X-106776738-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106776738
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106776738
    reference: chr 0
allele count: 1
allele frequency: 1.231390609415213e-5
allele num: 81209
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000398668
  ensembl transcript: ENST00000439554
  gene symbol: FRMPD3
  hgvsc: ENST00000439554.1:c.198C>T
  hgvsp: ENST00000439554.1:c.198C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000227610
  ensembl transcript: ENST00000415252
  gene symbol: FRMPD3-AS1
  hgvsc: ENST00000415252.1:n.107+12207G>A
  variant of: http://identifiers.org/hgnc/41239
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000276185
  ensembl transcript: ENST00000276185
  gene symbol: FRMPD3
  hgvsc: ENST00000276185.4:c.354C>T
  hgvsp: ENST00000276185.4:c.354C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29382
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1842
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1726
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2019
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3868
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3316
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 3.75e1
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genotype depth: GenotypeDepth
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  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1903
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2265
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2353
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 2.5e0
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genotype quality: GenotypeQuality
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  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 655
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 8.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4967
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ser118Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: DP

X-106776739-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106776739
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106776739
    reference: chr 0
allele count: 1
allele frequency: 1.231193518997316e-5
allele num: 81222
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000398668
  ensembl transcript: ENST00000439554
  gene symbol: FRMPD3
  hgvsc: ENST00000439554.1:c.199G>A
  hgvsp: ENSP00000398668.1:p.Ala67Thr
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000227610
  ensembl transcript: ENST00000415252
  gene symbol: FRMPD3-AS1
  hgvsc: ENST00000415252.1:n.107+12206C>T
  variant of: http://identifiers.org/hgnc/41239
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000276185
  ensembl transcript: ENST00000276185
  gene symbol: FRMPD3
  hgvsc: ENST00000276185.4:c.355G>A
  hgvsp: ENSP00000276185.4:p.Ala119Thr
  variant of: http://identifiers.org/hgnc/29382
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3469
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 1
genotype depth: GenotypeDepth
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  bin: 9.75e1
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genotype depth: GenotypeDepth
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  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2019
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2836
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1106
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genotype quality: GenotypeQuality
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  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5014
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1372
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 168
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1143
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ala119Thr
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: African
reference allele: G
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP

X-106776741-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106776741
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106776741
    reference: chr 0
allele count: 1
allele frequency: 1.230284687876775e-5
allele num: 81282
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000227610
  ensembl transcript: ENST00000415252
  gene symbol: FRMPD3-AS1
  hgvsc: ENST00000415252.1:n.107+12204A>G
  variant of: http://identifiers.org/hgnc/41239
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000276185
  ensembl transcript: ENST00000276185
  gene symbol: FRMPD3
  hgvsc: ENST00000276185.4:c.357T>C
  hgvsp: ENST00000276185.4:c.357T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000398668
  ensembl transcript: ENST00000439554
  gene symbol: FRMPD3
  hgvsc: ENST00000439554.1:c.201T>C
  hgvsp: ENST00000439554.1:c.201T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29382
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2818
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2058
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3470
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15864
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1903
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2019
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3746
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3316
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.75e1
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genotype depth: GenotypeDepth
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  bin: 4.75e1
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genotype depth: GenotypeDepth
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  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1372
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genotype quality: GenotypeQuality
  all individuals: 77
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ala119Ala
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP

X-106776744-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106776744
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106776744
    reference: chr 0
allele count: 1
allele frequency: 1.229664424578532e-5
allele num: 81323
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000276185
  ensembl transcript: ENST00000276185
  gene symbol: FRMPD3
  hgvsc: ENST00000276185.4:c.360G>A
  hgvsp: ENST00000276185.4:c.360G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000227610
  ensembl transcript: ENST00000415252
  gene symbol: FRMPD3-AS1
  hgvsc: ENST00000415252.1:n.107+12201C>T
  variant of: http://identifiers.org/hgnc/41239
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000398668
  ensembl transcript: ENST00000439554
  gene symbol: FRMPD3
  hgvsc: ENST00000439554.1:c.204G>A
  hgvsp: ENST00000439554.1:c.204G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29382
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2835
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3316
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3746
  bin: 5.25e1
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2019
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15865
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 3.75e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 1903
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genotype depth: GenotypeDepth
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  bin: 7.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 653
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Lys120Lys
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD

X-106776754-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106776754
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106776754
    reference: chr 0
allele count: 6
allele frequency: 7.375084506176634e-5
allele num: 81355
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000227610
  ensembl transcript: ENST00000415252
  gene symbol: FRMPD3-AS1
  hgvsc: ENST00000415252.1:n.107+12191C>T
  variant of: http://identifiers.org/hgnc/41239
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000398668
  ensembl transcript: ENST00000439554
  gene symbol: FRMPD3
  hgvsc: ENST00000439554.1:c.214G>A
  hgvsp: ENSP00000398668.1:p.Val72Ile
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000276185
  ensembl transcript: ENST00000276185
  gene symbol: FRMPD3
  hgvsc: ENST00000276185.4:c.370G>A
  hgvsp: ENSP00000276185.4:p.Val124Ile
  variant of: http://identifiers.org/hgnc/29382
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4016
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3316
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
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  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3868
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2355
  bin: 6.75e1
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genotype depth: GenotypeDepth
  all individuals: 1902
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2019
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1841
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.25e1
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genotype depth: GenotypeDepth
  all individuals: 2835
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15865
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2275
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5008
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genotype quality: GenotypeQuality
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  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 437
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 1.25e1
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genotype quality: GenotypeQuality
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  bin: 8.75e1
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genotype quality: GenotypeQuality
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  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1145
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Val124Ile
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

X-106776755-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106776755
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106776755
    reference: chr 0
allele count: 1
allele frequency: 1.229074998156387e-5
allele num: 81362
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000276185
  ensembl transcript: ENST00000276185
  gene symbol: FRMPD3
  hgvsc: ENST00000276185.4:c.371T>G
  hgvsp: ENSP00000276185.4:p.Val124Gly
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000227610
  ensembl transcript: ENST00000415252
  gene symbol: FRMPD3-AS1
  hgvsc: ENST00000415252.1:n.107+12190A>C
  variant of: http://identifiers.org/hgnc/41239
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000398668
  ensembl transcript: ENST00000439554
  gene symbol: FRMPD3
  hgvsc: ENST00000439554.1:c.215T>G
  hgvsp: ENSP00000398668.1:p.Val72Gly
  variant of: http://identifiers.org/hgnc/29382
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1842
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1725
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2019
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 6.75e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1372
  bin: 9.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1124
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Val124Gly
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum

X-106776772-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106776772
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106776772
    reference: chr 0
allele count: 32
allele frequency: 3.935845714847978e-4
allele num: 81304
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000227610
  ensembl transcript: ENST00000415252
  gene symbol: FRMPD3-AS1
  hgvsc: ENST00000415252.1:n.107+12173T>C
  variant of: http://identifiers.org/hgnc/41239
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000398668
  ensembl transcript: ENST00000439554
  gene symbol: FRMPD3
  hgvsc: ENST00000439554.1:c.232A>G
  hgvsp: ENSP00000398668.1:p.Thr78Ala
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000276185
  ensembl transcript: ENST00000276185
  gene symbol: FRMPD3
  hgvsc: ENST00000276185.4:c.388A>G
  hgvsp: ENSP00000276185.4:p.Thr130Ala
  variant of: http://identifiers.org/hgnc/29382
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2267
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1842
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3870
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  variant carriers: 1
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 1
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 2354
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.75e1
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 25
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1371
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4836
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Thr130Ala
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

X-106776773-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106776773
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106776773
    reference: chr 0
allele count: 6
allele frequency: 7.3807092861624e-5
allele num: 81293
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000227610
  ensembl transcript: ENST00000415252
  gene symbol: FRMPD3-AS1
  hgvsc: ENST00000415252.1:n.107+12172G>C
  variant of: http://identifiers.org/hgnc/41239
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000276185
  ensembl transcript: ENST00000276185
  gene symbol: FRMPD3
  hgvsc: ENST00000276185.4:c.389C>G
  hgvsp: ENSP00000276185.4:p.Thr130Ser
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000398668
  ensembl transcript: ENST00000439554
  gene symbol: FRMPD3
  hgvsc: ENST00000439554.1:c.233C>G
  hgvsp: ENSP00000398668.1:p.Thr78Ser
  variant of: http://identifiers.org/hgnc/29382
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2269
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1844
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3744
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 6.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1270
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Thr130Ser
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ

X-106776777-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106776777
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106776777
    reference: chr 0
allele count: 4
allele frequency: 4.922107646494229e-5
allele num: 81266
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000227610
  ensembl transcript: ENST00000415252
  gene symbol: FRMPD3-AS1
  hgvsc: ENST00000415252.1:n.107+12168A>T
  variant of: http://identifiers.org/hgnc/41239
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000398668
  ensembl transcript: ENST00000439554
  gene symbol: FRMPD3
  hgvsc: ENST00000439554.1:c.237T>A
  hgvsp: ENSP00000398668.1:p.His79Gln
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000276185
  ensembl transcript: ENST00000276185
  gene symbol: FRMPD3
  hgvsc: ENST00000276185.4:c.393T>A
  hgvsp: ENSP00000276185.4:p.His131Gln
  variant of: http://identifiers.org/hgnc/29382
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1900
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2195
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2267
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2022
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1723
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15865
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3744
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1844
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2355
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3315
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3470
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3869
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2810
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3405
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1841
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2834
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 639
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4615
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 237
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 234
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 519
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1366
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1032
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1093
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1370
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 750
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44677
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
hgvs: p.His131Gln
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

X-106776780-G-GGTGA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106776780
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106776784
    reference: chr 0
allele count: 3
allele frequency: 3.693626032676278e-5
allele num: 81221
alternate allele: GGTGA
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000398668
  ensembl transcript: ENST00000439554
  gene symbol: FRMPD3
  hgvsc: ENST00000439554.1:c.240+6_240+9dupTGAG
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000276185
  ensembl transcript: ENST00000276185
  gene symbol: FRMPD3
  hgvsc: ENST00000276185.4:c.396+6_396+9dupTGAG
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000227610
  ensembl transcript: ENST00000415252
  gene symbol: FRMPD3-AS1
  hgvsc: ENST00000415252.1:n.107+12161_107+12164dupTCAC
  variant of: http://identifiers.org/hgnc/41239
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 1724
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2810
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3744
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2196
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2022
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 949
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15864
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3315
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1899
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3870
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2263
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2355
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3472
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2834
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1843
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4410
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44678
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1459
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 279
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 750
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1086
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 526
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1030
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 261
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 635
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1143
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum

X-106776801-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106776801
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106776801
    reference: chr 0
allele count: 1
allele frequency: 1.235986997416787e-5
allele num: 80907
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000398668
  ensembl transcript: ENST00000439554
  gene symbol: FRMPD3
  hgvsc: ENST00000439554.1:c.240+21T>C
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000276185
  ensembl transcript: ENST00000276185
  gene symbol: FRMPD3
  hgvsc: ENST00000276185.4:c.396+21T>C
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000227610
  ensembl transcript: ENST00000415252
  gene symbol: FRMPD3-AS1
  hgvsc: ENST00000415252.1:n.107+12144A>G
  variant of: http://identifiers.org/hgnc/41239
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1843
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3871
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1825
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3315
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1899
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2241
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3471
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2037
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3744
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2355
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2835
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1168
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1842
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15863
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2809
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1723
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2022
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1899
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 556
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  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 622
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 76
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genotype quality: GenotypeQuality
  all individuals: 44677
  bin: 9.75e1
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 2841
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genotype quality: GenotypeQuality
  all individuals: 2076
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genotype quality: GenotypeQuality
  all individuals: 349
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 628
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1019
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum

X-106776812-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106776812
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106776812
    reference: chr 0
allele count: 1
allele frequency: 1.240617827678184e-5
allele num: 80605
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000227610
  ensembl transcript: ENST00000415252
  gene symbol: FRMPD3-AS1
  hgvsc: ENST00000415252.1:n.107+12133A>G
  variant of: http://identifiers.org/hgnc/41239
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000398668
  ensembl transcript: ENST00000439554
  gene symbol: FRMPD3
  hgvsc: ENST00000439554.1:c.240+32T>C
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000276185
  ensembl transcript: ENST00000276185
  gene symbol: FRMPD3
  hgvsc: ENST00000276185.4:c.396+32T>C
  variant of: http://identifiers.org/hgnc/29382
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1213
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2022
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2805
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3873
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2835
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3315
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3744
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1842
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1688
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1353
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2240
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1843
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2214
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1097
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1899
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2355
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15863
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1723
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3468
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44674
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2031
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 163
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 541
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1130
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
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genotype quality: GenotypeQuality
  all individuals: 1004
  bin: 7.75e1
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genotype quality: GenotypeQuality
  all individuals: 175
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genotype quality: GenotypeQuality
  all individuals: 1369
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genotype quality: GenotypeQuality
  all individuals: 784
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genotype quality: GenotypeQuality
  all individuals: 135
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genotype quality: GenotypeQuality
  all individuals: 686
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 162
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 747
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 611
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff

X-106788927-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106788927
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106788927
    reference: chr 0
allele count: 3
allele frequency: 4.336701504835422e-5
allele num: 69177
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000276185
  ensembl transcript: ENST00000276185
  gene symbol: FRMPD3
  hgvsc: ENST00000276185.4:c.397-40T>C
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000398668
  ensembl transcript: ENST00000439554
  gene symbol: FRMPD3
  hgvsc: ENST00000439554.1:c.241-40T>C
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147234
  ensembl transcript: ENST00000477796
  gene symbol: FRMPD3
  hgvsc: ENST00000477796.1:n.1115T>C
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000227610
  ensembl transcript: ENST00000415252
  gene symbol: FRMPD3-AS1
  hgvsc: ENST00000415252.1:n.107+18A>G
  variant of: http://identifiers.org/hgnc/41239
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6894
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7046
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genotype depth: GenotypeDepth
  all individuals: 183
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12146
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1739
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2002
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1181
  bin: 1.75e1
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genotype quality: GenotypeQuality
  all individuals: 1430
  bin: 7.5e0
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 892
  bin: 5.25e1
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genotype quality: GenotypeQuality
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  bin: 2.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 6149
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 672
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 308
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16242
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3930
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1965
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
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  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2497
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2113
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 625
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 366
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
reference allele: T
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

X-106788949-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106788949
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106788949
    reference: chr 0
allele count: 2
allele frequency: 2.768281035890764e-5
allele num: 72247
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000398668
  ensembl transcript: ENST00000439554
  gene symbol: FRMPD3
  hgvsc: ENST00000439554.1:c.241-18T>C
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000227610
  ensembl transcript: ENST00000415252
  gene symbol: FRMPD3-AS1
  hgvsc: ENST00000415252.1:n.103A>G
  variant of: http://identifiers.org/hgnc/41239
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000276185
  ensembl transcript: ENST00000276185
  gene symbol: FRMPD3
  hgvsc: ENST00000276185.4:c.397-18T>C
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147234
  ensembl transcript: ENST00000477796
  gene symbol: FRMPD3
  hgvsc: ENST00000477796.1:n.1137T>C
  variant of: http://identifiers.org/hgnc/29382
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9405
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 771
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1592
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9005
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
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  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 3188
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10117
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1787
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1965
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 675
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 382
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 673
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 481
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 234
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: QD

X-106788950-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106788950
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106788950
    reference: chr 0
allele count: 2
allele frequency: 2.760181619950593e-5
allele num: 72459
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000276185
  ensembl transcript: ENST00000276185
  gene symbol: FRMPD3
  hgvsc: ENST00000276185.4:c.397-17C>G
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000227610
  ensembl transcript: ENST00000415252
  gene symbol: FRMPD3-AS1
  hgvsc: ENST00000415252.1:n.102G>C
  variant of: http://identifiers.org/hgnc/41239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147234
  ensembl transcript: ENST00000477796
  gene symbol: FRMPD3
  hgvsc: ENST00000477796.1:n.1138C>G
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000398668
  ensembl transcript: ENST00000439554
  gene symbol: FRMPD3
  hgvsc: ENST00000439554.1:c.241-17C>G
  variant of: http://identifiers.org/hgnc/29382
canonical: true
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 25405
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7226
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2253
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  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9183
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9111
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
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  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 434
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31475
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1965
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  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 414
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 229
  bin: 5.75e1
  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: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: DP

X-106788957-CT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106788957
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106788956
    reference: chr 0
allele count: 3
allele frequency: 4.03801114491076e-5
allele num: 74294
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000227610
  ensembl transcript: ENST00000415252
  gene symbol: FRMPD3-AS1
  hgvsc: ENST00000415252.1:n.94delA
  variant of: http://identifiers.org/hgnc/41239
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000398668
  ensembl transcript: ENST00000439554
  gene symbol: FRMPD3
  hgvsc: ENST00000439554.1:c.241-5delT
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147234
  ensembl transcript: ENST00000477796
  gene symbol: FRMPD3
  hgvsc: ENST00000477796.1:n.1150delT
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000276185
  ensembl transcript: ENST00000276185
  gene symbol: FRMPD3
  hgvsc: ENST00000276185.4:c.397-5delT
  variant of: http://identifiers.org/hgnc/29382
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1018
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
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  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7448
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 302
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 382
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 385
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3137
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: CT
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff

X-106788986-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106788986
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106788986
    reference: chr 0
allele count: 1
allele frequency: 1.257940750990628e-5
allele num: 79495
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000276185
  ensembl transcript: ENST00000276185
  gene symbol: FRMPD3
  hgvsc: ENST00000276185.4:c.416T>C
  hgvsp: ENSP00000276185.4:p.Ile139Thr
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000227610
  ensembl transcript: ENST00000415252
  gene symbol: FRMPD3-AS1
  hgvsc: ENST00000415252.1:n.66A>G
  variant of: http://identifiers.org/hgnc/41239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147234
  ensembl transcript: ENST00000477796
  gene symbol: FRMPD3
  hgvsc: ENST00000477796.1:n.1174T>C
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000398668
  ensembl transcript: ENST00000439554
  gene symbol: FRMPD3
  hgvsc: ENST00000439554.1:c.260T>C
  hgvsp: ENSP00000398668.1:p.Ile87Thr
  variant of: http://identifiers.org/hgnc/29382
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12033
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 1.25e1
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genotype quality: GenotypeQuality
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  bin: 7.5e0
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 5.25e1
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
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  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3730
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.5e0
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genotype quality: GenotypeQuality
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  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1965
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 189
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Ile139Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: African
reference allele: T
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: DP
site quality: QD

X-106788987-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106788987
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106788987
    reference: chr 0
allele count: 1
allele frequency: 1.257308103350726e-5
allele num: 79535
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000276185
  ensembl transcript: ENST00000276185
  gene symbol: FRMPD3
  hgvsc: ENST00000276185.4:c.417C>T
  hgvsp: ENST00000276185.4:c.417C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000398668
  ensembl transcript: ENST00000439554
  gene symbol: FRMPD3
  hgvsc: ENST00000439554.1:c.261C>T
  hgvsp: ENST00000439554.1:c.261C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147234
  ensembl transcript: ENST00000477796
  gene symbol: FRMPD3
  hgvsc: ENST00000477796.1:n.1175C>T
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000227610
  ensembl transcript: ENST00000415252
  gene symbol: FRMPD3-AS1
  hgvsc: ENST00000415252.1:n.65G>A
  variant of: http://identifiers.org/hgnc/41239
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 12119
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 2.5e0
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genotype quality: GenotypeQuality
  all individuals: 191
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 230
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
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  variant carriers: 0
hgvs: p.Ile139Ile
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: BaseQRankSum

X-106788994-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106788994
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106788994
    reference: chr 0
allele count: 31
allele frequency: 3.883203266901329e-4
allele num: 79831
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000398668
  ensembl transcript: ENST00000439554
  gene symbol: FRMPD3
  hgvsc: ENST00000439554.1:c.268G>A
  hgvsp: ENSP00000398668.1:p.Ala90Thr
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000276185
  ensembl transcript: ENST00000276185
  gene symbol: FRMPD3
  hgvsc: ENST00000276185.4:c.424G>A
  hgvsp: ENSP00000276185.4:p.Ala142Thr
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000227610
  ensembl transcript: ENST00000415252
  gene symbol: FRMPD3-AS1
  hgvsc: ENST00000415252.1:n.58C>T
  variant of: http://identifiers.org/hgnc/41239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147234
  ensembl transcript: ENST00000477796
  gene symbol: FRMPD3
  hgvsc: ENST00000477796.1:n.1182G>A
  variant of: http://identifiers.org/hgnc/29382
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 472
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  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
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  variant carriers: 2
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 25
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 44622
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ala142Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: East Asian
population: African
population: European (Finnish)
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ

X-106788995-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106788995
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106788995
    reference: chr 0
allele count: 1
allele frequency: 1.252191334835963e-5
allele num: 79860
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000276185
  ensembl transcript: ENST00000276185
  gene symbol: FRMPD3
  hgvsc: ENST00000276185.4:c.425C>T
  hgvsp: ENSP00000276185.4:p.Ala142Val
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147234
  ensembl transcript: ENST00000477796
  gene symbol: FRMPD3
  hgvsc: ENST00000477796.1:n.1183C>T
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000398668
  ensembl transcript: ENST00000439554
  gene symbol: FRMPD3
  hgvsc: ENST00000439554.1:c.269C>T
  hgvsp: ENSP00000398668.1:p.Ala90Val
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000227610
  ensembl transcript: ENST00000415252
  gene symbol: FRMPD3-AS1
  hgvsc: ENST00000415252.1:n.57G>A
  variant of: http://identifiers.org/hgnc/41239
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 12526
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2645
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2354
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.25e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.75e1
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 304
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 444
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  variant carriers: 1
hgvs: p.Ala142Val
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: QD

X-106788996-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106788996
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106788996
    reference: chr 0
allele count: 2
allele frequency: 2.50278434758669e-5
allele num: 79911
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000276185
  ensembl transcript: ENST00000276185
  gene symbol: FRMPD3
  hgvsc: ENST00000276185.4:c.426G>A
  hgvsp: ENST00000276185.4:c.426G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000227610
  ensembl transcript: ENST00000415252
  gene symbol: FRMPD3-AS1
  hgvsc: ENST00000415252.1:n.56C>T
  variant of: http://identifiers.org/hgnc/41239
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147234
  ensembl transcript: ENST00000477796
  gene symbol: FRMPD3
  hgvsc: ENST00000477796.1:n.1184G>A
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000398668
  ensembl transcript: ENST00000439554
  gene symbol: FRMPD3
  hgvsc: ENST00000439554.1:c.270G>A
  hgvsp: ENST00000439554.1:c.270G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29382
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 6.75e1
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genotype quality: GenotypeQuality
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  bin: 4.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 1.25e1
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genotype quality: GenotypeQuality
  all individuals: 44937
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ala142Ala
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ

X-106789004-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106789004
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106789004
    reference: chr 0
allele count: 1
allele frequency: 1.249437753011145e-5
allele num: 80036
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147234
  ensembl transcript: ENST00000477796
  gene symbol: FRMPD3
  hgvsc: ENST00000477796.1:n.1192C>G
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000398668
  ensembl transcript: ENST00000439554
  gene symbol: FRMPD3
  hgvsc: ENST00000439554.1:c.278C>G
  hgvsp: ENSP00000398668.1:p.Ala93Gly
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000276185
  ensembl transcript: ENST00000276185
  gene symbol: FRMPD3
  hgvsc: ENST00000276185.4:c.434C>G
  hgvsp: ENSP00000276185.4:p.Ala145Gly
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000227610
  ensembl transcript: ENST00000415252
  gene symbol: FRMPD3-AS1
  hgvsc: ENST00000415252.1:n.48G>C
  variant of: http://identifiers.org/hgnc/41239
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1967
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 241
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  variant carriers: 0
hgvs: p.Ala145Gly
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: QD

X-106789012-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106789012
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106789012
    reference: chr 0
allele count: 1
allele frequency: 1.24979690800245e-5
allele num: 80013
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000398668
  ensembl transcript: ENST00000439554
  gene symbol: FRMPD3
  hgvsc: ENST00000439554.1:c.286A>G
  hgvsp: ENSP00000398668.1:p.Arg96Gly
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000227610
  ensembl transcript: ENST00000415252
  gene symbol: FRMPD3-AS1
  hgvsc: ENST00000415252.1:n.40T>C
  variant of: http://identifiers.org/hgnc/41239
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000276185
  ensembl transcript: ENST00000276185
  gene symbol: FRMPD3
  hgvsc: ENST00000276185.4:c.442A>G
  hgvsp: ENSP00000276185.4:p.Arg148Gly
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147234
  ensembl transcript: ENST00000477796
  gene symbol: FRMPD3
  hgvsc: ENST00000477796.1:n.1200A>G
  variant of: http://identifiers.org/hgnc/29382
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2654
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2207
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13028
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35586
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  variant carriers: 1
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 732
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1005
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 2805
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1967
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genotype quality: GenotypeQuality
  all individuals: 239
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genotype quality: GenotypeQuality
  all individuals: 413
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Arg148Gly
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ

X-106789025-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106789025
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106789025
    reference: chr 0
allele count: 1
allele frequency: 1.259366538631069e-5
allele num: 79405
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147234
  ensembl transcript: ENST00000477796
  gene symbol: FRMPD3
  hgvsc: ENST00000477796.1:n.1213T>C
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000276185
  ensembl transcript: ENST00000276185
  gene symbol: FRMPD3
  hgvsc: ENST00000276185.4:c.455T>C
  hgvsp: ENSP00000276185.4:p.Val152Ala
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000227610
  ensembl transcript: ENST00000415252
  gene symbol: FRMPD3-AS1
  hgvsc: ENST00000415252.1:n.27A>G
  variant of: http://identifiers.org/hgnc/41239
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000398668
  ensembl transcript: ENST00000439554
  gene symbol: FRMPD3
  hgvsc: ENST00000439554.1:c.299T>C
  hgvsp: ENSP00000398668.1:p.Val100Ala
  variant of: http://identifiers.org/hgnc/29382
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33994
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1771
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 354
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Val152Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

X-106789033-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106789033
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106789033
    reference: chr 0
allele count: 1
allele frequency: 1.26972840509415e-5
allele num: 78757
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000227610
  ensembl transcript: ENST00000415252
  gene symbol: FRMPD3-AS1
  hgvsc: ENST00000415252.1:n.19G>A
  variant of: http://identifiers.org/hgnc/41239
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000276185
  ensembl transcript: ENST00000276185
  gene symbol: FRMPD3
  hgvsc: ENST00000276185.4:c.463C>T
  hgvsp: ENSP00000276185.4:p.Arg155Ter
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000398668
  ensembl transcript: ENST00000439554
  gene symbol: FRMPD3
  hgvsc: ENST00000439554.1:c.307C>T
  hgvsp: ENSP00000398668.1:p.Arg103Ter
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147234
  ensembl transcript: ENST00000477796
  gene symbol: FRMPD3
  hgvsc: ENST00000477796.1:n.1221C>T
  variant of: http://identifiers.org/hgnc/29382
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3397
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 4.25e1
  variant carriers: 0
hgvs: p.Arg155Ter
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum

X-106789034-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106789034
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106789034
    reference: chr 0
allele count: 1
allele frequency: 1.273204145552698e-5
allele num: 78542
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147234
  ensembl transcript: ENST00000477796
  gene symbol: FRMPD3
  hgvsc: ENST00000477796.1:n.1222G>A
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000398668
  ensembl transcript: ENST00000439554
  gene symbol: FRMPD3
  hgvsc: ENST00000439554.1:c.308G>A
  hgvsp: ENSP00000398668.1:p.Arg103Gln
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000227610
  ensembl transcript: ENST00000415252
  gene symbol: FRMPD3-AS1
  hgvsc: ENST00000415252.1:n.18C>T
  variant of: http://identifiers.org/hgnc/41239
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000276185
  ensembl transcript: ENST00000276185
  gene symbol: FRMPD3
  hgvsc: ENST00000276185.4:c.464G>A
  hgvsp: ENSP00000276185.4:p.Arg155Gln
  variant of: http://identifiers.org/hgnc/29382
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
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  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
hgvs: p.Arg155Gln
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: QD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
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X-106789048-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106789048
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106789048
    reference: chr 0
allele count: 1
allele frequency: 1.3064893325146e-5
allele num: 76541
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147234
  ensembl transcript: ENST00000477796
  gene symbol: FRMPD3
  hgvsc: ENST00000477796.1:n.1236G>A
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000398668
  ensembl transcript: ENST00000439554
  gene symbol: FRMPD3
  hgvsc: ENST00000439554.1:c.322G>A
  hgvsp: ENSP00000398668.1:p.Val108Met
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000276185
  ensembl transcript: ENST00000276185
  gene symbol: FRMPD3
  hgvsc: ENST00000276185.4:c.478G>A
  hgvsp: ENSP00000276185.4:p.Val160Met
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000227610
  ensembl transcript: ENST00000415252
  gene symbol: FRMPD3-AS1
  hgvsc: ENST00000415252.1:n.4C>T
  variant of: http://identifiers.org/hgnc/41239
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 672
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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hgvs: p.Val160Met
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD

X-106789051-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106789051
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106789051
    reference: chr 0
allele count: 1
allele frequency: 1.312956252297673e-5
allele num: 76164
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000276185
  ensembl transcript: ENST00000276185
  gene symbol: FRMPD3
  hgvsc: ENST00000276185.4:c.481G>A
  hgvsp: ENSP00000276185.4:p.Ala161Thr
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000227610
  ensembl transcript: ENST00000415252
  gene symbol: FRMPD3-AS1
  hgvsc: ENST00000415252.1:n.1C>T
  variant of: http://identifiers.org/hgnc/41239
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000398668
  ensembl transcript: ENST00000439554
  gene symbol: FRMPD3
  hgvsc: ENST00000439554.1:c.325G>A
  hgvsp: ENSP00000398668.1:p.Ala109Thr
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147234
  ensembl transcript: ENST00000477796
  gene symbol: FRMPD3
  hgvsc: ENST00000477796.1:n.1239G>A
  variant of: http://identifiers.org/hgnc/29382
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 256
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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hgvs: p.Ala161Thr
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: South Asian
reference allele: G
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

X-106789052-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106789052
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106789052
    reference: chr 0
allele count: 1
allele frequency: 1.316551687819264e-5
allele num: 75956
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000276185
  ensembl transcript: ENST00000276185
  gene symbol: FRMPD3
  hgvsc: ENST00000276185.4:c.482C>T
  hgvsp: ENSP00000276185.4:p.Ala161Val
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000398668
  ensembl transcript: ENST00000439554
  gene symbol: FRMPD3
  hgvsc: ENST00000439554.1:c.326C>T
  hgvsp: ENSP00000398668.1:p.Ala109Val
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147234
  ensembl transcript: ENST00000477796
  gene symbol: FRMPD3
  hgvsc: ENST00000477796.1:n.1240C>T
  variant of: http://identifiers.org/hgnc/29382
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27095
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 2.75e1
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genotype quality: GenotypeQuality
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  bin: 3.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 678
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Ala161Val
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP

X-106789055-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106789055
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106789055
    reference: chr 0
allele count: 17
allele frequency: 2.251894240449319e-4
allele num: 75492
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000398668
  ensembl transcript: ENST00000439554
  gene symbol: FRMPD3
  hgvsc: ENST00000439554.1:c.329T>C
  hgvsp: ENSP00000398668.1:p.Val110Ala
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000276185
  ensembl transcript: ENST00000276185
  gene symbol: FRMPD3
  hgvsc: ENST00000276185.4:c.485T>C
  hgvsp: ENSP00000276185.4:p.Val162Ala
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147234
  ensembl transcript: ENST00000477796
  gene symbol: FRMPD3
  hgvsc: ENST00000477796.1:n.1243T>C
  variant of: http://identifiers.org/hgnc/29382
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1223
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 8.75e1
  variant carriers: 1
hgvs: p.Val162Ala
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum

X-106789066-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106789066
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106789066
    reference: chr 0
allele count: 1
allele frequency: 1.373003995441627e-5
allele num: 72833
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000276185
  ensembl transcript: ENST00000276185
  gene symbol: FRMPD3
  hgvsc: ENST00000276185.4:c.496G>C
  hgvsp: ENSP00000276185.4:p.Asp166His
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000398668
  ensembl transcript: ENST00000439554
  gene symbol: FRMPD3
  hgvsc: ENST00000439554.1:c.340G>C
  hgvsp: ENSP00000398668.1:p.Asp114His
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147234
  ensembl transcript: ENST00000477796
  gene symbol: FRMPD3
  hgvsc: ENST00000477796.1:n.1254G>C
  variant of: http://identifiers.org/hgnc/29382
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 87
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 228
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Asp166His
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP

X-106789068-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106789068
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106789068
    reference: chr 0
allele count: 1
allele frequency: 1.381349025458263e-5
allele num: 72393
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147234
  ensembl transcript: ENST00000477796
  gene symbol: FRMPD3
  hgvsc: ENST00000477796.1:n.1256T>C
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000276185
  ensembl transcript: ENST00000276185
  gene symbol: FRMPD3
  hgvsc: ENST00000276185.4:c.498T>C
  hgvsp: ENST00000276185.4:c.498T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000398668
  ensembl transcript: ENST00000439554
  gene symbol: FRMPD3
  hgvsc: ENST00000439554.1:c.342T>C
  hgvsp: ENST00000439554.1:c.342T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29382
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2429
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19891
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 210
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Asp166Asp
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQ

X-106789075-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106789075
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106789075
    reference: chr 0
allele count: 1
allele frequency: 1.417253645885004e-5
allele num: 70559
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl transcript: ENST00000477796
  gene symbol: FRMPD3
  hgvsc: ENST00000477796.1:n.1259+4A>C
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000276185
  ensembl transcript: ENST00000276185
  gene symbol: FRMPD3
  hgvsc: ENST00000276185.4:c.501+4A>C
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000398668
  ensembl transcript: ENST00000439554
  gene symbol: FRMPD3
  hgvsc: ENST00000439554.1:c.345+4A>C
  variant of: http://identifiers.org/hgnc/29382
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2340
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1354
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: c.501+4A>C
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
reference allele: A
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
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site quality: FS

X-106789076-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106789076
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106789076
    reference: chr 0
allele count: 1
allele frequency: 1.431700717282059e-5
allele num: 69847
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000276185
  ensembl transcript: ENST00000276185
  gene symbol: FRMPD3
  hgvsc: ENST00000276185.4:c.501+5G>T
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000398668
  ensembl transcript: ENST00000439554
  gene symbol: FRMPD3
  hgvsc: ENST00000439554.1:c.345+5G>T
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
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  ensembl gene: ENSG00000147234
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  gene symbol: FRMPD3
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  variant of: http://identifiers.org/hgnc/29382
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: c.501+5G>T
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: Latino
reference allele: G
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
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site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
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X-106789078-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106789078
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106789078
    reference: chr 0
allele count: 1
allele frequency: 1.438579833987887e-5
allele num: 69513
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000276185
  ensembl transcript: ENST00000276185
  gene symbol: FRMPD3
  hgvsc: ENST00000276185.4:c.501+7G>A
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000398668
  ensembl transcript: ENST00000439554
  gene symbol: FRMPD3
  hgvsc: ENST00000439554.1:c.345+7G>A
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
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  ensembl gene: ENSG00000147234
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  gene symbol: FRMPD3
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  variant of: http://identifiers.org/hgnc/29382
canonical: true
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genotype depth: GenotypeDepth
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hgvs: c.501+7G>A
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population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
population: African
reference allele: G
site quality: ReadPosRankSum
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site quality: MQRankSum
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site quality: DP
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X-106789090-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106789090
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106789090
    reference: chr 0
allele count: 1
allele frequency: 1.516898246465627e-5
allele num: 65924
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl transcript: ENST00000477796
  gene symbol: FRMPD3
  hgvsc: ENST00000477796.1:n.1259+19C>T
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000276185
  ensembl transcript: ENST00000276185
  gene symbol: FRMPD3
  hgvsc: ENST00000276185.4:c.501+19C>T
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
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  consequence: intron_variant
  ensembl gene: ENSG00000147234
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  ensembl transcript: ENST00000439554
  gene symbol: FRMPD3
  hgvsc: ENST00000439554.1:c.345+19C>T
  variant of: http://identifiers.org/hgnc/29382
canonical: true
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
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site quality: InbreedingCoeff
site quality: VQSLOD
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site quality: BaseQRankSum
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X-106789106-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106789106
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106789106
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 61062
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000276185
  ensembl transcript: ENST00000276185
  gene symbol: FRMPD3
  hgvsc: ENST00000276185.4:c.501+35T>C
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000398668
  ensembl transcript: ENST00000439554
  gene symbol: FRMPD3
  hgvsc: ENST00000439554.1:c.345+35T>C
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
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  ensembl gene: ENSG00000147234
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  gene symbol: FRMPD3
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  variant of: http://identifiers.org/hgnc/29382
canonical: true
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: QD

X-106789107-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106789107
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106789107
    reference: chr 0
allele count: 4
allele frequency: 6.589894396942289e-5
allele num: 60699
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000398668
  ensembl transcript: ENST00000439554
  gene symbol: FRMPD3
  hgvsc: ENST00000439554.1:c.345+36G>A
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl transcript: ENST00000477796
  gene symbol: FRMPD3
  hgvsc: ENST00000477796.1:n.1259+36G>A
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000276185
  ensembl transcript: ENST00000276185
  gene symbol: FRMPD3
  hgvsc: ENST00000276185.4:c.501+36G>A
  variant of: http://identifiers.org/hgnc/29382
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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  bin: 9.25e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

X-106789108-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106789108
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106789108
    reference: chr 0
allele count: 44
allele frequency: 7.418772867524322e-4
allele num: 59309
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl transcript: ENST00000477796
  gene symbol: FRMPD3
  hgvsc: ENST00000477796.1:n.1259+37G>C
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000398668
  ensembl transcript: ENST00000439554
  gene symbol: FRMPD3
  hgvsc: ENST00000439554.1:c.345+37G>C
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000276185
  ensembl transcript: ENST00000276185
  gene symbol: FRMPD3
  hgvsc: ENST00000276185.4:c.501+37G>C
  variant of: http://identifiers.org/hgnc/29382
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ReadPosRankSum

X-106789109-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106789109
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106789109
    reference: chr 0
allele count: 9
allele frequency: 1.517911353976928e-4
allele num: 59292
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000398668
  ensembl transcript: ENST00000439554
  gene symbol: FRMPD3
  hgvsc: ENST00000439554.1:c.345+38C>T
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl transcript: ENST00000477796
  gene symbol: FRMPD3
  hgvsc: ENST00000477796.1:n.1259+38C>T
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000276185
  ensembl transcript: ENST00000276185
  gene symbol: FRMPD3
  hgvsc: ENST00000276185.4:c.501+38C>T
  variant of: http://identifiers.org/hgnc/29382
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: Latino
population: Other
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: FS

X-106789113-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106789113
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106789113
    reference: chr 0
allele count: 1
allele frequency: 1.695748757864035e-5
allele num: 58971
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl transcript: ENST00000477796
  gene symbol: FRMPD3
  hgvsc: ENST00000477796.1:n.1259+42A>C
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000398668
  ensembl transcript: ENST00000439554
  gene symbol: FRMPD3
  hgvsc: ENST00000439554.1:c.345+42A>C
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000276185
  ensembl transcript: ENST00000276185
  gene symbol: FRMPD3
  hgvsc: ENST00000276185.4:c.501+42A>C
  variant of: http://identifiers.org/hgnc/29382
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 143
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

X-106793229-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106793229
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106793229
    reference: chr 0
allele count: 1
allele frequency: 3.340571237681643e-5
allele num: 29935
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000276185
  ensembl transcript: ENST00000276185
  gene symbol: FRMPD3
  hgvsc: ENST00000276185.4:c.502-50C>T
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000398668
  ensembl transcript: ENST00000439554
  gene symbol: FRMPD3
  hgvsc: ENST00000439554.1:c.346-50C>T
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl transcript: ENST00000477796
  gene symbol: FRMPD3
  hgvsc: ENST00000477796.1:n.1260-50C>T
  variant of: http://identifiers.org/hgnc/29382
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 2141
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum

X-106793232-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106793232
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106793232
    reference: chr 0
allele count: 1
allele frequency: 3.332222592469177e-5
allele num: 30010
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000398668
  ensembl transcript: ENST00000439554
  gene symbol: FRMPD3
  hgvsc: ENST00000439554.1:c.346-47C>A
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl transcript: ENST00000477796
  gene symbol: FRMPD3
  hgvsc: ENST00000477796.1:n.1260-47C>A
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000276185
  ensembl transcript: ENST00000276185
  gene symbol: FRMPD3
  hgvsc: ENST00000276185.4:c.502-47C>A
  variant of: http://identifiers.org/hgnc/29382
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1135
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: European (Finnish)
population: East Asian
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: QD
site quality: VQSLOD

X-106793233-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106793233
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106793233
    reference: chr 0
allele count: 1
allele frequency: 3.328783995206551e-5
allele num: 30041
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000398668
  ensembl transcript: ENST00000439554
  gene symbol: FRMPD3
  hgvsc: ENST00000439554.1:c.346-46C>G
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl transcript: ENST00000477796
  gene symbol: FRMPD3
  hgvsc: ENST00000477796.1:n.1260-46C>G
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000276185
  ensembl transcript: ENST00000276185
  gene symbol: FRMPD3
  hgvsc: ENST00000276185.4:c.502-46C>G
  variant of: http://identifiers.org/hgnc/29382
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

X-106793247-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106793247
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106793247
    reference: chr 0
allele count: 1
allele frequency: 3.19959045242209e-5
allele num: 31254
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl transcript: ENST00000477796
  gene symbol: FRMPD3
  hgvsc: ENST00000477796.1:n.1260-32G>A
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000398668
  ensembl transcript: ENST00000439554
  gene symbol: FRMPD3
  hgvsc: ENST00000439554.1:c.346-32G>A
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000276185
  ensembl transcript: ENST00000276185
  gene symbol: FRMPD3
  hgvsc: ENST00000276185.4:c.502-32G>A
  variant of: http://identifiers.org/hgnc/29382
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1607
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff

X-106793250-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106793250
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106793250
    reference: chr 0
allele count: 3
allele frequency: 9.346667912889055e-5
allele num: 32097
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl transcript: ENST00000477796
  gene symbol: FRMPD3
  hgvsc: ENST00000477796.1:n.1260-29C>A
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000398668
  ensembl transcript: ENST00000439554
  gene symbol: FRMPD3
  hgvsc: ENST00000439554.1:c.346-29C>A
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000276185
  ensembl transcript: ENST00000276185
  gene symbol: FRMPD3
  hgvsc: ENST00000276185.4:c.502-29C>A
  variant of: http://identifiers.org/hgnc/29382
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 125
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: East Asian
population: Latino
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: QD

X-106793256-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106793256
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106793256
    reference: chr 0
allele count: 1
allele frequency: 2.997512064986062e-5
allele num: 33361
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000398668
  ensembl transcript: ENST00000439554
  gene symbol: FRMPD3
  hgvsc: ENST00000439554.1:c.346-23G>A
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000276185
  ensembl transcript: ENST00000276185
  gene symbol: FRMPD3
  hgvsc: ENST00000276185.4:c.502-23G>A
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl transcript: ENST00000477796
  gene symbol: FRMPD3
  hgvsc: ENST00000477796.1:n.1260-23G>A
  variant of: http://identifiers.org/hgnc/29382
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
reference allele: G
site quality: FS
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ

X-106793260-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106793260
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106793260
    reference: chr 0
allele count: 1
allele frequency: 2.887753039360074e-5
allele num: 34629
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000276185
  ensembl transcript: ENST00000276185
  gene symbol: FRMPD3
  hgvsc: ENST00000276185.4:c.502-19T>A
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl transcript: ENST00000477796
  gene symbol: FRMPD3
  hgvsc: ENST00000477796.1:n.1260-19T>A
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000398668
  ensembl transcript: ENST00000439554
  gene symbol: FRMPD3
  hgvsc: ENST00000439554.1:c.346-19T>A
  variant of: http://identifiers.org/hgnc/29382
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 114
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
reference allele: T
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum

X-106793265-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106793265
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106793265
    reference: chr 0
allele count: 1
allele frequency: 2.75072894316994e-5
allele num: 36354
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000276185
  ensembl transcript: ENST00000276185
  gene symbol: FRMPD3
  hgvsc: ENST00000276185.4:c.502-14C>A
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl transcript: ENST00000477796
  gene symbol: FRMPD3
  hgvsc: ENST00000477796.1:n.1260-14C>A
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000398668
  ensembl transcript: ENST00000439554
  gene symbol: FRMPD3
  hgvsc: ENST00000439554.1:c.346-14C>A
  variant of: http://identifiers.org/hgnc/29382
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: South Asian
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP

X-106793272-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106793272
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106793272
    reference: chr 0
allele count: 3
allele frequency: 7.539582809751194e-5
allele num: 39790
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000276185
  ensembl transcript: ENST00000276185
  gene symbol: FRMPD3
  hgvsc: ENST00000276185.4:c.502-7T>C
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl transcript: ENST00000477796
  gene symbol: FRMPD3
  hgvsc: ENST00000477796.1:n.1260-7T>C
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000398668
  ensembl transcript: ENST00000439554
  gene symbol: FRMPD3
  hgvsc: ENST00000439554.1:c.346-7T>C
  variant of: http://identifiers.org/hgnc/29382
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: c.502-7T>C
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum

X-106793274-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106793274
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106793274
    reference: chr 0
allele count: 1
allele frequency: 2.465908810692181e-5
allele num: 40553
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000398668
  ensembl transcript: ENST00000439554
  gene symbol: FRMPD3
  hgvsc: ENST00000439554.1:c.346-5C>T
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl transcript: ENST00000477796
  gene symbol: FRMPD3
  hgvsc: ENST00000477796.1:n.1260-5C>T
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000276185
  ensembl transcript: ENST00000276185
  gene symbol: FRMPD3
  hgvsc: ENST00000276185.4:c.502-5C>T
  variant of: http://identifiers.org/hgnc/29382
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: c.502-5C>T
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQ

X-106793281-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106793281
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106793281
    reference: chr 0
allele count: 1
allele frequency: 2.279773846434434e-5
allele num: 43864
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000147234
  ensembl transcript: ENST00000477796
  gene symbol: FRMPD3
  hgvsc: ENST00000477796.1:n.1262A>G
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000398668
  ensembl transcript: ENST00000439554
  gene symbol: FRMPD3
  hgvsc: ENST00000439554.1:c.348A>G
  hgvsp: ENST00000439554.1:c.348A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000276185
  ensembl transcript: ENST00000276185
  gene symbol: FRMPD3
  hgvsc: ENST00000276185.4:c.504A>G
  hgvsp: ENST00000276185.4:c.504A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29382
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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hgvs: c.504A>G
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ

X-106793282-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106793282
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106793282
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 44244
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000398668
  ensembl transcript: ENST00000439554
  gene symbol: FRMPD3
  hgvsc: ENST00000439554.1:c.349A>G
  hgvsp: ENSP00000398668.1:p.Met117Val
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000276185
  ensembl transcript: ENST00000276185
  gene symbol: FRMPD3
  hgvsc: ENST00000276185.4:c.505A>G
  hgvsp: ENSP00000276185.4:p.Met169Val
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147234
  ensembl transcript: ENST00000477796
  gene symbol: FRMPD3
  hgvsc: ENST00000477796.1:n.1263A>G
  variant of: http://identifiers.org/hgnc/29382
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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hgvs: p.Met169Val
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: QD
site quality: MQ

X-106793283-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106793283
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106793283
    reference: chr 0
allele count: 10
allele frequency: 2.238638907544213e-4
allele num: 44670
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147234
  ensembl transcript: ENST00000477796
  gene symbol: FRMPD3
  hgvsc: ENST00000477796.1:n.1264T>C
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000398668
  ensembl transcript: ENST00000439554
  gene symbol: FRMPD3
  hgvsc: ENST00000439554.1:c.350T>C
  hgvsp: ENSP00000398668.1:p.Met117Thr
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000276185
  ensembl transcript: ENST00000276185
  gene symbol: FRMPD3
  hgvsc: ENST00000276185.4:c.506T>C
  hgvsp: ENSP00000276185.4:p.Met169Thr
  variant of: http://identifiers.org/hgnc/29382
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 289
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  variant carriers: 1
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 6.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 8.75e1
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genotype quality: GenotypeQuality
  all individuals: 540
  bin: 5.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 1.75e1
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genotype quality: GenotypeQuality
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  bin: 3.25e1
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genotype quality: GenotypeQuality
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  bin: 9.25e1
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genotype quality: GenotypeQuality
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  bin: 4.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 2150
  bin: 9.75e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 604
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Met169Thr
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: African
reference allele: T
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

X-106793284-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106793284
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106793284
    reference: chr 0
allele count: 1
allele frequency: 2.222666755573337e-5
allele num: 44991
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000398668
  ensembl transcript: ENST00000439554
  gene symbol: FRMPD3
  hgvsc: ENST00000439554.1:c.351G>A
  hgvsp: ENSP00000398668.1:p.Met117Ile
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000276185
  ensembl transcript: ENST00000276185
  gene symbol: FRMPD3
  hgvsc: ENST00000276185.4:c.507G>A
  hgvsp: ENSP00000276185.4:p.Met169Ile
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147234
  ensembl transcript: ENST00000477796
  gene symbol: FRMPD3
  hgvsc: ENST00000477796.1:n.1265G>A
  variant of: http://identifiers.org/hgnc/29382
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 724
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  variant carriers: 0
hgvs: p.Met169Ile
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD

X-106793298-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106793298
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106793298
    reference: chr 0
allele count: 1
allele frequency: 1.936520846646914e-5
allele num: 51639
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147234
  ensembl transcript: ENST00000477796
  gene symbol: FRMPD3
  hgvsc: ENST00000477796.1:n.1279C>G
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000276185
  ensembl transcript: ENST00000276185
  gene symbol: FRMPD3
  hgvsc: ENST00000276185.4:c.521C>G
  hgvsp: ENSP00000276185.4:p.Ala174Gly
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000398668
  ensembl transcript: ENST00000439554
  gene symbol: FRMPD3
  hgvsc: ENST00000439554.1:c.365C>G
  hgvsp: ENSP00000398668.1:p.Ala122Gly
  variant of: http://identifiers.org/hgnc/29382
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23785
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.25e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 3.25e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 174
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  variant carriers: 0
hgvs: p.Ala174Gly
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
reference allele: C
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ

X-106793300-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106793300
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106793300
    reference: chr 0
allele count: 1
allele frequency: 1.89897455374098e-5
allele num: 52660
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000398668
  ensembl transcript: ENST00000439554
  gene symbol: FRMPD3
  hgvsc: ENST00000439554.1:c.367C>G
  hgvsp: ENSP00000398668.1:p.Leu123Val
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147234
  ensembl transcript: ENST00000477796
  gene symbol: FRMPD3
  hgvsc: ENST00000477796.1:n.1281C>G
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000276185
  ensembl transcript: ENST00000276185
  gene symbol: FRMPD3
  hgvsc: ENST00000276185.4:c.523C>G
  hgvsp: ENSP00000276185.4:p.Leu175Val
  variant of: http://identifiers.org/hgnc/29382
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3378
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 197
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 233
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  variant carriers: 0
hgvs: p.Leu175Val
num of homozygotes: 0
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP

X-106793302-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106793302
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106793302
    reference: chr 0
allele count: 1
allele frequency: 1.878145894373075e-5
allele num: 53244
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000276185
  ensembl transcript: ENST00000276185
  gene symbol: FRMPD3
  hgvsc: ENST00000276185.4:c.525C>T
  hgvsp: ENST00000276185.4:c.525C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147234
  ensembl transcript: ENST00000477796
  gene symbol: FRMPD3
  hgvsc: ENST00000477796.1:n.1283C>T
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000398668
  ensembl transcript: ENST00000439554
  gene symbol: FRMPD3
  hgvsc: ENST00000439554.1:c.369C>T
  hgvsp: ENST00000439554.1:c.369C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29382
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 9.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 3.75e1
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genotype quality: GenotypeQuality
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  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 6.75e1
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genotype quality: GenotypeQuality
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  bin: 7.5e0
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genotype quality: GenotypeQuality
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  bin: 2.25e1
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genotype quality: GenotypeQuality
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  bin: 9.75e1
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genotype quality: GenotypeQuality
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  bin: 7.75e1
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genotype quality: GenotypeQuality
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  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1077
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Leu175Leu
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ReadPosRankSum

X-106793317-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106793317
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106793317
    reference: chr 0
allele count: 1
allele frequency: 1.728339584161496e-5
allele num: 57859
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147234
  ensembl transcript: ENST00000477796
  gene symbol: FRMPD3
  hgvsc: ENST00000477796.1:n.1298T>C
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000276185
  ensembl transcript: ENST00000276185
  gene symbol: FRMPD3
  hgvsc: ENST00000276185.4:c.540T>C
  hgvsp: ENST00000276185.4:c.540T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000398668
  ensembl transcript: ENST00000439554
  gene symbol: FRMPD3
  hgvsc: ENST00000439554.1:c.384T>C
  hgvsp: ENST00000439554.1:c.384T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29382
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 236
  bin: 4.25e1
  variant carriers: 1
hgvs: p.Asn180Asn
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQ
site quality: FS

X-106793331-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106793331
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106793331
    reference: chr 0
allele count: 1
allele frequency: 1.658044833532299e-5
allele num: 60312
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000398668
  ensembl transcript: ENST00000439554
  gene symbol: FRMPD3
  hgvsc: ENST00000439554.1:c.398T>C
  hgvsp: ENSP00000398668.1:p.Phe133Ser
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000276185
  ensembl transcript: ENST00000276185
  gene symbol: FRMPD3
  hgvsc: ENST00000276185.4:c.554T>C
  hgvsp: ENSP00000276185.4:p.Phe185Ser
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147234
  ensembl transcript: ENST00000477796
  gene symbol: FRMPD3
  hgvsc: ENST00000477796.1:n.1312T>C
  variant of: http://identifiers.org/hgnc/29382
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Phe185Ser
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP

X-106793338-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106793338
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106793338
    reference: chr 0
allele count: 1
allele frequency: 1.645792531393493e-5
allele num: 60761
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147234
  ensembl transcript: ENST00000477796
  gene symbol: FRMPD3
  hgvsc: ENST00000477796.1:n.1319A>G
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000276185
  ensembl transcript: ENST00000276185
  gene symbol: FRMPD3
  hgvsc: ENST00000276185.4:c.561A>G
  hgvsp: ENST00000276185.4:c.561A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000398668
  ensembl transcript: ENST00000439554
  gene symbol: FRMPD3
  hgvsc: ENST00000439554.1:c.405A>G
  hgvsp: ENST00000439554.1:c.405A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29382
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 6.25e1
  variant carriers: 0
hgvs: p.Glu187Glu
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: DP

X-106793348-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106793348
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106793348
    reference: chr 0
allele count: 1
allele frequency: 1.64766361299677e-5
allele num: 60692
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000276185
  ensembl transcript: ENST00000276185
  gene symbol: FRMPD3
  hgvsc: ENST00000276185.4:c.571A>G
  hgvsp: ENSP00000276185.4:p.Ile191Val
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000398668
  ensembl transcript: ENST00000439554
  gene symbol: FRMPD3
  hgvsc: ENST00000439554.1:c.415A>G
  hgvsp: ENSP00000398668.1:p.Ile139Val
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147234
  ensembl transcript: ENST00000477796
  gene symbol: FRMPD3
  hgvsc: ENST00000477796.1:n.1329A>G
  variant of: http://identifiers.org/hgnc/29382
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18426
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 476
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1623
  bin: 6.75e1
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genotype quality: GenotypeQuality
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  bin: 9.25e1
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genotype quality: GenotypeQuality
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  bin: 2.5e0
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genotype quality: GenotypeQuality
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  bin: 2.75e1
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genotype quality: GenotypeQuality
  all individuals: 2144
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 26451
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 263
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ile191Val
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: East Asian
population: African
reference allele: A
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

X-106793350-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106793350
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106793350
    reference: chr 0
allele count: 1
allele frequency: 1.653521173338625e-5
allele num: 60477
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000276185
  ensembl transcript: ENST00000276185
  gene symbol: FRMPD3
  hgvsc: ENST00000276185.4:c.573C>G
  hgvsp: ENSP00000276185.4:p.Ile191Met
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000398668
  ensembl transcript: ENST00000439554
  gene symbol: FRMPD3
  hgvsc: ENST00000439554.1:c.417C>G
  hgvsp: ENSP00000398668.1:p.Ile139Met
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147234
  ensembl transcript: ENST00000477796
  gene symbol: FRMPD3
  hgvsc: ENST00000477796.1:n.1331C>G
  variant of: http://identifiers.org/hgnc/29382
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4661
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 775
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ile191Met
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD

X-106793353-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106793353
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106793353
    reference: chr 0
allele count: 1
allele frequency: 1.655026314918407e-5
allele num: 60422
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000276185
  ensembl transcript: ENST00000276185
  gene symbol: FRMPD3
  hgvsc: ENST00000276185.4:c.576G>A
  hgvsp: ENST00000276185.4:c.576G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000398668
  ensembl transcript: ENST00000439554
  gene symbol: FRMPD3
  hgvsc: ENST00000439554.1:c.420G>A
  hgvsp: ENST00000439554.1:c.420G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147234
  ensembl transcript: ENST00000477796
  gene symbol: FRMPD3
  hgvsc: ENST00000477796.1:n.1334G>A
  variant of: http://identifiers.org/hgnc/29382
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.25e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 2.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 428
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 174
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Lys192Lys
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP

X-106793353-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106793353
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106793353
    reference: chr 0
allele count: 1
allele frequency: 1.655026314918407e-5
allele num: 60422
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000276185
  ensembl transcript: ENST00000276185
  gene symbol: FRMPD3
  hgvsc: ENST00000276185.4:c.576G>C
  hgvsp: ENSP00000276185.4:p.Lys192Asn
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000398668
  ensembl transcript: ENST00000439554
  gene symbol: FRMPD3
  hgvsc: ENST00000439554.1:c.420G>C
  hgvsp: ENSP00000398668.1:p.Lys140Asn
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147234
  ensembl transcript: ENST00000477796
  gene symbol: FRMPD3
  hgvsc: ENST00000477796.1:n.1334G>C
  variant of: http://identifiers.org/hgnc/29382
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1180
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22548
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 21311
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Lys192Asn
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: Other
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum

X-106793361-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106793361
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106793361
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 59440
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147234
  ensembl transcript: ENST00000477796
  gene symbol: FRMPD3
  hgvsc: ENST00000477796.1:n.1342C>T
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000398668
  ensembl transcript: ENST00000439554
  gene symbol: FRMPD3
  hgvsc: ENST00000439554.1:c.428C>T
  hgvsp: ENSP00000398668.1:p.Thr143Ile
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000276185
  ensembl transcript: ENST00000276185
  gene symbol: FRMPD3
  hgvsc: ENST00000276185.4:c.584C>T
  hgvsp: ENSP00000276185.4:p.Thr195Ile
  variant of: http://identifiers.org/hgnc/29382
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20483
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 444
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Thr195Ile
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: Other
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum

X-106793367-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106793367
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106793367
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 58313
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000398668
  ensembl transcript: ENST00000439554
  gene symbol: FRMPD3
  hgvsc: ENST00000439554.1:c.434A>T
  hgvsp: ENSP00000398668.1:p.Asp145Val
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147234
  ensembl transcript: ENST00000477796
  gene symbol: FRMPD3
  hgvsc: ENST00000477796.1:n.1348A>T
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000276185
  ensembl transcript: ENST00000276185
  gene symbol: FRMPD3
  hgvsc: ENST00000276185.4:c.590A>T
  hgvsp: ENSP00000276185.4:p.Asp197Val
  variant of: http://identifiers.org/hgnc/29382
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 9.25e1
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 2.5e0
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genotype quality: GenotypeQuality
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  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 1.75e1
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genotype quality: GenotypeQuality
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  bin: 4.25e1
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genotype quality: GenotypeQuality
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  bin: 4.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 1.25e1
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genotype quality: GenotypeQuality
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  bin: 8.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 6.25e1
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genotype quality: GenotypeQuality
  all individuals: 430
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 325
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Asp197Val
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: VQSLOD

X-106793368-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106793368
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106793368
    reference: chr 0
allele count: 1
allele frequency: 1.720814977973568e-5
allele num: 58112
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000276185
  ensembl transcript: ENST00000276185
  gene symbol: FRMPD3
  hgvsc: ENST00000276185.4:c.591T>C
  hgvsp: ENST00000276185.4:c.591T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147234
  ensembl transcript: ENST00000477796
  gene symbol: FRMPD3
  hgvsc: ENST00000477796.1:n.1349T>C
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000398668
  ensembl transcript: ENST00000439554
  gene symbol: FRMPD3
  hgvsc: ENST00000439554.1:c.435T>C
  hgvsp: ENST00000439554.1:c.435T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29382
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1139
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
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  variant carriers: 1
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 9.25e1
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 293
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Asp197Asp
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: T
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

X-106793372-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106793372
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106793372
    reference: chr 0
allele count: 2
allele frequency: 3.498766684743628e-5
allele num: 57163
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147234
  ensembl transcript: ENST00000477796
  gene symbol: FRMPD3
  hgvsc: ENST00000477796.1:n.1353C>T
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000276185
  ensembl transcript: ENST00000276185
  gene symbol: FRMPD3
  hgvsc: ENST00000276185.4:c.595C>T
  hgvsp: ENSP00000276185.4:p.Arg199Trp
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000398668
  ensembl transcript: ENST00000439554
  gene symbol: FRMPD3
  hgvsc: ENST00000439554.1:c.439C>T
  hgvsp: ENSP00000398668.1:p.Arg147Trp
  variant of: http://identifiers.org/hgnc/29382
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3431
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 1.25e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
hgvs: p.Arg199Trp
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: C
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP

X-106793373-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106793373
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106793373
    reference: chr 0
allele count: 1
allele frequency: 1.760439405675657e-5
allele num: 56804
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000276185
  ensembl transcript: ENST00000276185
  gene symbol: FRMPD3
  hgvsc: ENST00000276185.4:c.596G>A
  hgvsp: ENSP00000276185.4:p.Arg199Gln
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000398668
  ensembl transcript: ENST00000439554
  gene symbol: FRMPD3
  hgvsc: ENST00000439554.1:c.440G>A
  hgvsp: ENSP00000398668.1:p.Arg147Gln
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147234
  ensembl transcript: ENST00000477796
  gene symbol: FRMPD3
  hgvsc: ENST00000477796.1:n.1354G>A
  variant of: http://identifiers.org/hgnc/29382
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 416
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  variant carriers: 0
hgvs: p.Arg199Gln
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum

X-106793392-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106793392
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106793392
    reference: chr 0
allele count: 1
allele frequency: 2.003887541831152e-5
allele num: 49903
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl transcript: ENST00000477796
  gene symbol: FRMPD3
  hgvsc: ENST00000477796.1:n.1367+6T>A
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000276185
  ensembl transcript: ENST00000276185
  gene symbol: FRMPD3
  hgvsc: ENST00000276185.4:c.609+6T>A
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000398668
  ensembl transcript: ENST00000439554
  gene symbol: FRMPD3
  hgvsc: ENST00000439554.1:c.453+6T>A
  variant of: http://identifiers.org/hgnc/29382
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
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  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 5.25e1
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genotype depth: GenotypeDepth
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  bin: 1.25e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 9.75e1
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genotype depth: GenotypeDepth
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  bin: 9.25e1
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genotype depth: GenotypeDepth
  all individuals: 291
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 7.75e1
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genotype quality: GenotypeQuality
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  bin: 6.25e1
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genotype quality: GenotypeQuality
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  bin: 5.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 8.75e1
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genotype quality: GenotypeQuality
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  bin: 5.25e1
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genotype quality: GenotypeQuality
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  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 1.25e1
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genotype quality: GenotypeQuality
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  bin: 3.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 9.25e1
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genotype quality: GenotypeQuality
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  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2140
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2346
  bin: 3.25e1
  variant carriers: 0
hgvs: c.609+6T>A
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: FS

X-106793396-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106793396
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106793396
    reference: chr 0
allele count: 4329
allele frequency: 8.868720806359091e-2
allele num: 48812
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl transcript: ENST00000477796
  gene symbol: FRMPD3
  hgvsc: ENST00000477796.1:n.1367+10G>A
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000398668
  ensembl transcript: ENST00000439554
  gene symbol: FRMPD3
  hgvsc: ENST00000439554.1:c.453+10G>A
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000276185
  ensembl transcript: ENST00000276185
  gene symbol: FRMPD3
  hgvsc: ENST00000276185.4:c.609+10G>A
  variant of: http://identifiers.org/hgnc/29382
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 6.25e1
  variant carriers: 39
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.75e1
  variant carriers: 28
genotype quality: GenotypeQuality
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  variant carriers: 86
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 7.5e0
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genotype quality: GenotypeQuality
  all individuals: 23845
  bin: 2.25e1
  variant carriers: 175
genotype quality: GenotypeQuality
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  bin: 1.25e1
  variant carriers: 77
genotype quality: GenotypeQuality
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  bin: 8.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 128
genotype quality: GenotypeQuality
  all individuals: 4395
  bin: 9.75e1
  variant carriers: 2537
num of homozygotes: 576
population: East Asian
population: South Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff

X-106793402-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106793402
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106793402
    reference: chr 0
allele count: 1
allele frequency: 2.257540184215279e-5
allele num: 44296
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000276185
  ensembl transcript: ENST00000276185
  gene symbol: FRMPD3
  hgvsc: ENST00000276185.4:c.609+16T>A
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl transcript: ENST00000477796
  gene symbol: FRMPD3
  hgvsc: ENST00000477796.1:n.1367+16T>A
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000398668
  ensembl transcript: ENST00000439554
  gene symbol: FRMPD3
  hgvsc: ENST00000439554.1:c.453+16T>A
  variant of: http://identifiers.org/hgnc/29382
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2703
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  variant carriers: 1
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 192
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

X-106793404-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106793404
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106793404
    reference: chr 0
allele count: 224
allele frequency: 5.114739125470944e-3
allele num: 43795
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000398668
  ensembl transcript: ENST00000439554
  gene symbol: FRMPD3
  hgvsc: ENST00000439554.1:c.453+18C>T
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000276185
  ensembl transcript: ENST00000276185
  gene symbol: FRMPD3
  hgvsc: ENST00000276185.4:c.609+18C>T
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl transcript: ENST00000477796
  gene symbol: FRMPD3
  hgvsc: ENST00000477796.1:n.1367+18C>T
  variant of: http://identifiers.org/hgnc/29382
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 3.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
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  variant carriers: 52
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 24
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 60
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 17
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 2238
  bin: 9.75e1
  variant carriers: 109
num of homozygotes: 5
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: DP

X-106793410-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106793410
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106793410
    reference: chr 0
allele count: 1
allele frequency: 2.466030430815516e-5
allele num: 40551
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl transcript: ENST00000477796
  gene symbol: FRMPD3
  hgvsc: ENST00000477796.1:n.1367+24G>T
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000276185
  ensembl transcript: ENST00000276185
  gene symbol: FRMPD3
  hgvsc: ENST00000276185.4:c.609+24G>T
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000398668
  ensembl transcript: ENST00000439554
  gene symbol: FRMPD3
  hgvsc: ENST00000439554.1:c.453+24G>T
  variant of: http://identifiers.org/hgnc/29382
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1967
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2979
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13535
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2896
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14404
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18545
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 324
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3931
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 696
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14826
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2135
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 225
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 903
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21207
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1333
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2852
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 241
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 261
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2789
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2810
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

X-106793419-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106793419
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106793419
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 36543
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000276185
  ensembl transcript: ENST00000276185
  gene symbol: FRMPD3
  hgvsc: ENST00000276185.4:c.609+33G>A
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000398668
  ensembl transcript: ENST00000439554
  gene symbol: FRMPD3
  hgvsc: ENST00000439554.1:c.453+33G>A
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl transcript: ENST00000477796
  gene symbol: FRMPD3
  hgvsc: ENST00000477796.1:n.1367+33G>A
  variant of: http://identifiers.org/hgnc/29382
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 2013
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1513
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15911
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11906
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19122
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3608
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2848
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4221
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQ
site quality: InbreedingCoeff

X-106793423-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24106793423
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24106793423
    reference: chr 0
allele count: 1
allele frequency: 2.818727626349466e-5
allele num: 35477
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000276185
  ensembl transcript: ENST00000276185
  gene symbol: FRMPD3
  hgvsc: ENST00000276185.4:c.609+37T>G
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl transcript: ENST00000477796
  gene symbol: FRMPD3
  hgvsc: ENST00000477796.1:n.1367+37T>G
  variant of: http://identifiers.org/hgnc/29382
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147234
  ensembl protein: ENSP00000398668
  ensembl transcript: ENST00000439554
  gene symbol: FRMPD3
  hgvsc: ENST00000439554.1:c.453+37T>G
  variant of: http://identifiers.org/hgnc/29382
canonical: true
consequence: intron
filter: PASS
num of homozygotes: 0
reference allele: T

GenotypeQuality
all individuals: 1372
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.25017438851511e-5
allele num: 44441
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6769
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6478
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4525
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9184
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9232
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.015e0

VQSLOD
type: SiteQuality
SIO_000300: -3.431e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.95e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.31e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.32e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.98e-1

MQ
type: SiteQuality
SIO_000300: 5.979e1

QD
type: SiteQuality
SIO_000300: 3.503e1

DP
type: SiteQuality
SIO_000300: 4.27373e6

GenotypeQuality
all individuals: 1121
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.080964220084315e-4
allele num: 9251
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44444
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6478
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9185
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4525
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6759
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.953e1

FS
type: SiteQuality
SIO_000300: 1.429e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.35e0

MQRankSum
type: SiteQuality
SIO_000300: -2.72e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.19e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.885e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.6e-2

QD
type: SiteQuality
SIO_000300: 2.113e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.879999999999999e-1

DP
type: SiteQuality
SIO_000300: 4.274216e6

GenotypeQuality
all individuals: 1045
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9291
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6478
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6761
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4525
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44462
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.088731627653783e-4
allele num: 9185
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.24e0

FS
type: SiteQuality
SIO_000300: 9.99e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.0e-3

MQ
type: SiteQuality
SIO_000300: 5.936e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

VQSLOD
type: SiteQuality
SIO_000300: 9.8e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 6.2e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.688e0

QD
type: SiteQuality
SIO_000300: 1.615e1

DP
type: SiteQuality
SIO_000300: 4.275395e6

GenotypeQuality
all individuals: 1372
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4525
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9322
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6478
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.088494611951671e-4
allele num: 9187
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6763
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44468
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.986e1

DP
type: SiteQuality
SIO_000300: 4.276119e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.11e-2

QD
type: SiteQuality
SIO_000300: 3.366e1

VQSLOD
type: SiteQuality
SIO_000300: -1.836e-1

GenotypeQuality
all individuals: 44682
bin: 9.75e1
variant carriers: 6

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 581
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 4.439183190292986e-4
allele num: 6758
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.24870699347875e-5
allele num: 44470
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9188
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4525
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 9355
num of homozygotes: 0

East Asian
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allele count: 2
allele frequency: 3.087372645878358e-4
allele num: 6478
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 7.35e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.11e-2

MQ
type: SiteQuality
SIO_000300: 5.958e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.92e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.06e0

FS
type: SiteQuality
SIO_000300: 5.21e-1

DP
type: SiteQuality
SIO_000300: 4.277188e6

BaseQRankSum
type: SiteQuality
SIO_000300: -7.75e-1

QD
type: SiteQuality
SIO_000300: 1.378e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.47e-1

GenotypeQuality
all individuals: 71
bin: 5.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6478
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4525
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9360
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9187
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.478852410529429e-4
allele num: 6762
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 581
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44469
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.16e-2

QD
type: SiteQuality
SIO_000300: 2.154e1

MQ
type: SiteQuality
SIO_000300: 5.99e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.296e0

DP
type: SiteQuality
SIO_000300: 4.276744e6

MQRankSum
type: SiteQuality
SIO_000300: -1.14e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.742e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.33e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.4e0

GenotypeQuality
all individuals: 17
bin: 1.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6478
num of homozygotes: 0

African
type: Population
allele count: 32
allele frequency: 4.734428169847611e-3
allele num: 6759
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9186
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9310
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44466
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4525
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.6e-1

QD
type: SiteQuality
SIO_000300: 1.668e1

FS
type: SiteQuality
SIO_000300: 5.23e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.48e0

MQ
type: SiteQuality
SIO_000300: 5.979e1

VQSLOD
type: SiteQuality
SIO_000300: 1.98e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.169999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.799999999999999e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -5.48e-1

DP
type: SiteQuality
SIO_000300: 4.276676e6

GenotypeQuality
all individuals: 4784
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6755
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4525
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6478
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9302
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9189
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 1.349406261245052e-4
allele num: 44464
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 4.273831e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.97e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.81e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.5e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.6e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -9.31e-1

QD
type: SiteQuality
SIO_000300: 1.605e1

VQSLOD
type: SiteQuality
SIO_000300: 9.03e-1

MQ
type: SiteQuality
SIO_000300: 5.954e1

GenotypeQuality
all individuals: 1141
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6478
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4525
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6757
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9278
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 4.353978447806683e-4
allele num: 9187
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44460
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 581
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.46e-1

QD
type: SiteQuality
SIO_000300: 1.5e1

VQSLOD
type: SiteQuality
SIO_000300: 3.31e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.35e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.33e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.07e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.17e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.15e-1

MQ
type: SiteQuality
SIO_000300: 5.98e1

DP
type: SiteQuality
SIO_000300: 4.271805e6

GenotypeQuality
all individuals: 1370
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9246
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9189
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4525
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6478
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 581
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6753
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 6.749308195909919e-5
allele num: 44449
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 2.733e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.08e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.281e0

FS
type: SiteQuality
SIO_000300: 1.965e0

VQSLOD
type: SiteQuality
SIO_000300: -2.554e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.64e0

DP
type: SiteQuality
SIO_000300: 4.269739e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.41e-2

MQ
type: SiteQuality
SIO_000300: 5.698e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.329e0

GenotypeQuality
all individuals: 1370
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9180
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4525
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9003
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6749
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.252455176141995e-5
allele num: 44396
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6475
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 579
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.047e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.2e-2

DP
type: SiteQuality
SIO_000300: 4.25149e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

MQ
type: SiteQuality
SIO_000300: 5.982e1

VQSLOD
type: SiteQuality
SIO_000300: 9.5e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 7.64e0

MQRankSum
type: SiteQuality
SIO_000300: 6.909999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.718e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.16e-1

GenotypeQuality
all individuals: 933
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44332
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 576
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6739
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8786
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6473
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4525
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.090037061260083e-4
allele num: 9174
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.07e0

FS
type: SiteQuality
SIO_000300: 3.384e0

MQ
type: SiteQuality
SIO_000300: 5.975e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.15e0

VQSLOD
type: SiteQuality
SIO_000300: 3.81e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.045e0

MQRankSum
type: SiteQuality
SIO_000300: 1.02e0

DP
type: SiteQuality
SIO_000300: 4.242039e6

QD
type: SiteQuality
SIO_000300: 1.176e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

GenotypeQuality
all individuals: 5053
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2427
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 180
bin: 8.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 480
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6205
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 7.876289742445325e-5
allele num: 38089
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8216
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3933
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5652
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.56e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 1.04e0

VQSLOD
type: SiteQuality
SIO_000300: -4.59e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.66e-1

FS
type: SiteQuality
SIO_000300: 1.231e0

DP
type: SiteQuality
SIO_000300: 1.034315e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.65e-1

QD
type: SiteQuality
SIO_000300: 1.821e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 732
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 459
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2925
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 2
allele frequency: 3.391555027980329e-4
allele num: 5897
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8480
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 510
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6354
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4039
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7195
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 39772
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.53e0

MQRankSum
type: SiteQuality
SIO_000300: -5.669999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.21e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.39e0

DP
type: SiteQuality
SIO_000300: 1.180182e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -3.52e-1

FS
type: SiteQuality
SIO_000300: 1.191e0

QD
type: SiteQuality
SIO_000300: 1.261e1

GenotypeQuality
all individuals: 181
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 236
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 380
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 39902
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6360
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4050
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8495
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 509
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5913
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 2.76625172890733e-4
allele num: 7230
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.96e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.49e0

FS
type: SiteQuality
SIO_000300: 1.859e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.12e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.96e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.029e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.93e-1

QD
type: SiteQuality
SIO_000300: 2.994e1

DP
type: SiteQuality
SIO_000300: 1.189367e6

GenotypeQuality
all individuals: 236
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1966
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 178
bin: 8.75e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4131
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6440
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7585
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 519
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 4.966065220989903e-4
allele num: 6041
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 40934
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 9.02e-1

FS
type: SiteQuality
SIO_000300: 6.616e0

DP
type: SiteQuality
SIO_000300: 1.247598e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.14e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.669999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.294e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.62e-1

MQ
type: SiteQuality
SIO_000300: 6.057e1

VQSLOD
type: SiteQuality
SIO_000300: 1.54e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.4e-3

GenotypeQuality
all individuals: 206
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 784
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 240
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.294999196750281e-5
allele num: 43573
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6348
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9020
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 562
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4399
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8937
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6656
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -4.095e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.9e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.368165e6

QD
type: SiteQuality
SIO_000300: 2.935e1

GenotypeQuality
all individuals: 319
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1965
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6657
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4400
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6347
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8951
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.294051524397238e-5
allele num: 43591
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 563
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9026
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.206e0

QD
type: SiteQuality
SIO_000300: 2.78e0

MQRankSum
type: SiteQuality
SIO_000300: -4.48e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.194e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.62e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

MQ
type: SiteQuality
SIO_000300: 5.805e1

DP
type: SiteQuality
SIO_000300: 1.370346e6

BaseQRankSum
type: SiteQuality
SIO_000300: -7.19e-1

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 893
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2780
bin: 2.25e1
variant carriers: 2

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 43730
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9046
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9034
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 564
num of homozygotes: 0

East Asian
type: Population
allele count: 31
allele frequency: 4.868855033767865e-3
allele num: 6367
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6674
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4416
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.379082e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.734e0

VQSLOD
type: SiteQuality
SIO_000300: 3.21e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.480000000000001e-2

MQRankSum
type: SiteQuality
SIO_000300: -2.69e-1

QD
type: SiteQuality
SIO_000300: 1.389e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.75e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.59e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.992e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 417
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 211
bin: 3.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4415
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6675
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6370
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 564
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9044
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 43745
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.105338786338013e-4
allele num: 9047
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.16e0

FS
type: SiteQuality
SIO_000300: 2.318e0

MQRankSum
type: SiteQuality
SIO_000300: -2.51e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.54e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.357e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.1e-3

DP
type: SiteQuality
SIO_000300: 1.379746e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -2.694e0

QD
type: SiteQuality
SIO_000300: 2.76e1

GenotypeQuality
all individuals: 380
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 774
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 237
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9072
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 565
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4416
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6678
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 43762
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9046
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 3.138731952291275e-4
allele num: 6372
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.85e-1

DP
type: SiteQuality
SIO_000300: 1.381782e6

FS
type: SiteQuality
SIO_000300: 8.010999999999999e0

QD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -1.008e0

VQSLOD
type: SiteQuality
SIO_000300: -1.922e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.500000000000001e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -5.97e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.05e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9105
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9055
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6685
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.281438218653039e-5
allele num: 43832
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4422
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 564
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6373
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.48e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -7.6e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.27e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.843e0

DP
type: SiteQuality
SIO_000300: 1.385431e6

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 173
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6371
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6682
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4418
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.282583884957772e-5
allele num: 43810
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9048
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 568
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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ReadPosRankSum
type: SiteQuality
SIO_000300: -5.44e-1

VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 6.6e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 5.44e-1

DP
type: SiteQuality
SIO_000300: 1.385281e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.129e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 88
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.301125250247371e-5
allele num: 43457
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6654
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 559
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4377
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6354
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8993
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9011
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.592e0

MQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.370167e6

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.126e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.7e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.43e0

MQ
type: SiteQuality
SIO_000300: 5.933e1

QD
type: SiteQuality
SIO_000300: 1.296e1

GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 356
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 557
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4339
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 8947
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.321478317392515e-5
allele num: 43076
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 8904
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6326
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

QD
type: SiteQuality
SIO_000300: 1.129e1

DP
type: SiteQuality
SIO_000300: 1.353359e6

MQ
type: SiteQuality
SIO_000300: 5.965e1

BaseQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 1.4e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.0e-3

FS
type: SiteQuality
SIO_000300: 1.55e0

MQRankSum
type: SiteQuality
SIO_000300: 3.2e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 5.2e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8869
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4323
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.583280557314756e-4
allele num: 6316
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 8934
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 42948
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 556
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 2.912e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.973e1

BaseQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.347722e6

VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 3.47e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1025
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4168
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 540
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6500
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8759
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.391143205566581e-5
allele num: 41821
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
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FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.13e-1

BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.288672e6

QD
type: SiteQuality
SIO_000300: 1.114e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 476
bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 1.147052076164258e-4
allele num: 8718
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6147
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 41618
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4151
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 6478
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 537
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South Asian
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num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.512e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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InbreedingCoeff
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ClippingRankSum
type: SiteQuality
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QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 534
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6466
num of homozygotes: 0

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

South Asian
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allele count: 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: 2.410684152162384e-5
allele num: 41482
num of homozygotes: 0

Latino
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East Asian
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BaseQRankSum
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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InbreedingCoeff
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ClippingRankSum
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ReadPosRankSum
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VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.934e1

DP
type: SiteQuality
SIO_000300: 1.274528e6

GenotypeQuality
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bin: 4.25e1
variant carriers: 1

Other
type: Population
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allele frequency: 1.883239171374765e-3
allele num: 531
num of homozygotes: 0

African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 2.425830240399777e-5
allele num: 41223
num of homozygotes: 0

Latino
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allele frequency: 1.155134573177775e-4
allele num: 8657
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
allele num: 4113
num of homozygotes: 0

East Asian
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allele count: 5
allele frequency: 8.190008190008191e-4
allele num: 6105
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South Asian
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allele frequency: 1.067362428842505e-3
allele num: 8432
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 39732
num of homozygotes: 0

Other
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allele num: 503
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South Asian
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African
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Latino
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East Asian
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allele frequency: 1.692906720839682e-4
allele num: 5907
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European (Finnish)
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allele frequency: 0.0e0
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VQSLOD
type: SiteQuality
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ReadPosRankSum
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InbreedingCoeff
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ClippingRankSum
type: SiteQuality
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FS
type: SiteQuality
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MQ
type: SiteQuality
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QD
type: SiteQuality
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BaseQRankSum
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MQRankSum
type: SiteQuality
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DP
type: SiteQuality
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GenotypeQuality
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bin: 3.75e1
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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Latino
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South Asian
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European (Non-Finnish)
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allele frequency: 2.531004808909137e-5
allele num: 39510
num of homozygotes: 0

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

South Asian
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East Asian
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 2.599428125812321e-5
allele num: 38470
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
allele num: 493
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Latino
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ReadPosRankSum
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MQRankSum
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QD
type: SiteQuality
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DP
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MQ
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InbreedingCoeff
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ClippingRankSum
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VQSLOD
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BaseQRankSum
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FS
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GenotypeQuality
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variant carriers: 0

South Asian
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 2.627637491131724e-5
allele num: 38057
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

FS
type: SiteQuality
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MQ
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ReadPosRankSum
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InbreedingCoeff
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BaseQRankSum
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VQSLOD
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DP
type: SiteQuality
SIO_000300: 1.082182e6

MQRankSum
type: SiteQuality
SIO_000300: 1.22e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.08e-1

QD
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

European (Finnish)
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allele frequency: 0.0e0
allele num: 3810
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 37871
num of homozygotes: 0

East Asian
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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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Latino
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allele frequency: 1.246105919003115e-4
allele num: 8025
num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
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QD
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MQRankSum
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VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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DP
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InbreedingCoeff
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MQ
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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FS
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SIO_000300: 0.0e0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

South Asian
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allele frequency: 0.0e0
allele num: 7160
num of homozygotes: 0

African
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allele frequency: 0.0e0
allele num: 5865
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 5352
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 2.788700186842913e-5
allele num: 35859
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 7588
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3650
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 450
num of homozygotes: 0

InbreedingCoeff
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VQSLOD
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FS
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MQRankSum
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BaseQRankSum
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QD
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ClippingRankSum
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ReadPosRankSum
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MQ
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DP
type: SiteQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 412
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
allele num: 7042
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 33034
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3459
num of homozygotes: 0

MQRankSum
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 5.659999999999999e-1

DP
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ReadPosRankSum
type: SiteQuality
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FS
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MQ
type: SiteQuality
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QD
type: SiteQuality
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GenotypeQuality
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bin: 2.75e1
variant carriers: 1

Latino
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allele frequency: 0.0e0
allele num: 6981
num of homozygotes: 0

South Asian
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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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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3441
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African
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allele count: 0
allele frequency: 0.0e0
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 408
num of homozygotes: 0

European (Non-Finnish)
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allele count: 4
allele frequency: 1.21747070461117e-4
allele num: 32855
num of homozygotes: 0

InbreedingCoeff
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FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
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ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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QD
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VQSLOD
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BaseQRankSum
type: SiteQuality
SIO_000300: 6.37e-1

DP
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 5.73e-1

GenotypeQuality
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bin: 3.25e1
variant carriers: 6

Latino
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allele frequency: 0.0e0
allele num: 6817
num of homozygotes: 0

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

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 402
num of homozygotes: 0

African
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allele frequency: 1.836547291092746e-4
allele num: 5445
num of homozygotes: 0

South Asian
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allele count: 43
allele frequency: 6.742982593696096e-3
allele num: 6377
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3374
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 32078
num of homozygotes: 0

VQSLOD
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MQ
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 4.8e-2

DP
type: SiteQuality
SIO_000300: 8.44092e5

BaseQRankSum
type: SiteQuality
SIO_000300: 5.73e-1

MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-2

FS
type: SiteQuality
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QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 2.38e-1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

Latino
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allele count: 1
allele frequency: 1.471020888496617e-4
allele num: 6798
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 401
num of homozygotes: 0

African
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allele count: 8
allele frequency: 1.465738365701722e-3
allele num: 5458
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 4822
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3368
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6352
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 32093
num of homozygotes: 0

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

ReadPosRankSum
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ClippingRankSum
type: SiteQuality
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InbreedingCoeff
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VQSLOD
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MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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FS
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

Other
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allele frequency: 0.0e0
allele num: 396
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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African
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East Asian
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allele frequency: 2.085505735140772e-4
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European (Non-Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

VQSLOD
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QD
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FS
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DP
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ReadPosRankSum
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MQ
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InbreedingCoeff
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MQRankSum
type: SiteQuality
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BaseQRankSum
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ClippingRankSum
type: SiteQuality
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 4.761904761904762e-4
allele num: 2100
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Latino
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allele frequency: 0.0e0
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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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allele frequency: 0.0e0
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African
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South Asian
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InbreedingCoeff
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QD
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BaseQRankSum
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ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
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VQSLOD
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DP
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MQRankSum
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MQ
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ClippingRankSum
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GenotypeQuality
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variant carriers: 0

South Asian
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allele frequency: 2.029632636492795e-4
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num of homozygotes: 0

European (Non-Finnish)
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Latino
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African
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Other
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European (Finnish)
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allele frequency: 0.0e0
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East Asian
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FS
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InbreedingCoeff
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MQ
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DP
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QD
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VQSLOD
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

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

European (Non-Finnish)
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European (Finnish)
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African
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Other
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East Asian
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Latino
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allele frequency: 1.234567901234568e-3
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South Asian
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InbreedingCoeff
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ClippingRankSum
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DP
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BaseQRankSum
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MQRankSum
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MQ
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ReadPosRankSum
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FS
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VQSLOD
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QD
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GenotypeQuality
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African
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South Asian
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East Asian
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European (Non-Finnish)
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European (Finnish)
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Other
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Latino
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FS
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DP
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QD
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VQSLOD
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InbreedingCoeff
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MQ
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GenotypeQuality
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African
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European (Non-Finnish)
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Other
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East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 2802
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2358
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 5289
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 9.01e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.72e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.9e-2

DP
type: SiteQuality
SIO_000300: 7.16974e5

FS
type: SiteQuality
SIO_000300: 2.993e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.5e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.83e-1

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.824e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.98e-1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

Other
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allele frequency: 0.0e0
allele num: 285
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 18700
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 3077
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2419
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 3666
num of homozygotes: 0

South Asian
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allele frequency: 1.845699520118125e-4
allele num: 5418
num of homozygotes: 0

FS
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -3.8e-1

MQRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 7.42e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.3e-1

ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.985e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.54e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 7.4811e5

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 313
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 20508
num of homozygotes: 0

Latino
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allele count: 3
allele frequency: 8.105917319643339e-4
allele num: 3701
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 3981
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 3090
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2527
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.38e-2

MQ
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 7.02e-1

QD
type: SiteQuality
SIO_000300: 1.418e1

BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 7.98641e5

MQRankSum
type: SiteQuality
SIO_000300: 2.15e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.032e0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2548
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 311
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 3173
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 4045
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 5700
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 3858
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 4.780571756382063e-5
allele num: 20918
num of homozygotes: 0

DP
type: SiteQuality
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QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.988e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2672
num of homozygotes: 0

African
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allele frequency: 2.297266253158741e-4
allele num: 4353
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 3479
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 22625
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 4487
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
allele num: 333
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.59e0

QD
type: SiteQuality
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DP
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.12e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 6.94e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.41e-1

FS
type: SiteQuality
SIO_000300: 2.2e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.23e0

VQSLOD
type: SiteQuality
SIO_000300: 5.01e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2688
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 22833
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 4391
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 4553
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 335
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South Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.900000000000001e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -7.42e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.42e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.42e-1

ReadPosRankSum
type: SiteQuality
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VQSLOD
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FS
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 8.56272e5

QD
type: SiteQuality
SIO_000300: 2.378e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

East Asian
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allele frequency: 0.0e0
allele num: 3537
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 5959
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2699
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 335
num of homozygotes: 0

European (Non-Finnish)
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allele count: 10
allele frequency: 4.333506673600277e-4
allele num: 23076
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 4641
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 4423
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.21e0

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

MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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FS
type: SiteQuality
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DP
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -3.11e-1

VQSLOD
type: SiteQuality
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InbreedingCoeff
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 3573
num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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South Asian
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allele count: 1
allele frequency: 1.674480910917615e-4
allele num: 5972
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 23263
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 336
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2714
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
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DP
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.169e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.46e-1

QD
type: SiteQuality
SIO_000300: 1.361e1

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2936
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 5010
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South Asian
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 3.718301479883989e-5
allele num: 26894
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 5801
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 380
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.257e0

DP
type: SiteQuality
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MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -3.81e-1

VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -7.3e-3

MQ
type: SiteQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

African
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allele frequency: 0.0e0
allele num: 5067
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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Latino
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allele count: 1
allele frequency: 1.672240802675585e-4
allele num: 5980
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQ
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VQSLOD
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BaseQRankSum
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FS
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ClippingRankSum
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QD
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InbreedingCoeff
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DP
type: SiteQuality
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2996
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 394
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European (Non-Finnish)
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allele frequency: 3.592083048960092e-5
allele num: 27839
num of homozygotes: 0

East Asian
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Latino
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allele frequency: 0.0e0
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African
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South Asian
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DP
type: SiteQuality
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BaseQRankSum
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ClippingRankSum
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MQRankSum
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QD
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VQSLOD
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InbreedingCoeff
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FS
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MQ
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ReadPosRankSum
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GenotypeQuality
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variant carriers: 0

Other
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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: 3.272465475489233e-5
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num of homozygotes: 0

Latino
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South Asian
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African
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East Asian
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European (Finnish)
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VQSLOD
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InbreedingCoeff
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DP
type: SiteQuality
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QD
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MQ
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FS
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

East Asian
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num of homozygotes: 0

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

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

European (Non-Finnish)
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num of homozygotes: 0

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

BaseQRankSum
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MQ
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VQSLOD
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FS
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ReadPosRankSum
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DP
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MQRankSum
type: SiteQuality
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InbreedingCoeff
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ClippingRankSum
type: SiteQuality
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QD
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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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: 1.459427904261529e-4
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 32041
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

MQRankSum
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FS
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BaseQRankSum
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InbreedingCoeff
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DP
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ClippingRankSum
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MQ
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QD
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ReadPosRankSum
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VQSLOD
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

South Asian
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 3.124316555753429e-5
allele num: 32007
num of homozygotes: 0

African
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num of homozygotes: 0

Other
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QD
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ClippingRankSum
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VQSLOD
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ReadPosRankSum
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MQRankSum
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FS
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MQ
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InbreedingCoeff
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BaseQRankSum
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DP
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

Latino
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allele frequency: 0.0e0
allele num: 7120
num of homozygotes: 0

European (Non-Finnish)
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allele num: 32007
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European (Finnish)
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allele frequency: 0.0e0
allele num: 3266
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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East Asian
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MQRankSum
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
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MQ
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BaseQRankSum
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QD
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DP
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FS
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VQSLOD
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ClippingRankSum
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

East Asian
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allele frequency: 0.0e0
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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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allele frequency: 0.0e0
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African
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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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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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ReadPosRankSum
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InbreedingCoeff
type: SiteQuality
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VQSLOD
type: SiteQuality
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DP
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QD
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ClippingRankSum
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FS
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MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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

Other
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allele frequency: 0.0e0
allele num: 430
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South Asian
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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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African
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allele frequency: 0.0e0
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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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allele num: 3176
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MQ
type: SiteQuality
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DP
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InbreedingCoeff
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QD
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FS
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VQSLOD
type: SiteQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

Latino
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South Asian
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allele frequency: 1.491869312248247e-4
allele num: 6703
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Other
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
allele num: 3164
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East Asian
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allele frequency: 0.0e0
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FS
type: SiteQuality
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MQ
type: SiteQuality
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MQRankSum
type: SiteQuality
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ClippingRankSum
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InbreedingCoeff
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VQSLOD
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DP
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BaseQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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QD
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GenotypeQuality
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variant carriers: 0

East Asian
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allele frequency: 0.0e0
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South Asian
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allele num: 6650
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Latino
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 3.33555703802535e-5
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European (Finnish)
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Other
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allele frequency: 0.0e0
allele num: 415
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FS
type: SiteQuality
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QD
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BaseQRankSum
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MQ
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ReadPosRankSum
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ClippingRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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VQSLOD
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InbreedingCoeff
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DP
type: SiteQuality
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

African
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allele frequency: 0.0e0
allele num: 5630
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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East Asian
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Other
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Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 29741
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South Asian
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DP
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VQSLOD
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ClippingRankSum
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QD
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MQRankSum
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InbreedingCoeff
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FS
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ReadPosRankSum
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MQ
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BaseQRankSum
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

South Asian
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num of homozygotes: 0

African
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East Asian
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Latino
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Other
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allele frequency: 0.0e0
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European (Finnish)
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European (Non-Finnish)
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DP
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MQ
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InbreedingCoeff
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VQSLOD
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QD
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FS
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GenotypeQuality
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bin: 8.25e1
variant carriers: 62

East Asian
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allele frequency: 4.172031934071594e-2
allele num: 3883
num of homozygotes: 1

South Asian
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allele frequency: 5.403624382207578e-2
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African
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allele frequency: 5.190713101160862e-1
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Latino
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allele frequency: 1.585976627712855e-1
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Other
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allele frequency: 3.794037940379404e-2
allele num: 369
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European (Non-Finnish)
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allele frequency: 6.150506512301013e-3
allele num: 24876
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European (Finnish)
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VQSLOD
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BaseQRankSum
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ReadPosRankSum
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MQRankSum
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QD
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MQ
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ClippingRankSum
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FS
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DP
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InbreedingCoeff
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GenotypeQuality
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variant carriers: 0

African
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Other
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East Asian
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South Asian
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European (Non-Finnish)
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Latino
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European (Finnish)
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BaseQRankSum
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DP
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ClippingRankSum
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VQSLOD
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InbreedingCoeff
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FS
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MQ
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MQRankSum
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ReadPosRankSum
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QD
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GenotypeQuality
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variant carriers: 13

African
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Other
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European (Non-Finnish)
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European (Finnish)
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South Asian
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Latino
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East Asian
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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QD
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MQRankSum
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BaseQRankSum
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MQ
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FS
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ClippingRankSum
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DP
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GenotypeQuality
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African
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Latino
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European (Finnish)
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European (Non-Finnish)
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South Asian
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East Asian
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Other
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MQRankSum
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QD
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VQSLOD
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BaseQRankSum
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InbreedingCoeff
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FS
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MQ
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DP
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ReadPosRankSum
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ClippingRankSum
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GenotypeQuality
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South Asian
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East Asian
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African
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European (Finnish)
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Other
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3344
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 18731
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 6.44709e5

VQSLOD
type: SiteQuality
SIO_000300: -5.204e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 2.324e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.41e-2