAG
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381246
  ensembl transcript: ENST00000398185
  gene symbol: PCSK6
  hgvsc: ENST00000398185.2:c.758_759delAG
  hgvsp: ENSP00000381246.2:p.Glu253GlyfsTer49
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000351193
  ensembl transcript: ENST00000358417
  gene symbol: PCSK6
  hgvsc: ENST00000358417.3:c.1049_1050delAG
  hgvsp: ENSP00000351193.3:p.Glu350GlyfsTer49
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561444
  gene symbol: PCSK6
  hgvsc: ENST00000561444.1:n.1219_1220delAG
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381243
  ensembl transcript: ENST00000398181
  gene symbol: PCSK6
  hgvsc: ENST00000398181.2:c.1049_1050delAG
  hgvsp: ENSP00000381243.2:p.Glu350GlyfsTer49
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000559678
  gene symbol: PCSK6
  hgvsc: ENST00000559678.1:n.1124_1125delAG
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000332052
  ensembl transcript: ENST00000331826
  gene symbol: PCSK6
  hgvsc: ENST00000331826.7:c.554_555delAG
  hgvsp: ENSP00000332052.7:p.Glu185GlyfsTer49
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560921
  gene symbol: PCSK6
  hgvsc: ENST00000560921.1:n.1124_1125delAG
  variant of: http://identifiers.org/hgnc/8569
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1062
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2217
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2595
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu350GlyfsTer49
num of homozygotes: 0
population: Other
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: CCT
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum

15-101933581-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101933581
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101933581
    reference: chr 15
allele count: 2
allele frequency: 1.69586378822053e-5
allele num: 117934
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560921
  gene symbol: PCSK6
  hgvsc: ENST00000560921.1:n.1117G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000559678
  gene symbol: PCSK6
  hgvsc: ENST00000559678.1:n.1117G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381243
  ensembl transcript: ENST00000398181
  gene symbol: PCSK6
  hgvsc: ENST00000398181.2:c.1042G>A
  hgvsp: ENSP00000381243.2:p.Gly348Arg
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561109
  gene symbol: PCSK6
  hgvsc: ENST00000561109.1:n.1117G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561444
  gene symbol: PCSK6
  hgvsc: ENST00000561444.1:n.1212G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560271
  gene symbol: PCSK6
  hgvsc: ENST00000560271.1:n.1070G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000351193
  ensembl transcript: ENST00000358417
  gene symbol: PCSK6
  hgvsc: ENST00000358417.3:c.1042G>A
  hgvsp: ENSP00000351193.3:p.Gly348Arg
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000452997
  ensembl transcript: ENST00000559417
  gene symbol: PCSK6
  hgvsc: ENST00000559417.1:c.666G>A
  hgvsp: ENSP00000452997.1:p.Gly223Arg
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000557794
  gene symbol: PCSK6
  hgvsc: ENST00000557794.1:n.124-79871G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000344410
  ensembl transcript: ENST00000344273
  gene symbol: PCSK6
  hgvsc: ENST00000344273.2:c.1042G>A
  hgvsp: ENSP00000344410.2:p.Gly348Arg
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000558716
  gene symbol: PCSK6
  hgvsc: ENST00000558716.1:n.1070G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561177
  gene symbol: PCSK6
  hgvsc: ENST00000561177.1:n.1212G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000332052
  ensembl transcript: ENST00000331826
  gene symbol: PCSK6
  hgvsc: ENST00000331826.7:c.547G>A
  hgvsp: ENSP00000332052.7:p.Gly183Arg
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381246
  ensembl transcript: ENST00000398185
  gene symbol: PCSK6
  hgvsc: ENST00000398185.2:c.751G>A
  hgvsp: ENSP00000381246.2:p.Gly251Arg
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000305056
  ensembl transcript: ENST00000348070
  gene symbol: PCSK6
  hgvsc: ENST00000348070.1:c.1042G>A
  hgvsp: ENSP00000305056.4:p.Gly348Arg
  variant of: http://identifiers.org/hgnc/8569
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13279
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2701
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2242
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38825
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly348Arg
num of homozygotes: 0
population: Latino
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD

15-101933582-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101933582
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101933582
    reference: chr 15
allele count: 1
allele frequency: 8.491270973439305e-6
allele num: 117768
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561444
  gene symbol: PCSK6
  hgvsc: ENST00000561444.1:n.1211C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560271
  gene symbol: PCSK6
  hgvsc: ENST00000560271.1:n.1069C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560921
  gene symbol: PCSK6
  hgvsc: ENST00000560921.1:n.1116C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561177
  gene symbol: PCSK6
  hgvsc: ENST00000561177.1:n.1211C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000452997
  ensembl transcript: ENST00000559417
  gene symbol: PCSK6
  hgvsc: ENST00000559417.1:c.665C>T
  hgvsp: ENST00000559417.1:c.665C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000344410
  ensembl transcript: ENST00000344273
  gene symbol: PCSK6
  hgvsc: ENST00000344273.2:c.1041C>T
  hgvsp: ENST00000344273.2:c.1041C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381246
  ensembl transcript: ENST00000398185
  gene symbol: PCSK6
  hgvsc: ENST00000398185.2:c.750C>T
  hgvsp: ENST00000398185.2:c.750C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000351193
  ensembl transcript: ENST00000358417
  gene symbol: PCSK6
  hgvsc: ENST00000358417.3:c.1041C>T
  hgvsp: ENST00000358417.3:c.1041C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000558716
  gene symbol: PCSK6
  hgvsc: ENST00000558716.1:n.1069C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000305056
  ensembl transcript: ENST00000348070
  gene symbol: PCSK6
  hgvsc: ENST00000348070.1:c.1041C>T
  hgvsp: ENST00000348070.1:c.1041C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561109
  gene symbol: PCSK6
  hgvsc: ENST00000561109.1:n.1116C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381243
  ensembl transcript: ENST00000398181
  gene symbol: PCSK6
  hgvsc: ENST00000398181.2:c.1041C>T
  hgvsp: ENST00000398181.2:c.1041C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000559678
  gene symbol: PCSK6
  hgvsc: ENST00000559678.1:n.1116C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000332052
  ensembl transcript: ENST00000331826
  gene symbol: PCSK6
  hgvsc: ENST00000331826.7:c.546C>T
  hgvsp: ENST00000331826.7:c.546C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000557794
  gene symbol: PCSK6
  hgvsc: ENST00000557794.1:n.124-79872C>T
  variant of: http://identifiers.org/hgnc/8569
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2260
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38798
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13269
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1448
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly347Gly
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

15-101933588-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101933588
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101933588
    reference: chr 15
allele count: 1
allele frequency: 8.516001566944289e-6
allele num: 117426
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560921
  gene symbol: PCSK6
  hgvsc: ENST00000560921.1:n.1110G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000305056
  ensembl transcript: ENST00000348070
  gene symbol: PCSK6
  hgvsc: ENST00000348070.1:c.1035G>A
  hgvsp: ENST00000348070.1:c.1035G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000558716
  gene symbol: PCSK6
  hgvsc: ENST00000558716.1:n.1063G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000332052
  ensembl transcript: ENST00000331826
  gene symbol: PCSK6
  hgvsc: ENST00000331826.7:c.540G>A
  hgvsp: ENST00000331826.7:c.540G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381243
  ensembl transcript: ENST00000398181
  gene symbol: PCSK6
  hgvsc: ENST00000398181.2:c.1035G>A
  hgvsp: ENST00000398181.2:c.1035G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000452997
  ensembl transcript: ENST00000559417
  gene symbol: PCSK6
  hgvsc: ENST00000559417.1:c.659G>A
  hgvsp: ENST00000559417.1:c.659G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000559678
  gene symbol: PCSK6
  hgvsc: ENST00000559678.1:n.1110G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561109
  gene symbol: PCSK6
  hgvsc: ENST00000561109.1:n.1110G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000351193
  ensembl transcript: ENST00000358417
  gene symbol: PCSK6
  hgvsc: ENST00000358417.3:c.1035G>A
  hgvsp: ENST00000358417.3:c.1035G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000344410
  ensembl transcript: ENST00000344273
  gene symbol: PCSK6
  hgvsc: ENST00000344273.2:c.1035G>A
  hgvsp: ENST00000344273.2:c.1035G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381246
  ensembl transcript: ENST00000398185
  gene symbol: PCSK6
  hgvsc: ENST00000398185.2:c.744G>A
  hgvsp: ENST00000398185.2:c.744G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561444
  gene symbol: PCSK6
  hgvsc: ENST00000561444.1:n.1205G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000557794
  gene symbol: PCSK6
  hgvsc: ENST00000557794.1:n.124-79878G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561177
  gene symbol: PCSK6
  hgvsc: ENST00000561177.1:n.1205G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560271
  gene symbol: PCSK6
  hgvsc: ENST00000560271.1:n.1063G>A
  variant of: http://identifiers.org/hgnc/8569
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2663
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2314
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38707
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly345Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: Other
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ

15-101933594-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101933594
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101933594
    reference: chr 15
allele count: 1
allele frequency: 8.517597356137781e-6
allele num: 117404
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000332052
  ensembl transcript: ENST00000331826
  gene symbol: PCSK6
  hgvsc: ENST00000331826.7:c.534A>G
  hgvsp: ENST00000331826.7:c.534A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000351193
  ensembl transcript: ENST00000358417
  gene symbol: PCSK6
  hgvsc: ENST00000358417.3:c.1029A>G
  hgvsp: ENST00000358417.3:c.1029A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000452997
  ensembl transcript: ENST00000559417
  gene symbol: PCSK6
  hgvsc: ENST00000559417.1:c.653A>G
  hgvsp: ENST00000559417.1:c.653A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381243
  ensembl transcript: ENST00000398181
  gene symbol: PCSK6
  hgvsc: ENST00000398181.2:c.1029A>G
  hgvsp: ENST00000398181.2:c.1029A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000344410
  ensembl transcript: ENST00000344273
  gene symbol: PCSK6
  hgvsc: ENST00000344273.2:c.1029A>G
  hgvsp: ENST00000344273.2:c.1029A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000559678
  gene symbol: PCSK6
  hgvsc: ENST00000559678.1:n.1104A>G
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000558716
  gene symbol: PCSK6
  hgvsc: ENST00000558716.1:n.1057A>G
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561109
  gene symbol: PCSK6
  hgvsc: ENST00000561109.1:n.1104A>G
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560271
  gene symbol: PCSK6
  hgvsc: ENST00000560271.1:n.1057A>G
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561444
  gene symbol: PCSK6
  hgvsc: ENST00000561444.1:n.1199A>G
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381246
  ensembl transcript: ENST00000398185
  gene symbol: PCSK6
  hgvsc: ENST00000398185.2:c.738A>G
  hgvsp: ENST00000398185.2:c.738A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000305056
  ensembl transcript: ENST00000348070
  gene symbol: PCSK6
  hgvsc: ENST00000348070.1:c.1029A>G
  hgvsp: ENST00000348070.1:c.1029A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560921
  gene symbol: PCSK6
  hgvsc: ENST00000560921.1:n.1104A>G
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561177
  gene symbol: PCSK6
  hgvsc: ENST00000561177.1:n.1199A>G
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000557794
  gene symbol: PCSK6
  hgvsc: ENST00000557794.1:n.124-79884A>G
  variant of: http://identifiers.org/hgnc/8569
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38833
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1647
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2639
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13010
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala343Ala
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ

http://identifiers.org/exac.variant/15-101933597-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101933597
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101933597
    reference: chr 15
allele count: 2
allele frequency: 1.705233361185478e-5
allele num: 117286
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561109
  gene symbol: PCSK6
  hgvsc: ENST00000561109.1:n.1101G>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000452997
  ensembl transcript: ENST00000559417
  gene symbol: PCSK6
  hgvsc: ENST00000559417.1:c.650G>T
  hgvsp: ENSP00000452997.1:p.Trp217Cys
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561177
  gene symbol: PCSK6
  hgvsc: ENST00000561177.1:n.1196G>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000559678
  gene symbol: PCSK6
  hgvsc: ENST00000559678.1:n.1101G>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561444
  gene symbol: PCSK6
  hgvsc: ENST00000561444.1:n.1196G>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000351193
  ensembl transcript: ENST00000358417
  gene symbol: PCSK6
  hgvsc: ENST00000358417.3:c.1026G>T
  hgvsp: ENSP00000351193.3:p.Trp342Cys
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560921
  gene symbol: PCSK6
  hgvsc: ENST00000560921.1:n.1101G>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000305056
  ensembl transcript: ENST00000348070
  gene symbol: PCSK6
  hgvsc: ENST00000348070.1:c.1026G>T
  hgvsp: ENSP00000305056.4:p.Trp342Cys
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000332052
  ensembl transcript: ENST00000331826
  gene symbol: PCSK6
  hgvsc: ENST00000331826.7:c.531G>T
  hgvsp: ENSP00000332052.7:p.Trp177Cys
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381243
  ensembl transcript: ENST00000398181
  gene symbol: PCSK6
  hgvsc: ENST00000398181.2:c.1026G>T
  hgvsp: ENSP00000381243.2:p.Trp342Cys
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000344410
  ensembl transcript: ENST00000344273
  gene symbol: PCSK6
  hgvsc: ENST00000344273.2:c.1026G>T
  hgvsp: ENSP00000344410.2:p.Trp342Cys
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381246
  ensembl transcript: ENST00000398185
  gene symbol: PCSK6
  hgvsc: ENST00000398185.2:c.735G>T
  hgvsp: ENSP00000381246.2:p.Trp245Cys
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000557794
  gene symbol: PCSK6
  hgvsc: ENST00000557794.1:n.124-79887G>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560271
  gene symbol: PCSK6
  hgvsc: ENST00000560271.1:n.1054G>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000558716
  gene symbol: PCSK6
  hgvsc: ENST00000558716.1:n.1054G>T
  variant of: http://identifiers.org/hgnc/8569
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2637
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38843
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1684
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2301
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Trp342Cys
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

15-101933602-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101933602
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101933602
    reference: chr 15
allele count: 1
allele frequency: 8.544379507160189e-6
allele num: 117036
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381243
  ensembl transcript: ENST00000398181
  gene symbol: PCSK6
  hgvsc: ENST00000398181.2:c.1021G>C
  hgvsp: ENSP00000381243.2:p.Val341Leu
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561177
  gene symbol: PCSK6
  hgvsc: ENST00000561177.1:n.1191G>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000559678
  gene symbol: PCSK6
  hgvsc: ENST00000559678.1:n.1096G>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561444
  gene symbol: PCSK6
  hgvsc: ENST00000561444.1:n.1191G>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000305056
  ensembl transcript: ENST00000348070
  gene symbol: PCSK6
  hgvsc: ENST00000348070.1:c.1021G>C
  hgvsp: ENSP00000305056.4:p.Val341Leu
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381246
  ensembl transcript: ENST00000398185
  gene symbol: PCSK6
  hgvsc: ENST00000398185.2:c.730G>C
  hgvsp: ENSP00000381246.2:p.Val244Leu
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000351193
  ensembl transcript: ENST00000358417
  gene symbol: PCSK6
  hgvsc: ENST00000358417.3:c.1021G>C
  hgvsp: ENSP00000351193.3:p.Val341Leu
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000332052
  ensembl transcript: ENST00000331826
  gene symbol: PCSK6
  hgvsc: ENST00000331826.7:c.526G>C
  hgvsp: ENSP00000332052.7:p.Val176Leu
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560271
  gene symbol: PCSK6
  hgvsc: ENST00000560271.1:n.1049G>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560921
  gene symbol: PCSK6
  hgvsc: ENST00000560921.1:n.1096G>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000344410
  ensembl transcript: ENST00000344273
  gene symbol: PCSK6
  hgvsc: ENST00000344273.2:c.1021G>C
  hgvsp: ENSP00000344410.2:p.Val341Leu
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561109
  gene symbol: PCSK6
  hgvsc: ENST00000561109.1:n.1096G>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000557794
  gene symbol: PCSK6
  hgvsc: ENST00000557794.1:n.124-79892G>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000558716
  gene symbol: PCSK6
  hgvsc: ENST00000558716.1:n.1049G>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000452997
  ensembl transcript: ENST00000559417
  gene symbol: PCSK6
  hgvsc: ENST00000559417.1:c.645G>C
  hgvsp: ENSP00000452997.1:p.Val216Leu
  variant of: http://identifiers.org/hgnc/8569
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2313
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12921
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1754
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2634
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val341Leu
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD

15-101933602-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101933602
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101933602
    reference: chr 15
allele count: 5
allele frequency: 4.272189753580095e-5
allele num: 117036
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000305056
  ensembl transcript: ENST00000348070
  gene symbol: PCSK6
  hgvsc: ENST00000348070.1:c.1021G>A
  hgvsp: ENSP00000305056.4:p.Val341Ile
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560271
  gene symbol: PCSK6
  hgvsc: ENST00000560271.1:n.1049G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381243
  ensembl transcript: ENST00000398181
  gene symbol: PCSK6
  hgvsc: ENST00000398181.2:c.1021G>A
  hgvsp: ENSP00000381243.2:p.Val341Ile
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000559678
  gene symbol: PCSK6
  hgvsc: ENST00000559678.1:n.1096G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561444
  gene symbol: PCSK6
  hgvsc: ENST00000561444.1:n.1191G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560921
  gene symbol: PCSK6
  hgvsc: ENST00000560921.1:n.1096G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000557794
  gene symbol: PCSK6
  hgvsc: ENST00000557794.1:n.124-79892G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561109
  gene symbol: PCSK6
  hgvsc: ENST00000561109.1:n.1096G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000332052
  ensembl transcript: ENST00000331826
  gene symbol: PCSK6
  hgvsc: ENST00000331826.7:c.526G>A
  hgvsp: ENSP00000332052.7:p.Val176Ile
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000452997
  ensembl transcript: ENST00000559417
  gene symbol: PCSK6
  hgvsc: ENST00000559417.1:c.645G>A
  hgvsp: ENSP00000452997.1:p.Val216Ile
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000351193
  ensembl transcript: ENST00000358417
  gene symbol: PCSK6
  hgvsc: ENST00000358417.3:c.1021G>A
  hgvsp: ENSP00000351193.3:p.Val341Ile
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561177
  gene symbol: PCSK6
  hgvsc: ENST00000561177.1:n.1191G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381246
  ensembl transcript: ENST00000398185
  gene symbol: PCSK6
  hgvsc: ENST00000398185.2:c.730G>A
  hgvsp: ENSP00000381246.2:p.Val244Ile
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000344410
  ensembl transcript: ENST00000344273
  gene symbol: PCSK6
  hgvsc: ENST00000344273.2:c.1021G>A
  hgvsp: ENSP00000344410.2:p.Val341Ile
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000558716
  gene symbol: PCSK6
  hgvsc: ENST00000558716.1:n.1049G>A
  variant of: http://identifiers.org/hgnc/8569
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12921
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2313
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38876
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val341Ile
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

15-101933603-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101933603
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101933603
    reference: chr 15
allele count: 1
allele frequency: 8.544671542825894e-6
allele num: 117032
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000344410
  ensembl transcript: ENST00000344273
  gene symbol: PCSK6
  hgvsc: ENST00000344273.2:c.1020C>T
  hgvsp: ENST00000344273.2:c.1020C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381243
  ensembl transcript: ENST00000398181
  gene symbol: PCSK6
  hgvsc: ENST00000398181.2:c.1020C>T
  hgvsp: ENST00000398181.2:c.1020C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000559678
  gene symbol: PCSK6
  hgvsc: ENST00000559678.1:n.1095C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000557794
  gene symbol: PCSK6
  hgvsc: ENST00000557794.1:n.124-79893C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000351193
  ensembl transcript: ENST00000358417
  gene symbol: PCSK6
  hgvsc: ENST00000358417.3:c.1020C>T
  hgvsp: ENST00000358417.3:c.1020C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560271
  gene symbol: PCSK6
  hgvsc: ENST00000560271.1:n.1048C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560921
  gene symbol: PCSK6
  hgvsc: ENST00000560921.1:n.1095C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561444
  gene symbol: PCSK6
  hgvsc: ENST00000561444.1:n.1190C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000305056
  ensembl transcript: ENST00000348070
  gene symbol: PCSK6
  hgvsc: ENST00000348070.1:c.1020C>T
  hgvsp: ENST00000348070.1:c.1020C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381246
  ensembl transcript: ENST00000398185
  gene symbol: PCSK6
  hgvsc: ENST00000398185.2:c.729C>T
  hgvsp: ENST00000398185.2:c.729C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000452997
  ensembl transcript: ENST00000559417
  gene symbol: PCSK6
  hgvsc: ENST00000559417.1:c.644C>T
  hgvsp: ENST00000559417.1:c.644C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561177
  gene symbol: PCSK6
  hgvsc: ENST00000561177.1:n.1190C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000332052
  ensembl transcript: ENST00000331826
  gene symbol: PCSK6
  hgvsc: ENST00000331826.7:c.525C>T
  hgvsp: ENST00000331826.7:c.525C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000558716
  gene symbol: PCSK6
  hgvsc: ENST00000558716.1:n.1048C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561109
  gene symbol: PCSK6
  hgvsc: ENST00000561109.1:n.1095C>T
  variant of: http://identifiers.org/hgnc/8569
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38871
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1786
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2337
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe340Phe
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff

15-101933609-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101933609
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101933609
    reference: chr 15
allele count: 1
allele frequency: 8.554173581290312e-6
allele num: 116902
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000559678
  gene symbol: PCSK6
  hgvsc: ENST00000559678.1:n.1089C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381246
  ensembl transcript: ENST00000398185
  gene symbol: PCSK6
  hgvsc: ENST00000398185.2:c.723C>T
  hgvsp: ENST00000398185.2:c.723C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561444
  gene symbol: PCSK6
  hgvsc: ENST00000561444.1:n.1184C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381243
  ensembl transcript: ENST00000398181
  gene symbol: PCSK6
  hgvsc: ENST00000398181.2:c.1014C>T
  hgvsp: ENST00000398181.2:c.1014C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000557794
  gene symbol: PCSK6
  hgvsc: ENST00000557794.1:n.124-79899C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000351193
  ensembl transcript: ENST00000358417
  gene symbol: PCSK6
  hgvsc: ENST00000358417.3:c.1014C>T
  hgvsp: ENST00000358417.3:c.1014C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000558716
  gene symbol: PCSK6
  hgvsc: ENST00000558716.1:n.1042C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561177
  gene symbol: PCSK6
  hgvsc: ENST00000561177.1:n.1184C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000332052
  ensembl transcript: ENST00000331826
  gene symbol: PCSK6
  hgvsc: ENST00000331826.7:c.519C>T
  hgvsp: ENST00000331826.7:c.519C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000344410
  ensembl transcript: ENST00000344273
  gene symbol: PCSK6
  hgvsc: ENST00000344273.2:c.1014C>T
  hgvsp: ENST00000344273.2:c.1014C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561109
  gene symbol: PCSK6
  hgvsc: ENST00000561109.1:n.1089C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000452997
  ensembl transcript: ENST00000559417
  gene symbol: PCSK6
  hgvsc: ENST00000559417.1:c.638C>T
  hgvsp: ENST00000559417.1:c.638C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000305056
  ensembl transcript: ENST00000348070
  gene symbol: PCSK6
  hgvsc: ENST00000348070.1:c.1014C>T
  hgvsp: ENST00000348070.1:c.1014C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560271
  gene symbol: PCSK6
  hgvsc: ENST00000560271.1:n.1042C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560921
  gene symbol: PCSK6
  hgvsc: ENST00000560921.1:n.1089C>T
  variant of: http://identifiers.org/hgnc/8569
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2623
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38742
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12870
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2453
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1872
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser338Ser
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: DP

15-101933613-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101933613
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101933613
    reference: chr 15
allele count: 1
allele frequency: 8.573388203017833e-6
allele num: 116640
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381246
  ensembl transcript: ENST00000398185
  gene symbol: PCSK6
  hgvsc: ENST00000398185.2:c.719G>A
  hgvsp: ENSP00000381246.2:p.Gly240Asp
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560921
  gene symbol: PCSK6
  hgvsc: ENST00000560921.1:n.1085G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381243
  ensembl transcript: ENST00000398181
  gene symbol: PCSK6
  hgvsc: ENST00000398181.2:c.1010G>A
  hgvsp: ENSP00000381243.2:p.Gly337Asp
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000332052
  ensembl transcript: ENST00000331826
  gene symbol: PCSK6
  hgvsc: ENST00000331826.7:c.515G>A
  hgvsp: ENSP00000332052.7:p.Gly172Asp
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000559678
  gene symbol: PCSK6
  hgvsc: ENST00000559678.1:n.1085G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000344410
  ensembl transcript: ENST00000344273
  gene symbol: PCSK6
  hgvsc: ENST00000344273.2:c.1010G>A
  hgvsp: ENSP00000344410.2:p.Gly337Asp
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561109
  gene symbol: PCSK6
  hgvsc: ENST00000561109.1:n.1085G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000452997
  ensembl transcript: ENST00000559417
  gene symbol: PCSK6
  hgvsc: ENST00000559417.1:c.634G>A
  hgvsp: ENSP00000452997.1:p.Gly212Asp
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000351193
  ensembl transcript: ENST00000358417
  gene symbol: PCSK6
  hgvsc: ENST00000358417.3:c.1010G>A
  hgvsp: ENSP00000351193.3:p.Gly337Asp
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000558716
  gene symbol: PCSK6
  hgvsc: ENST00000558716.1:n.1038G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560271
  gene symbol: PCSK6
  hgvsc: ENST00000560271.1:n.1038G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000305056
  ensembl transcript: ENST00000348070
  gene symbol: PCSK6
  hgvsc: ENST00000348070.1:c.1010G>A
  hgvsp: ENSP00000305056.4:p.Gly337Asp
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561177
  gene symbol: PCSK6
  hgvsc: ENST00000561177.1:n.1180G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000557794
  gene symbol: PCSK6
  hgvsc: ENST00000557794.1:n.124-79903G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561444
  gene symbol: PCSK6
  hgvsc: ENST00000561444.1:n.1180G>A
  variant of: http://identifiers.org/hgnc/8569
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2562
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38598
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2605
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly337Asp
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
reference allele: C
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

15-101933647-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101933647
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101933647
    reference: chr 15
allele count: 1
allele frequency: 8.801887124599515e-6
allele num: 113612
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000558716
  gene symbol: PCSK6
  hgvsc: ENST00000558716.1:n.1022-18T>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000559678
  gene symbol: PCSK6
  hgvsc: ENST00000559678.1:n.1069-18T>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560921
  gene symbol: PCSK6
  hgvsc: ENST00000560921.1:n.1069-18T>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381243
  ensembl transcript: ENST00000398181
  gene symbol: PCSK6
  hgvsc: ENST00000398181.2:c.994-18T>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000305056
  ensembl transcript: ENST00000348070
  gene symbol: PCSK6
  hgvsc: ENST00000348070.1:c.994-18T>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000332052
  ensembl transcript: ENST00000331826
  gene symbol: PCSK6
  hgvsc: ENST00000331826.7:c.499-18T>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000557794
  gene symbol: PCSK6
  hgvsc: ENST00000557794.1:n.124-79937T>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000344410
  ensembl transcript: ENST00000344273
  gene symbol: PCSK6
  hgvsc: ENST00000344273.2:c.994-18T>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560271
  gene symbol: PCSK6
  hgvsc: ENST00000560271.1:n.1022-18T>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561177
  gene symbol: PCSK6
  hgvsc: ENST00000561177.1:n.1164-18T>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561444
  gene symbol: PCSK6
  hgvsc: ENST00000561444.1:n.1164-18T>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561109
  gene symbol: PCSK6
  hgvsc: ENST00000561109.1:n.1069-18T>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381246
  ensembl transcript: ENST00000398185
  gene symbol: PCSK6
  hgvsc: ENST00000398185.2:c.703-18T>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000351193
  ensembl transcript: ENST00000358417
  gene symbol: PCSK6
  hgvsc: ENST00000358417.3:c.994-18T>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000452997
  ensembl transcript: ENST00000559417
  gene symbol: PCSK6
  hgvsc: ENST00000559417.1:c.618-18T>C
  variant of: http://identifiers.org/hgnc/8569
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2161
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2293
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33119
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7426
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3261
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: QD

15-101933648-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101933648
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101933648
    reference: chr 15
allele count: 1
allele frequency: 8.826281134706703e-6
allele num: 113298
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000351193
  ensembl transcript: ENST00000358417
  gene symbol: PCSK6
  hgvsc: ENST00000358417.3:c.994-19G>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000557794
  gene symbol: PCSK6
  hgvsc: ENST00000557794.1:n.124-79938G>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000344410
  ensembl transcript: ENST00000344273
  gene symbol: PCSK6
  hgvsc: ENST00000344273.2:c.994-19G>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381246
  ensembl transcript: ENST00000398185
  gene symbol: PCSK6
  hgvsc: ENST00000398185.2:c.703-19G>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381243
  ensembl transcript: ENST00000398181
  gene symbol: PCSK6
  hgvsc: ENST00000398181.2:c.994-19G>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000452997
  ensembl transcript: ENST00000559417
  gene symbol: PCSK6
  hgvsc: ENST00000559417.1:c.618-19G>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561444
  gene symbol: PCSK6
  hgvsc: ENST00000561444.1:n.1164-19G>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000305056
  ensembl transcript: ENST00000348070
  gene symbol: PCSK6
  hgvsc: ENST00000348070.1:c.994-19G>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000332052
  ensembl transcript: ENST00000331826
  gene symbol: PCSK6
  hgvsc: ENST00000331826.7:c.499-19G>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560921
  gene symbol: PCSK6
  hgvsc: ENST00000560921.1:n.1069-19G>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561109
  gene symbol: PCSK6
  hgvsc: ENST00000561109.1:n.1069-19G>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000558716
  gene symbol: PCSK6
  hgvsc: ENST00000558716.1:n.1022-19G>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560271
  gene symbol: PCSK6
  hgvsc: ENST00000560271.1:n.1022-19G>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000559678
  gene symbol: PCSK6
  hgvsc: ENST00000559678.1:n.1069-19G>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561177
  gene symbol: PCSK6
  hgvsc: ENST00000561177.1:n.1164-19G>C
  variant of: http://identifiers.org/hgnc/8569
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31994
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10560
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2146
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

http://identifiers.org/exac.variant/15-101933650-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101933650
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101933650
    reference: chr 15
allele count: 2
allele frequency: 1.766503559504672e-5
allele num: 113218
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381243
  ensembl transcript: ENST00000398181
  gene symbol: PCSK6
  hgvsc: ENST00000398181.2:c.994-21T>G
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000351193
  ensembl transcript: ENST00000358417
  gene symbol: PCSK6
  hgvsc: ENST00000358417.3:c.994-21T>G
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000344410
  ensembl transcript: ENST00000344273
  gene symbol: PCSK6
  hgvsc: ENST00000344273.2:c.994-21T>G
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561444
  gene symbol: PCSK6
  hgvsc: ENST00000561444.1:n.1164-21T>G
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561109
  gene symbol: PCSK6
  hgvsc: ENST00000561109.1:n.1069-21T>G
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000557794
  gene symbol: PCSK6
  hgvsc: ENST00000557794.1:n.124-79940T>G
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560921
  gene symbol: PCSK6
  hgvsc: ENST00000560921.1:n.1069-21T>G
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000452997
  ensembl transcript: ENST00000559417
  gene symbol: PCSK6
  hgvsc: ENST00000559417.1:c.618-21T>G
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000305056
  ensembl transcript: ENST00000348070
  gene symbol: PCSK6
  hgvsc: ENST00000348070.1:c.994-21T>G
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000558716
  gene symbol: PCSK6
  hgvsc: ENST00000558716.1:n.1022-21T>G
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000332052
  ensembl transcript: ENST00000331826
  gene symbol: PCSK6
  hgvsc: ENST00000331826.7:c.499-21T>G
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561177
  gene symbol: PCSK6
  hgvsc: ENST00000561177.1:n.1164-21T>G
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381246
  ensembl transcript: ENST00000398185
  gene symbol: PCSK6
  hgvsc: ENST00000398185.2:c.703-21T>G
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000559678
  gene symbol: PCSK6
  hgvsc: ENST00000559678.1:n.1069-21T>G
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560271
  gene symbol: PCSK6
  hgvsc: ENST00000560271.1:n.1022-21T>G
  variant of: http://identifiers.org/hgnc/8569
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3398
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3108
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8822
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 1
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD

15-101933653-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101933653
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101933653
    reference: chr 15
allele count: 1
allele frequency: 8.882414595583663e-6
allele num: 112582
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000557794
  gene symbol: PCSK6
  hgvsc: ENST00000557794.1:n.124-79943G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381246
  ensembl transcript: ENST00000398185
  gene symbol: PCSK6
  hgvsc: ENST00000398185.2:c.703-24G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000559678
  gene symbol: PCSK6
  hgvsc: ENST00000559678.1:n.1069-24G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000344410
  ensembl transcript: ENST00000344273
  gene symbol: PCSK6
  hgvsc: ENST00000344273.2:c.994-24G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000305056
  ensembl transcript: ENST00000348070
  gene symbol: PCSK6
  hgvsc: ENST00000348070.1:c.994-24G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561109
  gene symbol: PCSK6
  hgvsc: ENST00000561109.1:n.1069-24G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561177
  gene symbol: PCSK6
  hgvsc: ENST00000561177.1:n.1164-24G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560921
  gene symbol: PCSK6
  hgvsc: ENST00000560921.1:n.1069-24G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000351193
  ensembl transcript: ENST00000358417
  gene symbol: PCSK6
  hgvsc: ENST00000358417.3:c.994-24G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560271
  gene symbol: PCSK6
  hgvsc: ENST00000560271.1:n.1022-24G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381243
  ensembl transcript: ENST00000398181
  gene symbol: PCSK6
  hgvsc: ENST00000398181.2:c.994-24G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000558716
  gene symbol: PCSK6
  hgvsc: ENST00000558716.1:n.1022-24G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000452997
  ensembl transcript: ENST00000559417
  gene symbol: PCSK6
  hgvsc: ENST00000559417.1:c.618-24G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000332052
  ensembl transcript: ENST00000331826
  gene symbol: PCSK6
  hgvsc: ENST00000331826.7:c.499-24G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561444
  gene symbol: PCSK6
  hgvsc: ENST00000561444.1:n.1164-24G>A
  variant of: http://identifiers.org/hgnc/8569
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28633
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9348
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4716
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1946
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10843
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: DP

15-101933658-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101933658
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101933658
    reference: chr 15
allele count: 231
allele frequency: 2.062905213524085e-3
allele num: 111978
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000344410
  ensembl transcript: ENST00000344273
  gene symbol: PCSK6
  hgvsc: ENST00000344273.2:c.994-29G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561109
  gene symbol: PCSK6
  hgvsc: ENST00000561109.1:n.1069-29G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000351193
  ensembl transcript: ENST00000358417
  gene symbol: PCSK6
  hgvsc: ENST00000358417.3:c.994-29G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381243
  ensembl transcript: ENST00000398181
  gene symbol: PCSK6
  hgvsc: ENST00000398181.2:c.994-29G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000558716
  gene symbol: PCSK6
  hgvsc: ENST00000558716.1:n.1022-29G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000305056
  ensembl transcript: ENST00000348070
  gene symbol: PCSK6
  hgvsc: ENST00000348070.1:c.994-29G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560921
  gene symbol: PCSK6
  hgvsc: ENST00000560921.1:n.1069-29G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000452997
  ensembl transcript: ENST00000559417
  gene symbol: PCSK6
  hgvsc: ENST00000559417.1:c.618-29G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561444
  gene symbol: PCSK6
  hgvsc: ENST00000561444.1:n.1164-29G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000559678
  gene symbol: PCSK6
  hgvsc: ENST00000559678.1:n.1069-29G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560271
  gene symbol: PCSK6
  hgvsc: ENST00000560271.1:n.1022-29G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561177
  gene symbol: PCSK6
  hgvsc: ENST00000561177.1:n.1164-29G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000557794
  gene symbol: PCSK6
  hgvsc: ENST00000557794.1:n.124-79948G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381246
  ensembl transcript: ENST00000398185
  gene symbol: PCSK6
  hgvsc: ENST00000398185.2:c.703-29G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000332052
  ensembl transcript: ENST00000331826
  gene symbol: PCSK6
  hgvsc: ENST00000331826.7:c.499-29G>A
  variant of: http://identifiers.org/hgnc/8569
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3679
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8419
  bin: 2.75e1
  variant carriers: 64
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12302
  bin: 1.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 3.75e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25638
  bin: 2.25e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 4
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: Other
reference allele: C
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum

15-101933661-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101933661
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101933661
    reference: chr 15
allele count: 1
allele frequency: 8.980530210503629e-6
allele num: 111352
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561177
  gene symbol: PCSK6
  hgvsc: ENST00000561177.1:n.1164-32G>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561444
  gene symbol: PCSK6
  hgvsc: ENST00000561444.1:n.1164-32G>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000305056
  ensembl transcript: ENST00000348070
  gene symbol: PCSK6
  hgvsc: ENST00000348070.1:c.994-32G>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000559678
  gene symbol: PCSK6
  hgvsc: ENST00000559678.1:n.1069-32G>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000332052
  ensembl transcript: ENST00000331826
  gene symbol: PCSK6
  hgvsc: ENST00000331826.7:c.499-32G>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000344410
  ensembl transcript: ENST00000344273
  gene symbol: PCSK6
  hgvsc: ENST00000344273.2:c.994-32G>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561109
  gene symbol: PCSK6
  hgvsc: ENST00000561109.1:n.1069-32G>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000558716
  gene symbol: PCSK6
  hgvsc: ENST00000558716.1:n.1022-32G>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560271
  gene symbol: PCSK6
  hgvsc: ENST00000560271.1:n.1022-32G>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000557794
  gene symbol: PCSK6
  hgvsc: ENST00000557794.1:n.124-79951G>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560921
  gene symbol: PCSK6
  hgvsc: ENST00000560921.1:n.1069-32G>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381243
  ensembl transcript: ENST00000398181
  gene symbol: PCSK6
  hgvsc: ENST00000398181.2:c.994-32G>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381246
  ensembl transcript: ENST00000398185
  gene symbol: PCSK6
  hgvsc: ENST00000398185.2:c.703-32G>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000351193
  ensembl transcript: ENST00000358417
  gene symbol: PCSK6
  hgvsc: ENST00000358417.3:c.994-32G>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000452997
  ensembl transcript: ENST00000559417
  gene symbol: PCSK6
  hgvsc: ENST00000559417.1:c.618-32G>C
  variant of: http://identifiers.org/hgnc/8569
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9550
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13056
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3833
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7680
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: Other
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum

15-101933661-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101933661
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101933661
    reference: chr 15
allele count: 7
allele frequency: 6.28637114735254e-5
allele num: 111352
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000344410
  ensembl transcript: ENST00000344273
  gene symbol: PCSK6
  hgvsc: ENST00000344273.2:c.994-32G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000559678
  gene symbol: PCSK6
  hgvsc: ENST00000559678.1:n.1069-32G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560921
  gene symbol: PCSK6
  hgvsc: ENST00000560921.1:n.1069-32G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560271
  gene symbol: PCSK6
  hgvsc: ENST00000560271.1:n.1022-32G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000305056
  ensembl transcript: ENST00000348070
  gene symbol: PCSK6
  hgvsc: ENST00000348070.1:c.994-32G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561177
  gene symbol: PCSK6
  hgvsc: ENST00000561177.1:n.1164-32G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381243
  ensembl transcript: ENST00000398181
  gene symbol: PCSK6
  hgvsc: ENST00000398181.2:c.994-32G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000557794
  gene symbol: PCSK6
  hgvsc: ENST00000557794.1:n.124-79951G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000558716
  gene symbol: PCSK6
  hgvsc: ENST00000558716.1:n.1022-32G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561109
  gene symbol: PCSK6
  hgvsc: ENST00000561109.1:n.1069-32G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000332052
  ensembl transcript: ENST00000331826
  gene symbol: PCSK6
  hgvsc: ENST00000331826.7:c.499-32G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561444
  gene symbol: PCSK6
  hgvsc: ENST00000561444.1:n.1164-32G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381246
  ensembl transcript: ENST00000398185
  gene symbol: PCSK6
  hgvsc: ENST00000398185.2:c.703-32G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000452997
  ensembl transcript: ENST00000559417
  gene symbol: PCSK6
  hgvsc: ENST00000559417.1:c.618-32G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000351193
  ensembl transcript: ENST00000358417
  gene symbol: PCSK6
  hgvsc: ENST00000358417.3:c.994-32G>A
  variant of: http://identifiers.org/hgnc/8569
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13056
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1594
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9550
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 23173
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3833
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: BaseQRankSum

15-101933662-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101933662
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101933662
    reference: chr 15
allele count: 107
allele frequency: 9.629749626509711e-4
allele num: 111114
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000344410
  ensembl transcript: ENST00000344273
  gene symbol: PCSK6
  hgvsc: ENST00000344273.2:c.994-33C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561444
  gene symbol: PCSK6
  hgvsc: ENST00000561444.1:n.1164-33C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000305056
  ensembl transcript: ENST00000348070
  gene symbol: PCSK6
  hgvsc: ENST00000348070.1:c.994-33C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381243
  ensembl transcript: ENST00000398181
  gene symbol: PCSK6
  hgvsc: ENST00000398181.2:c.994-33C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560921
  gene symbol: PCSK6
  hgvsc: ENST00000560921.1:n.1069-33C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561109
  gene symbol: PCSK6
  hgvsc: ENST00000561109.1:n.1069-33C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560271
  gene symbol: PCSK6
  hgvsc: ENST00000560271.1:n.1022-33C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381246
  ensembl transcript: ENST00000398185
  gene symbol: PCSK6
  hgvsc: ENST00000398185.2:c.703-33C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000332052
  ensembl transcript: ENST00000331826
  gene symbol: PCSK6
  hgvsc: ENST00000331826.7:c.499-33C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000557794
  gene symbol: PCSK6
  hgvsc: ENST00000557794.1:n.124-79952C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000559678
  gene symbol: PCSK6
  hgvsc: ENST00000559678.1:n.1069-33C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000558716
  gene symbol: PCSK6
  hgvsc: ENST00000558716.1:n.1022-33C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561177
  gene symbol: PCSK6
  hgvsc: ENST00000561177.1:n.1164-33C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000351193
  ensembl transcript: ENST00000358417
  gene symbol: PCSK6
  hgvsc: ENST00000358417.3:c.994-33C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000452997
  ensembl transcript: ENST00000559417
  gene symbol: PCSK6
  hgvsc: ENST00000559417.1:c.618-33C>T
  variant of: http://identifiers.org/hgnc/8569
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9511
  bin: 1.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7859
  bin: 2.75e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1580
  bin: 3.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 13135
  bin: 1.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 4.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/15-101933664-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101933664
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101933664
    reference: chr 15
allele count: 59
allele frequency: 5.309575233981282e-4
allele num: 111120
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000332052
  ensembl transcript: ENST00000331826
  gene symbol: PCSK6
  hgvsc: ENST00000331826.7:c.499-35T>G
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561109
  gene symbol: PCSK6
  hgvsc: ENST00000561109.1:n.1069-35T>G
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560921
  gene symbol: PCSK6
  hgvsc: ENST00000560921.1:n.1069-35T>G
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000344410
  ensembl transcript: ENST00000344273
  gene symbol: PCSK6
  hgvsc: ENST00000344273.2:c.994-35T>G
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561444
  gene symbol: PCSK6
  hgvsc: ENST00000561444.1:n.1164-35T>G
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000557794
  gene symbol: PCSK6
  hgvsc: ENST00000557794.1:n.124-79954T>G
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381243
  ensembl transcript: ENST00000398181
  gene symbol: PCSK6
  hgvsc: ENST00000398181.2:c.994-35T>G
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000558716
  gene symbol: PCSK6
  hgvsc: ENST00000558716.1:n.1022-35T>G
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000305056
  ensembl transcript: ENST00000348070
  gene symbol: PCSK6
  hgvsc: ENST00000348070.1:c.994-35T>G
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000452997
  ensembl transcript: ENST00000559417
  gene symbol: PCSK6
  hgvsc: ENST00000559417.1:c.618-35T>G
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000559678
  gene symbol: PCSK6
  hgvsc: ENST00000559678.1:n.1069-35T>G
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000351193
  ensembl transcript: ENST00000358417
  gene symbol: PCSK6
  hgvsc: ENST00000358417.3:c.994-35T>G
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560271
  gene symbol: PCSK6
  hgvsc: ENST00000560271.1:n.1022-35T>G
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561177
  gene symbol: PCSK6
  hgvsc: ENST00000561177.1:n.1164-35T>G
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381246
  ensembl transcript: ENST00000398185
  gene symbol: PCSK6
  hgvsc: ENST00000398185.2:c.703-35T>G
  variant of: http://identifiers.org/hgnc/8569
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7174
  bin: 2.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1389
  bin: 3.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 21327
  bin: 2.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13419
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 3.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 11520
  bin: 1.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 1
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
reference allele: A
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

15-101933672-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101933672
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101933672
    reference: chr 15
allele count: 5
allele frequency: 4.601678692386982e-5
allele num: 108656
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000558716
  gene symbol: PCSK6
  hgvsc: ENST00000558716.1:n.1022-43G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381246
  ensembl transcript: ENST00000398185
  gene symbol: PCSK6
  hgvsc: ENST00000398185.2:c.703-43G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000305056
  ensembl transcript: ENST00000348070
  gene symbol: PCSK6
  hgvsc: ENST00000348070.1:c.994-43G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560271
  gene symbol: PCSK6
  hgvsc: ENST00000560271.1:n.1022-43G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381243
  ensembl transcript: ENST00000398181
  gene symbol: PCSK6
  hgvsc: ENST00000398181.2:c.994-43G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560921
  gene symbol: PCSK6
  hgvsc: ENST00000560921.1:n.1069-43G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000351193
  ensembl transcript: ENST00000358417
  gene symbol: PCSK6
  hgvsc: ENST00000358417.3:c.994-43G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561109
  gene symbol: PCSK6
  hgvsc: ENST00000561109.1:n.1069-43G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000332052
  ensembl transcript: ENST00000331826
  gene symbol: PCSK6
  hgvsc: ENST00000331826.7:c.499-43G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561177
  gene symbol: PCSK6
  hgvsc: ENST00000561177.1:n.1164-43G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561444
  gene symbol: PCSK6
  hgvsc: ENST00000561444.1:n.1164-43G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000559678
  gene symbol: PCSK6
  hgvsc: ENST00000559678.1:n.1069-43G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000557794
  gene symbol: PCSK6
  hgvsc: ENST00000557794.1:n.124-79962G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000452997
  ensembl transcript: ENST00000559417
  gene symbol: PCSK6
  hgvsc: ENST00000559417.1:c.618-43G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000344410
  ensembl transcript: ENST00000344273
  gene symbol: PCSK6
  hgvsc: ENST00000344273.2:c.994-43G>A
  variant of: http://identifiers.org/hgnc/8569
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13020
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19023
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4976
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4854
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15863
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum

15-101933675-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101933675
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101933675
    reference: chr 15
allele count: 2
allele frequency: 1.870662401556391e-5
allele num: 106914
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561177
  gene symbol: PCSK6
  hgvsc: ENST00000561177.1:n.1164-46C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560921
  gene symbol: PCSK6
  hgvsc: ENST00000560921.1:n.1069-46C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000557794
  gene symbol: PCSK6
  hgvsc: ENST00000557794.1:n.124-79965C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000452997
  ensembl transcript: ENST00000559417
  gene symbol: PCSK6
  hgvsc: ENST00000559417.1:c.618-46C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000559678
  gene symbol: PCSK6
  hgvsc: ENST00000559678.1:n.1069-46C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000558716
  gene symbol: PCSK6
  hgvsc: ENST00000558716.1:n.1022-46C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000305056
  ensembl transcript: ENST00000348070
  gene symbol: PCSK6
  hgvsc: ENST00000348070.1:c.994-46C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381243
  ensembl transcript: ENST00000398181
  gene symbol: PCSK6
  hgvsc: ENST00000398181.2:c.994-46C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000344410
  ensembl transcript: ENST00000344273
  gene symbol: PCSK6
  hgvsc: ENST00000344273.2:c.994-46C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381246
  ensembl transcript: ENST00000398185
  gene symbol: PCSK6
  hgvsc: ENST00000398185.2:c.703-46C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560271
  gene symbol: PCSK6
  hgvsc: ENST00000560271.1:n.1022-46C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000332052
  ensembl transcript: ENST00000331826
  gene symbol: PCSK6
  hgvsc: ENST00000331826.7:c.499-46C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000351193
  ensembl transcript: ENST00000358417
  gene symbol: PCSK6
  hgvsc: ENST00000358417.3:c.994-46C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561444
  gene symbol: PCSK6
  hgvsc: ENST00000561444.1:n.1164-46C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561109
  gene symbol: PCSK6
  hgvsc: ENST00000561109.1:n.1069-46C>T
  variant of: http://identifiers.org/hgnc/8569
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15689
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5494
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19442
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
reference allele: G
site quality: QD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum

15-101933679-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101933679
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101933679
    reference: chr 15
allele count: 1
allele frequency: 9.417614706547127e-6
allele num: 106184
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000351193
  ensembl transcript: ENST00000358417
  gene symbol: PCSK6
  hgvsc: ENST00000358417.3:c.994-50C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000344410
  ensembl transcript: ENST00000344273
  gene symbol: PCSK6
  hgvsc: ENST00000344273.2:c.994-50C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000305056
  ensembl transcript: ENST00000348070
  gene symbol: PCSK6
  hgvsc: ENST00000348070.1:c.994-50C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381243
  ensembl transcript: ENST00000398181
  gene symbol: PCSK6
  hgvsc: ENST00000398181.2:c.994-50C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000559678
  gene symbol: PCSK6
  hgvsc: ENST00000559678.1:n.1069-50C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000452997
  ensembl transcript: ENST00000559417
  gene symbol: PCSK6
  hgvsc: ENST00000559417.1:c.618-50C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560921
  gene symbol: PCSK6
  hgvsc: ENST00000560921.1:n.1069-50C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560271
  gene symbol: PCSK6
  hgvsc: ENST00000560271.1:n.1022-50C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000557794
  gene symbol: PCSK6
  hgvsc: ENST00000557794.1:n.124-79969C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000558716
  gene symbol: PCSK6
  hgvsc: ENST00000558716.1:n.1022-50C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561444
  gene symbol: PCSK6
  hgvsc: ENST00000561444.1:n.1164-50C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381246
  ensembl transcript: ENST00000398185
  gene symbol: PCSK6
  hgvsc: ENST00000398185.2:c.703-50C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561177
  gene symbol: PCSK6
  hgvsc: ENST00000561177.1:n.1164-50C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561109
  gene symbol: PCSK6
  hgvsc: ENST00000561109.1:n.1069-50C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000332052
  ensembl transcript: ENST00000331826
  gene symbol: PCSK6
  hgvsc: ENST00000331826.7:c.499-50C>T
  variant of: http://identifiers.org/hgnc/8569
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4920
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12757
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5596
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQ

http://identifiers.org/exac.variant/15-101938559-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101938559
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101938559
    reference: chr 15
allele count: 1
allele frequency: 8.922039221284417e-6
allele num: 112082
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381243
  ensembl transcript: ENST00000398181
  gene symbol: PCSK6
  hgvsc: ENST00000398181.2:c.993+50T>G
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561109
  gene symbol: PCSK6
  hgvsc: ENST00000561109.1:n.1068+50T>G
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560271
  gene symbol: PCSK6
  hgvsc: ENST00000560271.1:n.1021+50T>G
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000332052
  ensembl transcript: ENST00000331826
  gene symbol: PCSK6
  hgvsc: ENST00000331826.7:c.498+50T>G
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561177
  gene symbol: PCSK6
  hgvsc: ENST00000561177.1:n.1163+50T>G
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560921
  gene symbol: PCSK6
  hgvsc: ENST00000560921.1:n.1068+50T>G
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000344410
  ensembl transcript: ENST00000344273
  gene symbol: PCSK6
  hgvsc: ENST00000344273.2:c.993+50T>G
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000305056
  ensembl transcript: ENST00000348070
  gene symbol: PCSK6
  hgvsc: ENST00000348070.1:c.993+50T>G
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000559678
  gene symbol: PCSK6
  hgvsc: ENST00000559678.1:n.1068+50T>G
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561444
  gene symbol: PCSK6
  hgvsc: ENST00000561444.1:n.1163+50T>G
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000558716
  gene symbol: PCSK6
  hgvsc: ENST00000558716.1:n.1021+50T>G
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000351193
  ensembl transcript: ENST00000358417
  gene symbol: PCSK6
  hgvsc: ENST00000358417.3:c.993+50T>G
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000557794
  gene symbol: PCSK6
  hgvsc: ENST00000557794.1:n.124-84849T>G
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000452997
  ensembl transcript: ENST00000559417
  gene symbol: PCSK6
  hgvsc: ENST00000559417.1:c.617+50T>G
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381246
  ensembl transcript: ENST00000398185
  gene symbol: PCSK6
  hgvsc: ENST00000398185.2:c.702+50T>G
  variant of: http://identifiers.org/hgnc/8569
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1376
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1878
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3014
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14732
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2859
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8855
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14394
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum

15-101938566-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101938566
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101938566
    reference: chr 15
allele count: 3
allele frequency: 2.674941151294672e-5
allele num: 112152
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000452997
  ensembl transcript: ENST00000559417
  gene symbol: PCSK6
  hgvsc: ENST00000559417.1:c.617+43G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381246
  ensembl transcript: ENST00000398185
  gene symbol: PCSK6
  hgvsc: ENST00000398185.2:c.702+43G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560921
  gene symbol: PCSK6
  hgvsc: ENST00000560921.1:n.1068+43G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000559678
  gene symbol: PCSK6
  hgvsc: ENST00000559678.1:n.1068+43G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561177
  gene symbol: PCSK6
  hgvsc: ENST00000561177.1:n.1163+43G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000305056
  ensembl transcript: ENST00000348070
  gene symbol: PCSK6
  hgvsc: ENST00000348070.1:c.993+43G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000344410
  ensembl transcript: ENST00000344273
  gene symbol: PCSK6
  hgvsc: ENST00000344273.2:c.993+43G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381243
  ensembl transcript: ENST00000398181
  gene symbol: PCSK6
  hgvsc: ENST00000398181.2:c.993+43G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561109
  gene symbol: PCSK6
  hgvsc: ENST00000561109.1:n.1068+43G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000557794
  gene symbol: PCSK6
  hgvsc: ENST00000557794.1:n.124-84856G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000351193
  ensembl transcript: ENST00000358417
  gene symbol: PCSK6
  hgvsc: ENST00000358417.3:c.993+43G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000332052
  ensembl transcript: ENST00000331826
  gene symbol: PCSK6
  hgvsc: ENST00000331826.7:c.498+43G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561444
  gene symbol: PCSK6
  hgvsc: ENST00000561444.1:n.1163+43G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000558716
  gene symbol: PCSK6
  hgvsc: ENST00000558716.1:n.1021+43G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560271
  gene symbol: PCSK6
  hgvsc: ENST00000560271.1:n.1021+43G>A
  variant of: http://identifiers.org/hgnc/8569
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3100
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14730
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5612
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1018
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1230
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14396
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8853
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

15-101938572-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101938572
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101938572
    reference: chr 15
allele count: 8
allele frequency: 7.117564369472767e-5
allele num: 112398
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000558716
  gene symbol: PCSK6
  hgvsc: ENST00000558716.1:n.1021+37A>G
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000452997
  ensembl transcript: ENST00000559417
  gene symbol: PCSK6
  hgvsc: ENST00000559417.1:c.617+37A>G
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000344410
  ensembl transcript: ENST00000344273
  gene symbol: PCSK6
  hgvsc: ENST00000344273.2:c.993+37A>G
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000557794
  gene symbol: PCSK6
  hgvsc: ENST00000557794.1:n.124-84862A>G
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561177
  gene symbol: PCSK6
  hgvsc: ENST00000561177.1:n.1163+37A>G
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381243
  ensembl transcript: ENST00000398181
  gene symbol: PCSK6
  hgvsc: ENST00000398181.2:c.993+37A>G
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561444
  gene symbol: PCSK6
  hgvsc: ENST00000561444.1:n.1163+37A>G
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381246
  ensembl transcript: ENST00000398185
  gene symbol: PCSK6
  hgvsc: ENST00000398185.2:c.702+37A>G
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000305056
  ensembl transcript: ENST00000348070
  gene symbol: PCSK6
  hgvsc: ENST00000348070.1:c.993+37A>G
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000559678
  gene symbol: PCSK6
  hgvsc: ENST00000559678.1:n.1068+37A>G
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561109
  gene symbol: PCSK6
  hgvsc: ENST00000561109.1:n.1068+37A>G
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000332052
  ensembl transcript: ENST00000331826
  gene symbol: PCSK6
  hgvsc: ENST00000331826.7:c.498+37A>G
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000351193
  ensembl transcript: ENST00000358417
  gene symbol: PCSK6
  hgvsc: ENST00000358417.3:c.993+37A>G
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560921
  gene symbol: PCSK6
  hgvsc: ENST00000560921.1:n.1068+37A>G
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560271
  gene symbol: PCSK6
  hgvsc: ENST00000560271.1:n.1021+37A>G
  variant of: http://identifiers.org/hgnc/8569
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3245
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14395
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2964
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14740
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1878
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3493
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8856
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD

15-101938579-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101938579
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101938579
    reference: chr 15
allele count: 12
allele frequency: 1.063245379312789e-4
allele num: 112862
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000305056
  ensembl transcript: ENST00000348070
  gene symbol: PCSK6
  hgvsc: ENST00000348070.1:c.993+30C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561177
  gene symbol: PCSK6
  hgvsc: ENST00000561177.1:n.1163+30C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381243
  ensembl transcript: ENST00000398181
  gene symbol: PCSK6
  hgvsc: ENST00000398181.2:c.993+30C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000557794
  gene symbol: PCSK6
  hgvsc: ENST00000557794.1:n.124-84869C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000452997
  ensembl transcript: ENST00000559417
  gene symbol: PCSK6
  hgvsc: ENST00000559417.1:c.617+30C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000332052
  ensembl transcript: ENST00000331826
  gene symbol: PCSK6
  hgvsc: ENST00000331826.7:c.498+30C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561109
  gene symbol: PCSK6
  hgvsc: ENST00000561109.1:n.1068+30C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000558716
  gene symbol: PCSK6
  hgvsc: ENST00000558716.1:n.1021+30C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000344410
  ensembl transcript: ENST00000344273
  gene symbol: PCSK6
  hgvsc: ENST00000344273.2:c.993+30C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560921
  gene symbol: PCSK6
  hgvsc: ENST00000560921.1:n.1068+30C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000559678
  gene symbol: PCSK6
  hgvsc: ENST00000559678.1:n.1068+30C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560271
  gene symbol: PCSK6
  hgvsc: ENST00000560271.1:n.1021+30C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000351193
  ensembl transcript: ENST00000358417
  gene symbol: PCSK6
  hgvsc: ENST00000358417.3:c.993+30C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381246
  ensembl transcript: ENST00000398185
  gene symbol: PCSK6
  hgvsc: ENST00000398185.2:c.702+30C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561444
  gene symbol: PCSK6
  hgvsc: ENST00000561444.1:n.1163+30C>T
  variant of: http://identifiers.org/hgnc/8569
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1103
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14758
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8858
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14393
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5612
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3339
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum

15-101938579-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101938579
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101938579
    reference: chr 15
allele count: 2
allele frequency: 1.772075632187982e-5
allele num: 112862
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000557794
  gene symbol: PCSK6
  hgvsc: ENST00000557794.1:n.124-84869C>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000559678
  gene symbol: PCSK6
  hgvsc: ENST00000559678.1:n.1068+30C>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561444
  gene symbol: PCSK6
  hgvsc: ENST00000561444.1:n.1163+30C>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381243
  ensembl transcript: ENST00000398181
  gene symbol: PCSK6
  hgvsc: ENST00000398181.2:c.993+30C>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381246
  ensembl transcript: ENST00000398185
  gene symbol: PCSK6
  hgvsc: ENST00000398185.2:c.702+30C>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000305056
  ensembl transcript: ENST00000348070
  gene symbol: PCSK6
  hgvsc: ENST00000348070.1:c.993+30C>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561109
  gene symbol: PCSK6
  hgvsc: ENST00000561109.1:n.1068+30C>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560271
  gene symbol: PCSK6
  hgvsc: ENST00000560271.1:n.1021+30C>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000344410
  ensembl transcript: ENST00000344273
  gene symbol: PCSK6
  hgvsc: ENST00000344273.2:c.993+30C>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000351193
  ensembl transcript: ENST00000358417
  gene symbol: PCSK6
  hgvsc: ENST00000358417.3:c.993+30C>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561177
  gene symbol: PCSK6
  hgvsc: ENST00000561177.1:n.1163+30C>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000558716
  gene symbol: PCSK6
  hgvsc: ENST00000558716.1:n.1021+30C>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560921
  gene symbol: PCSK6
  hgvsc: ENST00000560921.1:n.1068+30C>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000332052
  ensembl transcript: ENST00000331826
  gene symbol: PCSK6
  hgvsc: ENST00000331826.7:c.498+30C>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000452997
  ensembl transcript: ENST00000559417
  gene symbol: PCSK6
  hgvsc: ENST00000559417.1:c.617+30C>A
  variant of: http://identifiers.org/hgnc/8569
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8858
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3493
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14758
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1103
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14393
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3097
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/15-101938580-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101938580
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101938580
    reference: chr 15
allele count: 5
allele frequency: 4.432781304301571e-5
allele num: 112796
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000344410
  ensembl transcript: ENST00000344273
  gene symbol: PCSK6
  hgvsc: ENST00000344273.2:c.993+29G>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000558716
  gene symbol: PCSK6
  hgvsc: ENST00000558716.1:n.1021+29G>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000305056
  ensembl transcript: ENST00000348070
  gene symbol: PCSK6
  hgvsc: ENST00000348070.1:c.993+29G>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000452997
  ensembl transcript: ENST00000559417
  gene symbol: PCSK6
  hgvsc: ENST00000559417.1:c.617+29G>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381246
  ensembl transcript: ENST00000398185
  gene symbol: PCSK6
  hgvsc: ENST00000398185.2:c.702+29G>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560921
  gene symbol: PCSK6
  hgvsc: ENST00000560921.1:n.1068+29G>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560271
  gene symbol: PCSK6
  hgvsc: ENST00000560271.1:n.1021+29G>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000557794
  gene symbol: PCSK6
  hgvsc: ENST00000557794.1:n.124-84870G>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381243
  ensembl transcript: ENST00000398181
  gene symbol: PCSK6
  hgvsc: ENST00000398181.2:c.993+29G>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561109
  gene symbol: PCSK6
  hgvsc: ENST00000561109.1:n.1068+29G>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000559678
  gene symbol: PCSK6
  hgvsc: ENST00000559678.1:n.1068+29G>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000351193
  ensembl transcript: ENST00000358417
  gene symbol: PCSK6
  hgvsc: ENST00000358417.3:c.993+29G>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000332052
  ensembl transcript: ENST00000331826
  gene symbol: PCSK6
  hgvsc: ENST00000331826.7:c.498+29G>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561444
  gene symbol: PCSK6
  hgvsc: ENST00000561444.1:n.1163+29G>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561177
  gene symbol: PCSK6
  hgvsc: ENST00000561177.1:n.1163+29G>T
  variant of: http://identifiers.org/hgnc/8569
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5613
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1879
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1130
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14397
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14773
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3295
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

15-101938580-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101938580
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101938580
    reference: chr 15
allele count: 3
allele frequency: 2.659668782580943e-5
allele num: 112796
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000344410
  ensembl transcript: ENST00000344273
  gene symbol: PCSK6
  hgvsc: ENST00000344273.2:c.993+29G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000558716
  gene symbol: PCSK6
  hgvsc: ENST00000558716.1:n.1021+29G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560271
  gene symbol: PCSK6
  hgvsc: ENST00000560271.1:n.1021+29G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560921
  gene symbol: PCSK6
  hgvsc: ENST00000560921.1:n.1068+29G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000557794
  gene symbol: PCSK6
  hgvsc: ENST00000557794.1:n.124-84870G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000559678
  gene symbol: PCSK6
  hgvsc: ENST00000559678.1:n.1068+29G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000305056
  ensembl transcript: ENST00000348070
  gene symbol: PCSK6
  hgvsc: ENST00000348070.1:c.993+29G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381243
  ensembl transcript: ENST00000398181
  gene symbol: PCSK6
  hgvsc: ENST00000398181.2:c.993+29G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561177
  gene symbol: PCSK6
  hgvsc: ENST00000561177.1:n.1163+29G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000452997
  ensembl transcript: ENST00000559417
  gene symbol: PCSK6
  hgvsc: ENST00000559417.1:c.617+29G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381246
  ensembl transcript: ENST00000398185
  gene symbol: PCSK6
  hgvsc: ENST00000398185.2:c.702+29G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000332052
  ensembl transcript: ENST00000331826
  gene symbol: PCSK6
  hgvsc: ENST00000331826.7:c.498+29G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000351193
  ensembl transcript: ENST00000358417
  gene symbol: PCSK6
  hgvsc: ENST00000358417.3:c.993+29G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561444
  gene symbol: PCSK6
  hgvsc: ENST00000561444.1:n.1163+29G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561109
  gene symbol: PCSK6
  hgvsc: ENST00000561109.1:n.1068+29G>A
  variant of: http://identifiers.org/hgnc/8569
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8859
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1130
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3107
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3295
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
reference allele: C
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: VQSLOD

15-101938581-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101938581
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101938581
    reference: chr 15
allele count: 1
allele frequency: 8.844235327413593e-6
allele num: 113068
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561177
  gene symbol: PCSK6
  hgvsc: ENST00000561177.1:n.1163+28C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000351193
  ensembl transcript: ENST00000358417
  gene symbol: PCSK6
  hgvsc: ENST00000358417.3:c.993+28C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381246
  ensembl transcript: ENST00000398185
  gene symbol: PCSK6
  hgvsc: ENST00000398185.2:c.702+28C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561444
  gene symbol: PCSK6
  hgvsc: ENST00000561444.1:n.1163+28C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560921
  gene symbol: PCSK6
  hgvsc: ENST00000560921.1:n.1068+28C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560271
  gene symbol: PCSK6
  hgvsc: ENST00000560271.1:n.1021+28C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000332052
  ensembl transcript: ENST00000331826
  gene symbol: PCSK6
  hgvsc: ENST00000331826.7:c.498+28C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000305056
  ensembl transcript: ENST00000348070
  gene symbol: PCSK6
  hgvsc: ENST00000348070.1:c.993+28C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000558716
  gene symbol: PCSK6
  hgvsc: ENST00000558716.1:n.1021+28C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381243
  ensembl transcript: ENST00000398181
  gene symbol: PCSK6
  hgvsc: ENST00000398181.2:c.993+28C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000557794
  gene symbol: PCSK6
  hgvsc: ENST00000557794.1:n.124-84871C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000344410
  ensembl transcript: ENST00000344273
  gene symbol: PCSK6
  hgvsc: ENST00000344273.2:c.993+28C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000559678
  gene symbol: PCSK6
  hgvsc: ENST00000559678.1:n.1068+28C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561109
  gene symbol: PCSK6
  hgvsc: ENST00000561109.1:n.1068+28C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000452997
  ensembl transcript: ENST00000559417
  gene symbol: PCSK6
  hgvsc: ENST00000559417.1:c.617+28C>T
  variant of: http://identifiers.org/hgnc/8569
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3307
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3176
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1879
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8861
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5615
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP

15-101938594-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101938594
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101938594
    reference: chr 15
allele count: 1
allele frequency: 8.725698928484172e-6
allele num: 114604
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561177
  gene symbol: PCSK6
  hgvsc: ENST00000561177.1:n.1163+15G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560921
  gene symbol: PCSK6
  hgvsc: ENST00000560921.1:n.1068+15G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000557794
  gene symbol: PCSK6
  hgvsc: ENST00000557794.1:n.124-84884G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561109
  gene symbol: PCSK6
  hgvsc: ENST00000561109.1:n.1068+15G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000559678
  gene symbol: PCSK6
  hgvsc: ENST00000559678.1:n.1068+15G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381243
  ensembl transcript: ENST00000398181
  gene symbol: PCSK6
  hgvsc: ENST00000398181.2:c.993+15G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000351193
  ensembl transcript: ENST00000358417
  gene symbol: PCSK6
  hgvsc: ENST00000358417.3:c.993+15G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381246
  ensembl transcript: ENST00000398185
  gene symbol: PCSK6
  hgvsc: ENST00000398185.2:c.702+15G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000344410
  ensembl transcript: ENST00000344273
  gene symbol: PCSK6
  hgvsc: ENST00000344273.2:c.993+15G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000452997
  ensembl transcript: ENST00000559417
  gene symbol: PCSK6
  hgvsc: ENST00000559417.1:c.617+15G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000558716
  gene symbol: PCSK6
  hgvsc: ENST00000558716.1:n.1021+15G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560271
  gene symbol: PCSK6
  hgvsc: ENST00000560271.1:n.1021+15G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000305056
  ensembl transcript: ENST00000348070
  gene symbol: PCSK6
  hgvsc: ENST00000348070.1:c.993+15G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000332052
  ensembl transcript: ENST00000331826
  gene symbol: PCSK6
  hgvsc: ENST00000331826.7:c.498+15G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561444
  gene symbol: PCSK6
  hgvsc: ENST00000561444.1:n.1163+15G>A
  variant of: http://identifiers.org/hgnc/8569
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2837
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1878
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3914
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14852
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: African
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum

15-101938595-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101938595
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101938595
    reference: chr 15
allele count: 1
allele frequency: 8.712622847982157e-6
allele num: 114776
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561444
  gene symbol: PCSK6
  hgvsc: ENST00000561444.1:n.1163+14G>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560271
  gene symbol: PCSK6
  hgvsc: ENST00000560271.1:n.1021+14G>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560921
  gene symbol: PCSK6
  hgvsc: ENST00000560921.1:n.1068+14G>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000558716
  gene symbol: PCSK6
  hgvsc: ENST00000558716.1:n.1021+14G>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381243
  ensembl transcript: ENST00000398181
  gene symbol: PCSK6
  hgvsc: ENST00000398181.2:c.993+14G>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000305056
  ensembl transcript: ENST00000348070
  gene symbol: PCSK6
  hgvsc: ENST00000348070.1:c.993+14G>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000557794
  gene symbol: PCSK6
  hgvsc: ENST00000557794.1:n.124-84885G>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000351193
  ensembl transcript: ENST00000358417
  gene symbol: PCSK6
  hgvsc: ENST00000358417.3:c.993+14G>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381246
  ensembl transcript: ENST00000398185
  gene symbol: PCSK6
  hgvsc: ENST00000398185.2:c.702+14G>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561109
  gene symbol: PCSK6
  hgvsc: ENST00000561109.1:n.1068+14G>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000559678
  gene symbol: PCSK6
  hgvsc: ENST00000559678.1:n.1068+14G>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000332052
  ensembl transcript: ENST00000331826
  gene symbol: PCSK6
  hgvsc: ENST00000331826.7:c.498+14G>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561177
  gene symbol: PCSK6
  hgvsc: ENST00000561177.1:n.1163+14G>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000344410
  ensembl transcript: ENST00000344273
  gene symbol: PCSK6
  hgvsc: ENST00000344273.2:c.993+14G>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000452997
  ensembl transcript: ENST00000559417
  gene symbol: PCSK6
  hgvsc: ENST00000559417.1:c.617+14G>C
  variant of: http://identifiers.org/hgnc/8569
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 987
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3984
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14860
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14406
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1878
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8862
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

15-101938598-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101938598
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101938598
    reference: chr 15
allele count: 1
allele frequency: 8.688097306689835e-6
allele num: 115100
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381243
  ensembl transcript: ENST00000398181
  gene symbol: PCSK6
  hgvsc: ENST00000398181.2:c.993+11C>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381246
  ensembl transcript: ENST00000398185
  gene symbol: PCSK6
  hgvsc: ENST00000398185.2:c.702+11C>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000558716
  gene symbol: PCSK6
  hgvsc: ENST00000558716.1:n.1021+11C>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000305056
  ensembl transcript: ENST00000348070
  gene symbol: PCSK6
  hgvsc: ENST00000348070.1:c.993+11C>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560271
  gene symbol: PCSK6
  hgvsc: ENST00000560271.1:n.1021+11C>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561109
  gene symbol: PCSK6
  hgvsc: ENST00000561109.1:n.1068+11C>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000332052
  ensembl transcript: ENST00000331826
  gene symbol: PCSK6
  hgvsc: ENST00000331826.7:c.498+11C>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560921
  gene symbol: PCSK6
  hgvsc: ENST00000560921.1:n.1068+11C>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000557794
  gene symbol: PCSK6
  hgvsc: ENST00000557794.1:n.124-84888C>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561177
  gene symbol: PCSK6
  hgvsc: ENST00000561177.1:n.1163+11C>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000452997
  ensembl transcript: ENST00000559417
  gene symbol: PCSK6
  hgvsc: ENST00000559417.1:c.617+11C>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000344410
  ensembl transcript: ENST00000344273
  gene symbol: PCSK6
  hgvsc: ENST00000344273.2:c.993+11C>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000559678
  gene symbol: PCSK6
  hgvsc: ENST00000559678.1:n.1068+11C>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561444
  gene symbol: PCSK6
  hgvsc: ENST00000561444.1:n.1163+11C>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000351193
  ensembl transcript: ENST00000358417
  gene symbol: PCSK6
  hgvsc: ENST00000358417.3:c.993+11C>A
  variant of: http://identifiers.org/hgnc/8569
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14409
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4210
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14882
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2659
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8862
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

15-101938603-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101938603
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101938603
    reference: chr 15
allele count: 2
allele frequency: 1.726042529687932e-5
allele num: 115872
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000452997
  ensembl transcript: ENST00000559417
  gene symbol: PCSK6
  hgvsc: ENST00000559417.1:c.617+6A>G
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000332052
  ensembl transcript: ENST00000331826
  gene symbol: PCSK6
  hgvsc: ENST00000331826.7:c.498+6A>G
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000344410
  ensembl transcript: ENST00000344273
  gene symbol: PCSK6
  hgvsc: ENST00000344273.2:c.993+6A>G
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381243
  ensembl transcript: ENST00000398181
  gene symbol: PCSK6
  hgvsc: ENST00000398181.2:c.993+6A>G
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000305056
  ensembl transcript: ENST00000348070
  gene symbol: PCSK6
  hgvsc: ENST00000348070.1:c.993+6A>G
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561444
  gene symbol: PCSK6
  hgvsc: ENST00000561444.1:n.1163+6A>G
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000351193
  ensembl transcript: ENST00000358417
  gene symbol: PCSK6
  hgvsc: ENST00000358417.3:c.993+6A>G
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560921
  gene symbol: PCSK6
  hgvsc: ENST00000560921.1:n.1068+6A>G
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381246
  ensembl transcript: ENST00000398185
  gene symbol: PCSK6
  hgvsc: ENST00000398185.2:c.702+6A>G
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000558716
  gene symbol: PCSK6
  hgvsc: ENST00000558716.1:n.1021+6A>G
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560271
  gene symbol: PCSK6
  hgvsc: ENST00000560271.1:n.1021+6A>G
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561109
  gene symbol: PCSK6
  hgvsc: ENST00000561109.1:n.1068+6A>G
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000559678
  gene symbol: PCSK6
  hgvsc: ENST00000559678.1:n.1068+6A>G
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000557794
  gene symbol: PCSK6
  hgvsc: ENST00000557794.1:n.124-84893A>G
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561177
  gene symbol: PCSK6
  hgvsc: ENST00000561177.1:n.1163+6A>G
  variant of: http://identifiers.org/hgnc/8569
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14414
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8863
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1877
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2331
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14939
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.993+6A>G
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: VQSLOD

15-101938608-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101938608
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101938608
    reference: chr 15
allele count: 1
allele frequency: 8.575740944017563e-6
allele num: 116608
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000344410
  ensembl transcript: ENST00000344273
  gene symbol: PCSK6
  hgvsc: ENST00000344273.2:c.993+1G>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560271
  gene symbol: PCSK6
  hgvsc: ENST00000560271.1:n.1021+1G>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561177
  gene symbol: PCSK6
  hgvsc: ENST00000561177.1:n.1163+1G>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560921
  gene symbol: PCSK6
  hgvsc: ENST00000560921.1:n.1068+1G>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381243
  ensembl transcript: ENST00000398181
  gene symbol: PCSK6
  hgvsc: ENST00000398181.2:c.993+1G>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381246
  ensembl transcript: ENST00000398185
  gene symbol: PCSK6
  hgvsc: ENST00000398185.2:c.702+1G>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561109
  gene symbol: PCSK6
  hgvsc: ENST00000561109.1:n.1068+1G>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000351193
  ensembl transcript: ENST00000358417
  gene symbol: PCSK6
  hgvsc: ENST00000358417.3:c.993+1G>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000557794
  gene symbol: PCSK6
  hgvsc: ENST00000557794.1:n.124-84898G>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000559678
  gene symbol: PCSK6
  hgvsc: ENST00000559678.1:n.1068+1G>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000558716
  gene symbol: PCSK6
  hgvsc: ENST00000558716.1:n.1021+1G>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000305056
  ensembl transcript: ENST00000348070
  gene symbol: PCSK6
  hgvsc: ENST00000348070.1:c.993+1G>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561444
  gene symbol: PCSK6
  hgvsc: ENST00000561444.1:n.1163+1G>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000332052
  ensembl transcript: ENST00000331826
  gene symbol: PCSK6
  hgvsc: ENST00000331826.7:c.498+1G>C
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000452997
  ensembl transcript: ENST00000559417
  gene symbol: PCSK6
  hgvsc: ENST00000559417.1:c.617+1G>C
  variant of: http://identifiers.org/hgnc/8569
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3492
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5615
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5015
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1877
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8864
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15047
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1951
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.993+1G>C
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: European (Finnish)
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

15-101938626-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101938626
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101938626
    reference: chr 15
allele count: 1
allele frequency: 8.416374899003501e-6
allele num: 118816
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561109
  gene symbol: PCSK6
  hgvsc: ENST00000561109.1:n.1051G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000344410
  ensembl transcript: ENST00000344273
  gene symbol: PCSK6
  hgvsc: ENST00000344273.2:c.976G>A
  hgvsp: ENSP00000344410.2:p.Glu326Lys
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000305056
  ensembl transcript: ENST00000348070
  gene symbol: PCSK6
  hgvsc: ENST00000348070.1:c.976G>A
  hgvsp: ENSP00000305056.4:p.Glu326Lys
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561177
  gene symbol: PCSK6
  hgvsc: ENST00000561177.1:n.1146G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381243
  ensembl transcript: ENST00000398181
  gene symbol: PCSK6
  hgvsc: ENST00000398181.2:c.976G>A
  hgvsp: ENSP00000381243.2:p.Glu326Lys
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000351193
  ensembl transcript: ENST00000358417
  gene symbol: PCSK6
  hgvsc: ENST00000358417.3:c.976G>A
  hgvsp: ENSP00000351193.3:p.Glu326Lys
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000559678
  gene symbol: PCSK6
  hgvsc: ENST00000559678.1:n.1051G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561444
  gene symbol: PCSK6
  hgvsc: ENST00000561444.1:n.1146G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000558716
  gene symbol: PCSK6
  hgvsc: ENST00000558716.1:n.1004G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560271
  gene symbol: PCSK6
  hgvsc: ENST00000560271.1:n.1004G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000452997
  ensembl transcript: ENST00000559417
  gene symbol: PCSK6
  hgvsc: ENST00000559417.1:c.600G>A
  hgvsp: ENSP00000452997.1:p.Glu201Lys
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000332052
  ensembl transcript: ENST00000331826
  gene symbol: PCSK6
  hgvsc: ENST00000331826.7:c.481G>A
  hgvsp: ENSP00000332052.7:p.Glu161Lys
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560921
  gene symbol: PCSK6
  hgvsc: ENST00000560921.1:n.1051G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381246
  ensembl transcript: ENST00000398185
  gene symbol: PCSK6
  hgvsc: ENST00000398185.2:c.685G>A
  hgvsp: ENSP00000381246.2:p.Glu229Lys
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000557794
  gene symbol: PCSK6
  hgvsc: ENST00000557794.1:n.124-84916G>A
  variant of: http://identifiers.org/hgnc/8569
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8862
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1877
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15466
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6034
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3492
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Glu326Lys
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQRankSum

15-101938627-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101938627
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101938627
    reference: chr 15
allele count: 8
allele frequency: 6.716029483369432e-5
allele num: 119118
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000559678
  gene symbol: PCSK6
  hgvsc: ENST00000559678.1:n.1050C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000305056
  ensembl transcript: ENST00000348070
  gene symbol: PCSK6
  hgvsc: ENST00000348070.1:c.975C>T
  hgvsp: ENST00000348070.1:c.975C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000351193
  ensembl transcript: ENST00000358417
  gene symbol: PCSK6
  hgvsc: ENST00000358417.3:c.975C>T
  hgvsp: ENST00000358417.3:c.975C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000332052
  ensembl transcript: ENST00000331826
  gene symbol: PCSK6
  hgvsc: ENST00000331826.7:c.480C>T
  hgvsp: ENST00000331826.7:c.480C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560271
  gene symbol: PCSK6
  hgvsc: ENST00000560271.1:n.1003C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000557794
  gene symbol: PCSK6
  hgvsc: ENST00000557794.1:n.124-84917C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561177
  gene symbol: PCSK6
  hgvsc: ENST00000561177.1:n.1145C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381246
  ensembl transcript: ENST00000398185
  gene symbol: PCSK6
  hgvsc: ENST00000398185.2:c.684C>T
  hgvsp: ENST00000398185.2:c.684C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561109
  gene symbol: PCSK6
  hgvsc: ENST00000561109.1:n.1050C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000558716
  gene symbol: PCSK6
  hgvsc: ENST00000558716.1:n.1003C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381243
  ensembl transcript: ENST00000398181
  gene symbol: PCSK6
  hgvsc: ENST00000398181.2:c.975C>T
  hgvsp: ENST00000398181.2:c.975C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000344410
  ensembl transcript: ENST00000344273
  gene symbol: PCSK6
  hgvsc: ENST00000344273.2:c.975C>T
  hgvsp: ENST00000344273.2:c.975C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560921
  gene symbol: PCSK6
  hgvsc: ENST00000560921.1:n.1050C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561444
  gene symbol: PCSK6
  hgvsc: ENST00000561444.1:n.1145C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000452997
  ensembl transcript: ENST00000559417
  gene symbol: PCSK6
  hgvsc: ENST00000559417.1:c.599C>T
  hgvsp: ENST00000559417.1:c.599C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6186
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 14466
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1877
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5614
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe325Phe
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/15-101938646-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101938646
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101938646
    reference: chr 15
allele count: 1
allele frequency: 8.326810664979099e-6
allele num: 120094
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381243
  ensembl transcript: ENST00000398181
  gene symbol: PCSK6
  hgvsc: ENST00000398181.2:c.956G>T
  hgvsp: ENSP00000381243.2:p.Arg319Leu
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561177
  gene symbol: PCSK6
  hgvsc: ENST00000561177.1:n.1126G>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561444
  gene symbol: PCSK6
  hgvsc: ENST00000561444.1:n.1126G>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560271
  gene symbol: PCSK6
  hgvsc: ENST00000560271.1:n.984G>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561109
  gene symbol: PCSK6
  hgvsc: ENST00000561109.1:n.1031G>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381246
  ensembl transcript: ENST00000398185
  gene symbol: PCSK6
  hgvsc: ENST00000398185.2:c.665G>T
  hgvsp: ENSP00000381246.2:p.Arg222Leu
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000351193
  ensembl transcript: ENST00000358417
  gene symbol: PCSK6
  hgvsc: ENST00000358417.3:c.956G>T
  hgvsp: ENSP00000351193.3:p.Arg319Leu
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000344410
  ensembl transcript: ENST00000344273
  gene symbol: PCSK6
  hgvsc: ENST00000344273.2:c.956G>T
  hgvsp: ENSP00000344410.2:p.Arg319Leu
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000559678
  gene symbol: PCSK6
  hgvsc: ENST00000559678.1:n.1031G>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000558716
  gene symbol: PCSK6
  hgvsc: ENST00000558716.1:n.984G>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000332052
  ensembl transcript: ENST00000331826
  gene symbol: PCSK6
  hgvsc: ENST00000331826.7:c.461G>T
  hgvsp: ENSP00000332052.7:p.Arg154Leu
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000452997
  ensembl transcript: ENST00000559417
  gene symbol: PCSK6
  hgvsc: ENST00000559417.1:c.580G>T
  hgvsp: ENSP00000452997.1:p.Arg194Leu
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000305056
  ensembl transcript: ENST00000348070
  gene symbol: PCSK6
  hgvsc: ENST00000348070.1:c.956G>T
  hgvsp: ENSP00000305056.4:p.Arg319Leu
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000557794
  gene symbol: PCSK6
  hgvsc: ENST00000557794.1:n.124-84936G>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560921
  gene symbol: PCSK6
  hgvsc: ENST00000560921.1:n.1031G>T
  variant of: http://identifiers.org/hgnc/8569
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3475
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16052
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6485
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14580
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8858
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg319Leu
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: QD
site quality: BaseQRankSum

15-101938646-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101938646
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101938646
    reference: chr 15
allele count: 2
allele frequency: 1.66536213299582e-5
allele num: 120094
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381243
  ensembl transcript: ENST00000398181
  gene symbol: PCSK6
  hgvsc: ENST00000398181.2:c.956G>A
  hgvsp: ENSP00000381243.2:p.Arg319Gln
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000557794
  gene symbol: PCSK6
  hgvsc: ENST00000557794.1:n.124-84936G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560921
  gene symbol: PCSK6
  hgvsc: ENST00000560921.1:n.1031G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000305056
  ensembl transcript: ENST00000348070
  gene symbol: PCSK6
  hgvsc: ENST00000348070.1:c.956G>A
  hgvsp: ENSP00000305056.4:p.Arg319Gln
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000452997
  ensembl transcript: ENST00000559417
  gene symbol: PCSK6
  hgvsc: ENST00000559417.1:c.580G>A
  hgvsp: ENSP00000452997.1:p.Arg194Gln
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561177
  gene symbol: PCSK6
  hgvsc: ENST00000561177.1:n.1126G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000351193
  ensembl transcript: ENST00000358417
  gene symbol: PCSK6
  hgvsc: ENST00000358417.3:c.956G>A
  hgvsp: ENSP00000351193.3:p.Arg319Gln
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000344410
  ensembl transcript: ENST00000344273
  gene symbol: PCSK6
  hgvsc: ENST00000344273.2:c.956G>A
  hgvsp: ENSP00000344410.2:p.Arg319Gln
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561109
  gene symbol: PCSK6
  hgvsc: ENST00000561109.1:n.1031G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381246
  ensembl transcript: ENST00000398185
  gene symbol: PCSK6
  hgvsc: ENST00000398185.2:c.665G>A
  hgvsp: ENSP00000381246.2:p.Arg222Gln
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560271
  gene symbol: PCSK6
  hgvsc: ENST00000560271.1:n.984G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000332052
  ensembl transcript: ENST00000331826
  gene symbol: PCSK6
  hgvsc: ENST00000331826.7:c.461G>A
  hgvsp: ENSP00000332052.7:p.Arg154Gln
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000558716
  gene symbol: PCSK6
  hgvsc: ENST00000558716.1:n.984G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000559678
  gene symbol: PCSK6
  hgvsc: ENST00000559678.1:n.1031G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561444
  gene symbol: PCSK6
  hgvsc: ENST00000561444.1:n.1126G>A
  variant of: http://identifiers.org/hgnc/8569
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6485
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5595
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3475
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14580
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8858
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1864
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg319Gln
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: African
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

15-101938647-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101938647
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101938647
    reference: chr 15
allele count: 4
allele frequency: 3.328119279794988e-5
allele num: 120188
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000344410
  ensembl transcript: ENST00000344273
  gene symbol: PCSK6
  hgvsc: ENST00000344273.2:c.955C>T
  hgvsp: ENSP00000344410.2:p.Arg319Ter
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561109
  gene symbol: PCSK6
  hgvsc: ENST00000561109.1:n.1030C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000332052
  ensembl transcript: ENST00000331826
  gene symbol: PCSK6
  hgvsc: ENST00000331826.7:c.460C>T
  hgvsp: ENSP00000332052.7:p.Arg154Ter
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000305056
  ensembl transcript: ENST00000348070
  gene symbol: PCSK6
  hgvsc: ENST00000348070.1:c.955C>T
  hgvsp: ENSP00000305056.4:p.Arg319Ter
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561177
  gene symbol: PCSK6
  hgvsc: ENST00000561177.1:n.1125C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560921
  gene symbol: PCSK6
  hgvsc: ENST00000560921.1:n.1030C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000557794
  gene symbol: PCSK6
  hgvsc: ENST00000557794.1:n.124-84937C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381243
  ensembl transcript: ENST00000398181
  gene symbol: PCSK6
  hgvsc: ENST00000398181.2:c.955C>T
  hgvsp: ENSP00000381243.2:p.Arg319Ter
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000351193
  ensembl transcript: ENST00000358417
  gene symbol: PCSK6
  hgvsc: ENST00000358417.3:c.955C>T
  hgvsp: ENSP00000351193.3:p.Arg319Ter
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561444
  gene symbol: PCSK6
  hgvsc: ENST00000561444.1:n.1125C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381246
  ensembl transcript: ENST00000398185
  gene symbol: PCSK6
  hgvsc: ENST00000398185.2:c.664C>T
  hgvsp: ENSP00000381246.2:p.Arg222Ter
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000452997
  ensembl transcript: ENST00000559417
  gene symbol: PCSK6
  hgvsc: ENST00000559417.1:c.579C>T
  hgvsp: ENSP00000452997.1:p.Arg194Ter
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560271
  gene symbol: PCSK6
  hgvsc: ENST00000560271.1:n.983C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000559678
  gene symbol: PCSK6
  hgvsc: ENST00000559678.1:n.1030C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000558716
  gene symbol: PCSK6
  hgvsc: ENST00000558716.1:n.983C>T
  variant of: http://identifiers.org/hgnc/8569
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5596
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14558
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16108
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg319Ter
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
reference allele: G
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

15-101938651-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101938651
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101938651
    reference: chr 15
allele count: 14
allele frequency: 1.163177135260884e-4
allele num: 120360
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000351193
  ensembl transcript: ENST00000358417
  gene symbol: PCSK6
  hgvsc: ENST00000358417.3:c.951C>T
  hgvsp: ENST00000358417.3:c.951C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000557794
  gene symbol: PCSK6
  hgvsc: ENST00000557794.1:n.124-84941C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000559678
  gene symbol: PCSK6
  hgvsc: ENST00000559678.1:n.1026C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560271
  gene symbol: PCSK6
  hgvsc: ENST00000560271.1:n.979C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000558716
  gene symbol: PCSK6
  hgvsc: ENST00000558716.1:n.979C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560921
  gene symbol: PCSK6
  hgvsc: ENST00000560921.1:n.1026C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381246
  ensembl transcript: ENST00000398185
  gene symbol: PCSK6
  hgvsc: ENST00000398185.2:c.660C>T
  hgvsp: ENST00000398185.2:c.660C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000332052
  ensembl transcript: ENST00000331826
  gene symbol: PCSK6
  hgvsc: ENST00000331826.7:c.456C>T
  hgvsp: ENST00000331826.7:c.456C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381243
  ensembl transcript: ENST00000398181
  gene symbol: PCSK6
  hgvsc: ENST00000398181.2:c.951C>T
  hgvsp: ENST00000398181.2:c.951C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000344410
  ensembl transcript: ENST00000344273
  gene symbol: PCSK6
  hgvsc: ENST00000344273.2:c.951C>T
  hgvsp: ENST00000344273.2:c.951C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000452997
  ensembl transcript: ENST00000559417
  gene symbol: PCSK6
  hgvsc: ENST00000559417.1:c.575C>T
  hgvsp: ENST00000559417.1:c.575C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561177
  gene symbol: PCSK6
  hgvsc: ENST00000561177.1:n.1121C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561444
  gene symbol: PCSK6
  hgvsc: ENST00000561444.1:n.1121C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000305056
  ensembl transcript: ENST00000348070
  gene symbol: PCSK6
  hgvsc: ENST00000348070.1:c.951C>T
  hgvsp: ENST00000348070.1:c.951C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561109
  gene symbol: PCSK6
  hgvsc: ENST00000561109.1:n.1026C>T
  variant of: http://identifiers.org/hgnc/8569
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6540
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8853
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5595
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1864
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3471
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14585
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro317Pro
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: Latino
reference allele: G
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

15-101938656-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101938656
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101938656
    reference: chr 15
allele count: 1
allele frequency: 8.299995020002988e-6
allele num: 120482
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000557794
  gene symbol: PCSK6
  hgvsc: ENST00000557794.1:n.124-84946G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000452997
  ensembl transcript: ENST00000559417
  gene symbol: PCSK6
  hgvsc: ENST00000559417.1:c.570G>A
  hgvsp: ENSP00000452997.1:p.Gly191Arg
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000332052
  ensembl transcript: ENST00000331826
  gene symbol: PCSK6
  hgvsc: ENST00000331826.7:c.451G>A
  hgvsp: ENSP00000332052.7:p.Gly151Arg
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560271
  gene symbol: PCSK6
  hgvsc: ENST00000560271.1:n.974G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381243
  ensembl transcript: ENST00000398181
  gene symbol: PCSK6
  hgvsc: ENST00000398181.2:c.946G>A
  hgvsp: ENSP00000381243.2:p.Gly316Arg
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000559678
  gene symbol: PCSK6
  hgvsc: ENST00000559678.1:n.1021G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561177
  gene symbol: PCSK6
  hgvsc: ENST00000561177.1:n.1116G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000351193
  ensembl transcript: ENST00000358417
  gene symbol: PCSK6
  hgvsc: ENST00000358417.3:c.946G>A
  hgvsp: ENSP00000351193.3:p.Gly316Arg
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561444
  gene symbol: PCSK6
  hgvsc: ENST00000561444.1:n.1116G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560921
  gene symbol: PCSK6
  hgvsc: ENST00000560921.1:n.1021G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000344410
  ensembl transcript: ENST00000344273
  gene symbol: PCSK6
  hgvsc: ENST00000344273.2:c.946G>A
  hgvsp: ENSP00000344410.2:p.Gly316Arg
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561109
  gene symbol: PCSK6
  hgvsc: ENST00000561109.1:n.1021G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000558716
  gene symbol: PCSK6
  hgvsc: ENST00000558716.1:n.974G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000305056
  ensembl transcript: ENST00000348070
  gene symbol: PCSK6
  hgvsc: ENST00000348070.1:c.946G>A
  hgvsp: ENSP00000305056.4:p.Gly316Arg
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381246
  ensembl transcript: ENST00000398185
  gene symbol: PCSK6
  hgvsc: ENST00000398185.2:c.655G>A
  hgvsp: ENSP00000381246.2:p.Gly219Arg
  variant of: http://identifiers.org/hgnc/8569
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16289
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14604
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5591
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8857
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6552
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Gly316Arg
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

15-101938657-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101938657
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101938657
    reference: chr 15
allele count: 7
allele frequency: 5.807875479149727e-5
allele num: 120526
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381243
  ensembl transcript: ENST00000398181
  gene symbol: PCSK6
  hgvsc: ENST00000398181.2:c.945C>T
  hgvsp: ENST00000398181.2:c.945C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560921
  gene symbol: PCSK6
  hgvsc: ENST00000560921.1:n.1020C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000452997
  ensembl transcript: ENST00000559417
  gene symbol: PCSK6
  hgvsc: ENST00000559417.1:c.569C>T
  hgvsp: ENST00000559417.1:c.569C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000559678
  gene symbol: PCSK6
  hgvsc: ENST00000559678.1:n.1020C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000332052
  ensembl transcript: ENST00000331826
  gene symbol: PCSK6
  hgvsc: ENST00000331826.7:c.450C>T
  hgvsp: ENST00000331826.7:c.450C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000558716
  gene symbol: PCSK6
  hgvsc: ENST00000558716.1:n.973C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381246
  ensembl transcript: ENST00000398185
  gene symbol: PCSK6
  hgvsc: ENST00000398185.2:c.654C>T
  hgvsp: ENST00000398185.2:c.654C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561109
  gene symbol: PCSK6
  hgvsc: ENST00000561109.1:n.1020C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561177
  gene symbol: PCSK6
  hgvsc: ENST00000561177.1:n.1115C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000344410
  ensembl transcript: ENST00000344273
  gene symbol: PCSK6
  hgvsc: ENST00000344273.2:c.945C>T
  hgvsp: ENST00000344273.2:c.945C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000305056
  ensembl transcript: ENST00000348070
  gene symbol: PCSK6
  hgvsc: ENST00000348070.1:c.945C>T
  hgvsp: ENST00000348070.1:c.945C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000351193
  ensembl transcript: ENST00000358417
  gene symbol: PCSK6
  hgvsc: ENST00000358417.3:c.945C>T
  hgvsp: ENST00000358417.3:c.945C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560271
  gene symbol: PCSK6
  hgvsc: ENST00000560271.1:n.973C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561444
  gene symbol: PCSK6
  hgvsc: ENST00000561444.1:n.1115C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000557794
  gene symbol: PCSK6
  hgvsc: ENST00000557794.1:n.124-84947C>T
  variant of: http://identifiers.org/hgnc/8569
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14603
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6574
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8858
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp315Asp
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: DP

15-101938663-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101938663
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101938663
    reference: chr 15
allele count: 7
allele frequency: 5.80286827489016e-5
allele num: 120630
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560921
  gene symbol: PCSK6
  hgvsc: ENST00000560921.1:n.1014G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381243
  ensembl transcript: ENST00000398181
  gene symbol: PCSK6
  hgvsc: ENST00000398181.2:c.939G>A
  hgvsp: ENST00000398181.2:c.939G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000305056
  ensembl transcript: ENST00000348070
  gene symbol: PCSK6
  hgvsc: ENST00000348070.1:c.939G>A
  hgvsp: ENST00000348070.1:c.939G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560271
  gene symbol: PCSK6
  hgvsc: ENST00000560271.1:n.967G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000558716
  gene symbol: PCSK6
  hgvsc: ENST00000558716.1:n.967G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000452997
  ensembl transcript: ENST00000559417
  gene symbol: PCSK6
  hgvsc: ENST00000559417.1:c.563G>A
  hgvsp: ENST00000559417.1:c.563G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000559678
  gene symbol: PCSK6
  hgvsc: ENST00000559678.1:n.1014G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000351193
  ensembl transcript: ENST00000358417
  gene symbol: PCSK6
  hgvsc: ENST00000358417.3:c.939G>A
  hgvsp: ENST00000358417.3:c.939G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561444
  gene symbol: PCSK6
  hgvsc: ENST00000561444.1:n.1109G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561177
  gene symbol: PCSK6
  hgvsc: ENST00000561177.1:n.1109G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561109
  gene symbol: PCSK6
  hgvsc: ENST00000561109.1:n.1014G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000557794
  gene symbol: PCSK6
  hgvsc: ENST00000557794.1:n.124-84953G>A
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381246
  ensembl transcript: ENST00000398185
  gene symbol: PCSK6
  hgvsc: ENST00000398185.2:c.648G>A
  hgvsp: ENST00000398185.2:c.648G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000344410
  ensembl transcript: ENST00000344273
  gene symbol: PCSK6
  hgvsc: ENST00000344273.2:c.939G>A
  hgvsp: ENST00000344273.2:c.939G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000332052
  ensembl transcript: ENST00000331826
  gene symbol: PCSK6
  hgvsc: ENST00000331826.7:c.444G>A
  hgvsp: ENST00000331826.7:c.444G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14609
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5590
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3471
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6624
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16351
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8857
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Thr313Thr
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP

15-101938664-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101938664
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101938664
    reference: chr 15
allele count: 2
allele frequency: 1.657797450307521e-5
allele num: 120642
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000558716
  gene symbol: PCSK6
  hgvsc: ENST00000558716.1:n.966C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000351193
  ensembl transcript: ENST00000358417
  gene symbol: PCSK6
  hgvsc: ENST00000358417.3:c.938C>T
  hgvsp: ENSP00000351193.3:p.Thr313Met
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381243
  ensembl transcript: ENST00000398181
  gene symbol: PCSK6
  hgvsc: ENST00000398181.2:c.938C>T
  hgvsp: ENSP00000381243.2:p.Thr313Met
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000305056
  ensembl transcript: ENST00000348070
  gene symbol: PCSK6
  hgvsc: ENST00000348070.1:c.938C>T
  hgvsp: ENSP00000305056.4:p.Thr313Met
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000344410
  ensembl transcript: ENST00000344273
  gene symbol: PCSK6
  hgvsc: ENST00000344273.2:c.938C>T
  hgvsp: ENSP00000344410.2:p.Thr313Met
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561109
  gene symbol: PCSK6
  hgvsc: ENST00000561109.1:n.1013C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000452997
  ensembl transcript: ENST00000559417
  gene symbol: PCSK6
  hgvsc: ENST00000559417.1:c.562C>T
  hgvsp: ENSP00000452997.1:p.Thr188Met
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000332052
  ensembl transcript: ENST00000331826
  gene symbol: PCSK6
  hgvsc: ENST00000331826.7:c.443C>T
  hgvsp: ENSP00000332052.7:p.Thr148Met
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000559678
  gene symbol: PCSK6
  hgvsc: ENST00000559678.1:n.1013C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561444
  gene symbol: PCSK6
  hgvsc: ENST00000561444.1:n.1108C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000557794
  gene symbol: PCSK6
  hgvsc: ENST00000557794.1:n.124-84954C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560921
  gene symbol: PCSK6
  hgvsc: ENST00000560921.1:n.1013C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381246
  ensembl transcript: ENST00000398185
  gene symbol: PCSK6
  hgvsc: ENST00000398185.2:c.647C>T
  hgvsp: ENSP00000381246.2:p.Thr216Met
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561177
  gene symbol: PCSK6
  hgvsc: ENST00000561177.1:n.1108C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560271
  gene symbol: PCSK6
  hgvsc: ENST00000560271.1:n.966C>T
  variant of: http://identifiers.org/hgnc/8569
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5589
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6630
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3472
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14617
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Thr313Met
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP

15-101938669-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101938669
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101938669
    reference: chr 15
allele count: 1
allele frequency: 8.285553309249991e-6
allele num: 120692
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381246
  ensembl transcript: ENST00000398185
  gene symbol: PCSK6
  hgvsc: ENST00000398185.2:c.642C>T
  hgvsp: ENST00000398185.2:c.642C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000558716
  gene symbol: PCSK6
  hgvsc: ENST00000558716.1:n.961C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561109
  gene symbol: PCSK6
  hgvsc: ENST00000561109.1:n.1008C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000305056
  ensembl transcript: ENST00000348070
  gene symbol: PCSK6
  hgvsc: ENST00000348070.1:c.933C>T
  hgvsp: ENST00000348070.1:c.933C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560271
  gene symbol: PCSK6
  hgvsc: ENST00000560271.1:n.961C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000452997
  ensembl transcript: ENST00000559417
  gene symbol: PCSK6
  hgvsc: ENST00000559417.1:c.557C>T
  hgvsp: ENST00000559417.1:c.557C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000332052
  ensembl transcript: ENST00000331826
  gene symbol: PCSK6
  hgvsc: ENST00000331826.7:c.438C>T
  hgvsp: ENST00000331826.7:c.438C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561177
  gene symbol: PCSK6
  hgvsc: ENST00000561177.1:n.1103C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381243
  ensembl transcript: ENST00000398181
  gene symbol: PCSK6
  hgvsc: ENST00000398181.2:c.933C>T
  hgvsp: ENST00000398181.2:c.933C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000351193
  ensembl transcript: ENST00000358417
  gene symbol: PCSK6
  hgvsc: ENST00000358417.3:c.933C>T
  hgvsp: ENST00000358417.3:c.933C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561444
  gene symbol: PCSK6
  hgvsc: ENST00000561444.1:n.1103C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000557794
  gene symbol: PCSK6
  hgvsc: ENST00000557794.1:n.124-84959C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000344410
  ensembl transcript: ENST00000344273
  gene symbol: PCSK6
  hgvsc: ENST00000344273.2:c.933C>T
  hgvsp: ENST00000344273.2:c.933C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000559678
  gene symbol: PCSK6
  hgvsc: ENST00000559678.1:n.1008C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560921
  gene symbol: PCSK6
  hgvsc: ENST00000560921.1:n.1008C>T
  variant of: http://identifiers.org/hgnc/8569
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3472
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1862
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16361
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14618
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6661
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly311Gly
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

15-101938672-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101938672
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101938672
    reference: chr 15
allele count: 19
allele frequency: 1.574098621420997e-4
allele num: 120704
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381243
  ensembl transcript: ENST00000398181
  gene symbol: PCSK6
  hgvsc: ENST00000398181.2:c.930C>T
  hgvsp: ENST00000398181.2:c.930C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000381246
  ensembl transcript: ENST00000398185
  gene symbol: PCSK6
  hgvsc: ENST00000398185.2:c.639C>T
  hgvsp: ENST00000398185.2:c.639C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000452997
  ensembl transcript: ENST00000559417
  gene symbol: PCSK6
  hgvsc: ENST00000559417.1:c.554C>T
  hgvsp: ENST00000559417.1:c.554C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560271
  gene symbol: PCSK6
  hgvsc: ENST00000560271.1:n.958C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000351193
  ensembl transcript: ENST00000358417
  gene symbol: PCSK6
  hgvsc: ENST00000358417.3:c.930C>T
  hgvsp: ENST00000358417.3:c.930C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000332052
  ensembl transcript: ENST00000331826
  gene symbol: PCSK6
  hgvsc: ENST00000331826.7:c.435C>T
  hgvsp: ENST00000331826.7:c.435C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000557794
  gene symbol: PCSK6
  hgvsc: ENST00000557794.1:n.124-84962C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000344410
  ensembl transcript: ENST00000344273
  gene symbol: PCSK6
  hgvsc: ENST00000344273.2:c.930C>T
  hgvsp: ENST00000344273.2:c.930C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561177
  gene symbol: PCSK6
  hgvsc: ENST00000561177.1:n.1100C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561444
  gene symbol: PCSK6
  hgvsc: ENST00000561444.1:n.1100C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000559678
  gene symbol: PCSK6
  hgvsc: ENST00000559678.1:n.1005C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000305056
  ensembl transcript: ENST00000348070
  gene symbol: PCSK6
  hgvsc: ENST00000348070.1:c.930C>T
  hgvsp: ENST00000348070.1:c.930C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000561109
  gene symbol: PCSK6
  hgvsc: ENST00000561109.1:n.1005C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560921
  gene symbol: PCSK6
  hgvsc: ENST00000560921.1:n.1005C>T
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000558716
  gene symbol: PCSK6
  hgvsc: ENST00000558716.1:n.958C>T
  variant of: http://identifiers.org/hgnc/8569
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6671
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14622
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16362
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8859
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3470
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp310Asp
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: VQSLOD

15-101938674-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 101938674
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 101938674
    reference: chr 15
allele count: 1
allele frequency: 8.284592315212168e-6
allele num: 120706
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140479
  ensembl protein: ENSP00000332052
  ensembl transcript: ENST00000331826
  gene symbol: PCSK6
  hgvsc: ENST00000331826.7:c.433G>A
  hgvsp: ENSP00000332052.7:p.Asp145Asn
  variant of: http://identifiers.org/hgnc/8569
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140479
  ensembl transcript: ENST00000560271
  gene symbol: PCSK6
  hgvsc: ENST00000560271.1:n.956G>A
  variant of: http://identifiers.org/hgnc/8569
canonical: true
consequence: missense
filter: PASS
hgvs: p.Asp310Asn
num of homozygotes: 0
reference allele: C

GenotypeDepth
all individuals: 1
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 222
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 126
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 927
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 52
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4666
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 339
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 326
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 334
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 1.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
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allele frequency: 0.0e0
allele num: 9922
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 6.361323155216285e-5
allele num: 15720
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66206
num of homozygotes: 0

DP
type: SiteQuality
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ReadPosRankSum
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InbreedingCoeff
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ClippingRankSum
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BaseQRankSum
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FS
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MQRankSum
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QD
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MQ
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66204
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9930
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele frequency: 6.370238246910434e-5
allele num: 15698
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VQSLOD
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DP
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ReadPosRankSum
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FS
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MQRankSum
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MQ
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele frequency: 0.0e0
allele num: 886
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.156604210039325e-4
allele num: 8646
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10032
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66236
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

BaseQRankSum
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SIO_000300: -2.516e0

MQ
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ReadPosRankSum
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SIO_000300: 1.82e0

FS
type: SiteQuality
SIO_000300: 1.0456e1

ClippingRankSum
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MQRankSum
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VQSLOD
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InbreedingCoeff
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QD
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DP
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SIO_000300: 1.416765e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11500
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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South Asian
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allele count: 0
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African
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allele count: 5
allele frequency: 4.970178926441351e-4
allele num: 10060
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

ClippingRankSum
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InbreedingCoeff
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BaseQRankSum
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VQSLOD
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DP
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ReadPosRankSum
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MQ
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FS
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MQRankSum
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QD
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.510026576467746e-5
allele num: 66224
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East Asian
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Latino
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African
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European (Finnish)
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Other
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South Asian
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BaseQRankSum
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MQ
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MQRankSum
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VQSLOD
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FS
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ClippingRankSum
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DP
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ReadPosRankSum
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InbreedingCoeff
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele num: 15586
num of homozygotes: 0

East Asian
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European (Non-Finnish)
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Latino
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African
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European (Finnish)
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Other
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MQ
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BaseQRankSum
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InbreedingCoeff
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MQRankSum
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DP
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FS
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ClippingRankSum
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VQSLOD
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QD
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 4.336513443191674e-4
allele num: 11530
num of homozygotes: 0

African
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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South Asian
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allele count: 22
allele frequency: 1.412248042110669e-3
allele num: 15578
num of homozygotes: 0

European (Non-Finnish)
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allele count: 4
allele frequency: 6.037006852002777e-5
allele num: 66258
num of homozygotes: 0

QD
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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VQSLOD
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FS
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DP
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InbreedingCoeff
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ReadPosRankSum
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 1.509297271190534e-5
allele num: 66256
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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South Asian
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Other
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ClippingRankSum
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InbreedingCoeff
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QD
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VQSLOD
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ReadPosRankSum
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FS
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MQ
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MQRankSum
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BaseQRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 1
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allele num: 66268
num of homozygotes: 0

Latino
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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African
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Other
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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ReadPosRankSum
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VQSLOD
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ClippingRankSum
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DP
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MQRankSum
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QD
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FS
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InbreedingCoeff
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MQ
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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East Asian
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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European (Finnish)
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South Asian
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European (Non-Finnish)
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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DP
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ClippingRankSum
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VQSLOD
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QD
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FS
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MQ
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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East Asian
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African
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European (Finnish)
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European (Non-Finnish)
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South Asian
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VQSLOD
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DP
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FS
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ClippingRankSum
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MQRankSum
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MQ
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InbreedingCoeff
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ReadPosRankSum
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BaseQRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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South Asian
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European (Finnish)
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Latino
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East Asian
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Other
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European (Non-Finnish)
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MQ
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FS
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DP
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QD
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ReadPosRankSum
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BaseQRankSum
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MQRankSum
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 355
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 5.75e1
variant carriers: 0

African
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allele count: 1
allele frequency: 9.828975820719482e-5
allele num: 10174
num of homozygotes: 0

East Asian
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allele count: 6
allele frequency: 6.938020351526364e-4
allele num: 8648
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15070
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.511898642315019e-5
allele num: 66142
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11544
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 880
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 6.05e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.54e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.17e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 5.961e0

DP
type: SiteQuality
SIO_000300: 1.40043e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.64e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.0e-2

QD
type: SiteQuality
SIO_000300: 1.385e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.75e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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variant carriers: 3

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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variant carriers: 5

GenotypeDepth
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variant carriers: 7

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 31

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 352
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14994
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10164
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 880
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11544
num of homozygotes: 0

East Asian
type: Population
allele count: 31
allele frequency: 3.583815028901734e-3
allele num: 8650
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.512630464377553e-5
allele num: 66110
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.399349e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.81e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.41e0

BaseQRankSum
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SIO_000300: -3.92e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.0e-3

QD
type: SiteQuality
SIO_000300: 1.207e1

ClippingRankSum
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SIO_000300: -2.07e-1

FS
type: SiteQuality
SIO_000300: 2.45e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.18e-1

MQ
type: SiteQuality
SIO_000300: 5.961e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 880
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66108
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.664009703690868e-5
allele num: 11542
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.664889362836577e-5
allele num: 15004
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.83671060397403e-5
allele num: 10166
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 8.02e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.397642e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.62e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.7e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.53e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.8e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.6e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.201e1

GenotypeDepth
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bin: 2.5e0
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14664
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 876
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11546
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10036
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.5148760831364e-5
allele num: 66012
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 6.76e-1

QD
type: SiteQuality
SIO_000300: 1.073e1

FS
type: SiteQuality
SIO_000300: 2.177e0

MQ
type: SiteQuality
SIO_000300: 5.951e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.9e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.12e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.6e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.19e-1

DP
type: SiteQuality
SIO_000300: 1.387971e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.78e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 1280
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 876
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11546
num of homozygotes: 0

African
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allele count: 1
allele frequency: 9.952229299363058e-5
allele num: 10048
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14670
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.029660375071954e-5
allele num: 66014
num of homozygotes: 0

VQSLOD
type: SiteQuality
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QD
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SIO_000300: 1.343e1

DP
type: SiteQuality
SIO_000300: 1.387997e6

BaseQRankSum
type: SiteQuality
SIO_000300: 5.33e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 3.9e-1

FS
type: SiteQuality
SIO_000300: 3.787e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.83e-1

MQ
type: SiteQuality
SIO_000300: 6.075e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.42e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11538
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.005631536604988e-4
allele num: 9944
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8644
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65926
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.943480072212192e-5
allele num: 14402
num of homozygotes: 0

MQRankSum
type: SiteQuality
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InbreedingCoeff
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FS
type: SiteQuality
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VQSLOD
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DP
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ReadPosRankSum
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MQ
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ClippingRankSum
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BaseQRankSum
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SIO_000300: -2.068e0

QD
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SIO_000300: 9.789999999999999e0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11536
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 6.993006993006993e-5
allele num: 14300
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9928
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65882
num of homozygotes: 0

InbreedingCoeff
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SIO_000300: -1.1e-3

QD
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MQRankSum
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MQ
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VQSLOD
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FS
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ReadPosRankSum
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BaseQRankSum
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SIO_000300: 8.2e-2

ClippingRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.519248883352071e-5
allele num: 65822
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11524
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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Other
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FS
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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DP
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MQRankSum
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QD
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ReadPosRankSum
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InbreedingCoeff
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MQ
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GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11522
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.519110408944522e-5
allele num: 65828
num of homozygotes: 0

QD
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SIO_000300: 1.168e1

VQSLOD
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SIO_000300: -1.073e-1

BaseQRankSum
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SIO_000300: -8.64e-1

ClippingRankSum
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DP
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SIO_000300: 1.378853e6

MQRankSum
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ReadPosRankSum
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FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
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SIO_000300: -5.999999999999999e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele frequency: 7.119464616260858e-5
allele num: 14046
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele count: 1
allele frequency: 1.019367991845056e-4
allele num: 9810
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65786
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

QD
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VQSLOD
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BaseQRankSum
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FS
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InbreedingCoeff
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MQRankSum
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MQ
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ReadPosRankSum
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ClippingRankSum
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DP
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 0
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East Asian
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allele frequency: 1.157407407407407e-4
allele num: 8640
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Latino
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allele count: 0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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South Asian
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Other
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European (Finnish)
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InbreedingCoeff
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ClippingRankSum
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MQ
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VQSLOD
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BaseQRankSum
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FS
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MQRankSum
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DP
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ReadPosRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Non-Finnish)
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allele num: 65720
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European (Finnish)
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Latino
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Other
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East Asian
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South Asian
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MQRankSum
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DP
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ReadPosRankSum
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MQ
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InbreedingCoeff
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BaseQRankSum
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FS
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VQSLOD
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ClippingRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele count: 0
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num of homozygotes: 0

South Asian
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African
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allele count: 1
allele frequency: 1.023960679909891e-4
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European (Non-Finnish)
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

BaseQRankSum
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SIO_000300: -9.370000000000001e-1

ClippingRankSum
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SIO_000300: 1.5e-2

FS
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MQ
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VQSLOD
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DP
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MQRankSum
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ReadPosRankSum
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QD
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InbreedingCoeff
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SIO_000300: -1.3e-3

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11498
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.157139551029854e-4
allele num: 8642
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

BaseQRankSum
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SIO_000300: -3.602e0

ClippingRankSum
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InbreedingCoeff
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MQ
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SIO_000300: 5.97e1

ReadPosRankSum
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MQRankSum
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VQSLOD
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QD
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FS
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 13818
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 858
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65532
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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East Asian
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allele count: 1
allele frequency: 1.158211721102618e-4
allele num: 8634
num of homozygotes: 0

QD
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SIO_000300: 9.789999999999999e0

MQ
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SIO_000300: 5.682e1

VQSLOD
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SIO_000300: -2.015e0

BaseQRankSum
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SIO_000300: -3.378e0

MQRankSum
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SIO_000300: -2.0e-2

ReadPosRankSum
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SIO_000300: 2.06e0

FS
type: SiteQuality
SIO_000300: 6.062e0

InbreedingCoeff
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SIO_000300: -1.3e-3

ClippingRankSum
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SIO_000300: -2.339e0

DP
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SIO_000300: 1.369857e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

East Asian
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allele count: 1
allele frequency: 1.190759704691593e-4
allele num: 8398
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64090
num of homozygotes: 0

South Asian
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ClippingRankSum
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ReadPosRankSum
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InbreedingCoeff
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DP
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MQRankSum
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VQSLOD
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MQ
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BaseQRankSum
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SIO_000300: 1.04e0

FS
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SIO_000300: 9.94e-1

QD
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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South Asian
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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Other
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European (Non-Finnish)
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allele frequency: 1.564504521418067e-5
allele num: 63918
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ClippingRankSum
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InbreedingCoeff
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MQ
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FS
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QD
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BaseQRankSum
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VQSLOD
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MQRankSum
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ReadPosRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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num of homozygotes: 0

East Asian
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allele frequency: 2.392916965781287e-4
allele num: 8358
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Latino
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European (Non-Finnish)
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European (Finnish)
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Other
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South Asian
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InbreedingCoeff
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VQSLOD
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MQ
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BaseQRankSum
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DP
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ClippingRankSum
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MQRankSum
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FS
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ReadPosRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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Latino
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African
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East Asian
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European (Non-Finnish)
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European (Finnish)
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South Asian
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MQRankSum
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QD
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VQSLOD
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BaseQRankSum
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MQ
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SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.12e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.4e-3

FS
type: SiteQuality
SIO_000300: 2.153e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.32e-1

DP
type: SiteQuality
SIO_000300: 1.214679e6

GenotypeDepth
all individuals: 124
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variant carriers: 4

GenotypeDepth
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bin: 9.25e1
variant carriers: 0

GenotypeDepth
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variant carriers: 42

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 22

GenotypeDepth
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GenotypeDepth
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variant carriers: 14

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 222

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
all individuals: 580
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GenotypeQuality
all individuals: 112
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 229
allele frequency: 2.771725974340353e-2
allele num: 8262
num of homozygotes: 4

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63232
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9064
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6496
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11124
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.540120129370091e-4
allele num: 12986
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 814
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.6e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.45e-1

DP
type: SiteQuality
SIO_000300: 1.179665e6

QD
type: SiteQuality
SIO_000300: 1.351e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.4e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-3

VQSLOD
type: SiteQuality
SIO_000300: 5.87e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.876e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 533
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GenotypeQuality
all individuals: 112
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8202
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62854
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.74233508826262e-5
allele num: 12916
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9008
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11086
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 808
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6478
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 7.3e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.6e-3

DP
type: SiteQuality
SIO_000300: 1.151144e6

FS
type: SiteQuality
SIO_000300: 3.01e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.46e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.25e0

QD
type: SiteQuality
SIO_000300: 1.579e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.1e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.29e-1

GenotypeDepth
all individuals: 7680
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variant carriers: 2

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1405
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variant carriers: 0

GenotypeQuality
all individuals: 533
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11086
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9008
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 808
num of homozygotes: 0

East Asian
type: Population
allele count: 5
allele frequency: 6.0960741282614e-4
allele num: 8202
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.74233508826262e-5
allele num: 12916
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.590988640341108e-5
allele num: 62854
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6478
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 7.3e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.6e-3

QD
type: SiteQuality
SIO_000300: 1.579e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.29e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.25e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.46e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 3.01e0

DP
type: SiteQuality
SIO_000300: 1.151144e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.1e0

GenotypeDepth
all individuals: 4
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variant carriers: 0

GenotypeDepth
all individuals: 22907
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variant carriers: 16

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 477
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GenotypeQuality
all individuals: 113
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variant carriers: 1

Latino
type: Population
allele count: 1
allele frequency: 9.061254077564335e-5
allele num: 11036
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 80
allele frequency: 1.274331772276912e-3
allele num: 62778
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 12
allele frequency: 1.850138760407031e-3
allele num: 6486
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.221001221001221e-4
allele num: 8190
num of homozygotes: 0

African
type: Population
allele count: 4
allele frequency: 4.452359750667854e-4
allele num: 8984
num of homozygotes: 0

South Asian
type: Population
allele count: 9
allele frequency: 7.011530071673418e-4
allele num: 12836
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 804
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BaseQRankSum
type: SiteQuality
SIO_000300: -2.752e0

DP
type: SiteQuality
SIO_000300: 1.151378e6

MQRankSum
type: SiteQuality
SIO_000300: 4.9e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.301e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.48e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 5.3e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.5e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.4e-3

GenotypeDepth
all individuals: 14
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variant carriers: 0

GenotypeDepth
all individuals: 4
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variant carriers: 0

GenotypeDepth
all individuals: 4014
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GenotypeDepth
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GenotypeDepth
all individuals: 6
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GenotypeDepth
all individuals: 28
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GenotypeDepth
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GenotypeDepth
all individuals: 2
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GenotypeQuality
all individuals: 231
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8194
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 22
allele frequency: 3.390875462392108e-3
allele num: 6488
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11062
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 36
allele frequency: 5.735589331803843e-4
allele num: 62766
num of homozygotes: 1

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8972
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.240694789081886e-3
allele num: 806
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12832
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

VQSLOD
type: SiteQuality
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DP
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -3.9e-2

QD
type: SiteQuality
SIO_000300: 1.242e1

BaseQRankSum
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ReadPosRankSum
type: SiteQuality
SIO_000300: -4.3e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 2.83e-1

GenotypeDepth
all individuals: 28
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variant carriers: 0

GenotypeDepth
all individuals: 2
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 439
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GenotypeQuality
all individuals: 112
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GenotypeQuality
all individuals: 258
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 800
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10830
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8010
num of homozygotes: 0

African
type: Population
allele count: 4
allele frequency: 4.564125969876769e-4
allele num: 8764
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6444
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12388
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.62813415825464e-5
allele num: 61420
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.5e-3

DP
type: SiteQuality
SIO_000300: 1.082999e6

BaseQRankSum
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QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -2.7e-1

VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 4.77e-1

GenotypeDepth
all individuals: 28
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variant carriers: 0

GenotypeDepth
all individuals: 118
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GenotypeDepth
all individuals: 6
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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Latino
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Other
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South Asian
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European (Non-Finnish)
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allele frequency: 3.305348053149996e-5
allele num: 60508
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African
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QD
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DP
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MQ
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InbreedingCoeff
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BaseQRankSum
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FS
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ReadPosRankSum
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VQSLOD
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MQRankSum
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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Other
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 60134
num of homozygotes: 0

DP
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FS
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ClippingRankSum
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ReadPosRankSum
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VQSLOD
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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QD
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 1.547125440930751e-5
allele num: 64636
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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East Asian
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num of homozygotes: 0

European (Finnish)
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num of homozygotes: 0

South Asian
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ReadPosRankSum
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BaseQRankSum
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VQSLOD
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FS
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MQRankSum
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QD
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DP
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InbreedingCoeff
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MQ
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele num: 10318
num of homozygotes: 0

Other
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num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

African
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num of homozygotes: 0

East Asian
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Latino
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European (Non-Finnish)
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InbreedingCoeff
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FS
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VQSLOD
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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DP
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MQ
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QD
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ReadPosRankSum
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SIO_000300: 5.42e-1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele num: 64714
num of homozygotes: 0

Other
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Latino
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East Asian
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African
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South Asian
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European (Finnish)
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MQRankSum
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DP
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InbreedingCoeff
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BaseQRankSum
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MQ
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VQSLOD
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ClippingRankSum
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FS
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ReadPosRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele frequency: 1.014011799410029e-3
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num of homozygotes: 0

African
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Other
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Latino
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East Asian
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European (Finnish)
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European (Non-Finnish)
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DP
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InbreedingCoeff
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ReadPosRankSum
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MQ
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MQRankSum
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FS
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QD
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VQSLOD
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BaseQRankSum
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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South Asian
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European (Finnish)
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European (Non-Finnish)
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East Asian
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FS
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InbreedingCoeff
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ClippingRankSum
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MQ
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VQSLOD
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BaseQRankSum
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MQRankSum
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DP
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Finnish)
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Other
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Latino
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European (Non-Finnish)
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African
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South Asian
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InbreedingCoeff
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MQRankSum
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FS
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VQSLOD
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DP
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BaseQRankSum
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ReadPosRankSum
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MQ
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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African
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South Asian
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European (Finnish)
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Other
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East Asian
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DP
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QD
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ClippingRankSum
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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InbreedingCoeff
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FS
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MQ
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Other
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South Asian
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European (Finnish)
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Latino
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African
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European (Non-Finnish)
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FS
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ReadPosRankSum
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VQSLOD
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MQ
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InbreedingCoeff
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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QD
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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European (Non-Finnish)
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South Asian
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East Asian
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African
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MQ
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BaseQRankSum
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VQSLOD
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ClippingRankSum
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InbreedingCoeff
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QD
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FS
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DP
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MQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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European (Non-Finnish)
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European (Finnish)
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South Asian
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Latino
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African
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East Asian
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QD
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VQSLOD
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FS
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MQ
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InbreedingCoeff
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ClippingRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 1.531252871099133e-5
allele num: 65306
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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East Asian
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Other
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QD
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InbreedingCoeff
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DP
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MQ
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ClippingRankSum
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VQSLOD
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FS
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
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allele num: 65498
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East Asian
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Other
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Latino
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South Asian
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InbreedingCoeff
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FS
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BaseQRankSum
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ClippingRankSum
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ReadPosRankSum
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MQ
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QD
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MQRankSum
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DP
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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African
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Other
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Latino
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European (Finnish)
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allele frequency: 0.0e0
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FS
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VQSLOD
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InbreedingCoeff
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MQ
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MQRankSum
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DP
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BaseQRankSum
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ClippingRankSum
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QD
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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num of homozygotes: 0

European (Finnish)
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num of homozygotes: 0

South Asian
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Latino
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East Asian
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Other
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European (Non-Finnish)
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ReadPosRankSum
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QD
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InbreedingCoeff
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MQ
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BaseQRankSum
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ClippingRankSum
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FS
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DP
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VQSLOD
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MQRankSum
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Latino
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South Asian
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European (Finnish)
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African
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European (Non-Finnish)
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Other
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MQRankSum
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MQ
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BaseQRankSum
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QD
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VQSLOD
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ClippingRankSum
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DP
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FS
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InbreedingCoeff
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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East Asian
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South Asian
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Latino
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European (Finnish)
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African
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European (Non-Finnish)
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MQ
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ClippingRankSum
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InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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VQSLOD
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DP
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FS
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QD
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele frequency: 6.225874735400324e-5
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 8.641548565502938e-5
allele num: 11572
num of homozygotes: 0

Other
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East Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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InbreedingCoeff
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SIO_000300: 1.5e-3

VQSLOD
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MQRankSum
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BaseQRankSum
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QD
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ClippingRankSum
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FS
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MQ
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ReadPosRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 3.061224489795918e-4
allele num: 9800
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 1.502765087761481e-5
allele num: 66544
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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South Asian
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MQ
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DP
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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VQSLOD
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FS
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QD
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ReadPosRankSum
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 14

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

African
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allele count: 8
allele frequency: 8.159934720522236e-4
allele num: 9804
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66598
num of homozygotes: 0

East Asian
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allele count: 6
allele frequency: 6.957328385899814e-4
allele num: 8624
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.277e1

MQ
type: SiteQuality
SIO_000300: 5.959e1

VQSLOD
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SIO_000300: 4.17e0

ReadPosRankSum
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SIO_000300: 5.77e-1

BaseQRankSum
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SIO_000300: 7.23e-1

FS
type: SiteQuality
SIO_000300: 5.28e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.78e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.629999999999999e-1

DP
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SIO_000300: 2.086909e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.501005673801447e-5
allele num: 66622
num of homozygotes: 0

East Asian
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allele count: 0
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num of homozygotes: 0

InbreedingCoeff
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VQSLOD
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FS
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SIO_000300: 1.2973e1

DP
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QD
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MQ
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SIO_000300: 5.93e1

BaseQRankSum
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SIO_000300: 4.33e0

MQRankSum
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SIO_000300: 1.92e-1

ClippingRankSum
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SIO_000300: -9.69e-1

ReadPosRankSum
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SIO_000300: 1.46e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.500690317546071e-5
allele num: 66636
num of homozygotes: 0

Other
type: Population
allele count: 0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.159285879897983e-4
allele num: 8626
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele count: 4
allele frequency: 2.443195699975568e-4
allele num: 16372
num of homozygotes: 0

European (Finnish)
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allele count: 1
allele frequency: 1.511944360447536e-4
allele num: 6614
num of homozygotes: 0

ClippingRankSum
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VQSLOD
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ReadPosRankSum
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BaseQRankSum
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FS
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SIO_000300: 1.807e0

MQRankSum
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InbreedingCoeff
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MQ
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QD
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DP
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SIO_000300: 2.087872e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele num: 8626
num of homozygotes: 0

Other
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European (Finnish)
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African
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European (Non-Finnish)
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allele num: 66662
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Latino
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South Asian
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allele frequency: 2.43161094224924e-4
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FS
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ReadPosRankSum
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BaseQRankSum
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ClippingRankSum
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MQ
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QD
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MQRankSum
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InbreedingCoeff
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VQSLOD
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele count: 1
allele frequency: 6.076072426783327e-5
allele num: 16458
num of homozygotes: 0

East Asian
type: Population
allele count: 0
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Latino
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allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9804
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499970000599988e-5
allele num: 66668
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

FS
type: SiteQuality
SIO_000300: 2.702e0

MQ
type: SiteQuality
SIO_000300: 5.939e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.3e-2

MQRankSum
type: SiteQuality
SIO_000300: -7.83e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.5e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.946e0

VQSLOD
type: SiteQuality
SIO_000300: 1.16e0

QD
type: SiteQuality
SIO_000300: 1.034e1

DP
type: SiteQuality
SIO_000300: 2.088255e6

GenotypeDepth
all individuals: 8858
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 167
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 39
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 296
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 458
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 92
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5591
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 108
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3425
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25171
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9085
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 10
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2747
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8803
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5013
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1898
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4126
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 3.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9804
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499610101373643e-5
allele num: 66684
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.64e-1

FS
type: SiteQuality
SIO_000300: 6.94e-1

DP
type: SiteQuality
SIO_000300: 2.088636e6

MQRankSum
type: SiteQuality
SIO_000300: -9.1e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.79e-1

MQ
type: SiteQuality
SIO_000300: 5.97e1

QD
type: SiteQuality
SIO_000300: 1.174e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.515e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.52e0

GenotypeDepth
all individuals: 527
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 166
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 118
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5590
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 107
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 15
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 51
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1862
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 464
bin: 9.75e1
variant carriers: 17

GenotypeQuality
all individuals: 12
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4123
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3424
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8807
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1896
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25172
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2748
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9086
bin: 9.75e1
variant carriers: 19

GenotypeQuality
all individuals: 5013
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.019991840065279e-4
allele num: 9804
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

East Asian
type: Population
allele count: 11
allele frequency: 1.275214467887781e-3
allele num: 8626
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.049695588279399e-4
allele num: 66686
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16498
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.38e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.471e0

DP
type: SiteQuality
SIO_000300: 2.090012e6

ClippingRankSum
type: SiteQuality
SIO_000300: -8.1e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.27e-1

QD
type: SiteQuality
SIO_000300: 1.29e1

MQ
type: SiteQuality
SIO_000300: 5.97e1

FS
type: SiteQuality
SIO_000300: 6.1e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.17e0