16-84228148-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84228148
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84228148
    reference: chr 16
allele count: 1
allele frequency: 1.12739571589628e-5
allele num: 88700
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000561900
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000561900.1:n.173G>A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000268624
  ensembl transcript: ENST00000268624
  gene symbol: ADAD2
  hgvsc: ENST00000268624.3:c.735C>T
  hgvsp: ENST00000268624.3:c.735C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000566526
  gene symbol: ADAD2
  hgvsc: ENST00000566526.1:n.1347C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000536986
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000536986.1:n.787G>A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000454950
  ensembl transcript: ENST00000567685
  gene symbol: ADAD2
  hgvsc: ENST00000567685.1:c.293C>T
  hgvsp: ENST00000567685.1:c.293C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564169
  gene symbol: ADAD2
  hgvsc: ENST00000564169.1:n.184C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000565643
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000565643.1:n.649G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000569221
  gene symbol: ADAD2
  hgvsc: ENST00000569221.1:n.148C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000325153
  ensembl transcript: ENST00000315906
  gene symbol: ADAD2
  hgvsc: ENST00000315906.5:c.519C>T
  hgvsp: ENST00000315906.5:c.519C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564430
  gene symbol: ADAD2
  hgvsc: ENST00000564430.1:n.819C>T
  variant of: http://identifiers.org/hgnc/30714
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4944
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1322
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16102
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15608
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1278
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14551
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5919
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1488
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 632
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Leu245Leu
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

16-84228148-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84228148
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84228148
    reference: chr 16
allele count: 2
allele frequency: 2.254791431792559e-5
allele num: 88700
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564430
  gene symbol: ADAD2
  hgvsc: ENST00000564430.1:n.819C>G
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000268624
  ensembl transcript: ENST00000268624
  gene symbol: ADAD2
  hgvsc: ENST00000268624.3:c.735C>G
  hgvsp: ENST00000268624.3:c.735C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000565643
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000565643.1:n.649G>C
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000536986
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000536986.1:n.787G>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000561900
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000561900.1:n.173G>C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000454950
  ensembl transcript: ENST00000567685
  gene symbol: ADAD2
  hgvsc: ENST00000567685.1:c.293C>G
  hgvsp: ENST00000567685.1:c.293C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000566526
  gene symbol: ADAD2
  hgvsc: ENST00000566526.1:n.1347C>G
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000569221
  gene symbol: ADAD2
  hgvsc: ENST00000569221.1:n.148C>G
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000325153
  ensembl transcript: ENST00000315906
  gene symbol: ADAD2
  hgvsc: ENST00000315906.5:c.519C>G
  hgvsp: ENST00000315906.5:c.519C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564169
  gene symbol: ADAD2
  hgvsc: ENST00000564169.1:n.184C>G
  variant of: http://identifiers.org/hgnc/30714
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4944
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1278
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1322
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14551
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5919
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15608
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16102
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 737
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22393
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1488
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Leu245Leu
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: ReadPosRankSum

16-84228150-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84228150
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84228150
    reference: chr 16
allele count: 3
allele frequency: 3.393434834739724e-5
allele num: 88406
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000268624
  ensembl transcript: ENST00000268624
  gene symbol: ADAD2
  hgvsc: ENST00000268624.3:c.737C>T
  hgvsp: ENSP00000268624.3:p.Ser246Phe
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564430
  gene symbol: ADAD2
  hgvsc: ENST00000564430.1:n.821C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000565643
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000565643.1:n.647G>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000325153
  ensembl transcript: ENST00000315906
  gene symbol: ADAD2
  hgvsc: ENST00000315906.5:c.521C>T
  hgvsp: ENSP00000325153.5:p.Ser174Phe
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000454950
  ensembl transcript: ENST00000567685
  gene symbol: ADAD2
  hgvsc: ENST00000567685.1:c.295C>T
  hgvsp: ENSP00000454950.1:p.Ser99Phe
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000566526
  gene symbol: ADAD2
  hgvsc: ENST00000566526.1:n.1349C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000536986
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000536986.1:n.785G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000561900
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000561900.1:n.171G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564169
  gene symbol: ADAD2
  hgvsc: ENST00000564169.1:n.186C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000569221
  gene symbol: ADAD2
  hgvsc: ENST00000569221.1:n.150C>T
  variant of: http://identifiers.org/hgnc/30714
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4852
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5716
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14734
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1362
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1246
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15658
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16157
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 946
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3937
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1524
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 520
  bin: 9.75e1
  variant carriers: 3
hgvs: p.Ser246Phe
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: Other
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: InbreedingCoeff

16-84228152-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84228152
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84228152
    reference: chr 16
allele count: 1
allele frequency: 1.134970717755482e-5
allele num: 88108
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000268624
  ensembl transcript: ENST00000268624
  gene symbol: ADAD2
  hgvsc: ENST00000268624.3:c.739G>A
  hgvsp: ENSP00000268624.3:p.Ala247Thr
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000566526
  gene symbol: ADAD2
  hgvsc: ENST00000566526.1:n.1351G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564430
  gene symbol: ADAD2
  hgvsc: ENST00000564430.1:n.823G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000565643
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000565643.1:n.645C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000561900
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000561900.1:n.169C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000569221
  gene symbol: ADAD2
  hgvsc: ENST00000569221.1:n.152G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000325153
  ensembl transcript: ENST00000315906
  gene symbol: ADAD2
  hgvsc: ENST00000315906.5:c.523G>A
  hgvsp: ENSP00000325153.5:p.Ala175Thr
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000454950
  ensembl transcript: ENST00000567685
  gene symbol: ADAD2
  hgvsc: ENST00000567685.1:c.297G>A
  hgvsp: ENSP00000454950.1:p.Ala100Thr
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564169
  gene symbol: ADAD2
  hgvsc: ENST00000564169.1:n.188G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000536986
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000536986.1:n.783C>T
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1233
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1365
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5640
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15824
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4658
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14841
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16164
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 681
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 186
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 863
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 515
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ala247Thr
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: Other
reference allele: G
site quality: QD
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD

16-84228154-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84228154
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84228154
    reference: chr 16
allele count: 1
allele frequency: 1.142935515578211e-5
allele num: 87494
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000565643
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000565643.1:n.643G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000561900
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000561900.1:n.167G>A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000268624
  ensembl transcript: ENST00000268624
  gene symbol: ADAD2
  hgvsc: ENST00000268624.3:c.741C>T
  hgvsp: ENST00000268624.3:c.741C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000454950
  ensembl transcript: ENST00000567685
  gene symbol: ADAD2
  hgvsc: ENST00000567685.1:c.299C>T
  hgvsp: ENST00000567685.1:c.299C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564169
  gene symbol: ADAD2
  hgvsc: ENST00000564169.1:n.190C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000569221
  gene symbol: ADAD2
  hgvsc: ENST00000569221.1:n.154C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000536986
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000536986.1:n.781G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000566526
  gene symbol: ADAD2
  hgvsc: ENST00000566526.1:n.1353C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000325153
  ensembl transcript: ENST00000315906
  gene symbol: ADAD2
  hgvsc: ENST00000315906.5:c.525C>T
  hgvsp: ENST00000315906.5:c.525C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564430
  gene symbol: ADAD2
  hgvsc: ENST00000564430.1:n.825C>T
  variant of: http://identifiers.org/hgnc/30714
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15138
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1211
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15477
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5512
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16474
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4498
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23485
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4093
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 718
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ala247Ala
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP

16-84228159-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84228159
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84228159
    reference: chr 16
allele count: 4
allele frequency: 4.678472011041194e-5
allele num: 85498
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564430
  gene symbol: ADAD2
  hgvsc: ENST00000564430.1:n.830G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000561900
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000561900.1:n.162C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000454950
  ensembl transcript: ENST00000567685
  gene symbol: ADAD2
  hgvsc: ENST00000567685.1:c.304G>A
  hgvsp: ENSP00000454950.1:p.Cys102Tyr
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000325153
  ensembl transcript: ENST00000315906
  gene symbol: ADAD2
  hgvsc: ENST00000315906.5:c.530G>A
  hgvsp: ENSP00000325153.5:p.Cys177Tyr
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000569221
  gene symbol: ADAD2
  hgvsc: ENST00000569221.1:n.159G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000565643
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000565643.1:n.638C>T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000268624
  ensembl transcript: ENST00000268624
  gene symbol: ADAD2
  hgvsc: ENST00000268624.3:c.746G>A
  hgvsp: ENSP00000268624.3:p.Cys249Tyr
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564169
  gene symbol: ADAD2
  hgvsc: ENST00000564169.1:n.195G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000566526
  gene symbol: ADAD2
  hgvsc: ENST00000566526.1:n.1358G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000536986
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000536986.1:n.776C>T
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1662
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13802
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17414
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1191
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5096
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15832
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4708
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2155
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4385
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 612
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1874
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Cys249Tyr
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum

16-84228163-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84228163
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84228163
    reference: chr 16
allele count: 1
allele frequency: 1.192975758732582e-5
allele num: 83824
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564430
  gene symbol: ADAD2
  hgvsc: ENST00000564430.1:n.834C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000566526
  gene symbol: ADAD2
  hgvsc: ENST00000566526.1:n.1362C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000561900
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000561900.1:n.158G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000569221
  gene symbol: ADAD2
  hgvsc: ENST00000569221.1:n.163C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000454950
  ensembl transcript: ENST00000567685
  gene symbol: ADAD2
  hgvsc: ENST00000567685.1:c.308C>T
  hgvsp: ENST00000567685.1:c.308C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564169
  gene symbol: ADAD2
  hgvsc: ENST00000564169.1:n.199C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000536986
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000536986.1:n.772G>A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000325153
  ensembl transcript: ENST00000315906
  gene symbol: ADAD2
  hgvsc: ENST00000315906.5:c.534C>T
  hgvsp: ENST00000315906.5:c.534C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000268624
  ensembl transcript: ENST00000268624
  gene symbol: ADAD2
  hgvsc: ENST00000268624.3:c.750C>T
  hgvsp: ENST00000268624.3:c.750C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000565643
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000565643.1:n.634G>A
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12293
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4942
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1939
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1203
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4893
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18094
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16321
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13106
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 665
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2151
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4382
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Tyr250Tyr
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS

16-84228167-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84228167
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84228167
    reference: chr 16
allele count: 3
allele frequency: 3.620302657302151e-5
allele num: 82866
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000268624
  ensembl transcript: ENST00000268624
  gene symbol: ADAD2
  hgvsc: ENST00000268624.3:c.754C>T
  hgvsp: ENSP00000268624.3:p.Arg252Trp
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564169
  gene symbol: ADAD2
  hgvsc: ENST00000564169.1:n.203C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000454950
  ensembl transcript: ENST00000567685
  gene symbol: ADAD2
  hgvsc: ENST00000567685.1:c.312C>T
  hgvsp: ENSP00000454950.1:p.Arg105Trp
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000569221
  gene symbol: ADAD2
  hgvsc: ENST00000569221.1:n.167C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000325153
  ensembl transcript: ENST00000315906
  gene symbol: ADAD2
  hgvsc: ENST00000315906.5:c.538C>T
  hgvsp: ENSP00000325153.5:p.Arg180Trp
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000566526
  gene symbol: ADAD2
  hgvsc: ENST00000566526.1:n.1366C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000536986
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000536986.1:n.768G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000561900
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000561900.1:n.154G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000565643
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000565643.1:n.630G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564430
  gene symbol: ADAD2
  hgvsc: ENST00000564430.1:n.838C>T
  variant of: http://identifiers.org/hgnc/30714
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11886
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4861
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4872
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16575
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2035
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18253
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1198
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 718
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1037
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 600
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Arg252Trp
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff

16-84228168-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84228168
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84228168
    reference: chr 16
allele count: 1
allele frequency: 1.23395853899309e-5
allele num: 81040
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000268624
  ensembl transcript: ENST00000268624
  gene symbol: ADAD2
  hgvsc: ENST00000268624.3:c.755G>A
  hgvsp: ENSP00000268624.3:p.Arg252Gln
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000454950
  ensembl transcript: ENST00000567685
  gene symbol: ADAD2
  hgvsc: ENST00000567685.1:c.313G>A
  hgvsp: ENSP00000454950.1:p.Arg105Gln
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000569221
  gene symbol: ADAD2
  hgvsc: ENST00000569221.1:n.168G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000536986
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000536986.1:n.767C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564169
  gene symbol: ADAD2
  hgvsc: ENST00000564169.1:n.204G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000325153
  ensembl transcript: ENST00000315906
  gene symbol: ADAD2
  hgvsc: ENST00000315906.5:c.539G>A
  hgvsp: ENSP00000325153.5:p.Arg180Gln
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000565643
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000565643.1:n.629C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564430
  gene symbol: ADAD2
  hgvsc: ENST00000564430.1:n.839G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000566526
  gene symbol: ADAD2
  hgvsc: ENST00000566526.1:n.1367G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000561900
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000561900.1:n.153C>T
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4591
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5279
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18482
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10816
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2322
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16970
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4792
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 286
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1556
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11151
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Arg252Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: Other
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: QD

16-84228168-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84228168
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84228168
    reference: chr 16
allele count: 1
allele frequency: 1.23395853899309e-5
allele num: 81040
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000268624
  ensembl transcript: ENST00000268624
  gene symbol: ADAD2
  hgvsc: ENST00000268624.3:c.755G>T
  hgvsp: ENSP00000268624.3:p.Arg252Leu
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000325153
  ensembl transcript: ENST00000315906
  gene symbol: ADAD2
  hgvsc: ENST00000315906.5:c.539G>T
  hgvsp: ENSP00000325153.5:p.Arg180Leu
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000561900
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000561900.1:n.153C>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000565643
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000565643.1:n.629C>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000569221
  gene symbol: ADAD2
  hgvsc: ENST00000569221.1:n.168G>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000566526
  gene symbol: ADAD2
  hgvsc: ENST00000566526.1:n.1367G>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564169
  gene symbol: ADAD2
  hgvsc: ENST00000564169.1:n.204G>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000454950
  ensembl transcript: ENST00000567685
  gene symbol: ADAD2
  hgvsc: ENST00000567685.1:c.313G>T
  hgvsp: ENSP00000454950.1:p.Arg105Leu
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000536986
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000536986.1:n.767C>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564430
  gene symbol: ADAD2
  hgvsc: ENST00000564430.1:n.839G>T
  variant of: http://identifiers.org/hgnc/30714
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4591
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5279
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16970
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18482
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2322
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10816
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4449
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11151
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 802
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 187
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Arg252Leu
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: African
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum

16-84228169-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84228169
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84228169
    reference: chr 16
allele count: 1
allele frequency: 1.228501228501229e-5
allele num: 81400
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000566526
  gene symbol: ADAD2
  hgvsc: ENST00000566526.1:n.1368G>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000325153
  ensembl transcript: ENST00000315906
  gene symbol: ADAD2
  hgvsc: ENST00000315906.5:c.540G>T
  hgvsp: ENST00000315906.5:c.540G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000561900
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000561900.1:n.152C>A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000536986
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000536986.1:n.766C>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000565643
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000565643.1:n.628C>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000569221
  gene symbol: ADAD2
  hgvsc: ENST00000569221.1:n.169G>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564430
  gene symbol: ADAD2
  hgvsc: ENST00000564430.1:n.840G>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000454950
  ensembl transcript: ENST00000567685
  gene symbol: ADAD2
  hgvsc: ENST00000567685.1:c.314G>T
  hgvsp: ENST00000567685.1:c.314G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564169
  gene symbol: ADAD2
  hgvsc: ENST00000564169.1:n.205G>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000268624
  ensembl transcript: ENST00000268624
  gene symbol: ADAD2
  hgvsc: ENST00000268624.3:c.756G>T
  hgvsp: ENST00000268624.3:c.756G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30714
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5109
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2331
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17109
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4559
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1179
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10879
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18498
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4451
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24935
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 188
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 787
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Arg252Arg
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ClippingRankSum

16-84228171-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84228171
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84228171
    reference: chr 16
allele count: 1
allele frequency: 1.227144434899988e-5
allele num: 81490
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000325153
  ensembl transcript: ENST00000315906
  gene symbol: ADAD2
  hgvsc: ENST00000315906.5:c.542G>A
  hgvsp: ENSP00000325153.5:p.Ser181Asn
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000561900
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000561900.1:n.150C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000566526
  gene symbol: ADAD2
  hgvsc: ENST00000566526.1:n.1370G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000454950
  ensembl transcript: ENST00000567685
  gene symbol: ADAD2
  hgvsc: ENST00000567685.1:c.316G>A
  hgvsp: ENSP00000454950.1:p.Ser106Asn
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000268624
  ensembl transcript: ENST00000268624
  gene symbol: ADAD2
  hgvsc: ENST00000268624.3:c.758G>A
  hgvsp: ENSP00000268624.3:p.Ser253Asn
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564169
  gene symbol: ADAD2
  hgvsc: ENST00000564169.1:n.207G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000565643
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000565643.1:n.626C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564430
  gene symbol: ADAD2
  hgvsc: ENST00000564430.1:n.842G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000536986
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000536986.1:n.764C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000569221
  gene symbol: ADAD2
  hgvsc: ENST00000569221.1:n.171G>A
  variant of: http://identifiers.org/hgnc/30714
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17212
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4487
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11036
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2348
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4951
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18460
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1170
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2555
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12231
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25499
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ser253Asn
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: G
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD

16-84228176-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84228176
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84228176
    reference: chr 16
allele count: 1
allele frequency: 1.256376108751916e-5
allele num: 79594
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000569221
  gene symbol: ADAD2
  hgvsc: ENST00000569221.1:n.176C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000454950
  ensembl transcript: ENST00000567685
  gene symbol: ADAD2
  hgvsc: ENST00000567685.1:c.321C>T
  hgvsp: ENST00000567685.1:c.321C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000566526
  gene symbol: ADAD2
  hgvsc: ENST00000566526.1:n.1375C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000325153
  ensembl transcript: ENST00000315906
  gene symbol: ADAD2
  hgvsc: ENST00000315906.5:c.547C>T
  hgvsp: ENST00000315906.5:c.547C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000536986
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000536986.1:n.759G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000561900
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000561900.1:n.145G>A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000268624
  ensembl transcript: ENST00000268624
  gene symbol: ADAD2
  hgvsc: ENST00000268624.3:c.763C>T
  hgvsp: ENST00000268624.3:c.763C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000565643
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000565643.1:n.621G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564430
  gene symbol: ADAD2
  hgvsc: ENST00000564430.1:n.847C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564169
  gene symbol: ADAD2
  hgvsc: ENST00000564169.1:n.212C>T
  variant of: http://identifiers.org/hgnc/30714
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4205
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18599
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1168
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2584
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5091
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17731
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10268
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1450
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11401
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4783
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2451
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Leu255Leu
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: DP

16-84228178-GGA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84228178
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84228176
    reference: chr 16
allele count: 2
allele frequency: 2.546019298826285e-5
allele num: 78554
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564169
  gene symbol: ADAD2
  hgvsc: ENST00000564169.1:n.217_218delGA
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000268624
  ensembl transcript: ENST00000268624
  gene symbol: ADAD2
  hgvsc: ENST00000268624.3:c.768_769delGA
  hgvsp: ENSP00000268624.3:p.Asn257ProfsTer24
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000566526
  gene symbol: ADAD2
  hgvsc: ENST00000566526.1:n.1380_1381delGA
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000536986
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000536986.1:n.755_756delTC
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000454950
  ensembl transcript: ENST00000567685
  gene symbol: ADAD2
  hgvsc: ENST00000567685.1:c.326_327delGA
  hgvsp: ENSP00000454950.1:p.Asn110ProfsTer8
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000569221
  gene symbol: ADAD2
  hgvsc: ENST00000569221.1:n.181_182delGA
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000565643
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000565643.1:n.617_618delTC
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000561900
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000561900.1:n.141_142delTC
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000325153
  ensembl transcript: ENST00000315906
  gene symbol: ADAD2
  hgvsc: ENST00000315906.5:c.552_553delGA
  hgvsp: ENSP00000325153.5:p.Asn185ProfsTer24
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564430
  gene symbol: ADAD2
  hgvsc: ENST00000564430.1:n.852_853delGA
  variant of: http://identifiers.org/hgnc/30714
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1157
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2768
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9666
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5325
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4046
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18640
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18022
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 759
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1077
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 534
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4862
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Asn257ProfsTer24
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: GGA
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: QD

16-84228188-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84228188
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84228188
    reference: chr 16
allele count: 1
allele frequency: 1.327245699723933e-5
allele num: 75344
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000569221
  gene symbol: ADAD2
  hgvsc: ENST00000569221.1:n.188G>C
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564430
  gene symbol: ADAD2
  hgvsc: ENST00000564430.1:n.859G>C
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564169
  gene symbol: ADAD2
  hgvsc: ENST00000564169.1:n.224G>C
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000561900
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000561900.1:n.133C>G
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000536986
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000536986.1:n.747C>G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000268624
  ensembl transcript: ENST00000268624
  gene symbol: ADAD2
  hgvsc: ENST00000268624.3:c.775G>C
  hgvsp: ENSP00000268624.3:p.Glu259Gln
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000454950
  ensembl transcript: ENST00000567685
  gene symbol: ADAD2
  hgvsc: ENST00000567685.1:c.333G>C
  hgvsp: ENSP00000454950.1:p.Glu112Gln
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000566526
  gene symbol: ADAD2
  hgvsc: ENST00000566526.1:n.1387G>C
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000325153
  ensembl transcript: ENST00000315906
  gene symbol: ADAD2
  hgvsc: ENST00000315906.5:c.559G>C
  hgvsp: ENSP00000325153.5:p.Glu187Gln
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000565643
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000565643.1:n.609C>G
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19064
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8470
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5556
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3620
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1160
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3299
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18382
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1457
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2714
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Glu259Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: Latino
population: South Asian
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

16-84228197-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84228197
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84228197
    reference: chr 16
allele count: 1
allele frequency: 1.379500620775279e-5
allele num: 72490
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000569221
  gene symbol: ADAD2
  hgvsc: ENST00000569221.1:n.197G>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564169
  gene symbol: ADAD2
  hgvsc: ENST00000564169.1:n.224+9G>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000268624
  ensembl transcript: ENST00000268624
  gene symbol: ADAD2
  hgvsc: ENST00000268624.3:c.775+9G>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000325153
  ensembl transcript: ENST00000315906
  gene symbol: ADAD2
  hgvsc: ENST00000315906.5:c.559+9G>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000561900
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000561900.1:n.124C>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000454950
  ensembl transcript: ENST00000567685
  gene symbol: ADAD2
  hgvsc: ENST00000567685.1:c.333+9G>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000566526
  gene symbol: ADAD2
  hgvsc: ENST00000566526.1:n.1387+9G>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564430
  gene symbol: ADAD2
  hgvsc: ENST00000564430.1:n.868G>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000565643
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000565643.1:n.600C>A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000536986
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000536986.1:n.738C>A
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3886
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7867
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1137
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5489
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3458
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19452
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18169
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1782
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5058
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2729
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 562
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: QD

16-84228198-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84228198
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84228198
    reference: chr 16
allele count: 2
allele frequency: 2.757403628743175e-5
allele num: 72532
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564430
  gene symbol: ADAD2
  hgvsc: ENST00000564430.1:n.869G>C
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000566526
  gene symbol: ADAD2
  hgvsc: ENST00000566526.1:n.1387+10G>C
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000561900
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000561900.1:n.123C>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000325153
  ensembl transcript: ENST00000315906
  gene symbol: ADAD2
  hgvsc: ENST00000315906.5:c.559+10G>C
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564169
  gene symbol: ADAD2
  hgvsc: ENST00000564169.1:n.224+10G>C
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000565643
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000565643.1:n.599C>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000454950
  ensembl transcript: ENST00000567685
  gene symbol: ADAD2
  hgvsc: ENST00000567685.1:c.333+10G>C
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000536986
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000536986.1:n.737C>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000569221
  gene symbol: ADAD2
  hgvsc: ENST00000569221.1:n.198G>C
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000268624
  ensembl transcript: ENST00000268624
  gene symbol: ADAD2
  hgvsc: ENST00000268624.3:c.775+10G>C
  variant of: http://identifiers.org/hgnc/30714
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18145
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19496
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1136
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3472
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7861
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5455
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3896
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5051
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1775
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1098
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1407
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: QD

16-84228199-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84228199
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84228199
    reference: chr 16
allele count: 21162
allele frequency: 2.914314044123723e-1
allele num: 72614
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000536986
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000536986.1:n.736C>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000565643
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000565643.1:n.598C>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000454950
  ensembl transcript: ENST00000567685
  gene symbol: ADAD2
  hgvsc: ENST00000567685.1:c.333+11G>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000325153
  ensembl transcript: ENST00000315906
  gene symbol: ADAD2
  hgvsc: ENST00000315906.5:c.559+11G>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000268624
  ensembl transcript: ENST00000268624
  gene symbol: ADAD2
  hgvsc: ENST00000268624.3:c.775+11G>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000561900
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000561900.1:n.122C>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000569221
  gene symbol: ADAD2
  hgvsc: ENST00000569221.1:n.199G>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564430
  gene symbol: ADAD2
  hgvsc: ENST00000564430.1:n.870G>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000566526
  gene symbol: ADAD2
  hgvsc: ENST00000566526.1:n.1387+11G>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564169
  gene symbol: ADAD2
  hgvsc: ENST00000564169.1:n.224+11G>T
  variant of: http://identifiers.org/hgnc/30714
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6017
  bin: 2.25e1
  variant carriers: 1564
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.75e1
  variant carriers: 207
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.75e1
  variant carriers: 218
genotype depth: GenotypeDepth
  all individuals: 2565
  bin: 2.75e1
  variant carriers: 611
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.75e1
  variant carriers: 241
genotype depth: GenotypeDepth
  all individuals: 18701
  bin: 7.5e0
  variant carriers: 4853
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.25e1
  variant carriers: 203
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 4.25e1
  variant carriers: 276
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 6.25e1
  variant carriers: 259
genotype depth: GenotypeDepth
  all individuals: 3551
  bin: 2.5e0
  variant carriers: 338
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 8.25e1
  variant carriers: 231
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 3.75e1
  variant carriers: 287
genotype depth: GenotypeDepth
  all individuals: 6175
  bin: 1.75e1
  variant carriers: 4568
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 4.75e1
  variant carriers: 271
genotype depth: GenotypeDepth
  all individuals: 18374
  bin: 1.25e1
  variant carriers: 8124
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 9.75e1
  variant carriers: 728
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 5.25e1
  variant carriers: 253
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 3.25e1
  variant carriers: 370
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.25e1
  variant carriers: 173
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 8.75e1
  variant carriers: 180
genotype quality: GenotypeQuality
  all individuals: 1166
  bin: 6.75e1
  variant carriers: 434
genotype quality: GenotypeQuality
  all individuals: 427
  bin: 4.25e1
  variant carriers: 266
genotype quality: GenotypeQuality
  all individuals: 1382
  bin: 1.75e1
  variant carriers: 524
genotype quality: GenotypeQuality
  all individuals: 15759
  bin: 9.75e1
  variant carriers: 15555
num of homozygotes: 2654
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQ

http://identifiers.org/exac.variant/16-84228205-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84228205
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84228205
    reference: chr 16
allele count: 1
allele frequency: 1.66461364317342e-5
allele num: 60074
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000565643
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000565643.1:n.592G>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000569221
  gene symbol: ADAD2
  hgvsc: ENST00000569221.1:n.205C>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000561900
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000561900.1:n.116G>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000566526
  gene symbol: ADAD2
  hgvsc: ENST00000566526.1:n.1387+17C>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000325153
  ensembl transcript: ENST00000315906
  gene symbol: ADAD2
  hgvsc: ENST00000315906.5:c.559+17C>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000536986
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000536986.1:n.730G>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564169
  gene symbol: ADAD2
  hgvsc: ENST00000564169.1:n.224+17C>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564430
  gene symbol: ADAD2
  hgvsc: ENST00000564430.1:n.876C>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000268624
  ensembl transcript: ENST00000268624
  gene symbol: ADAD2
  hgvsc: ENST00000268624.3:c.775+17C>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000454950
  ensembl transcript: ENST00000567685
  gene symbol: ADAD2
  hgvsc: ENST00000567685.1:c.333+17C>A
  variant of: http://identifiers.org/hgnc/30714
canonical: true
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 16932
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22901
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2158
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6994
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2521
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4590
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2639
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 269
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1171
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: Other
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

16-84228209-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84228209
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84228209
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 58278
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000569221
  gene symbol: ADAD2
  hgvsc: ENST00000569221.1:n.209C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000565643
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000565643.1:n.588G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000566526
  gene symbol: ADAD2
  hgvsc: ENST00000566526.1:n.1387+21C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000561900
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000561900.1:n.112G>A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000536986
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000536986.1:n.726G>A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000268624
  ensembl transcript: ENST00000268624
  gene symbol: ADAD2
  hgvsc: ENST00000268624.3:c.775+21C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564169
  gene symbol: ADAD2
  hgvsc: ENST00000564169.1:n.224+21C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000325153
  ensembl transcript: ENST00000315906
  gene symbol: ADAD2
  hgvsc: ENST00000315906.5:c.559+21C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564430
  gene symbol: ADAD2
  hgvsc: ENST00000564430.1:n.880C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000454950
  ensembl transcript: ENST00000567685
  gene symbol: ADAD2
  hgvsc: ENST00000567685.1:c.333+21C>T
  variant of: http://identifiers.org/hgnc/30714
canonical: true
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4283
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22917
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2362
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16408
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7795
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2288
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 959
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 236
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 340
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5205
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

16-84228211-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84228211
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84228211
    reference: chr 16
allele count: 1
allele frequency: 1.744287458573173e-5
allele num: 57330
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000536986
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000536986.1:n.724C>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000569221
  gene symbol: ADAD2
  hgvsc: ENST00000569221.1:n.211G>C
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564430
  gene symbol: ADAD2
  hgvsc: ENST00000564430.1:n.882G>C
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000566526
  gene symbol: ADAD2
  hgvsc: ENST00000566526.1:n.1387+23G>C
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000454950
  ensembl transcript: ENST00000567685
  gene symbol: ADAD2
  hgvsc: ENST00000567685.1:c.333+23G>C
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000325153
  ensembl transcript: ENST00000315906
  gene symbol: ADAD2
  hgvsc: ENST00000315906.5:c.559+23G>C
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000561900
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000561900.1:n.110C>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564169
  gene symbol: ADAD2
  hgvsc: ENST00000564169.1:n.224+23G>C
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000565643
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000565643.1:n.586C>G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000268624
  ensembl transcript: ENST00000268624
  gene symbol: ADAD2
  hgvsc: ENST00000268624.3:c.775+23G>C
  variant of: http://identifiers.org/hgnc/30714
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2344
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8176
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4150
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22973
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2319
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16083
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2516
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2639
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 438
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8760
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: Other
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum

http://identifiers.org/exac.variant/16-84228217-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84228217
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84228217
    reference: chr 16
allele count: 1
allele frequency: 1.852469341632396e-5
allele num: 53982
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000454950
  ensembl transcript: ENST00000567685
  gene symbol: ADAD2
  hgvsc: ENST00000567685.1:c.333+29C>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000566526
  gene symbol: ADAD2
  hgvsc: ENST00000566526.1:n.1387+29C>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000565643
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000565643.1:n.580G>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000561900
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000561900.1:n.104G>T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000536986
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000536986.1:n.718G>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564430
  gene symbol: ADAD2
  hgvsc: ENST00000564430.1:n.888C>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000325153
  ensembl transcript: ENST00000315906
  gene symbol: ADAD2
  hgvsc: ENST00000315906.5:c.559+29C>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564169
  gene symbol: ADAD2
  hgvsc: ENST00000564169.1:n.224+29C>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000569221
  gene symbol: ADAD2
  hgvsc: ENST00000569221.1:n.217C>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000268624
  ensembl transcript: ENST00000268624
  gene symbol: ADAD2
  hgvsc: ENST00000268624.3:c.775+29C>A
  variant of: http://identifiers.org/hgnc/30714
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9222
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2436
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2183
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14818
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3855
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23443
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 935
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3057
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10229
  bin: 7.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2863
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ClippingRankSum

16-84228218-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84228218
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84228218
    reference: chr 16
allele count: 123
allele frequency: 2.300011219566925e-3
allele num: 53478
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000561900
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000561900.1:n.103G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000325153
  ensembl transcript: ENST00000315906
  gene symbol: ADAD2
  hgvsc: ENST00000315906.5:c.559+30C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000536986
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000536986.1:n.717G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000565643
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000565643.1:n.579G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564169
  gene symbol: ADAD2
  hgvsc: ENST00000564169.1:n.224+30C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000566526
  gene symbol: ADAD2
  hgvsc: ENST00000566526.1:n.1387+30C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564430
  gene symbol: ADAD2
  hgvsc: ENST00000564430.1:n.889C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000454950
  ensembl transcript: ENST00000567685
  gene symbol: ADAD2
  hgvsc: ENST00000567685.1:c.333+30C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000268624
  ensembl transcript: ENST00000268624
  gene symbol: ADAD2
  hgvsc: ENST00000268624.3:c.775+30C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000569221
  gene symbol: ADAD2
  hgvsc: ENST00000569221.1:n.218C>T
  variant of: http://identifiers.org/hgnc/30714
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2165
  bin: 2.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23566
  bin: 7.5e0
  variant carriers: 56
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2440
  bin: 1.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 14597
  bin: 1.25e1
  variant carriers: 49
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 9344
  bin: 2.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 5.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 3819
  bin: 2.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 4.25e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 5.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 281
  bin: 4.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 949
  bin: 6.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 4659
  bin: 6.25e1
  variant carriers: 6
num of homozygotes: 2
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
population: African
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP

16-84228219-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84228219
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84228219
    reference: chr 16
allele count: 5
allele frequency: 9.534706331045004e-5
allele num: 52440
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564169
  gene symbol: ADAD2
  hgvsc: ENST00000564169.1:n.224+31G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000566526
  gene symbol: ADAD2
  hgvsc: ENST00000566526.1:n.1387+31G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000268624
  ensembl transcript: ENST00000268624
  gene symbol: ADAD2
  hgvsc: ENST00000268624.3:c.775+31G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000569221
  gene symbol: ADAD2
  hgvsc: ENST00000569221.1:n.219G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000561900
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000561900.1:n.102C>T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000536986
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000536986.1:n.716C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000454950
  ensembl transcript: ENST00000567685
  gene symbol: ADAD2
  hgvsc: ENST00000567685.1:c.333+31G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000325153
  ensembl transcript: ENST00000315906
  gene symbol: ADAD2
  hgvsc: ENST00000315906.5:c.559+31G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000565643
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000565643.1:n.578C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564430
  gene symbol: ADAD2
  hgvsc: ENST00000564430.1:n.890G>A
  variant of: http://identifiers.org/hgnc/30714
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2460
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 9523
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14330
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3778
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2153
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23679
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 387
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2771
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24460
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3104
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP

16-84228219-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84228219
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84228219
    reference: chr 16
allele count: 1
allele frequency: 1.906941266209001e-5
allele num: 52440
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564169
  gene symbol: ADAD2
  hgvsc: ENST00000564169.1:n.224+31G>C
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000268624
  ensembl transcript: ENST00000268624
  gene symbol: ADAD2
  hgvsc: ENST00000268624.3:c.775+31G>C
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000569221
  gene symbol: ADAD2
  hgvsc: ENST00000569221.1:n.219G>C
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000536986
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000536986.1:n.716C>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000565643
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000565643.1:n.578C>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000454950
  ensembl transcript: ENST00000567685
  gene symbol: ADAD2
  hgvsc: ENST00000567685.1:c.333+31G>C
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000561900
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000561900.1:n.102C>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000325153
  ensembl transcript: ENST00000315906
  gene symbol: ADAD2
  hgvsc: ENST00000315906.5:c.559+31G>C
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564430
  gene symbol: ADAD2
  hgvsc: ENST00000564430.1:n.890G>C
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000566526
  gene symbol: ADAD2
  hgvsc: ENST00000566526.1:n.1387+31G>C
  variant of: http://identifiers.org/hgnc/30714
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9523
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3778
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23679
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14330
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2153
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2460
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1171
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24460
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 768
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: Other
population: East Asian
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ReadPosRankSum

16-84228225-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84228225
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84228225
    reference: chr 16
allele count: 1
allele frequency: 2.042817453832326e-5
allele num: 48952
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000454950
  ensembl transcript: ENST00000567685
  gene symbol: ADAD2
  hgvsc: ENST00000567685.1:c.333+37G>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564169
  gene symbol: ADAD2
  hgvsc: ENST00000564169.1:n.224+37G>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000565643
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000565643.1:n.572C>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000325153
  ensembl transcript: ENST00000315906
  gene symbol: ADAD2
  hgvsc: ENST00000315906.5:c.559+37G>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000569221
  gene symbol: ADAD2
  hgvsc: ENST00000569221.1:n.225G>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000561900
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000561900.1:n.96C>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564430
  gene symbol: ADAD2
  hgvsc: ENST00000564430.1:n.896G>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000268624
  ensembl transcript: ENST00000268624
  gene symbol: ADAD2
  hgvsc: ENST00000268624.3:c.775+37G>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000536986
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000536986.1:n.710C>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000566526
  gene symbol: ADAD2
  hgvsc: ENST00000566526.1:n.1387+37G>T
  variant of: http://identifiers.org/hgnc/30714
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2403
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2085
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 921
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10020
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3681
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24800
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12662
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5027
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2721
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1201
  bin: 3.75e1
  variant carriers: 1
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP

16-84228228-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84228228
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84228228
    reference: chr 16
allele count: 1
allele frequency: 2.064324346641344e-5
allele num: 48442
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000565643
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000565643.1:n.569C>T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000536986
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000536986.1:n.707C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564430
  gene symbol: ADAD2
  hgvsc: ENST00000564430.1:n.899G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000561900
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000561900.1:n.93C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000454950
  ensembl transcript: ENST00000567685
  gene symbol: ADAD2
  hgvsc: ENST00000567685.1:c.333+40G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000325153
  ensembl transcript: ENST00000315906
  gene symbol: ADAD2
  hgvsc: ENST00000315906.5:c.559+40G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000566526
  gene symbol: ADAD2
  hgvsc: ENST00000566526.1:n.1387+40G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564169
  gene symbol: ADAD2
  hgvsc: ENST00000564169.1:n.224+40G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000569221
  gene symbol: ADAD2
  hgvsc: ENST00000569221.1:n.228G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000268624
  ensembl transcript: ENST00000268624
  gene symbol: ADAD2
  hgvsc: ENST00000268624.3:c.775+40G>A
  variant of: http://identifiers.org/hgnc/30714
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25090
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2080
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12349
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10096
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2321
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3674
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 233
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 288
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20295
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 480
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: BaseQRankSum

http://identifiers.org/exac.variant/16-84228237-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84228237
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84228237
    reference: chr 16
allele count: 29576
allele frequency: 6.324523137456163e-1
allele num: 46764
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000565643
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000565643.1:n.560T>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564430
  gene symbol: ADAD2
  hgvsc: ENST00000564430.1:n.908A>C
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000454950
  ensembl transcript: ENST00000567685
  gene symbol: ADAD2
  hgvsc: ENST00000567685.1:c.333+49A>C
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564169
  gene symbol: ADAD2
  hgvsc: ENST00000564169.1:n.224+49A>C
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000268624
  ensembl transcript: ENST00000268624
  gene symbol: ADAD2
  hgvsc: ENST00000268624.3:c.775+49A>C
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000561900
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000561900.1:n.84T>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000569221
  gene symbol: ADAD2
  hgvsc: ENST00000569221.1:n.237A>C
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000536986
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000536986.1:n.698T>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000325153
  ensembl transcript: ENST00000315906
  gene symbol: ADAD2
  hgvsc: ENST00000315906.5:c.559+49A>C
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000566526
  gene symbol: ADAD2
  hgvsc: ENST00000566526.1:n.1387+49A>C
  variant of: http://identifiers.org/hgnc/30714
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 7.75e1
  variant carriers: 401
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 4.25e1
  variant carriers: 577
genotype depth: GenotypeDepth
  all individuals: 1744
  bin: 2.25e1
  variant carriers: 781
genotype depth: GenotypeDepth
  all individuals: 1194
  bin: 2.75e1
  variant carriers: 671
genotype depth: GenotypeDepth
  all individuals: 2575
  bin: 1.75e1
  variant carriers: 2433
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 5.25e1
  variant carriers: 555
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 7.25e1
  variant carriers: 514
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 4.75e1
  variant carriers: 524
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 6.75e1
  variant carriers: 553
genotype depth: GenotypeDepth
  all individuals: 11866
  bin: 1.25e1
  variant carriers: 10278
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 3.25e1
  variant carriers: 644
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 6.25e1
  variant carriers: 582
genotype depth: GenotypeDepth
  all individuals: 25355
  bin: 7.5e0
  variant carriers: 18546
genotype depth: GenotypeDepth
  all individuals: 7775
  bin: 2.5e0
  variant carriers: 3355
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 3.75e1
  variant carriers: 615
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 5.75e1
  variant carriers: 598
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 8.25e1
  variant carriers: 335
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 8.75e1
  variant carriers: 299
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 9.75e1
  variant carriers: 485
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 9.25e1
  variant carriers: 189
genotype quality: GenotypeQuality
  all individuals: 2120
  bin: 2.75e1
  variant carriers: 1982
genotype quality: GenotypeQuality
  all individuals: 2255
  bin: 1.25e1
  variant carriers: 2018
genotype quality: GenotypeQuality
  all individuals: 918
  bin: 5.25e1
  variant carriers: 902
genotype quality: GenotypeQuality
  all individuals: 885
  bin: 8.25e1
  variant carriers: 872
num of homozygotes: 8889
population: East Asian
population: Latino
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum

16-84228237-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84228237
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84228237
    reference: chr 16
allele count: 108
allele frequency: 2.309468822170901e-3
allele num: 46764
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000566526
  gene symbol: ADAD2
  hgvsc: ENST00000566526.1:n.1387+49A>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000268624
  ensembl transcript: ENST00000268624
  gene symbol: ADAD2
  hgvsc: ENST00000268624.3:c.775+49A>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000325153
  ensembl transcript: ENST00000315906
  gene symbol: ADAD2
  hgvsc: ENST00000315906.5:c.559+49A>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000536986
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000536986.1:n.698T>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564169
  gene symbol: ADAD2
  hgvsc: ENST00000564169.1:n.224+49A>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000569221
  gene symbol: ADAD2
  hgvsc: ENST00000569221.1:n.237A>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564430
  gene symbol: ADAD2
  hgvsc: ENST00000564430.1:n.908A>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000454950
  ensembl transcript: ENST00000567685
  gene symbol: ADAD2
  hgvsc: ENST00000567685.1:c.333+49A>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000561900
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000561900.1:n.84T>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000565643
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000565643.1:n.560T>A
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7775
  bin: 2.5e0
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1744
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11866
  bin: 1.25e1
  variant carriers: 63
genotype depth: GenotypeDepth
  all individuals: 25355
  bin: 7.5e0
  variant carriers: 101
genotype depth: GenotypeDepth
  all individuals: 1194
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2575
  bin: 1.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 7.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 623
  bin: 7.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 820
  bin: 5.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 7948
  bin: 2.25e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 1821
  bin: 6.25e1
  variant carriers: 2
num of homozygotes: 2
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: A
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: QD

16-84228242-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84228242
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84228242
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 30912
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000566526
  gene symbol: ADAD2
  hgvsc: ENST00000566526.1:n.1387+54G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564430
  gene symbol: ADAD2
  hgvsc: ENST00000564430.1:n.913G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000536986
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000536986.1:n.693C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000565643
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000565643.1:n.555C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000454950
  ensembl transcript: ENST00000567685
  gene symbol: ADAD2
  hgvsc: ENST00000567685.1:c.333+54G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000561900
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000561900.1:n.79C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000569221
  gene symbol: ADAD2
  hgvsc: ENST00000569221.1:n.242G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000325153
  ensembl transcript: ENST00000315906
  gene symbol: ADAD2
  hgvsc: ENST00000315906.5:c.559+54G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000268624
  ensembl transcript: ENST00000268624
  gene symbol: ADAD2
  hgvsc: ENST00000268624.3:c.775+54G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564169
  gene symbol: ADAD2
  hgvsc: ENST00000564169.1:n.224+54G>A
  variant of: http://identifiers.org/hgnc/30714
canonical: true
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23793
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1826
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1996
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19378
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6160
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3221
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2322
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 565
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24155
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 4.75e1
  variant carriers: 0
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: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum

16-84228244-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84228244
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84228244
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 29176
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000561900
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000561900.1:n.77G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564430
  gene symbol: ADAD2
  hgvsc: ENST00000564430.1:n.915C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000566526
  gene symbol: ADAD2
  hgvsc: ENST00000566526.1:n.1387+56C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000268624
  ensembl transcript: ENST00000268624
  gene symbol: ADAD2
  hgvsc: ENST00000268624.3:c.775+56C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564169
  gene symbol: ADAD2
  hgvsc: ENST00000564169.1:n.224+56C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000454950
  ensembl transcript: ENST00000567685
  gene symbol: ADAD2
  hgvsc: ENST00000567685.1:c.333+56C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000565643
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000565643.1:n.553G>A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000536986
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000536986.1:n.691G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000325153
  ensembl transcript: ENST00000315906
  gene symbol: ADAD2
  hgvsc: ENST00000315906.5:c.559+56C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000569221
  gene symbol: ADAD2
  hgvsc: ENST00000569221.1:n.244C>T
  variant of: http://identifiers.org/hgnc/30714
canonical: true
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 3095
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5526
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25108
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18590
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1782
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1942
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1249
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25398
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16186
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: InbreedingCoeff

16-84228246-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84228246
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84228246
    reference: chr 16
allele count: 1
allele frequency: 3.487479946990305e-5
allele num: 28674
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000565643
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000565643.1:n.551C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564430
  gene symbol: ADAD2
  hgvsc: ENST00000564430.1:n.917G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000561900
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000561900.1:n.75C>T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000536986
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000536986.1:n.689C>T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000268624
  ensembl transcript: ENST00000268624
  gene symbol: ADAD2
  hgvsc: ENST00000268624.3:c.775+58G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000566526
  gene symbol: ADAD2
  hgvsc: ENST00000566526.1:n.1387+58G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000325153
  ensembl transcript: ENST00000315906
  gene symbol: ADAD2
  hgvsc: ENST00000315906.5:c.559+58G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000454950
  ensembl transcript: ENST00000567685
  gene symbol: ADAD2
  hgvsc: ENST00000567685.1:c.333+58G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564169
  gene symbol: ADAD2
  hgvsc: ENST00000564169.1:n.224+58G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000569221
  gene symbol: ADAD2
  hgvsc: ENST00000569221.1:n.246G>A
  variant of: http://identifiers.org/hgnc/30714
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3080
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1941
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25636
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1768
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18328
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5245
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 410
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 243
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 462
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

16-84228248-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84228248
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84228248
    reference: chr 16
allele count: 1
allele frequency: 3.635041802980734e-5
allele num: 27510
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000565643
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000565643.1:n.549G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000569221
  gene symbol: ADAD2
  hgvsc: ENST00000569221.1:n.248C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000454950
  ensembl transcript: ENST00000567685
  gene symbol: ADAD2
  hgvsc: ENST00000567685.1:c.333+60C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000566526
  gene symbol: ADAD2
  hgvsc: ENST00000566526.1:n.1387+60C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564430
  gene symbol: ADAD2
  hgvsc: ENST00000564430.1:n.919C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564169
  gene symbol: ADAD2
  hgvsc: ENST00000564169.1:n.224+60C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000561900
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000561900.1:n.73G>A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000536986
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000536986.1:n.687G>A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000268624
  ensembl transcript: ENST00000268624
  gene symbol: ADAD2
  hgvsc: ENST00000268624.3:c.775+60C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000325153
  ensembl transcript: ENST00000315906
  gene symbol: ADAD2
  hgvsc: ENST00000315906.5:c.559+60C>T
  variant of: http://identifiers.org/hgnc/30714
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3047
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1934
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1747
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17775
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4748
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26545
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 547
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26823
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 225
  bin: 3.75e1
  variant carriers: 0
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: C
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: DP

16-84228255-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84228255
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84228255
    reference: chr 16
allele count: 1
allele frequency: 4.081299485756264e-5
allele num: 24502
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564430
  gene symbol: ADAD2
  hgvsc: ENST00000564430.1:n.926G>C
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000566526
  gene symbol: ADAD2
  hgvsc: ENST00000566526.1:n.1387+67G>C
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000561900
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000561900.1:n.66C>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000569221
  gene symbol: ADAD2
  hgvsc: ENST00000569221.1:n.255G>C
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000454950
  ensembl transcript: ENST00000567685
  gene symbol: ADAD2
  hgvsc: ENST00000567685.1:c.333+67G>C
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564169
  gene symbol: ADAD2
  hgvsc: ENST00000564169.1:n.224+67G>C
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000536986
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000536986.1:n.680C>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000565643
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000565643.1:n.542C>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000325153
  ensembl transcript: ENST00000315906
  gene symbol: ADAD2
  hgvsc: ENST00000315906.5:c.559+67G>C
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000268624
  ensembl transcript: ENST00000268624
  gene symbol: ADAD2
  hgvsc: ENST00000268624.3:c.775+67G>C
  variant of: http://identifiers.org/hgnc/30714
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2851
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1899
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15357
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1657
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3462
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29198
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 534
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29098
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1638
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 387
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

16-84228265-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84228265
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84228265
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 22228
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000325153
  ensembl transcript: ENST00000315906
  gene symbol: ADAD2
  hgvsc: ENST00000315906.5:c.559+77G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564430
  gene symbol: ADAD2
  hgvsc: ENST00000564430.1:n.936G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000561900
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000561900.1:n.56C>T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000536986
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000536986.1:n.670C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000565643
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000565643.1:n.532C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000566526
  gene symbol: ADAD2
  hgvsc: ENST00000566526.1:n.1387+77G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000569221
  gene symbol: ADAD2
  hgvsc: ENST00000569221.1:n.265G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000454950
  ensembl transcript: ENST00000567685
  gene symbol: ADAD2
  hgvsc: ENST00000567685.1:c.333+77G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564169
  gene symbol: ADAD2
  hgvsc: ENST00000564169.1:n.224+77G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000268624
  ensembl transcript: ENST00000268624
  gene symbol: ADAD2
  hgvsc: ENST00000268624.3:c.775+77G>A
  variant of: http://identifiers.org/hgnc/30714
canonical: true
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2546
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13709
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29989
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2585
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1489
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1836
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 543
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29756
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 302
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

16-84228277-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84228277
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84228277
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 20772
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000566526
  gene symbol: ADAD2
  hgvsc: ENST00000566526.1:n.1387+89G>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564169
  gene symbol: ADAD2
  hgvsc: ENST00000564169.1:n.224+89G>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000569221
  gene symbol: ADAD2
  hgvsc: ENST00000569221.1:n.277G>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000561900
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000561900.1:n.44C>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000454950
  ensembl transcript: ENST00000567685
  gene symbol: ADAD2
  hgvsc: ENST00000567685.1:c.333+89G>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564430
  gene symbol: ADAD2
  hgvsc: ENST00000564430.1:n.948G>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000536986
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000536986.1:n.658C>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000325153
  ensembl transcript: ENST00000315906
  gene symbol: ADAD2
  hgvsc: ENST00000315906.5:c.559+89G>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000268624
  ensembl transcript: ENST00000268624
  gene symbol: ADAD2
  hgvsc: ENST00000268624.3:c.775+89G>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000565643
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000565643.1:n.520C>A
canonical: true
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1238
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28803
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2196
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2201
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12540
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2021
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4148
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 482
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 345
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: G
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP

http://identifiers.org/exac.variant/16-84228278-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84228278
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84228278
    reference: chr 16
allele count: 1
allele frequency: 4.846839860411012e-5
allele num: 20632
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000565643
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000565643.1:n.519G>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000454950
  ensembl transcript: ENST00000567685
  gene symbol: ADAD2
  hgvsc: ENST00000567685.1:c.333+90C>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000561900
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000561900.1:n.43G>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564430
  gene symbol: ADAD2
  hgvsc: ENST00000564430.1:n.949C>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000566526
  gene symbol: ADAD2
  hgvsc: ENST00000566526.1:n.1387+90C>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000536986
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000536986.1:n.657G>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564169
  gene symbol: ADAD2
  hgvsc: ENST00000564169.1:n.224+90C>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000325153
  ensembl transcript: ENST00000315906
  gene symbol: ADAD2
  hgvsc: ENST00000315906.5:c.559+90C>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000569221
  gene symbol: ADAD2
  hgvsc: ENST00000569221.1:n.278C>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000268624
  ensembl transcript: ENST00000268624
  gene symbol: ADAD2
  hgvsc: ENST00000268624.3:c.775+90C>A
  variant of: http://identifiers.org/hgnc/30714
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28510
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1990
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2217
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12452
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1235
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2173
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 303
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 561
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 853
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 430
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: C
site quality: DP
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ

16-84228278-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84228278
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84228278
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 20632
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000566526
  gene symbol: ADAD2
  hgvsc: ENST00000566526.1:n.1387+90C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564169
  gene symbol: ADAD2
  hgvsc: ENST00000564169.1:n.224+90C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000268624
  ensembl transcript: ENST00000268624
  gene symbol: ADAD2
  hgvsc: ENST00000268624.3:c.775+90C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000569221
  gene symbol: ADAD2
  hgvsc: ENST00000569221.1:n.278C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000325153
  ensembl transcript: ENST00000315906
  gene symbol: ADAD2
  hgvsc: ENST00000315906.5:c.559+90C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000561900
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000561900.1:n.43G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564430
  gene symbol: ADAD2
  hgvsc: ENST00000564430.1:n.949C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000565643
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000565643.1:n.519G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000454950
  ensembl transcript: ENST00000567685
  gene symbol: ADAD2
  hgvsc: ENST00000567685.1:c.333+90C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000536986
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000536986.1:n.657G>A
canonical: true
consequence: non coding transcript exon
filter: AC_Adj0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1235
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2217
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12452
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28510
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1990
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2173
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 224
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3545
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27998
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2075
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

16-84228279-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84228279
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84228279
    reference: chr 16
allele count: 7123
allele frequency: 3.386744009128946e-1
allele num: 21032
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000561900
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000561900.1:n.42C>T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000268624
  ensembl transcript: ENST00000268624
  gene symbol: ADAD2
  hgvsc: ENST00000268624.3:c.775+91G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000569221
  gene symbol: ADAD2
  hgvsc: ENST00000569221.1:n.279G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000325153
  ensembl transcript: ENST00000315906
  gene symbol: ADAD2
  hgvsc: ENST00000315906.5:c.559+91G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000565643
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000565643.1:n.518C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564169
  gene symbol: ADAD2
  hgvsc: ENST00000564169.1:n.224+91G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000536986
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000536986.1:n.656C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564430
  gene symbol: ADAD2
  hgvsc: ENST00000564430.1:n.950G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000566526
  gene symbol: ADAD2
  hgvsc: ENST00000566526.1:n.1387+91G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000454950
  ensembl transcript: ENST00000567685
  gene symbol: ADAD2
  hgvsc: ENST00000567685.1:c.333+91G>A
  variant of: http://identifiers.org/hgnc/30714
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 4.75e1
  variant carriers: 240
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.75e1
  variant carriers: 60
genotype depth: GenotypeDepth
  all individuals: 1932
  bin: 2.25e1
  variant carriers: 761
genotype depth: GenotypeDepth
  all individuals: 2376
  bin: 1.25e1
  variant carriers: 1110
genotype depth: GenotypeDepth
  all individuals: 1235
  bin: 3.25e1
  variant carriers: 865
genotype depth: GenotypeDepth
  all individuals: 13356
  bin: 7.5e0
  variant carriers: 7264
genotype depth: GenotypeDepth
  all individuals: 2161
  bin: 2.75e1
  variant carriers: 860
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 6.25e1
  variant carriers: 41
genotype depth: GenotypeDepth
  all individuals: 24192
  bin: 2.5e0
  variant carriers: 3577
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 3.75e1
  variant carriers: 709
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 5.25e1
  variant carriers: 131
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 1.75e1
  variant carriers: 674
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 4.25e1
  variant carriers: 434
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 2095
  bin: 1.75e1
  variant carriers: 1576
genotype quality: GenotypeQuality
  all individuals: 2695
  bin: 6.25e1
  variant carriers: 665
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 4.25e1
  variant carriers: 67
genotype quality: GenotypeQuality
  all individuals: 610
  bin: 8.75e1
  variant carriers: 577
num of homozygotes: 1197
population: African
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

16-84228289-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84228289
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84228289
    reference: chr 16
allele count: 1
allele frequency: 5.606638259699485e-5
allele num: 17836
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000566526
  gene symbol: ADAD2
  hgvsc: ENST00000566526.1:n.1387+101G>C
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564169
  gene symbol: ADAD2
  hgvsc: ENST00000564169.1:n.224+101G>C
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000565643
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000565643.1:n.508C>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000454950
  ensembl transcript: ENST00000567685
  gene symbol: ADAD2
  hgvsc: ENST00000567685.1:c.333+101G>C
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000268624
  ensembl transcript: ENST00000268624
  gene symbol: ADAD2
  hgvsc: ENST00000268624.3:c.775+101G>C
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000569221
  gene symbol: ADAD2
  hgvsc: ENST00000569221.1:n.289G>C
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000536986
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000536986.1:n.646C>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564430
  gene symbol: ADAD2
  hgvsc: ENST00000564430.1:n.960G>C
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000325153
  ensembl transcript: ENST00000315906
  gene symbol: ADAD2
  hgvsc: ENST00000315906.5:c.559+101G>C
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000561900
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000561900.1:n.32C>G
canonical: true
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1353
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6396
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32250
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1788
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2557
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2224
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 240
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 572
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1171
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29966
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: G
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum

16-84228291-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84228291
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84228291
    reference: chr 16
allele count: 1
allele frequency: 5.632533513574406e-5
allele num: 17754
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000569221
  gene symbol: ADAD2
  hgvsc: ENST00000569221.1:n.291G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564169
  gene symbol: ADAD2
  hgvsc: ENST00000564169.1:n.224+103G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564430
  gene symbol: ADAD2
  hgvsc: ENST00000564430.1:n.962G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000325153
  ensembl transcript: ENST00000315906
  gene symbol: ADAD2
  hgvsc: ENST00000315906.5:c.559+103G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000561900
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000561900.1:n.30C>T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000536986
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000536986.1:n.644C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000565643
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000565643.1:n.506C>T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000268624
  ensembl transcript: ENST00000268624
  gene symbol: ADAD2
  hgvsc: ENST00000268624.3:c.775+103G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000454950
  ensembl transcript: ENST00000567685
  gene symbol: ADAD2
  hgvsc: ENST00000567685.1:c.333+103G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000566526
  gene symbol: ADAD2
  hgvsc: ENST00000566526.1:n.1387+103G>A
  variant of: http://identifiers.org/hgnc/30714
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1372
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1783
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6324
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2579
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32193
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2161
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 226
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 225
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 608
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: European (Finnish)
population: South Asian
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum

16-84228295-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84228295
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84228295
    reference: chr 16
allele count: 1
allele frequency: 5.796429399489914e-5
allele num: 17252
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000325153
  ensembl transcript: ENST00000315906
  gene symbol: ADAD2
  hgvsc: ENST00000315906.5:c.559+107G>C
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564169
  gene symbol: ADAD2
  hgvsc: ENST00000564169.1:n.224+107G>C
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000561900
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000561900.1:n.26C>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000566526
  gene symbol: ADAD2
  hgvsc: ENST00000566526.1:n.1387+107G>C
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000569221
  gene symbol: ADAD2
  hgvsc: ENST00000569221.1:n.295G>C
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000268624
  ensembl transcript: ENST00000268624
  gene symbol: ADAD2
  hgvsc: ENST00000268624.3:c.775+107G>C
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000536986
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000536986.1:n.640C>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000565643
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000565643.1:n.502C>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000454950
  ensembl transcript: ENST00000567685
  gene symbol: ADAD2
  hgvsc: ENST00000567685.1:c.333+107G>C
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564430
  gene symbol: ADAD2
  hgvsc: ENST00000564430.1:n.966G>C
  variant of: http://identifiers.org/hgnc/30714
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1484
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1865
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31330
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6080
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2634
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1795
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 516
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 267
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: African
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum

16-84228305-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84228305
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84228305
    reference: chr 16
allele count: 4613
allele frequency: 2.846125370187562e-1
allele num: 16208
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000536986
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000536986.1:n.630G>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000566526
  gene symbol: ADAD2
  hgvsc: ENST00000566526.1:n.1387+117C>G
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564430
  gene symbol: ADAD2
  hgvsc: ENST00000564430.1:n.976C>G
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000561900
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000561900.1:n.16G>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000454950
  ensembl transcript: ENST00000567685
  gene symbol: ADAD2
  hgvsc: ENST00000567685.1:c.333+117C>G
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000565643
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000565643.1:n.492G>C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000268624
  ensembl transcript: ENST00000268624
  gene symbol: ADAD2
  hgvsc: ENST00000268624.3:c.775+117C>G
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000325153
  ensembl transcript: ENST00000315906
  gene symbol: ADAD2
  hgvsc: ENST00000315906.5:c.559+117C>G
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000569221
  gene symbol: ADAD2
  hgvsc: ENST00000569221.1:n.305C>G
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564169
  gene symbol: ADAD2
  hgvsc: ENST00000564169.1:n.224+117C>G
  variant of: http://identifiers.org/hgnc/30714
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1564
  bin: 1.75e1
  variant carriers: 1058
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 4.25e1
  variant carriers: 67
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1252
  bin: 2.75e1
  variant carriers: 495
genotype depth: GenotypeDepth
  all individuals: 1703
  bin: 2.25e1
  variant carriers: 788
genotype depth: GenotypeDepth
  all individuals: 6655
  bin: 7.5e0
  variant carriers: 2388
genotype depth: GenotypeDepth
  all individuals: 2954
  bin: 1.25e1
  variant carriers: 1055
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 5.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 4.75e1
  variant carriers: 45
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 25220
  bin: 2.5e0
  variant carriers: 2000
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 3.25e1
  variant carriers: 264
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 3.75e1
  variant carriers: 131
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.25e1
  variant carriers: 23
genotype quality: GenotypeQuality
  all individuals: 194
  bin: 5.25e1
  variant carriers: 123
genotype quality: GenotypeQuality
  all individuals: 774
  bin: 1.75e1
  variant carriers: 459
genotype quality: GenotypeQuality
  all individuals: 259
  bin: 3.75e1
  variant carriers: 95
genotype quality: GenotypeQuality
  all individuals: 214
  bin: 5.75e1
  variant carriers: 169
num of homozygotes: 665
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: C
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum

16-84228307-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84228307
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84228307
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 14334
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000325153
  ensembl transcript: ENST00000315906
  gene symbol: ADAD2
  hgvsc: ENST00000315906.5:c.559+119A>G
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000536986
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000536986.1:n.628T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000561900
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000561900.1:n.14T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000565643
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000565643.1:n.490T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564430
  gene symbol: ADAD2
  hgvsc: ENST00000564430.1:n.978A>G
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000569221
  gene symbol: ADAD2
  hgvsc: ENST00000569221.1:n.307A>G
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000268624
  ensembl transcript: ENST00000268624
  gene symbol: ADAD2
  hgvsc: ENST00000268624.3:c.775+119A>G
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000454950
  ensembl transcript: ENST00000567685
  gene symbol: ADAD2
  hgvsc: ENST00000567685.1:c.333+119A>G
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564169
  gene symbol: ADAD2
  hgvsc: ENST00000564169.1:n.224+119A>G
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000566526
  gene symbol: ADAD2
  hgvsc: ENST00000566526.1:n.1387+119A>G
  variant of: http://identifiers.org/hgnc/30714
canonical: true
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30786
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1192
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3442
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4959
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5789
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 9.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: DP

16-84228313-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84228313
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84228313
    reference: chr 16
allele count: 1
allele frequency: 7.51653638003608e-5
allele num: 13304
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000561900
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000561900.1:n.8G>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000569221
  gene symbol: ADAD2
  hgvsc: ENST00000569221.1:n.313C>G
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000566526
  gene symbol: ADAD2
  hgvsc: ENST00000566526.1:n.1387+125C>G
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000325153
  ensembl transcript: ENST00000315906
  gene symbol: ADAD2
  hgvsc: ENST00000315906.5:c.559+125C>G
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000565643
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000565643.1:n.484G>C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000268624
  ensembl transcript: ENST00000268624
  gene symbol: ADAD2
  hgvsc: ENST00000268624.3:c.775+125C>G
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564169
  gene symbol: ADAD2
  hgvsc: ENST00000564169.1:n.224+125C>G
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000536986
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000536986.1:n.622G>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564430
  gene symbol: ADAD2
  hgvsc: ENST00000564430.1:n.984C>G
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000454950
  ensembl transcript: ENST00000567685
  gene symbol: ADAD2
  hgvsc: ENST00000567685.1:c.333+125C>G
  variant of: http://identifiers.org/hgnc/30714
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30106
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3587
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4908
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3048
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27447
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 770
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: QD

16-84228321-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84228321
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84228321
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 11854
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000454950
  ensembl transcript: ENST00000567685
  gene symbol: ADAD2
  hgvsc: ENST00000567685.1:c.333+133C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564430
  gene symbol: ADAD2
  hgvsc: ENST00000564430.1:n.992C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564169
  gene symbol: ADAD2
  hgvsc: ENST00000564169.1:n.224+133C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000565643
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000565643.1:n.476G>A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000536986
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000536986.1:n.614G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000566526
  gene symbol: ADAD2
  hgvsc: ENST00000566526.1:n.1387+133C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000569221
  gene symbol: ADAD2
  hgvsc: ENST00000569221.1:n.321C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000325153
  ensembl transcript: ENST00000315906
  gene symbol: ADAD2
  hgvsc: ENST00000315906.5:c.559+133C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000268624
  ensembl transcript: ENST00000268624
  gene symbol: ADAD2
  hgvsc: ENST00000268624.3:c.775+133C>T
  variant of: http://identifiers.org/hgnc/30714
canonical: true
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3573
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4816
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29067
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 602
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 222
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 782
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 618
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: Other
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

16-84228323-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84228323
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84228323
    reference: chr 16
allele count: 1
allele frequency: 8.484642796538266e-5
allele num: 11786
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000536986
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000536986.1:n.612C>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000566526
  gene symbol: ADAD2
  hgvsc: ENST00000566526.1:n.1387+135G>C
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000325153
  ensembl transcript: ENST00000315906
  gene symbol: ADAD2
  hgvsc: ENST00000315906.5:c.559+135G>C
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564430
  gene symbol: ADAD2
  hgvsc: ENST00000564430.1:n.994G>C
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000565643
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000565643.1:n.474C>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564169
  gene symbol: ADAD2
  hgvsc: ENST00000564169.1:n.224+135G>C
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000569221
  gene symbol: ADAD2
  hgvsc: ENST00000569221.1:n.323G>C
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000454950
  ensembl transcript: ENST00000567685
  gene symbol: ADAD2
  hgvsc: ENST00000567685.1:c.333+135G>C
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000268624
  ensembl transcript: ENST00000268624
  gene symbol: ADAD2
  hgvsc: ENST00000268624.3:c.775+135G>C
  variant of: http://identifiers.org/hgnc/30714
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4824
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29135
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3562
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 675
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 281
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25985
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 216
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 894
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD

16-84228332-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84228332
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84228332
    reference: chr 16
allele count: 1
allele frequency: 1.045369015262388e-4
allele num: 9566
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000566526
  gene symbol: ADAD2
  hgvsc: ENST00000566526.1:n.1387+144C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000536986
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000536986.1:n.603G>A
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000565643
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000565643.1:n.466-1G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000569221
  gene symbol: ADAD2
  hgvsc: ENST00000569221.1:n.332C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564169
  gene symbol: ADAD2
  hgvsc: ENST00000564169.1:n.224+144C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000454950
  ensembl transcript: ENST00000567685
  gene symbol: ADAD2
  hgvsc: ENST00000567685.1:c.333+144C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000325153
  ensembl transcript: ENST00000315906
  gene symbol: ADAD2
  hgvsc: ENST00000315906.5:c.559+144C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000268624
  ensembl transcript: ENST00000268624
  gene symbol: ADAD2
  hgvsc: ENST00000268624.3:c.775+144C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564430
  gene symbol: ADAD2
  hgvsc: ENST00000564430.1:n.1003C>T
  variant of: http://identifiers.org/hgnc/30714
canonical: false
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4841
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28055
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3026
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 516
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 881
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 866
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 4.25e1
  variant carriers: 0
hgvs: n.466-1G>A
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/16-84228342-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84228342
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84228342
    reference: chr 16
allele count: 640
allele frequency: 7.703418391911411e-2
allele num: 8308
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000325153
  ensembl transcript: ENST00000315906
  gene symbol: ADAD2
  hgvsc: ENST00000315906.5:c.559+154C>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000536986
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000536986.1:n.593G>T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000268624
  ensembl transcript: ENST00000268624
  gene symbol: ADAD2
  hgvsc: ENST00000268624.3:c.775+154C>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564169
  gene symbol: ADAD2
  hgvsc: ENST00000564169.1:n.224+154C>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000569221
  gene symbol: ADAD2
  hgvsc: ENST00000569221.1:n.342C>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564430
  gene symbol: ADAD2
  hgvsc: ENST00000564430.1:n.1013C>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000565643
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000565643.1:n.466-11G>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000566526
  gene symbol: ADAD2
  hgvsc: ENST00000566526.1:n.1387+154C>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000454950
  ensembl transcript: ENST00000567685
  gene symbol: ADAD2
  hgvsc: ENST00000567685.1:c.333+154C>A
  variant of: http://identifiers.org/hgnc/30714
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 4.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 27456
  bin: 2.5e0
  variant carriers: 386
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 3.75e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 2.75e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 3.25e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2514
  bin: 1.25e1
  variant carriers: 295
genotype depth: GenotypeDepth
  all individuals: 5186
  bin: 7.5e0
  variant carriers: 605
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 1.75e1
  variant carriers: 133
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 4.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 2.25e1
  variant carriers: 61
genotype quality: GenotypeQuality
  all individuals: 835
  bin: 1.25e1
  variant carriers: 70
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 7.75e1
  variant carriers: 20
genotype quality: GenotypeQuality
  all individuals: 5738
  bin: 2.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 22060
  bin: 7.5e0
  variant carriers: 174
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 8.25e1
  variant carriers: 48
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 6.75e1
  variant carriers: 60
num of homozygotes: 31
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: Other
population: East Asian
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD

16-84228349-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84228349
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84228349
    reference: chr 16
allele count: 1
allele frequency: 1.421666192777936e-4
allele num: 7034
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000454950
  ensembl transcript: ENST00000567685
  gene symbol: ADAD2
  hgvsc: ENST00000567685.1:c.333+161G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000268624
  ensembl transcript: ENST00000268624
  gene symbol: ADAD2
  hgvsc: ENST00000268624.3:c.775+161G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564169
  gene symbol: ADAD2
  hgvsc: ENST00000564169.1:n.224+161G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000536986
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000536986.1:n.586C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000566526
  gene symbol: ADAD2
  hgvsc: ENST00000566526.1:n.1387+161G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564430
  gene symbol: ADAD2
  hgvsc: ENST00000564430.1:n.1020G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000569221
  gene symbol: ADAD2
  hgvsc: ENST00000569221.1:n.349G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000565643
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000565643.1:n.466-18C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000325153
  ensembl transcript: ENST00000315906
  gene symbol: ADAD2
  hgvsc: ENST00000315906.5:c.559+161G>A
  variant of: http://identifiers.org/hgnc/30714
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29552
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2024
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5022
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4500
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25258
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 168
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 475
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

16-84228350-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84228350
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84228350
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 6888
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000325153
  ensembl transcript: ENST00000315906
  gene symbol: ADAD2
  hgvsc: ENST00000315906.5:c.559+162G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000565643
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000565643.1:n.466-19C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000569221
  gene symbol: ADAD2
  hgvsc: ENST00000569221.1:n.350G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000566526
  gene symbol: ADAD2
  hgvsc: ENST00000566526.1:n.1387+162G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564169
  gene symbol: ADAD2
  hgvsc: ENST00000564169.1:n.224+162G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000268624
  ensembl transcript: ENST00000268624
  gene symbol: ADAD2
  hgvsc: ENST00000268624.3:c.775+162G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000536986
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000536986.1:n.585C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000454950
  ensembl transcript: ENST00000567685
  gene symbol: ADAD2
  hgvsc: ENST00000567685.1:c.333+162G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564430
  gene symbol: ADAD2
  hgvsc: ENST00000564430.1:n.1021G>A
  variant of: http://identifiers.org/hgnc/30714
canonical: true
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 1932
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5026
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29604
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1134
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24999
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4774
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 168
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD

16-84228356-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84228356
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84228356
    reference: chr 16
allele count: 2
allele frequency: 3.059975520195838e-4
allele num: 6536
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000454950
  ensembl transcript: ENST00000567685
  gene symbol: ADAD2
  hgvsc: ENST00000567685.1:c.333+168A>G
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000268624
  ensembl transcript: ENST00000268624
  gene symbol: ADAD2
  hgvsc: ENST00000268624.3:c.775+168A>G
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000569221
  gene symbol: ADAD2
  hgvsc: ENST00000569221.1:n.356A>G
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000566526
  gene symbol: ADAD2
  hgvsc: ENST00000566526.1:n.1387+168A>G
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564430
  gene symbol: ADAD2
  hgvsc: ENST00000564430.1:n.1027A>G
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000536986
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000536986.1:n.579T>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000325153
  ensembl transcript: ENST00000315906
  gene symbol: ADAD2
  hgvsc: ENST00000315906.5:c.559+168A>G
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564169
  gene symbol: ADAD2
  hgvsc: ENST00000564169.1:n.224+168A>G
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000565643
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000565643.1:n.466-25T>C
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5029
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30621
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1742
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 393
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26053
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 176
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
reference allele: A
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum

16-84228357-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84228357
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84228357
    reference: chr 16
allele count: 1
allele frequency: 1.545117428924598e-4
allele num: 6472
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000454950
  ensembl transcript: ENST00000567685
  gene symbol: ADAD2
  hgvsc: ENST00000567685.1:c.333+169T>G
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000569221
  gene symbol: ADAD2
  hgvsc: ENST00000569221.1:n.357T>G
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000536986
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000536986.1:n.578A>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564430
  gene symbol: ADAD2
  hgvsc: ENST00000564430.1:n.1028T>G
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000566526
  gene symbol: ADAD2
  hgvsc: ENST00000566526.1:n.1387+169T>G
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000325153
  ensembl transcript: ENST00000315906
  gene symbol: ADAD2
  hgvsc: ENST00000315906.5:c.559+169T>G
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564169
  gene symbol: ADAD2
  hgvsc: ENST00000564169.1:n.224+169T>G
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000565643
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000565643.1:n.466-26A>C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000268624
  ensembl transcript: ENST00000268624
  gene symbol: ADAD2
  hgvsc: ENST00000268624.3:c.775+169T>G
  variant of: http://identifiers.org/hgnc/30714
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5028
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30774
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1717
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 809
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 474
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 392
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: Other
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum

16-84228362-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84228362
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84228362
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 6038
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000569221
  gene symbol: ADAD2
  hgvsc: ENST00000569221.1:n.362C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000566526
  gene symbol: ADAD2
  hgvsc: ENST00000566526.1:n.1387+174C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000536986
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000536986.1:n.573G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564430
  gene symbol: ADAD2
  hgvsc: ENST00000564430.1:n.1033C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000325153
  ensembl transcript: ENST00000315906
  gene symbol: ADAD2
  hgvsc: ENST00000315906.5:c.559+174C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000454950
  ensembl transcript: ENST00000567685
  gene symbol: ADAD2
  hgvsc: ENST00000567685.1:c.333+174C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000565643
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000565643.1:n.466-31G>A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000268624
  ensembl transcript: ENST00000268624
  gene symbol: ADAD2
  hgvsc: ENST00000268624.3:c.775+174C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564169
  gene symbol: ADAD2
  hgvsc: ENST00000564169.1:n.224+174C>T
  variant of: http://identifiers.org/hgnc/30714
canonical: true
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 1520
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31566
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5170
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26671
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1397
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3467
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5094
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ

16-84228377-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84228377
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84228377
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 5730
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000569221
  gene symbol: ADAD2
  hgvsc: ENST00000569221.1:n.377C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000268624
  ensembl transcript: ENST00000268624
  gene symbol: ADAD2
  hgvsc: ENST00000268624.3:c.776-162C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000566526
  gene symbol: ADAD2
  hgvsc: ENST00000566526.1:n.1388-162C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000536986
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000536986.1:n.558G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000325153
  ensembl transcript: ENST00000315906
  gene symbol: ADAD2
  hgvsc: ENST00000315906.5:c.560-162C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000565643
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000565643.1:n.466-46G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564169
  gene symbol: ADAD2
  hgvsc: ENST00000564169.1:n.225-162C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564430
  gene symbol: ADAD2
  hgvsc: ENST00000564430.1:n.1048C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000454950
  ensembl transcript: ENST00000567685
  gene symbol: ADAD2
  hgvsc: ENST00000567685.1:c.333+189C>T
  variant of: http://identifiers.org/hgnc/30714
canonical: true
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5838
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34889
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1308
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5667
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 189
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 392
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3012
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

16-84228378-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84228378
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84228378
    reference: chr 16
allele count: 2
allele frequency: 3.485535029627048e-4
allele num: 5738
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564430
  gene symbol: ADAD2
  hgvsc: ENST00000564430.1:n.1049G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000454950
  ensembl transcript: ENST00000567685
  gene symbol: ADAD2
  hgvsc: ENST00000567685.1:c.333+190G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000569221
  gene symbol: ADAD2
  hgvsc: ENST00000569221.1:n.378G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000536986
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000536986.1:n.557C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000565643
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000565643.1:n.466-47C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000325153
  ensembl transcript: ENST00000315906
  gene symbol: ADAD2
  hgvsc: ENST00000315906.5:c.560-161G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564169
  gene symbol: ADAD2
  hgvsc: ENST00000564169.1:n.225-161G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000566526
  gene symbol: ADAD2
  hgvsc: ENST00000566526.1:n.1388-161G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000268624
  ensembl transcript: ENST00000268624
  gene symbol: ADAD2
  hgvsc: ENST00000268624.3:c.776-161G>A
  variant of: http://identifiers.org/hgnc/30714
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35252
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1297
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5936
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5780
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 392
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 187
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

16-84228380-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84228380
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84228380
    reference: chr 16
allele count: 1
allele frequency: 1.739130434782609e-4
allele num: 5750
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000569221
  gene symbol: ADAD2
  hgvsc: ENST00000569221.1:n.380C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564430
  gene symbol: ADAD2
  hgvsc: ENST00000564430.1:n.1051C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000566526
  gene symbol: ADAD2
  hgvsc: ENST00000566526.1:n.1388-159C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000268624
  ensembl transcript: ENST00000268624
  gene symbol: ADAD2
  hgvsc: ENST00000268624.3:c.776-159C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000565643
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000565643.1:n.466-49G>A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000536986
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000536986.1:n.555G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000454950
  ensembl transcript: ENST00000567685
  gene symbol: ADAD2
  hgvsc: ENST00000567685.1:c.333+192C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000325153
  ensembl transcript: ENST00000315906
  gene symbol: ADAD2
  hgvsc: ENST00000315906.5:c.560-159C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564169
  gene symbol: ADAD2
  hgvsc: ENST00000564169.1:n.225-159C>T
  variant of: http://identifiers.org/hgnc/30714
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6066
  bin: 7.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1309
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35688
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 402
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 391
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: African
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ

16-84228492-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84228492
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84228492
    reference: chr 16
allele count: 3
allele frequency: 3.025535519787002e-5
allele num: 99156
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000566526
  gene symbol: ADAD2
  hgvsc: ENST00000566526.1:n.1388-47G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564169
  gene symbol: ADAD2
  hgvsc: ENST00000564169.1:n.225-47G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000454950
  ensembl transcript: ENST00000567685
  gene symbol: ADAD2
  hgvsc: ENST00000567685.1:c.334-183G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564430
  gene symbol: ADAD2
  hgvsc: ENST00000564430.1:n.1163G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000536986
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000536986.1:n.443C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000325153
  ensembl transcript: ENST00000315906
  gene symbol: ADAD2
  hgvsc: ENST00000315906.5:c.560-47G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000565643
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000565643.1:n.465+159C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000569221
  gene symbol: ADAD2
  hgvsc: ENST00000569221.1:n.492G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000268624
  ensembl transcript: ENST00000268624
  gene symbol: ADAD2
  hgvsc: ENST00000268624.3:c.776-47G>A
  variant of: http://identifiers.org/hgnc/30714
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14824
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1802
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2026
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13454
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8557
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12369
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5354
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1665
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8428
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6035
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3042
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3203
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1128
  bin: 7.25e1
  variant carriers: 1
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: South Asian
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: DP

16-84228502-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84228502
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84228502
    reference: chr 16
allele count: 1
allele frequency: 9.994403134244822e-6
allele num: 100056
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000565643
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000565643.1:n.465+149C>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000569221
  gene symbol: ADAD2
  hgvsc: ENST00000569221.1:n.502G>C
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000325153
  ensembl transcript: ENST00000315906
  gene symbol: ADAD2
  hgvsc: ENST00000315906.5:c.560-37G>C
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000536986
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000536986.1:n.433C>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564430
  gene symbol: ADAD2
  hgvsc: ENST00000564430.1:n.1173G>C
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000566526
  gene symbol: ADAD2
  hgvsc: ENST00000566526.1:n.1388-37G>C
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000268624
  ensembl transcript: ENST00000268624
  gene symbol: ADAD2
  hgvsc: ENST00000268624.3:c.776-37G>C
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564169
  gene symbol: ADAD2
  hgvsc: ENST00000564169.1:n.225-37G>C
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000454950
  ensembl transcript: ENST00000567685
  gene symbol: ADAD2
  hgvsc: ENST00000567685.1:c.334-173G>C
  variant of: http://identifiers.org/hgnc/30714
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2068
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8035
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6214
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1771
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8409
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13980
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17904
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1128
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 266
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2631
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18452
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9356
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 861
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum

16-84228506-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84228506
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84228506
    reference: chr 16
allele count: 1
allele frequency: 9.943125323151573e-6
allele num: 100572
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000536986
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000536986.1:n.429G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564430
  gene symbol: ADAD2
  hgvsc: ENST00000564430.1:n.1177C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000569221
  gene symbol: ADAD2
  hgvsc: ENST00000569221.1:n.506C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000325153
  ensembl transcript: ENST00000315906
  gene symbol: ADAD2
  hgvsc: ENST00000315906.5:c.560-33C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000566526
  gene symbol: ADAD2
  hgvsc: ENST00000566526.1:n.1388-33C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000454950
  ensembl transcript: ENST00000567685
  gene symbol: ADAD2
  hgvsc: ENST00000567685.1:c.334-169C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000268624
  ensembl transcript: ENST00000268624
  gene symbol: ADAD2
  hgvsc: ENST00000268624.3:c.776-33C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564169
  gene symbol: ADAD2
  hgvsc: ENST00000564169.1:n.225-33C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000565643
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000565643.1:n.465+145G>A
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13199
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2253
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19500
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8303
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6800
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1625
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6688
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2211
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 288
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1486
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1174
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4167
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5239
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP

16-84228510-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84228510
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84228510
    reference: chr 16
allele count: 1
allele frequency: 9.875762902684232e-6
allele num: 101258
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000565643
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000565643.1:n.465+141G>A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000536986
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000536986.1:n.425G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000454950
  ensembl transcript: ENST00000567685
  gene symbol: ADAD2
  hgvsc: ENST00000567685.1:c.334-165C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000569221
  gene symbol: ADAD2
  hgvsc: ENST00000569221.1:n.510C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000325153
  ensembl transcript: ENST00000315906
  gene symbol: ADAD2
  hgvsc: ENST00000315906.5:c.560-29C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564430
  gene symbol: ADAD2
  hgvsc: ENST00000564430.1:n.1181C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000268624
  ensembl transcript: ENST00000268624
  gene symbol: ADAD2
  hgvsc: ENST00000268624.3:c.776-29C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000566526
  gene symbol: ADAD2
  hgvsc: ENST00000566526.1:n.1388-29C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564169
  gene symbol: ADAD2
  hgvsc: ENST00000564169.1:n.225-29C>T
  variant of: http://identifiers.org/hgnc/30714
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2379
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1513
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12406
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5783
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7194
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8177
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20912
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1270
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1778
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 579
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 275
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1229
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 225
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum

16-84228518-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84228518
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84228518
    reference: chr 16
allele count: 26
allele frequency: 2.536387403909939e-4
allele num: 102508
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000268624
  ensembl transcript: ENST00000268624
  gene symbol: ADAD2
  hgvsc: ENST00000268624.3:c.776-21C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000569221
  gene symbol: ADAD2
  hgvsc: ENST00000569221.1:n.518C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564430
  gene symbol: ADAD2
  hgvsc: ENST00000564430.1:n.1189C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000325153
  ensembl transcript: ENST00000315906
  gene symbol: ADAD2
  hgvsc: ENST00000315906.5:c.560-21C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564169
  gene symbol: ADAD2
  hgvsc: ENST00000564169.1:n.225-21C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000565643
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000565643.1:n.465+133G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000454950
  ensembl transcript: ENST00000567685
  gene symbol: ADAD2
  hgvsc: ENST00000567685.1:c.334-157C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000566526
  gene symbol: ADAD2
  hgvsc: ENST00000566526.1:n.1388-21C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000536986
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000536986.1:n.417G>A
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1234
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10134
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3799
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7771
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8174
  bin: 2.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2833
  bin: 3.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 24385
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 452
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 762
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 555
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3117
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8931
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1346
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum

16-84228519-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84228519
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84228519
    reference: chr 16
allele count: 6
allele frequency: 5.833738454059309e-5
allele num: 102850
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000565643
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000565643.1:n.465+132C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564169
  gene symbol: ADAD2
  hgvsc: ENST00000564169.1:n.225-20G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000325153
  ensembl transcript: ENST00000315906
  gene symbol: ADAD2
  hgvsc: ENST00000315906.5:c.560-20G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000536986
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000536986.1:n.416C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000454950
  ensembl transcript: ENST00000567685
  gene symbol: ADAD2
  hgvsc: ENST00000567685.1:c.334-156G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564430
  gene symbol: ADAD2
  hgvsc: ENST00000564430.1:n.1190G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000566526
  gene symbol: ADAD2
  hgvsc: ENST00000566526.1:n.1388-20G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000569221
  gene symbol: ADAD2
  hgvsc: ENST00000569221.1:n.519G>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000268624
  ensembl transcript: ENST00000268624
  gene symbol: ADAD2
  hgvsc: ENST00000268624.3:c.776-20G>A
  variant of: http://identifiers.org/hgnc/30714
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7687
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9713
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2948
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24754
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1174
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8427
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3627
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 422
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1378
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8801
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 754
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 1082
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 892
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

16-84228520-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84228520
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84228520
    reference: chr 16
allele count: 2
allele frequency: 1.937158575801015e-5
allele num: 103244
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564430
  gene symbol: ADAD2
  hgvsc: ENST00000564430.1:n.1191C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564169
  gene symbol: ADAD2
  hgvsc: ENST00000564169.1:n.225-19C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000566526
  gene symbol: ADAD2
  hgvsc: ENST00000566526.1:n.1388-19C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000454950
  ensembl transcript: ENST00000567685
  gene symbol: ADAD2
  hgvsc: ENST00000567685.1:c.334-155C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000268624
  ensembl transcript: ENST00000268624
  gene symbol: ADAD2
  hgvsc: ENST00000268624.3:c.776-19C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000536986
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000536986.1:n.415G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000325153
  ensembl transcript: ENST00000315906
  gene symbol: ADAD2
  hgvsc: ENST00000315906.5:c.560-19C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000569221
  gene symbol: ADAD2
  hgvsc: ENST00000569221.1:n.520C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000565643
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000565643.1:n.465+131G>A
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7606
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3342
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8581
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25363
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9286
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3013
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2445
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 418
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 735
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 192
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 976
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 281
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: MQ

16-84228529-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84228529
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84228529
    reference: chr 16
allele count: 1
allele frequency: 9.463065654749513e-6
allele num: 105674
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000454950
  ensembl transcript: ENST00000567685
  gene symbol: ADAD2
  hgvsc: ENST00000567685.1:c.334-146C>G
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000325153
  ensembl transcript: ENST00000315906
  gene symbol: ADAD2
  hgvsc: ENST00000315906.5:c.560-10C>G
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000566526
  gene symbol: ADAD2
  hgvsc: ENST00000566526.1:n.1388-10C>G
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000565643
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000565643.1:n.465+122G>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000569221
  gene symbol: ADAD2
  hgvsc: ENST00000569221.1:n.529C>G
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000536986
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000536986.1:n.406G>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564430
  gene symbol: ADAD2
  hgvsc: ENST00000564430.1:n.1200C>G
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000268624
  ensembl transcript: ENST00000268624
  gene symbol: ADAD2
  hgvsc: ENST00000268624.3:c.776-10C>G
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564169
  gene symbol: ADAD2
  hgvsc: ENST00000564169.1:n.225-10C>G
  variant of: http://identifiers.org/hgnc/30714
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6540
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3528
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2089
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28610
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9859
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6812
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7999
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 683
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 226
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5307
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2194
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum

16-84228533-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84228533
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84228533
    reference: chr 16
allele count: 2
allele frequency: 1.876771202822664e-5
allele num: 106566
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000565643
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000565643.1:n.465+118A>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564169
  gene symbol: ADAD2
  hgvsc: ENST00000564169.1:n.225-6T>G
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000325153
  ensembl transcript: ENST00000315906
  gene symbol: ADAD2
  hgvsc: ENST00000315906.5:c.560-6T>G
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000268624
  ensembl transcript: ENST00000268624
  gene symbol: ADAD2
  hgvsc: ENST00000268624.3:c.776-6T>G
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000569221
  gene symbol: ADAD2
  hgvsc: ENST00000569221.1:n.533T>G
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000454950
  ensembl transcript: ENST00000567685
  gene symbol: ADAD2
  hgvsc: ENST00000567685.1:c.334-142T>G
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564430
  gene symbol: ADAD2
  hgvsc: ENST00000564430.1:n.1204T>G
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000536986
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000536986.1:n.402A>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000566526
  gene symbol: ADAD2
  hgvsc: ENST00000566526.1:n.1388-6T>G
  variant of: http://identifiers.org/hgnc/30714
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29047
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10399
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1932
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6544
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5938
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3648
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 481
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1504
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33133
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2200
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 767
  bin: 9.75e1
  variant carriers: 2
hgvs: c.776-6T>G
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP

http://identifiers.org/exac.variant/16-84228542-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84228542
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84228542
    reference: chr 16
allele count: 5
allele frequency: 4.622268239470473e-5
allele num: 108172
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000268624
  ensembl transcript: ENST00000268624
  gene symbol: ADAD2
  hgvsc: ENST00000268624.3:c.779C>A
  hgvsp: ENSP00000268624.3:p.Ser260Tyr
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564169
  gene symbol: ADAD2
  hgvsc: ENST00000564169.1:n.228C>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000565643
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000565643.1:n.465+109G>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000569834
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000569834.1:n.573G>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000325153
  ensembl transcript: ENST00000315906
  gene symbol: ADAD2
  hgvsc: ENST00000315906.5:c.563C>A
  hgvsp: ENSP00000325153.5:p.Ser188Tyr
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564430
  gene symbol: ADAD2
  hgvsc: ENST00000564430.1:n.1213C>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000536986
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000536986.1:n.393G>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000454950
  ensembl transcript: ENST00000567685
  gene symbol: ADAD2
  hgvsc: ENST00000567685.1:c.334-133C>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000566526
  gene symbol: ADAD2
  hgvsc: ENST00000566526.1:n.1391C>A
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000569221
  gene symbol: ADAD2
  hgvsc: ENST00000569221.1:n.542C>A
  variant of: http://identifiers.org/hgnc/30714
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4141
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1779
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5670
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29854
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11440
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4626
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 469
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 272
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 782
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1094
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ser260Tyr
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

16-84228543-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84228543
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84228543
    reference: chr 16
allele count: 1
allele frequency: 9.20454336260378e-6
allele num: 108642
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564430
  gene symbol: ADAD2
  hgvsc: ENST00000564430.1:n.1214C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564169
  gene symbol: ADAD2
  hgvsc: ENST00000564169.1:n.229C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000565643
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000565643.1:n.465+108G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000569221
  gene symbol: ADAD2
  hgvsc: ENST00000569221.1:n.543C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000268624
  ensembl transcript: ENST00000268624
  gene symbol: ADAD2
  hgvsc: ENST00000268624.3:c.780C>T
  hgvsp: ENST00000268624.3:c.780C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000325153
  ensembl transcript: ENST00000315906
  gene symbol: ADAD2
  hgvsc: ENST00000315906.5:c.564C>T
  hgvsp: ENST00000315906.5:c.564C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000536986
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000536986.1:n.392G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000454950
  ensembl transcript: ENST00000567685
  gene symbol: ADAD2
  hgvsc: ENST00000567685.1:c.334-132C>T
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000569834
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000569834.1:n.572G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000566526
  gene symbol: ADAD2
  hgvsc: ENST00000566526.1:n.1392C>T
  variant of: http://identifiers.org/hgnc/30714
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1677
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11618
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4247
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5485
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30106
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4396
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 424
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 603
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 302
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Ser260Ser
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP

16-84228545-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 84228545
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 84228545
    reference: chr 16
allele count: 1
allele frequency: 9.104814625974215e-6
allele num: 109832
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000325153
  ensembl transcript: ENST00000315906
  gene symbol: ADAD2
  hgvsc: ENST00000315906.5:c.566C>G
  hgvsp: ENSP00000325153.5:p.Pro189Arg
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564430
  gene symbol: ADAD2
  hgvsc: ENST00000564430.1:n.1216C>G
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000566526
  gene symbol: ADAD2
  hgvsc: ENST00000566526.1:n.1394C>G
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000564169
  gene symbol: ADAD2
  hgvsc: ENST00000564169.1:n.231C>G
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000565643
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000565643.1:n.465+106G>C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000268624
  ensembl transcript: ENST00000268624
  gene symbol: ADAD2
  hgvsc: ENST00000268624.3:c.782C>G
  hgvsp: ENSP00000268624.3:p.Pro261Arg
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140955
  ensembl transcript: ENST00000569221
  gene symbol: ADAD2
  hgvsc: ENST00000569221.1:n.545C>G
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140955
  ensembl protein: ENSP00000454950
  ensembl transcript: ENST00000567685
  gene symbol: ADAD2
  hgvsc: ENST00000567685.1:c.334-130C>G
  variant of: http://identifiers.org/hgnc/30714
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000536986
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000536986.1:n.390G>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000250685
  ensembl transcript: ENST00000569834
  gene symbol: RP11-486L19.2
  hgvsc: ENST00000569834.1:n.570G>C
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 3959
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1524
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11892
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5126
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4380
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30659
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 347
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 898
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1657
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Pro261Arg
num of homozygotes: 0
population: European (Non-Finnish)
reference allele: C

GenotypeQuality
all individuals: 1851
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1101
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 500
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 683
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3953
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16121
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1507
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 934
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4114
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 737
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22393
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1045
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 518
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 383
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2185
bin: 3.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3914
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 646
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 49620
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6476
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7696
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.969397513547975e-5
allele num: 12548
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7800
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 9.70771e5

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.9e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -7.36e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.2e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.07e-1

FS
type: SiteQuality
SIO_000300: 9.330000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.62e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.26e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.045e1

GenotypeQuality
all individuals: 1045
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16121
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 500
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 518
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 4114
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1851
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3953
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 934
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 632
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1101
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2185
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 683
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 383
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1507
bin: 5.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12548
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7696
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7800
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6476
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3914
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 646
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.030632809351068e-5
allele num: 49620
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.07e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.36e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.62e-1

FS
type: SiteQuality
SIO_000300: 9.330000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.2e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.9e-3

QD
type: SiteQuality
SIO_000300: 1.045e1

DP
type: SiteQuality
SIO_000300: 9.70771e5

ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 frequency: 0.0e0
allele num: 49466
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 6454
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Latino
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allele frequency: 3.919519205644108e-4
allele num: 7654
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3888
num of homozygotes: 0

African
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allele frequency: 0.0e0
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South Asian
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Other
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DP
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BaseQRankSum
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ClippingRankSum
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SIO_000300: -8.51e-1

MQRankSum
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MQ
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ReadPosRankSum
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VQSLOD
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QD
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FS
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InbreedingCoeff
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SIO_000300: -5.2e-3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

European (Non-Finnish)
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allele frequency: 0.0e0
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Latino
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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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South Asian
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allele frequency: 0.0e0
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African
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allele frequency: 1.290322580645161e-4
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Other
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QD
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FS
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DP
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ReadPosRankSum
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ClippingRankSum
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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MQ
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 12440
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Latino
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Other
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African
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allele frequency: 0.0e0
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East Asian
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European (Non-Finnish)
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allele frequency: 0.0e0
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European (Finnish)
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num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.664e0

MQ
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SIO_000300: 5.914e1

InbreedingCoeff
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ClippingRankSum
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VQSLOD
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MQRankSum
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BaseQRankSum
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QD
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ReadPosRankSum
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DP
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
allele num: 6226
num of homozygotes: 0

African
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allele count: 4
allele frequency: 5.274261603375527e-4
allele num: 7584
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12238
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Latino
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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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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.34e-1

DP
type: SiteQuality
SIO_000300: 9.28478e5

QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -5.8e-3

FS
type: SiteQuality
SIO_000300: 3.577e0

ReadPosRankSum
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SIO_000300: 7.36e-1

MQ
type: SiteQuality
SIO_000300: 5.787e1

VQSLOD
type: SiteQuality
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BaseQRankSum
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SIO_000300: -1.584e0

ClippingRankSum
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SIO_000300: -5.97e-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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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num of homozygotes: 0

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

African
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East Asian
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European (Non-Finnish)
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allele num: 46432
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Latino
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Other
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South Asian
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allele num: 12028
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QD
type: SiteQuality
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BaseQRankSum
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MQ
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ClippingRankSum
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FS
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MQRankSum
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ReadPosRankSum
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VQSLOD
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DP
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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South Asian
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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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FS
type: SiteQuality
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BaseQRankSum
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ClippingRankSum
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ReadPosRankSum
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VQSLOD
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DP
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InbreedingCoeff
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MQ
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MQRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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South Asian
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East Asian
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Latino
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European (Non-Finnish)
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Other
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African
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BaseQRankSum
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DP
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InbreedingCoeff
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MQ
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MQRankSum
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ClippingRankSum
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FS
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QD
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VQSLOD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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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: 1

GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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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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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7258
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6680
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 596
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.191060473269062e-5
allele num: 45640
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5850
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3500
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11876
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.6e-3

MQRankSum
type: SiteQuality
SIO_000300: -2.05e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.128e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.32e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 8.79997e5

VQSLOD
type: SiteQuality
SIO_000300: 4.89e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.186e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.03e0

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
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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: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6696
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.189812989970656e-5
allele num: 45666
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 592
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7292
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5876
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3494
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11874
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.943e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.13e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.5e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 1.15e0

FS
type: SiteQuality
SIO_000300: 9.48e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.045e0

MQRankSum
type: SiteQuality
SIO_000300: 1.76e0

DP
type: SiteQuality
SIO_000300: 8.79154e5

ClippingRankSum
type: SiteQuality
SIO_000300: -1.13e-1

QD
type: SiteQuality
SIO_000300: 5.63e0

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11714
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7174
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5728
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.244265900623906e-5
allele num: 44558
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6448
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3392
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 580
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.166e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.500000000000001e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.05e0

VQSLOD
type: SiteQuality
SIO_000300: 5.55e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.46e-1

QD
type: SiteQuality
SIO_000300: 1.459e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 2.96e-1

FS
type: SiteQuality
SIO_000300: 3.707e0

DP
type: SiteQuality
SIO_000300: 8.62755e5

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

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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GenotypeQuality
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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: 2

GenotypeQuality
all individuals: 589
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variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6332
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3312
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5670
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11624
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7104
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.551661356395084e-5
allele num: 43940
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 572
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.800000000000001e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.259e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.9e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.8e-2

DP
type: SiteQuality
SIO_000300: 8.5162e5

FS
type: SiteQuality
SIO_000300: 8.05e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.97e0

MQRankSum
type: SiteQuality
SIO_000300: 3.37e-1

QD
type: SiteQuality
SIO_000300: 1.322e1

GenotypeQuality
all individuals: 24671
bin: 2.25e1
variant carriers: 0

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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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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variant carriers: 1

GenotypeQuality
all individuals: 159
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variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 42010
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3108
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.453065969195002e-4
allele num: 6882
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 544
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5972
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11440
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5388
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.22e-1

DP
type: SiteQuality
SIO_000300: 8.22973e5

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.8e-2

MQRankSum
type: SiteQuality
SIO_000300: -3.7e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.65e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.299999999999999e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.51e0

QD
type: SiteQuality
SIO_000300: 1.39e1

GenotypeQuality
all individuals: 7586
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
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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
all individuals: 4397
bin: 7.5e0
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5666
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5158
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.492091912861832e-4
allele num: 6702
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 40322
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11212
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2912
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 518
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.42e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.42e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.895e0

FS
type: SiteQuality
SIO_000300: 1.547e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.04e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.42e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.6e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 8.05681e5

QD
type: SiteQuality
SIO_000300: 3.93e0

GenotypeQuality
all individuals: 188
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 861
bin: 4.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 518
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6724
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.763046544428773e-4
allele num: 5672
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2908
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5132
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11222
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.47794627812469e-5
allele num: 40356
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.68e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.03e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.68e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.500000000000001e-3

MQRankSum
type: SiteQuality
SIO_000300: -5.21e-1

FS
type: SiteQuality
SIO_000300: 3.227e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.635e0

DP
type: SiteQuality
SIO_000300: 8.05416e5

QD
type: SiteQuality
SIO_000300: 7.94e0

GenotypeQuality
all individuals: 2283
bin: 2.75e1
variant carriers: 419

GenotypeQuality
all individuals: 1145
bin: 3.75e1
variant carriers: 539

GenotypeQuality
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bin: 8.75e1
variant carriers: 615

GenotypeQuality
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bin: 3.25e1
variant carriers: 616

GenotypeQuality
all individuals: 425
bin: 5.75e1
variant carriers: 389

GenotypeQuality
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bin: 2.5e0
variant carriers: 86

GenotypeQuality
all individuals: 1009
bin: 1.25e1
variant carriers: 252

GenotypeQuality
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variant carriers: 663

GenotypeQuality
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bin: 6.25e1
variant carriers: 485

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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variant carriers: 467

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 7.75e1
variant carriers: 516

GenotypeQuality
all individuals: 516
bin: 5.25e1
variant carriers: 396

GenotypeQuality
all individuals: 610
bin: 9.25e1
variant carriers: 531

GenotypeQuality
all individuals: 780
bin: 8.25e1
variant carriers: 595

Latino
type: Population
allele count: 1214
allele frequency: 2.193711601011926e-1
allele num: 5534
num of homozygotes: 85

East Asian
type: Population
allele count: 1117
allele frequency: 2.198818897637795e-1
allele num: 5080
num of homozygotes: 86

European (Non-Finnish)
type: Population
allele count: 12846
allele frequency: 3.17970297029703e-1
allele num: 40400
num of homozygotes: 1591

European (Finnish)
type: Population
allele count: 1030
allele frequency: 3.503401360544218e-1
allele num: 2940
num of homozygotes: 121

Other
type: Population
allele count: 164
allele frequency: 3.082706766917293e-1
allele num: 532
num of homozygotes: 18

African
type: Population
allele count: 3114
allele frequency: 4.544658493870403e-1
allele num: 6852
num of homozygotes: 645

South Asian
type: Population
allele count: 1677
allele frequency: 1.487229514012061e-1
allele num: 11276
num of homozygotes: 108

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.28e0

FS
type: SiteQuality
SIO_000300: 1.992e0

DP
type: SiteQuality
SIO_000300: 9.7722e5

MQRankSum
type: SiteQuality
SIO_000300: 1.01e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.754e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.06e-2

QD
type: SiteQuality
SIO_000300: 1.48e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.41e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 356
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 340
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2945
bin: 3.25e1
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GenotypeQuality
all individuals: 29459
bin: 2.25e1
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GenotypeQuality
all individuals: 985
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GenotypeQuality
all individuals: 196
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GenotypeQuality
all individuals: 7328
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GenotypeQuality
all individuals: 1891
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
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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variant carriers: 0

European (Non-Finnish)
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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 frequency: 0.0e0
allele num: 2060
num of homozygotes: 0

East Asian
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allele frequency: 2.361832782239018e-4
allele num: 4234
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 4476
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 frequency: 0.0e0
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num of homozygotes: 0

InbreedingCoeff
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SIO_000300: -1.49e-2

ClippingRankSum
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FS
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VQSLOD
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DP
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BaseQRankSum
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MQ
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SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -6.98e-1

QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -1.56e-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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 3.75e1
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European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 31584
num of homozygotes: 0

African
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allele frequency: 0.0e0
allele num: 5428
num of homozygotes: 0

Latino
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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: 4096
num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
allele num: 428
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10544
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1938
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.36e-1

DP
type: SiteQuality
SIO_000300: 8.02285e5

ReadPosRankSum
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FS
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -1.076e-1

MQRankSum
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MQ
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SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.71e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 7.36e-1

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 10480
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 3.225598348493646e-5
allele num: 31002
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 4152
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1884
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4012
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
allele num: 418
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.131e0

InbreedingCoeff
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SIO_000300: -1.81e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.33e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
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QD
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MQRankSum
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SIO_000300: 5.669999999999999e-1

VQSLOD
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SIO_000300: -2.267e0

DP
type: SiteQuality
SIO_000300: 7.9567e5

ClippingRankSum
type: SiteQuality
SIO_000300: -7.36e-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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1726
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10284
num of homozygotes: 0

African
type: Population
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: 396
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3724
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3740
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.449941350997033e-5
allele num: 28986
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.96e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.78e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
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BaseQRankSum
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SIO_000300: -1.231e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.01e-2

VQSLOD
type: SiteQuality
SIO_000300: 6.860000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.048e1

FS
type: SiteQuality
SIO_000300: 3.79e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.29e-1

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 7

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 3664
num of homozygotes: 0

European (Non-Finnish)
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allele count: 5
allele frequency: 1.744226609921161e-4
allele num: 28666
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1726
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.75800156128025e-5
allele num: 10248
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 2.525252525252525e-3
allele num: 396
num of homozygotes: 0

African
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allele count: 116
allele frequency: 2.272727272727273e-2
allele num: 5104
num of homozygotes: 2

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 3674
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.76e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.11e-1

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 3.61e-1

FS
type: SiteQuality
SIO_000300: 1.418e0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.51e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 7.71738e5

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 0.0e0
allele num: 5012
num of homozygotes: 0

South Asian
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allele frequency: 1.970443349753695e-4
allele num: 10150
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Latino
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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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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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East Asian
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allele frequency: 8.356545961002785e-4
allele num: 3590
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MQRankSum
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QD
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MQ
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ReadPosRankSum
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BaseQRankSum
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VQSLOD
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ClippingRankSum
type: SiteQuality
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InbreedingCoeff
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FS
type: SiteQuality
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DP
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 (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: 1
allele frequency: 3.564299971485601e-5
allele num: 28056
num of homozygotes: 0

South Asian
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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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Other
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East Asian
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allele num: 3590
num of homozygotes: 0

MQ
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SIO_000300: 6.0e1

MQRankSum
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BaseQRankSum
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ClippingRankSum
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VQSLOD
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QD
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InbreedingCoeff
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DP
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FS
type: SiteQuality
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1
allele frequency: 3.094059405940594e-4
allele num: 3232
num of homozygotes: 0

Latino
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Other
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European (Finnish)
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African
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South Asian
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European (Non-Finnish)
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VQSLOD
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QD
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BaseQRankSum
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MQ
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ClippingRankSum
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ReadPosRankSum
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MQRankSum
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FS
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InbreedingCoeff
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.88621172081455e-5
allele num: 25732
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4722
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1490
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3096
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 366
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3164
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9872
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.29e0

DP
type: SiteQuality
SIO_000300: 7.44861e5

QD
type: SiteQuality
SIO_000300: 1.569e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.38e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.026e0

MQRankSum
type: SiteQuality
SIO_000300: 2.03e0

VQSLOD
type: SiteQuality
SIO_000300: -1.101e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.386e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.026e0

GenotypeQuality
all individuals: 1507
bin: 3.75e1
variant carriers: 1471

GenotypeQuality
all individuals: 1193
bin: 8.75e1
variant carriers: 1182

GenotypeQuality
all individuals: 4868
bin: 7.5e0
variant carriers: 1408

GenotypeQuality
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bin: 4.25e1
variant carriers: 622

GenotypeQuality
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bin: 2.25e1
variant carriers: 4782

GenotypeQuality
all individuals: 1821
bin: 6.25e1
variant carriers: 500

GenotypeQuality
all individuals: 15472
bin: 9.75e1
variant carriers: 15404

GenotypeQuality
all individuals: 896
bin: 4.75e1
variant carriers: 883

GenotypeQuality
all individuals: 5582
bin: 2.5e0
variant carriers: 168

GenotypeQuality
all individuals: 1166
bin: 9.25e1
variant carriers: 1157

GenotypeQuality
all individuals: 410
bin: 7.25e1
variant carriers: 374

GenotypeQuality
all individuals: 2683
bin: 3.25e1
variant carriers: 2611

GenotypeQuality
all individuals: 5132
bin: 1.75e1
variant carriers: 4771

GenotypeQuality
all individuals: 567
bin: 6.75e1
variant carriers: 420

GenotypeQuality
all individuals: 623
bin: 7.75e1
variant carriers: 596

GenotypeQuality
all individuals: 820
bin: 5.75e1
variant carriers: 812

East Asian
type: Population
allele count: 1622
allele frequency: 5.554794520547945e-1
allele num: 2920
num of homozygotes: 419

Latino
type: Population
allele count: 2012
allele frequency: 7.180585296216988e-1
allele num: 2802
num of homozygotes: 676

African
type: Population
allele count: 3333
allele frequency: 7.097529812606473e-1
allele num: 4696
num of homozygotes: 1170

Other
type: Population
allele count: 231
allele frequency: 6.311475409836066e-1
allele num: 366
num of homozygotes: 70

European (Finnish)
type: Population
allele count: 977
allele frequency: 6.794158553546592e-1
allele num: 1438
num of homozygotes: 302

European (Non-Finnish)
type: Population
allele count: 15999
allele frequency: 6.489939964303099e-1
allele num: 24652
num of homozygotes: 4820

South Asian
type: Population
allele count: 5402
allele frequency: 5.462082912032356e-1
allele num: 9890
num of homozygotes: 1432

VQSLOD
type: SiteQuality
SIO_000300: 5.8e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.0e-1

DP
type: SiteQuality
SIO_000300: 8.824e5

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.512e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.43e-1

FS
type: SiteQuality
SIO_000300: 1.589e0

QD
type: SiteQuality
SIO_000300: 2.363e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.22e0

GenotypeQuality
all individuals: 2255
bin: 1.25e1
variant carriers: 5

GenotypeQuality
all individuals: 632
bin: 4.25e1
variant carriers: 1

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 8.75e1
variant carriers: 18

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 15

GenotypeQuality
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variant carriers: 2

GenotypeQuality
all individuals: 1507
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variant carriers: 1

GenotypeQuality
all individuals: 918
bin: 5.25e1
variant carriers: 3

GenotypeQuality
all individuals: 4868
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variant carriers: 10

GenotypeQuality
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variant carriers: 7

GenotypeQuality
all individuals: 15472
bin: 9.75e1
variant carriers: 115

GenotypeQuality
all individuals: 410
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variant carriers: 3

GenotypeQuality
all individuals: 1166
bin: 9.25e1
variant carriers: 13

GenotypeQuality
all individuals: 896
bin: 4.75e1
variant carriers: 2

GenotypeQuality
all individuals: 567
bin: 6.75e1
variant carriers: 6

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1438
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 3.568879371877231e-4
allele num: 2802
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4696
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 24652
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 3.033367037411527e-4
allele num: 9890
num of homozygotes: 0

East Asian
type: Population
allele count: 104
allele frequency: 3.561643835616438e-2
allele num: 2920
num of homozygotes: 2

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 366
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.43e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.512e-1

FS
type: SiteQuality
SIO_000300: 1.589e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.0e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.22e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 5.8e0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 8.824e5

QD
type: SiteQuality
SIO_000300: 2.363e1

GenotypeQuality
all individuals: 1308
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 305
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 828
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variant carriers: 0

GenotypeQuality
all individuals: 69
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variant carriers: 0

GenotypeQuality
all individuals: 690
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 36
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 218
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variant carriers: 0

GenotypeQuality
all individuals: 4674
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variant carriers: 0

GenotypeQuality
all individuals: 2524
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 425
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variant carriers: 0

GenotypeQuality
all individuals: 467
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1270
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14974
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 652
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1654
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3402
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8716
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 244
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -8.784e-1

DP
type: SiteQuality
SIO_000300: 5.63467e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.4e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.65e0

MQRankSum
type: SiteQuality
SIO_000300: -7.29e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.76e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 9.52e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.31e0

GenotypeQuality
all individuals: 796
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 413
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variant carriers: 0

GenotypeQuality
all individuals: 2562
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 218
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GenotypeQuality
all individuals: 2824
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variant carriers: 0

GenotypeQuality
all individuals: 75
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variant carriers: 0

GenotypeQuality
all individuals: 125
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variant carriers: 0

GenotypeQuality
all individuals: 4416
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variant carriers: 0

GenotypeQuality
all individuals: 245
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variant carriers: 0

GenotypeQuality
all individuals: 620
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variant carriers: 0

GenotypeQuality
all individuals: 985
bin: 2.5e0
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GenotypeQuality
all individuals: 556
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variant carriers: 0

GenotypeQuality
all individuals: 962
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variant carriers: 0

GenotypeQuality
all individuals: 81
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variant carriers: 0

GenotypeQuality
all individuals: 462
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 305
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1078
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3278
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13924
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 572
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8572
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1518
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 234
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.102e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.07e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.02e0

MQ
type: SiteQuality
SIO_000300: 5.967e1

MQRankSum
type: SiteQuality
SIO_000300: -9.11e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.663e0

QD
type: SiteQuality
SIO_000300: 1.955e1

DP
type: SiteQuality
SIO_000300: 5.47448e5

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.69e-2

GenotypeQuality
all individuals: 2610
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 770
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16017
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 587
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variant carriers: 0

GenotypeQuality
all individuals: 2459
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variant carriers: 0

GenotypeQuality
all individuals: 25945
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variant carriers: 0

GenotypeQuality
all individuals: 963
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GenotypeQuality
all individuals: 304
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variant carriers: 0

GenotypeQuality
all individuals: 35
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GenotypeQuality
all individuals: 1245
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GenotypeQuality
all individuals: 962
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GenotypeQuality
all individuals: 111
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GenotypeQuality
all individuals: 75
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GenotypeQuality
all individuals: 550
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variant carriers: 0

GenotypeQuality
all individuals: 218
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variant carriers: 0

GenotypeQuality
all individuals: 4448
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3226
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1028
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1460
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8556
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 530
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 7.330303474563847e-5
allele num: 13642
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 232
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.647e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -7.36e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.07e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.78e-2

FS
type: SiteQuality
SIO_000300: 1.756e0

QD
type: SiteQuality
SIO_000300: 7.58e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.36e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.48e0

DP
type: SiteQuality
SIO_000300: 5.42381e5

GenotypeQuality
all individuals: 217
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 545
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 5.25e1
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GenotypeQuality
all individuals: 706
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GenotypeQuality
all individuals: 2272
bin: 1.75e1
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GenotypeQuality
all individuals: 4421
bin: 6.25e1
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GenotypeQuality
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GenotypeQuality
all individuals: 1120
bin: 2.5e0
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GenotypeQuality
all individuals: 2681
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 962
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variant carriers: 1

GenotypeQuality
all individuals: 1230
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3156
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 924
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.183151916706105e-4
allele num: 8452
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 224
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 490
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12906
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1358
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.326e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.01e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.17e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.31e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.553e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.47e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 2.74e0

DP
type: SiteQuality
SIO_000300: 5.32637e5

GenotypeQuality
all individuals: 10612
bin: 2.25e1
variant carriers: 1

GenotypeQuality
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bin: 1.25e1
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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bin: 1.75e1
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GenotypeQuality
all individuals: 529
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GenotypeQuality
all individuals: 98
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GenotypeQuality
all individuals: 452
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GenotypeQuality
all individuals: 137
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 957
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GenotypeQuality
all individuals: 1155
bin: 6.75e1
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GenotypeQuality
all individuals: 599
bin: 2.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 340
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 212
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1086
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.223091976516634e-4
allele num: 8176
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 668
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11088
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2932
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 6.840000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.11e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.840000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.46e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.249e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.62e-2

DP
type: SiteQuality
SIO_000300: 4.96295e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.9e-1

GenotypeQuality
all individuals: 126
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 955
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GenotypeQuality
all individuals: 574
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GenotypeQuality
all individuals: 1050
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GenotypeQuality
all individuals: 364
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GenotypeQuality
all individuals: 2620
bin: 1.75e1
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GenotypeQuality
all individuals: 7175
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variant carriers: 0

GenotypeQuality
all individuals: 177
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GenotypeQuality
all individuals: 3834
bin: 1.25e1
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GenotypeQuality
all individuals: 380
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variant carriers: 0

GenotypeQuality
all individuals: 139
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GenotypeQuality
all individuals: 2064
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GenotypeQuality
all individuals: 3638
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variant carriers: 0

GenotypeQuality
all individuals: 502
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variant carriers: 0

GenotypeQuality
all individuals: 443
bin: 8.25e1
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GenotypeQuality
all individuals: 217
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 550
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9646
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 220
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2718
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8002
num of homozygotes: 0

FS
type: SiteQuality
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MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.04e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.219e0

DP
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SIO_000300: 4.60727e5

BaseQRankSum
type: SiteQuality
SIO_000300: -2.219e0

VQSLOD
type: SiteQuality
SIO_000300: -3.339e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.88e0

QD
type: SiteQuality
SIO_000300: 1.215e1

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 554
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 194
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 476
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 146
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 756
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8764
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2576
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7860
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 4.712e1

MQRankSum
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VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -7.2e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.594e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.57e-2

DP
type: SiteQuality
SIO_000300: 4.311e5

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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GenotypeQuality
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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: 6.25e1
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GenotypeQuality
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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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bin: 7.25e1
variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7830
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 192
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2566
num of homozygotes: 0

East Asian
type: Population
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allele frequency: 0.0e0
allele num: 740
num of homozygotes: 0

European (Non-Finnish)
type: Population
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allele frequency: 1.149954001839926e-4
allele num: 8696
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 468
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 140
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 4.29235e5

FS
type: SiteQuality
SIO_000300: 3.965e0

QD
type: SiteQuality
SIO_000300: 2.412e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.2e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
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SIO_000300: -2.286e0

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.25e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.22e-2

MQ
type: SiteQuality
SIO_000300: 5.959e1

GenotypeQuality
all individuals: 2710
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 212
bin: 8.75e1
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: 2.25e1
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GenotypeQuality
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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: 430
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GenotypeQuality
all individuals: 676
bin: 3.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 192
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8696
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2566
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 468
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 740
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7830
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 140
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.286e0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.22e-2

QD
type: SiteQuality
SIO_000300: 2.412e1

FS
type: SiteQuality
SIO_000300: 3.965e0

MQ
type: SiteQuality
SIO_000300: 5.959e1

MQRankSum
type: SiteQuality
SIO_000300: 2.25e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 4.29235e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.2e-1

GenotypeQuality
all individuals: 341
bin: 5.25e1
variant carriers: 281

GenotypeQuality
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variant carriers: 659

GenotypeQuality
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GenotypeQuality
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variant carriers: 437

GenotypeQuality
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variant carriers: 505

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 191

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1191

GenotypeQuality
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GenotypeQuality
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variant carriers: 979

GenotypeQuality
all individuals: 719
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variant carriers: 408

GenotypeQuality
all individuals: 5985
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variant carriers: 5861

African
type: Population
allele count: 558
allele frequency: 2.162790697674419e-1
allele num: 2580
num of homozygotes: 64

European (Finnish)
type: Population
allele count: 69
allele frequency: 4.156626506024096e-1
allele num: 166
num of homozygotes: 14

Latino
type: Population
allele count: 241
allele frequency: 4.858870967741936e-1
allele num: 496
num of homozygotes: 53

Other
type: Population
allele count: 60
allele frequency: 3.125e-1
allele num: 192
num of homozygotes: 8

East Asian
type: Population
allele count: 237
allele frequency: 3.062015503875969e-1
allele num: 774
num of homozygotes: 35

European (Non-Finnish)
type: Population
allele count: 3116
allele frequency: 3.473027195720018e-1
allele num: 8972
num of homozygotes: 507

South Asian
type: Population
allele count: 2842
allele frequency: 3.619460010188487e-1
allele num: 7852
num of homozygotes: 516

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.323e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 4.32434e5

BaseQRankSum
type: SiteQuality
SIO_000300: -1.231e0

VQSLOD
type: SiteQuality
SIO_000300: 4.94e0

MQRankSum
type: SiteQuality
SIO_000300: 2.89e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.62e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.01e-1

QD
type: SiteQuality
SIO_000300: 1.945e1

GenotypeQuality
all individuals: 226
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variant carriers: 1

GenotypeQuality
all individuals: 201
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 72
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2288
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 386
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7236
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 190
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 624
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.420454545454545e-4
allele num: 7040
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 3.349e1

DP
type: SiteQuality
SIO_000300: 3.16875e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.23e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.06e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -3.682e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.35e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -1.905e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.06e-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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 626
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7202
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 2.631578947368421e-3
allele num: 380
num of homozygotes: 0

African
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allele frequency: 0.0e0
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 186
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 70
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7012
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.14277e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.36e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.08e-2

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

ClippingRankSum
type: SiteQuality
SIO_000300: 2.17e-1

QD
type: SiteQuality
SIO_000300: 1.069e1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.75e-1

MQRankSum
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SIO_000300: 1.19e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 3.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 604
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
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6802
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.432664756446991e-4
allele num: 6980
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 372
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 186
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African
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allele count: 0
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allele num: 2242
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QD
type: SiteQuality
SIO_000300: 1.239e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.93e-1

MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.942e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.28e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.08e-2

DP
type: SiteQuality
SIO_000300: 3.00041e5

FS
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -7.326e-1

BaseQRankSum
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SIO_000300: -4.305e0

GenotypeQuality
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variant carriers: 9

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 2.25e1
variant carriers: 280

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 118
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GenotypeQuality
all individuals: 203
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GenotypeQuality
all individuals: 3784
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variant carriers: 3729

GenotypeQuality
all individuals: 136
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GenotypeQuality
all individuals: 121
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variant carriers: 92

Other
type: Population
allele count: 54
allele frequency: 3.103448275862069e-1
allele num: 174
num of homozygotes: 6

European (Non-Finnish)
type: Population
allele count: 2170
allele frequency: 3.245587795393359e-1
allele num: 6686
num of homozygotes: 291

African
type: Population
allele count: 1106
allele frequency: 5.096774193548387e-1
allele num: 2170
num of homozygotes: 271

European (Finnish)
type: Population
allele count: 25
allele frequency: 3.472222222222222e-1
allele num: 72
num of homozygotes: 2

East Asian
type: Population
allele count: 126
allele frequency: 2.226148409893993e-1
allele num: 566
num of homozygotes: 11

Latino
type: Population
allele count: 92
allele frequency: 2.674418604651163e-1
allele num: 344
num of homozygotes: 14

South Asian
type: Population
allele count: 1040
allele frequency: 1.678502259522272e-1
allele num: 6196
num of homozygotes: 70

FS
type: SiteQuality
SIO_000300: 7.39e-1

QD
type: SiteQuality
SIO_000300: 1.953e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.61e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.48e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.216e-1

DP
type: SiteQuality
SIO_000300: 2.82986e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 4.42e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.14e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.46e-1

GenotypeQuality
all individuals: 78
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 697
bin: 1.75e1
variant carriers: 1

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 528
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5602
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 152
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1844
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 326
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 50
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5832
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 7.36e-1

QD
type: SiteQuality
SIO_000300: 1.332e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.36e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.36e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.97e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 7.36e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.6e-2

DP
type: SiteQuality
SIO_000300: 2.47216e5

GenotypeQuality
all individuals: 111
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 8.75e1
variant carriers: 0

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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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 7.25e1
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GenotypeQuality
all individuals: 599
bin: 3.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 148
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1710
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5430
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 518
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.944012441679627e-4
allele num: 5144
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 310
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.77e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.787e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.26e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.389999999999999e-2

DP
type: SiteQuality
SIO_000300: 2.3013e5

MQRankSum
type: SiteQuality
SIO_000300: -6.28e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.062e0

QD
type: SiteQuality
SIO_000300: 1.065e1

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

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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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 869
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4842
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1524
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 498
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 128
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 288
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.495e0

MQRankSum
type: SiteQuality
SIO_000300: 1.98e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.37e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.84e-2

QD
type: SiteQuality
SIO_000300: 3.211e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.98e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.98e-1

DP
type: SiteQuality
SIO_000300: 2.08928e5

GenotypeQuality
all individuals: 72
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 28
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 600
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1510
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 504
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 288
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 124
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 2.219263204616067e-4
allele num: 4506
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4808
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.06696e5

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.344e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.65e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.383e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.84e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.07e0

QD
type: SiteQuality
SIO_000300: 3.14e0

GenotypeQuality
all individuals: 539
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4653
bin: 2.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 145
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GenotypeQuality
all individuals: 23783
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GenotypeQuality
all individuals: 75
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GenotypeQuality
all individuals: 595
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GenotypeQuality
all individuals: 62
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GenotypeQuality
all individuals: 173
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GenotypeQuality
all individuals: 53
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GenotypeQuality
all individuals: 236
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.471576866040534e-4
allele num: 4046
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1246
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 42
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3368
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 478
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 282
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 104
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 5.27e0

VQSLOD
type: SiteQuality
SIO_000300: -2.47e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.23e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.41e-1

DP
type: SiteQuality
SIO_000300: 1.86567e5

MQRankSum
type: SiteQuality
SIO_000300: 6.33e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.65e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.57e0

GenotypeQuality
all individuals: 174
bin: 3.75e1
variant carriers: 12

GenotypeQuality
all individuals: 67
bin: 4.75e1
variant carriers: 23

GenotypeQuality
all individuals: 87
bin: 8.75e1
variant carriers: 45

GenotypeQuality
all individuals: 4237
bin: 2.25e1
variant carriers: 64

GenotypeQuality
all individuals: 686
bin: 1.75e1
variant carriers: 57

GenotypeQuality
all individuals: 76
bin: 5.25e1
variant carriers: 26

GenotypeQuality
all individuals: 560
bin: 2.75e1
variant carriers: 99

GenotypeQuality
all individuals: 509
bin: 6.25e1
variant carriers: 59

GenotypeQuality
all individuals: 115
bin: 7.25e1
variant carriers: 37

GenotypeQuality
all individuals: 741
bin: 9.75e1
variant carriers: 612

GenotypeQuality
all individuals: 459
bin: 3.25e1
variant carriers: 78

GenotypeQuality
all individuals: 53
bin: 4.25e1
variant carriers: 11

GenotypeQuality
all individuals: 106
bin: 9.25e1
variant carriers: 57

GenotypeQuality
all individuals: 71
bin: 5.75e1
variant carriers: 49

South Asian
type: Population
allele count: 167
allele frequency: 6.482919254658386e-2
allele num: 2576
num of homozygotes: 5

European (Non-Finnish)
type: Population
allele count: 239
allele frequency: 6.515812431842966e-2
allele num: 3668
num of homozygotes: 10

European (Finnish)
type: Population
allele count: 4
allele frequency: 1.176470588235294e-1
allele num: 34
num of homozygotes: 0

African
type: Population
allele count: 169
allele frequency: 1.394389438943894e-1
allele num: 1212
num of homozygotes: 11

Latino
type: Population
allele count: 5
allele frequency: 1.937984496124031e-2
allele num: 258
num of homozygotes: 0

Other
type: Population
allele count: 6
allele frequency: 6.666666666666667e-2
allele num: 90
num of homozygotes: 0

East Asian
type: Population
allele count: 50
allele frequency: 1.063829787234043e-1
allele num: 470
num of homozygotes: 5

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.109e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.4e-1

FS
type: SiteQuality
SIO_000300: 5.55e-1

QD
type: SiteQuality
SIO_000300: 1.57e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.57e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.58e-1

DP
type: SiteQuality
SIO_000300: 1.80297e5

VQSLOD
type: SiteQuality
SIO_000300: 3.4e0

GenotypeQuality
all individuals: 419
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1061
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 729
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 89
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GenotypeQuality
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GenotypeQuality
all individuals: 454
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 22
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GenotypeQuality
all individuals: 75
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GenotypeQuality
all individuals: 56
bin: 4.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 74
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1832
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.010234798314269e-4
allele num: 3322
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 246
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 426
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1104
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 30
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.031e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.64e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.03e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.33e-2

DP
type: SiteQuality
SIO_000300: 1.71313e5

FS
type: SiteQuality
SIO_000300: 1.0964e1

VQSLOD
type: SiteQuality
SIO_000300: -6.213e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.17e-1

QD
type: SiteQuality
SIO_000300: 8.800000000000001e0

GenotypeQuality
all individuals: 164
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 454
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variant carriers: 0

GenotypeQuality
all individuals: 448
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GenotypeQuality
all individuals: 175
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GenotypeQuality
all individuals: 817
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GenotypeQuality
all individuals: 31
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GenotypeQuality
all individuals: 61
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 89
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GenotypeQuality
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GenotypeQuality
all individuals: 60
bin: 4.75e1
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GenotypeQuality
all individuals: 51
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1754
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 74
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 434
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 248
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1098
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3248
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 32
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.39e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.42e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.42e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.42e-1

DP
type: SiteQuality
SIO_000300: 1.69581e5

MQ
type: SiteQuality
SIO_000300: 5.728e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.42e-1

QD
type: SiteQuality
SIO_000300: 1.24e1

VQSLOD
type: SiteQuality
SIO_000300: -1.257e-1

GenotypeQuality
all individuals: 815
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1255
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GenotypeQuality
all individuals: 13
bin: 5.75e1
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GenotypeQuality
all individuals: 4709
bin: 2.5e0
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GenotypeQuality
all individuals: 478
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 44
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3808
bin: 2.25e1
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GenotypeQuality
all individuals: 85
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GenotypeQuality
all individuals: 442
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GenotypeQuality
all individuals: 23
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GenotypeQuality
all individuals: 57
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GenotypeQuality
all individuals: 166
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 52
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 6.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 34
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 72
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 418
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3180
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1490
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 4.0e-3
allele num: 250
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.157509157509158e-4
allele num: 1092
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.94e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.62e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 5.85e-1

QD
type: SiteQuality
SIO_000300: 1.239e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.56e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

FS
type: SiteQuality
SIO_000300: 1.114e0

DP
type: SiteQuality
SIO_000300: 1.68557e5

ClippingRankSum
type: SiteQuality
SIO_000300: 7.27e-1

GenotypeQuality
all individuals: 62
bin: 9.25e1
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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GenotypeQuality
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GenotypeQuality
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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: 5.75e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 36
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 422
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1444
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3160
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 250
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.174311926605505e-4
allele num: 1090
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 70
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.771e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.98e-1

DP
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SIO_000300: 1.68492e5

QD
type: SiteQuality
SIO_000300: 1.41e1

MQRankSum
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SIO_000300: 6.7e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.036e0

MQ
type: SiteQuality
SIO_000300: 5.811e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.59e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 3.65e-1

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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GenotypeQuality
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GenotypeQuality
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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: 6.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 34
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 412
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 244
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1038
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1182
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3060
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 68
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 6.14e0

VQSLOD
type: SiteQuality
SIO_000300: 6.59e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.58e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.83e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.23e0

DP
type: SiteQuality
SIO_000300: 1.68154e5

ClippingRankSum
type: SiteQuality
SIO_000300: 3.58e-1

MQ
type: SiteQuality
SIO_000300: 5.616e1

GenotypeQuality
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variant carriers: 0

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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GenotypeQuality
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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: 250
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 418
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 920
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3014
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1028
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 42
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -6.913e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.130000000000001e-2

DP
type: SiteQuality
SIO_000300: 1.77987e5

MQRankSum
type: SiteQuality
SIO_000300: 8.24e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.58e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.95e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.299e1

GenotypeQuality
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bin: 5.75e1
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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GenotypeQuality
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GenotypeQuality
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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: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 2
allele frequency: 4.784688995215311e-3
allele num: 418
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 248
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1042
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 926
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3000
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.79656e5

ClippingRankSum
type: SiteQuality
SIO_000300: 5.9e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.283e0

MQRankSum
type: SiteQuality
SIO_000300: 1.12e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.44e0

QD
type: SiteQuality
SIO_000300: 1.018e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.24e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.180000000000001e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.709e0

GenotypeQuality
all individuals: 198
bin: 3.75e1
variant carriers: 0

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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GenotypeQuality
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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: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1044
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 256
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 414
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.320053120849933e-4
allele num: 3012
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 922
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.69e-1

VQSLOD
type: SiteQuality
SIO_000300: -8.44e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.2e-2

DP
type: SiteQuality
SIO_000300: 1.82318e5

FS
type: SiteQuality
SIO_000300: 2.914e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.42e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.58e-1

QD
type: SiteQuality
SIO_000300: 1.223e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.49e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
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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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bin: 9.75e1
variant carriers: 2

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5246
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56060
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8178
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 680
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.267748478701826e-4
allele num: 7888
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.877581674802854e-4
allele num: 10652
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10452
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.2e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.95e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.04e0

ClippingRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 4.774e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.9e-3

ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.151e1

DP
type: SiteQuality
SIO_000300: 1.07187e6

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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GenotypeQuality
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GenotypeQuality
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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: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.771039954661377e-5
allele num: 56464
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8332
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 686
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5322
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: 7954
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.117909e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -2.202e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.043e0

GenotypeQuality
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bin: 3.75e1
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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GenotypeQuality
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GenotypeQuality
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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: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8406
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 56742
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 686
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10590
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7976
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.240436148586214e-5
allele num: 10822
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5350
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e0

QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -3.91e-1

FS
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQRankSum
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InbreedingCoeff
type: SiteQuality
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MQ
type: SiteQuality
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DP
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 695
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 57002
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8468
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10652
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5404
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 702
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.243781094527363e-4
allele num: 8040
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South Asian
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allele frequency: 0.0e0
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BaseQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.161967e6

VQSLOD
type: SiteQuality
SIO_000300: 7.099999999999999e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.928e1

MQRankSum
type: SiteQuality
SIO_000300: 1.05e0

QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -3.5e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 7.7e-2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 frequency: 0.0e0
allele num: 11264
num of homozygotes: 0

Latino
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allele count: 15
allele frequency: 1.393534002229654e-3
allele num: 10764
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 3.498134328358209e-4
allele num: 8576
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.388406803193336e-4
allele num: 57620
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8076
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5486
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.91e0

MQRankSum
type: SiteQuality
SIO_000300: 1.76e-1

DP
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SIO_000300: 1.215837e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -3.59e-1

FS
type: SiteQuality
SIO_000300: 3.408e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.86e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.09e-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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1
allele frequency: 8.838607035531201e-5
allele num: 11314
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 724
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5508
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10782
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8130
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8598
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European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 8.651417102121327e-5
allele num: 57794
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.187e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
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InbreedingCoeff
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MQRankSum
type: SiteQuality
SIO_000300: -1.86e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.71e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.71e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.27e0

DP
type: SiteQuality
SIO_000300: 1.225928e6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 2

South Asian
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allele count: 2
allele frequency: 1.761804087385483e-4
allele num: 11352
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10844
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 57986
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 728
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5540
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8140
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 9.27e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.4e-2

QD
type: SiteQuality
SIO_000300: 1.541e1

FS
type: SiteQuality
SIO_000300: 1.2026e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.44e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.356e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.6e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.34e-1

DP
type: SiteQuality
SIO_000300: 1.235503e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5626
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11026
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8268
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 752
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.690445601460545e-5
allele num: 59156
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11992
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VQSLOD
type: SiteQuality
SIO_000300: -1.032e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.9e-2

ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.300319e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

MQRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.712e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.5e-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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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)
type: Population
allele count: 1
allele frequency: 1.678133915086424e-5
allele num: 59590
num of homozygotes: 0

African
type: Population
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: 764
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8320
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5698
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Latino
type: Population
allele count: 1
allele frequency: 9.018759018759019e-5
allele num: 11088
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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InbreedingCoeff
type: SiteQuality
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MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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VQSLOD
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QD
type: SiteQuality
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FS
type: SiteQuality
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ClippingRankSum
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BaseQRankSum
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MQ
type: SiteQuality
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DP
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 8410
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5822
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 782
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9060
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European (Non-Finnish)
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allele count: 5
allele frequency: 8.291598951941892e-5
allele num: 60302
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 12622
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11174
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

MQ
type: SiteQuality
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QD
type: SiteQuality
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FS
type: SiteQuality
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MQRankSum
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DP
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VQSLOD
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ClippingRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5828
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 frequency: 0.0e0
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8430
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11206
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.651909607506277e-5
allele num: 60536
num of homozygotes: 0

Other
type: Population
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VQSLOD
type: SiteQuality
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MQRankSum
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BaseQRankSum
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InbreedingCoeff
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QD
type: SiteQuality
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FS
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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ClippingRankSum
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MQ
type: SiteQuality
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DP
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61032
num of homozygotes: 0