X-19032173-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24019032173
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24019032173
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 68305
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000346845
  ensembl transcript: ENST00000354791
  gene symbol: GPR64
  hgvsc: ENST00000354791.3:c.682G>T
  hgvsp: ENSP00000346845.3:p.Val228Phe
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350152
  ensembl transcript: ENST00000357544
  gene symbol: GPR64
  hgvsc: ENST00000357544.3:c.640G>T
  hgvsp: ENSP00000350152.3:p.Val214Phe
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000353421
  ensembl transcript: ENST00000360279
  gene symbol: GPR64
  hgvsc: ENST00000360279.4:c.664G>T
  hgvsp: ENSP00000353421.4:p.Val222Phe
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350680
  ensembl transcript: ENST00000357991
  gene symbol: GPR64
  hgvsc: ENST00000357991.3:c.721G>T
  hgvsp: ENSP00000350680.3:p.Val241Phe
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369207
  ensembl transcript: ENST00000379878
  gene symbol: GPR64
  hgvsc: ENST00000379878.3:c.682G>T
  hgvsp: ENSP00000369207.3:p.Val228Phe
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369205
  ensembl transcript: ENST00000379876
  gene symbol: GPR64
  hgvsc: ENST00000379876.1:c.658G>T
  hgvsp: ENSP00000369205.1:p.Val220Phe
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000344972
  ensembl transcript: ENST00000340581
  gene symbol: GPR64
  hgvsc: ENST00000340581.3:c.640G>T
  hgvsp: ENSP00000344972.3:p.Val214Phe
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369198
  ensembl transcript: ENST00000379869
  gene symbol: GPR64
  hgvsc: ENST00000379869.3:c.730G>T
  hgvsp: ENSP00000369198.3:p.Val244Phe
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369202
  ensembl transcript: ENST00000379873
  gene symbol: GPR64
  hgvsc: ENST00000379873.2:c.730G>T
  hgvsp: ENSP00000369202.2:p.Val244Phe
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000349015
  ensembl transcript: ENST00000356606
  gene symbol: GPR64
  hgvsc: ENST00000356606.4:c.688G>T
  hgvsp: ENSP00000349015.4:p.Val230Phe
  variant of: http://identifiers.org/hgnc/4516
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 3904
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8648
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1747
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14541
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2412
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14747
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13425
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 566
  bin: 9.75e1
  variant carriers: 0
hgvs: p.Val244Phe
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: FS

X-19032174-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24019032174
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24019032174
    reference: chr 0
allele count: 1
allele frequency: 1.460365675565161e-5
allele num: 68476
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000346845
  ensembl transcript: ENST00000354791
  gene symbol: GPR64
  hgvsc: ENST00000354791.3:c.681T>G
  hgvsp: ENSP00000346845.3:p.Ile227Met
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000353421
  ensembl transcript: ENST00000360279
  gene symbol: GPR64
  hgvsc: ENST00000360279.4:c.663T>G
  hgvsp: ENSP00000353421.4:p.Ile221Met
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369202
  ensembl transcript: ENST00000379873
  gene symbol: GPR64
  hgvsc: ENST00000379873.2:c.729T>G
  hgvsp: ENSP00000369202.2:p.Ile243Met
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350680
  ensembl transcript: ENST00000357991
  gene symbol: GPR64
  hgvsc: ENST00000357991.3:c.720T>G
  hgvsp: ENSP00000350680.3:p.Ile240Met
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369198
  ensembl transcript: ENST00000379869
  gene symbol: GPR64
  hgvsc: ENST00000379869.3:c.729T>G
  hgvsp: ENSP00000369198.3:p.Ile243Met
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369205
  ensembl transcript: ENST00000379876
  gene symbol: GPR64
  hgvsc: ENST00000379876.1:c.657T>G
  hgvsp: ENSP00000369205.1:p.Ile219Met
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350152
  ensembl transcript: ENST00000357544
  gene symbol: GPR64
  hgvsc: ENST00000357544.3:c.639T>G
  hgvsp: ENSP00000350152.3:p.Ile213Met
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000349015
  ensembl transcript: ENST00000356606
  gene symbol: GPR64
  hgvsc: ENST00000356606.4:c.687T>G
  hgvsp: ENSP00000349015.4:p.Ile229Met
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000344972
  ensembl transcript: ENST00000340581
  gene symbol: GPR64
  hgvsc: ENST00000340581.3:c.639T>G
  hgvsp: ENSP00000344972.3:p.Ile213Met
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369207
  ensembl transcript: ENST00000379878
  gene symbol: GPR64
  hgvsc: ENST00000379878.3:c.681T>G
  hgvsp: ENSP00000369207.3:p.Ile227Met
  variant of: http://identifiers.org/hgnc/4516
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13430
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1758
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14855
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8707
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14529
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2298
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3864
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2034
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ile243Met
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: FS
site quality: QD

X-19032182-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24019032182
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24019032182
    reference: chr 0
allele count: 2
allele frequency: 3.161105754793027e-5
allele num: 63269
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369202
  ensembl transcript: ENST00000379873
  gene symbol: GPR64
  hgvsc: ENST00000379873.2:c.721G>A
  hgvsp: ENSP00000369202.2:p.Asp241Asn
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000346845
  ensembl transcript: ENST00000354791
  gene symbol: GPR64
  hgvsc: ENST00000354791.3:c.673G>A
  hgvsp: ENSP00000346845.3:p.Asp225Asn
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369207
  ensembl transcript: ENST00000379878
  gene symbol: GPR64
  hgvsc: ENST00000379878.3:c.673G>A
  hgvsp: ENSP00000369207.3:p.Asp225Asn
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350152
  ensembl transcript: ENST00000357544
  gene symbol: GPR64
  hgvsc: ENST00000357544.3:c.631G>A
  hgvsp: ENSP00000350152.3:p.Asp211Asn
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350680
  ensembl transcript: ENST00000357991
  gene symbol: GPR64
  hgvsc: ENST00000357991.3:c.712G>A
  hgvsp: ENSP00000350680.3:p.Asp238Asn
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000344972
  ensembl transcript: ENST00000340581
  gene symbol: GPR64
  hgvsc: ENST00000340581.3:c.631G>A
  hgvsp: ENSP00000344972.3:p.Asp211Asn
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369205
  ensembl transcript: ENST00000379876
  gene symbol: GPR64
  hgvsc: ENST00000379876.1:c.649G>A
  hgvsp: ENSP00000369205.1:p.Asp217Asn
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000349015
  ensembl transcript: ENST00000356606
  gene symbol: GPR64
  hgvsc: ENST00000356606.4:c.679G>A
  hgvsp: ENSP00000349015.4:p.Asp227Asn
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369198
  ensembl transcript: ENST00000379869
  gene symbol: GPR64
  hgvsc: ENST00000379869.3:c.721G>A
  hgvsp: ENSP00000369198.3:p.Asp241Asn
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000353421
  ensembl transcript: ENST00000360279
  gene symbol: GPR64
  hgvsc: ENST00000360279.4:c.655G>A
  hgvsp: ENSP00000353421.4:p.Asp219Asn
  variant of: http://identifiers.org/hgnc/4516
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 15365
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11641
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2347
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17099
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3158
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3165
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6748
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 270
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Asp241Asn
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: C
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD

X-19032186-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24019032186
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24019032186
    reference: chr 0
allele count: 1
allele frequency: 1.654861984510492e-5
allele num: 60428
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000346845
  ensembl transcript: ENST00000354791
  gene symbol: GPR64
  hgvsc: ENST00000354791.3:c.669G>T
  hgvsp: ENST00000354791.3:c.669G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350680
  ensembl transcript: ENST00000357991
  gene symbol: GPR64
  hgvsc: ENST00000357991.3:c.708G>T
  hgvsp: ENST00000357991.3:c.708G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000344972
  ensembl transcript: ENST00000340581
  gene symbol: GPR64
  hgvsc: ENST00000340581.3:c.627G>T
  hgvsp: ENST00000340581.3:c.627G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369205
  ensembl transcript: ENST00000379876
  gene symbol: GPR64
  hgvsc: ENST00000379876.1:c.645G>T
  hgvsp: ENST00000379876.1:c.645G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350152
  ensembl transcript: ENST00000357544
  gene symbol: GPR64
  hgvsc: ENST00000357544.3:c.627G>T
  hgvsp: ENST00000357544.3:c.627G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369202
  ensembl transcript: ENST00000379873
  gene symbol: GPR64
  hgvsc: ENST00000379873.2:c.717G>T
  hgvsp: ENST00000379873.2:c.717G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369207
  ensembl transcript: ENST00000379878
  gene symbol: GPR64
  hgvsc: ENST00000379878.3:c.669G>T
  hgvsp: ENST00000379878.3:c.669G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000353421
  ensembl transcript: ENST00000360279
  gene symbol: GPR64
  hgvsc: ENST00000360279.4:c.651G>T
  hgvsp: ENST00000360279.4:c.651G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369198
  ensembl transcript: ENST00000379869
  gene symbol: GPR64
  hgvsc: ENST00000379869.3:c.717G>T
  hgvsp: ENST00000379869.3:c.717G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000349015
  ensembl transcript: ENST00000356606
  gene symbol: GPR64
  hgvsc: ENST00000356606.4:c.675G>T
  hgvsp: ENST00000356606.4:c.675G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4516
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18234
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4059
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2631
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6085
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10339
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2155
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16098
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 414
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Leu239Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: African
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: QD

X-19032199-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24019032199
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24019032199
    reference: chr 0
allele count: 1
allele frequency: 1.941672168071143e-5
allele num: 51502
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350152
  ensembl transcript: ENST00000357544
  gene symbol: GPR64
  hgvsc: ENST00000357544.3:c.621-7C>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369198
  ensembl transcript: ENST00000379869
  gene symbol: GPR64
  hgvsc: ENST00000379869.3:c.711-7C>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000353421
  ensembl transcript: ENST00000360279
  gene symbol: GPR64
  hgvsc: ENST00000360279.4:c.645-7C>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000344972
  ensembl transcript: ENST00000340581
  gene symbol: GPR64
  hgvsc: ENST00000340581.3:c.621-7C>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350680
  ensembl transcript: ENST00000357991
  gene symbol: GPR64
  hgvsc: ENST00000357991.3:c.702-7C>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000349015
  ensembl transcript: ENST00000356606
  gene symbol: GPR64
  hgvsc: ENST00000356606.4:c.669-7C>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369205
  ensembl transcript: ENST00000379876
  gene symbol: GPR64
  hgvsc: ENST00000379876.1:c.639-7C>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000346845
  ensembl transcript: ENST00000354791
  gene symbol: GPR64
  hgvsc: ENST00000354791.3:c.663-7C>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369202
  ensembl transcript: ENST00000379873
  gene symbol: GPR64
  hgvsc: ENST00000379873.2:c.711-7C>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369207
  ensembl transcript: ENST00000379878
  gene symbol: GPR64
  hgvsc: ENST00000379878.3:c.663-7C>T
  variant of: http://identifiers.org/hgnc/4516
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17681
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8383
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2017
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1332
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20350
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4076
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5701
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 8.25e1
  variant carriers: 0
hgvs: c.711-7C>T
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQ

X-19032206-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24019032206
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24019032206
    reference: chr 0
allele count: 1
allele frequency: 2.031611880866279e-5
allele num: 49222
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000349015
  ensembl transcript: ENST00000356606
  gene symbol: GPR64
  hgvsc: ENST00000356606.4:c.669-14A>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369207
  ensembl transcript: ENST00000379878
  gene symbol: GPR64
  hgvsc: ENST00000379878.3:c.663-14A>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350152
  ensembl transcript: ENST00000357544
  gene symbol: GPR64
  hgvsc: ENST00000357544.3:c.621-14A>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000346845
  ensembl transcript: ENST00000354791
  gene symbol: GPR64
  hgvsc: ENST00000354791.3:c.663-14A>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369202
  ensembl transcript: ENST00000379873
  gene symbol: GPR64
  hgvsc: ENST00000379873.2:c.711-14A>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000353421
  ensembl transcript: ENST00000360279
  gene symbol: GPR64
  hgvsc: ENST00000360279.4:c.645-14A>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369198
  ensembl transcript: ENST00000379869
  gene symbol: GPR64
  hgvsc: ENST00000379869.3:c.711-14A>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369205
  ensembl transcript: ENST00000379876
  gene symbol: GPR64
  hgvsc: ENST00000379876.1:c.639-14A>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350680
  ensembl transcript: ENST00000357991
  gene symbol: GPR64
  hgvsc: ENST00000357991.3:c.702-14A>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000344972
  ensembl transcript: ENST00000340581
  gene symbol: GPR64
  hgvsc: ENST00000340581.3:c.621-14A>G
  variant of: http://identifiers.org/hgnc/4516
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17778
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1965
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10070
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4565
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1076
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20535
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3467
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30274
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1312
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 926
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
reference allele: T
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: QD

X-19032217-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24019032217
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24019032217
    reference: chr 0
allele count: 14
allele frequency: 3.232285918777272e-4
allele num: 43313
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369207
  ensembl transcript: ENST00000379878
  gene symbol: GPR64
  hgvsc: ENST00000379878.3:c.663-25G>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369198
  ensembl transcript: ENST00000379869
  gene symbol: GPR64
  hgvsc: ENST00000379869.3:c.711-25G>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350152
  ensembl transcript: ENST00000357544
  gene symbol: GPR64
  hgvsc: ENST00000357544.3:c.621-25G>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350680
  ensembl transcript: ENST00000357991
  gene symbol: GPR64
  hgvsc: ENST00000357991.3:c.702-25G>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000346845
  ensembl transcript: ENST00000354791
  gene symbol: GPR64
  hgvsc: ENST00000354791.3:c.663-25G>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000349015
  ensembl transcript: ENST00000356606
  gene symbol: GPR64
  hgvsc: ENST00000356606.4:c.669-25G>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369202
  ensembl transcript: ENST00000379873
  gene symbol: GPR64
  hgvsc: ENST00000379873.2:c.711-25G>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369205
  ensembl transcript: ENST00000379876
  gene symbol: GPR64
  hgvsc: ENST00000379876.1:c.639-25G>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000353421
  ensembl transcript: ENST00000360279
  gene symbol: GPR64
  hgvsc: ENST00000360279.4:c.645-25G>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000344972
  ensembl transcript: ENST00000340581
  gene symbol: GPR64
  hgvsc: ENST00000340581.3:c.621-25G>A
  variant of: http://identifiers.org/hgnc/4516
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17230
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2618
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 14505
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19779
  bin: 7.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1782
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2376
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 276
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1259
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

X-19032228-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24019032228
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24019032228
    reference: chr 0
allele count: 34
allele frequency: 9.167138504677937e-4
allele num: 37089
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369207
  ensembl transcript: ENST00000379878
  gene symbol: GPR64
  hgvsc: ENST00000379878.3:c.663-36G>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350152
  ensembl transcript: ENST00000357544
  gene symbol: GPR64
  hgvsc: ENST00000357544.3:c.621-36G>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369202
  ensembl transcript: ENST00000379873
  gene symbol: GPR64
  hgvsc: ENST00000379873.2:c.711-36G>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369205
  ensembl transcript: ENST00000379876
  gene symbol: GPR64
  hgvsc: ENST00000379876.1:c.639-36G>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000346845
  ensembl transcript: ENST00000354791
  gene symbol: GPR64
  hgvsc: ENST00000354791.3:c.663-36G>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000353421
  ensembl transcript: ENST00000360279
  gene symbol: GPR64
  hgvsc: ENST00000360279.4:c.645-36G>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350680
  ensembl transcript: ENST00000357991
  gene symbol: GPR64
  hgvsc: ENST00000357991.3:c.702-36G>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000349015
  ensembl transcript: ENST00000356606
  gene symbol: GPR64
  hgvsc: ENST00000356606.4:c.669-36G>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000344972
  ensembl transcript: ENST00000340581
  gene symbol: GPR64
  hgvsc: ENST00000340581.3:c.621-36G>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369198
  ensembl transcript: ENST00000379869
  gene symbol: GPR64
  hgvsc: ENST00000379869.3:c.711-36G>A
  variant of: http://identifiers.org/hgnc/4516
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17346
  bin: 2.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 14397
  bin: 1.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3490
  bin: 1.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 1208
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20557
  bin: 7.5e0
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 384
  bin: 4.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 424
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3291
  bin: 3.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 5.25e1
  variant carriers: 1
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: Latino
reference allele: C
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ

X-19032229-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24019032229
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24019032229
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 36238
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369207
  ensembl transcript: ENST00000379878
  gene symbol: GPR64
  hgvsc: ENST00000379878.3:c.663-37C>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000353421
  ensembl transcript: ENST00000360279
  gene symbol: GPR64
  hgvsc: ENST00000360279.4:c.645-37C>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369198
  ensembl transcript: ENST00000379869
  gene symbol: GPR64
  hgvsc: ENST00000379869.3:c.711-37C>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369202
  ensembl transcript: ENST00000379873
  gene symbol: GPR64
  hgvsc: ENST00000379873.2:c.711-37C>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369205
  ensembl transcript: ENST00000379876
  gene symbol: GPR64
  hgvsc: ENST00000379876.1:c.639-37C>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350152
  ensembl transcript: ENST00000357544
  gene symbol: GPR64
  hgvsc: ENST00000357544.3:c.621-37C>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000344972
  ensembl transcript: ENST00000340581
  gene symbol: GPR64
  hgvsc: ENST00000340581.3:c.621-37C>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000346845
  ensembl transcript: ENST00000354791
  gene symbol: GPR64
  hgvsc: ENST00000354791.3:c.663-37C>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000349015
  ensembl transcript: ENST00000356606
  gene symbol: GPR64
  hgvsc: ENST00000356606.4:c.669-37C>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350680
  ensembl transcript: ENST00000357991
  gene symbol: GPR64
  hgvsc: ENST00000357991.3:c.702-37C>T
  variant of: http://identifiers.org/hgnc/4516
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17499
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3531
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20784
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1112
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14082
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2962
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1722
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: African
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP

X-19032242-A-AG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24019032242
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24019032243
    reference: chr 0
allele count: 11
allele frequency: 3.738698932771396e-4
allele num: 29422
alternate allele: AG
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369198
  ensembl transcript: ENST00000379869
  gene symbol: GPR64
  hgvsc: ENST00000379869.3:c.711-51dupC
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350680
  ensembl transcript: ENST00000357991
  gene symbol: GPR64
  hgvsc: ENST00000357991.3:c.702-51dupC
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369205
  ensembl transcript: ENST00000379876
  gene symbol: GPR64
  hgvsc: ENST00000379876.1:c.639-51dupC
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000346845
  ensembl transcript: ENST00000354791
  gene symbol: GPR64
  hgvsc: ENST00000354791.3:c.663-51dupC
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000353421
  ensembl transcript: ENST00000360279
  gene symbol: GPR64
  hgvsc: ENST00000360279.4:c.645-51dupC
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000344972
  ensembl transcript: ENST00000340581
  gene symbol: GPR64
  hgvsc: ENST00000340581.3:c.621-51dupC
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369207
  ensembl transcript: ENST00000379878
  gene symbol: GPR64
  hgvsc: ENST00000379878.3:c.663-51dupC
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369202
  ensembl transcript: ENST00000379873
  gene symbol: GPR64
  hgvsc: ENST00000379873.2:c.711-51dupC
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350152
  ensembl transcript: ENST00000357544
  gene symbol: GPR64
  hgvsc: ENST00000357544.3:c.621-51dupC
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000349015
  ensembl transcript: ENST00000356606
  gene symbol: GPR64
  hgvsc: ENST00000356606.4:c.669-51dupC
  variant of: http://identifiers.org/hgnc/4516
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18005
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3469
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 10422
  bin: 1.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23890
  bin: 7.5e0
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1175
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3254
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2816
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16810
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 237
  bin: 6.75e1
  variant carriers: 1
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: European (Finnish)
population: East Asian
reference allele: A
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD

X-19032244-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24019032244
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24019032244
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 28729
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369207
  ensembl transcript: ENST00000379878
  gene symbol: GPR64
  hgvsc: ENST00000379878.3:c.663-52C>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000346845
  ensembl transcript: ENST00000354791
  gene symbol: GPR64
  hgvsc: ENST00000354791.3:c.663-52C>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000353421
  ensembl transcript: ENST00000360279
  gene symbol: GPR64
  hgvsc: ENST00000360279.4:c.645-52C>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350680
  ensembl transcript: ENST00000357991
  gene symbol: GPR64
  hgvsc: ENST00000357991.3:c.702-52C>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369205
  ensembl transcript: ENST00000379876
  gene symbol: GPR64
  hgvsc: ENST00000379876.1:c.639-52C>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000349015
  ensembl transcript: ENST00000356606
  gene symbol: GPR64
  hgvsc: ENST00000356606.4:c.669-52C>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000344972
  ensembl transcript: ENST00000340581
  gene symbol: GPR64
  hgvsc: ENST00000340581.3:c.621-52C>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350152
  ensembl transcript: ENST00000357544
  gene symbol: GPR64
  hgvsc: ENST00000357544.3:c.621-52C>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369198
  ensembl transcript: ENST00000379869
  gene symbol: GPR64
  hgvsc: ENST00000379869.3:c.711-52C>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369202
  ensembl transcript: ENST00000379873
  gene symbol: GPR64
  hgvsc: ENST00000379873.2:c.711-52C>A
  variant of: http://identifiers.org/hgnc/4516
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23891
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10414
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18034
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3455
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6851
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 567
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9508
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: Latino
reference allele: G
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: InbreedingCoeff

X-19037666-A-AT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24019037666
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24019037667
    reference: chr 0
allele count: 2203
allele frequency: 4.6979293284712e-2
allele num: 46893
alternate allele: AT
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369198
  ensembl transcript: ENST00000379869
  gene symbol: GPR64
  hgvsc: ENST00000379869.3:c.710+50dupA
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000353421
  ensembl transcript: ENST00000360279
  gene symbol: GPR64
  hgvsc: ENST00000360279.4:c.644+50dupA
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369202
  ensembl transcript: ENST00000379873
  gene symbol: GPR64
  hgvsc: ENST00000379873.2:c.710+50dupA
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350152
  ensembl transcript: ENST00000357544
  gene symbol: GPR64
  hgvsc: ENST00000357544.3:c.620+50dupA
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000349015
  ensembl transcript: ENST00000356606
  gene symbol: GPR64
  hgvsc: ENST00000356606.4:c.668+50dupA
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000346845
  ensembl transcript: ENST00000354791
  gene symbol: GPR64
  hgvsc: ENST00000354791.3:c.662+50dupA
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000344972
  ensembl transcript: ENST00000340581
  gene symbol: GPR64
  hgvsc: ENST00000340581.3:c.620+50dupA
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369207
  ensembl transcript: ENST00000379878
  gene symbol: GPR64
  hgvsc: ENST00000379878.3:c.662+50dupA
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350680
  ensembl transcript: ENST00000357991
  gene symbol: GPR64
  hgvsc: ENST00000357991.3:c.701+50dupA
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369205
  ensembl transcript: ENST00000379876
  gene symbol: GPR64
  hgvsc: ENST00000379876.1:c.638+50dupA
  variant of: http://identifiers.org/hgnc/4516
canonical: true
consequence: intron
filter: VQSRTrancheINDEL96.00to97.00
genotype depth: GenotypeDepth
  all individuals: 15042
  bin: 1.75e1
  variant carriers: 1323
genotype depth: GenotypeDepth
  all individuals: 2361
  bin: 3.25e1
  variant carriers: 168
genotype depth: GenotypeDepth
  all individuals: 7541
  bin: 7.5e0
  variant carriers: 1391
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 4.25e1
  variant carriers: 76
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 16361
  bin: 1.25e1
  variant carriers: 2007
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 4.75e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 9567
  bin: 2.25e1
  variant carriers: 728
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 5.25e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 2.5e0
  variant carriers: 89
genotype depth: GenotypeDepth
  all individuals: 4963
  bin: 2.75e1
  variant carriers: 323
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 5.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1215
  bin: 3.75e1
  variant carriers: 84
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1801
  bin: 6.75e1
  variant carriers: 106
genotype quality: GenotypeQuality
  all individuals: 2338
  bin: 2.75e1
  variant carriers: 431
genotype quality: GenotypeQuality
  all individuals: 3123
  bin: 7.5e0
  variant carriers: 734
genotype quality: GenotypeQuality
  all individuals: 1324
  bin: 7.75e1
  variant carriers: 94
num of homozygotes: 1
population: African
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum

X-19037666-A-ATT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24019037666
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24019037668
    reference: chr 0
allele count: 230
allele frequency: 4.904783229906382e-3
allele num: 46893
alternate allele: ATT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000349015
  ensembl transcript: ENST00000356606
  gene symbol: GPR64
  hgvsc: ENST00000356606.4:c.668+49_668+50dupAA
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000344972
  ensembl transcript: ENST00000340581
  gene symbol: GPR64
  hgvsc: ENST00000340581.3:c.620+49_620+50dupAA
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369205
  ensembl transcript: ENST00000379876
  gene symbol: GPR64
  hgvsc: ENST00000379876.1:c.638+49_638+50dupAA
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350152
  ensembl transcript: ENST00000357544
  gene symbol: GPR64
  hgvsc: ENST00000357544.3:c.620+49_620+50dupAA
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369202
  ensembl transcript: ENST00000379873
  gene symbol: GPR64
  hgvsc: ENST00000379873.2:c.710+49_710+50dupAA
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000353421
  ensembl transcript: ENST00000360279
  gene symbol: GPR64
  hgvsc: ENST00000360279.4:c.644+49_644+50dupAA
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369207
  ensembl transcript: ENST00000379878
  gene symbol: GPR64
  hgvsc: ENST00000379878.3:c.662+49_662+50dupAA
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000346845
  ensembl transcript: ENST00000354791
  gene symbol: GPR64
  hgvsc: ENST00000354791.3:c.662+49_662+50dupAA
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350680
  ensembl transcript: ENST00000357991
  gene symbol: GPR64
  hgvsc: ENST00000357991.3:c.701+49_701+50dupAA
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369198
  ensembl transcript: ENST00000379869
  gene symbol: GPR64
  hgvsc: ENST00000379869.3:c.710+49_710+50dupAA
  variant of: http://identifiers.org/hgnc/4516
canonical: true
consequence: intron
filter: VQSRTrancheINDEL96.00to97.00
genotype depth: GenotypeDepth
  all individuals: 1215
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2361
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7541
  bin: 7.5e0
  variant carriers: 165
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 2.5e0
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 9567
  bin: 2.25e1
  variant carriers: 70
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16361
  bin: 1.25e1
  variant carriers: 233
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15042
  bin: 1.75e1
  variant carriers: 139
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4963
  bin: 2.75e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 4.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 4981
  bin: 9.75e1
  variant carriers: 28
genotype quality: GenotypeQuality
  all individuals: 2375
  bin: 5.25e1
  variant carriers: 37
genotype quality: GenotypeQuality
  all individuals: 976
  bin: 8.75e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 1498
  bin: 7.25e1
  variant carriers: 23
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum

X-19037666-A-ATTT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24019037666
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24019037669
    reference: chr 0
allele count: 24
allele frequency: 5.118034674684921e-4
allele num: 46893
alternate allele: ATTT
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369198
  ensembl transcript: ENST00000379869
  gene symbol: GPR64
  hgvsc: ENST00000379869.3:c.710+48_710+50dupAAA
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000344972
  ensembl transcript: ENST00000340581
  gene symbol: GPR64
  hgvsc: ENST00000340581.3:c.620+48_620+50dupAAA
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350152
  ensembl transcript: ENST00000357544
  gene symbol: GPR64
  hgvsc: ENST00000357544.3:c.620+48_620+50dupAAA
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000346845
  ensembl transcript: ENST00000354791
  gene symbol: GPR64
  hgvsc: ENST00000354791.3:c.662+48_662+50dupAAA
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369207
  ensembl transcript: ENST00000379878
  gene symbol: GPR64
  hgvsc: ENST00000379878.3:c.662+48_662+50dupAAA
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000349015
  ensembl transcript: ENST00000356606
  gene symbol: GPR64
  hgvsc: ENST00000356606.4:c.668+48_668+50dupAAA
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000353421
  ensembl transcript: ENST00000360279
  gene symbol: GPR64
  hgvsc: ENST00000360279.4:c.644+48_644+50dupAAA
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350680
  ensembl transcript: ENST00000357991
  gene symbol: GPR64
  hgvsc: ENST00000357991.3:c.701+48_701+50dupAAA
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369202
  ensembl transcript: ENST00000379873
  gene symbol: GPR64
  hgvsc: ENST00000379873.2:c.710+48_710+50dupAAA
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369205
  ensembl transcript: ENST00000379876
  gene symbol: GPR64
  hgvsc: ENST00000379876.1:c.638+48_638+50dupAAA
  variant of: http://identifiers.org/hgnc/4516
canonical: true
consequence: intron
filter: VQSRTrancheINDEL96.00to97.00
genotype depth: GenotypeDepth
  all individuals: 9567
  bin: 2.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 1215
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4963
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7541
  bin: 7.5e0
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15042
  bin: 1.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2361
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16361
  bin: 1.25e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2447
  bin: 4.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 1324
  bin: 7.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 1859
  bin: 6.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 17039
  bin: 2.5e0
  variant carriers: 6
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: Other
reference allele: A
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: MQ

X-19037666-AT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24019037666
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24019037665
    reference: chr 0
allele count: 15510
allele frequency: 3.30752990851513e-1
allele num: 46893
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369202
  ensembl transcript: ENST00000379873
  gene symbol: GPR64
  hgvsc: ENST00000379873.2:c.710+50delA
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350152
  ensembl transcript: ENST00000357544
  gene symbol: GPR64
  hgvsc: ENST00000357544.3:c.620+50delA
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369198
  ensembl transcript: ENST00000379869
  gene symbol: GPR64
  hgvsc: ENST00000379869.3:c.710+50delA
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000346845
  ensembl transcript: ENST00000354791
  gene symbol: GPR64
  hgvsc: ENST00000354791.3:c.662+50delA
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369205
  ensembl transcript: ENST00000379876
  gene symbol: GPR64
  hgvsc: ENST00000379876.1:c.638+50delA
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000349015
  ensembl transcript: ENST00000356606
  gene symbol: GPR64
  hgvsc: ENST00000356606.4:c.668+50delA
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369207
  ensembl transcript: ENST00000379878
  gene symbol: GPR64
  hgvsc: ENST00000379878.3:c.662+50delA
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000353421
  ensembl transcript: ENST00000360279
  gene symbol: GPR64
  hgvsc: ENST00000360279.4:c.644+50delA
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000344972
  ensembl transcript: ENST00000340581
  gene symbol: GPR64
  hgvsc: ENST00000340581.3:c.620+50delA
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350680
  ensembl transcript: ENST00000357991
  gene symbol: GPR64
  hgvsc: ENST00000357991.3:c.701+50delA
  variant of: http://identifiers.org/hgnc/4516
canonical: true
consequence: intron
filter: VQSRTrancheINDEL96.00to97.00
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.25e1
  variant carriers: 40
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 2.5e0
  variant carriers: 148
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 4.25e1
  variant carriers: 497
genotype depth: GenotypeDepth
  all individuals: 2361
  bin: 3.25e1
  variant carriers: 1292
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.75e1
  variant carriers: 62
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 4963
  bin: 2.75e1
  variant carriers: 2548
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1215
  bin: 3.75e1
  variant carriers: 731
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 4.75e1
  variant carriers: 270
genotype depth: GenotypeDepth
  all individuals: 15042
  bin: 1.75e1
  variant carriers: 6906
genotype depth: GenotypeDepth
  all individuals: 9567
  bin: 2.25e1
  variant carriers: 4502
genotype depth: GenotypeDepth
  all individuals: 7541
  bin: 7.5e0
  variant carriers: 4001
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 5.25e1
  variant carriers: 256
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 16361
  bin: 1.25e1
  variant carriers: 8586
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.75e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 5.75e1
  variant carriers: 149
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.25e1
  variant carriers: 106
genotype quality: GenotypeQuality
  all individuals: 1168
  bin: 8.25e1
  variant carriers: 794
genotype quality: GenotypeQuality
  all individuals: 2707
  bin: 2.25e1
  variant carriers: 1767
genotype quality: GenotypeQuality
  all individuals: 2137
  bin: 5.75e1
  variant carriers: 1660
genotype quality: GenotypeQuality
  all individuals: 1324
  bin: 7.75e1
  variant carriers: 882
num of homozygotes: 0
population: Other
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: AT
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

X-19037666-ATT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24019037666
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24019037664
    reference: chr 0
allele count: 4471
allele frequency: 9.534472096048451e-2
allele num: 46893
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000346845
  ensembl transcript: ENST00000354791
  gene symbol: GPR64
  hgvsc: ENST00000354791.3:c.662+49_662+50delAA
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369207
  ensembl transcript: ENST00000379878
  gene symbol: GPR64
  hgvsc: ENST00000379878.3:c.662+49_662+50delAA
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369205
  ensembl transcript: ENST00000379876
  gene symbol: GPR64
  hgvsc: ENST00000379876.1:c.638+49_638+50delAA
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000353421
  ensembl transcript: ENST00000360279
  gene symbol: GPR64
  hgvsc: ENST00000360279.4:c.644+49_644+50delAA
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350152
  ensembl transcript: ENST00000357544
  gene symbol: GPR64
  hgvsc: ENST00000357544.3:c.620+49_620+50delAA
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000349015
  ensembl transcript: ENST00000356606
  gene symbol: GPR64
  hgvsc: ENST00000356606.4:c.668+49_668+50delAA
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369198
  ensembl transcript: ENST00000379869
  gene symbol: GPR64
  hgvsc: ENST00000379869.3:c.710+49_710+50delAA
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369202
  ensembl transcript: ENST00000379873
  gene symbol: GPR64
  hgvsc: ENST00000379873.2:c.710+49_710+50delAA
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000344972
  ensembl transcript: ENST00000340581
  gene symbol: GPR64
  hgvsc: ENST00000340581.3:c.620+49_620+50delAA
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350680
  ensembl transcript: ENST00000357991
  gene symbol: GPR64
  hgvsc: ENST00000357991.3:c.701+49_701+50delAA
  variant of: http://identifiers.org/hgnc/4516
canonical: true
consequence: intron
filter: VQSRTrancheINDEL96.00to97.00
genotype depth: GenotypeDepth
  all individuals: 15042
  bin: 1.75e1
  variant carriers: 3173
genotype depth: GenotypeDepth
  all individuals: 16361
  bin: 1.25e1
  variant carriers: 3098
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 5.25e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 7541
  bin: 7.5e0
  variant carriers: 885
genotype depth: GenotypeDepth
  all individuals: 4963
  bin: 2.75e1
  variant carriers: 1115
genotype depth: GenotypeDepth
  all individuals: 2361
  bin: 3.25e1
  variant carriers: 495
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 2.5e0
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 1215
  bin: 3.75e1
  variant carriers: 201
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 4.75e1
  variant carriers: 48
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 5.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 4.25e1
  variant carriers: 117
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9567
  bin: 2.25e1
  variant carriers: 2246
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 2137
  bin: 5.75e1
  variant carriers: 406
genotype quality: GenotypeQuality
  all individuals: 2707
  bin: 2.25e1
  variant carriers: 669
genotype quality: GenotypeQuality
  all individuals: 2447
  bin: 4.75e1
  variant carriers: 402
genotype quality: GenotypeQuality
  all individuals: 2488
  bin: 3.25e1
  variant carriers: 584
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: ATT
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum

X-19037666-ATTT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24019037666
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24019037663
    reference: chr 0
allele count: 390
allele frequency: 8.316806346362997e-3
allele num: 46893
alternate allele: A
canonical: false
filter: VQSRTrancheINDEL96.00to97.00
genotype depth: GenotypeDepth
  all individuals: 9567
  bin: 2.25e1
  variant carriers: 228
genotype depth: GenotypeDepth
  all individuals: 15042
  bin: 1.75e1
  variant carriers: 431
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4963
  bin: 2.75e1
  variant carriers: 121
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1215
  bin: 3.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 4.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 16361
  bin: 1.25e1
  variant carriers: 406
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7541
  bin: 7.5e0
  variant carriers: 60
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2361
  bin: 3.25e1
  variant carriers: 48
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2707
  bin: 2.25e1
  variant carriers: 82
genotype quality: GenotypeQuality
  all individuals: 1324
  bin: 7.75e1
  variant carriers: 32
genotype quality: GenotypeQuality
  all individuals: 1168
  bin: 8.25e1
  variant carriers: 32
genotype quality: GenotypeQuality
  all individuals: 3123
  bin: 7.5e0
  variant carriers: 138
genotype quality: GenotypeQuality
  all individuals: 2137
  bin: 5.75e1
  variant carriers: 43
genotype quality: GenotypeQuality
  all individuals: 2447
  bin: 4.75e1
  variant carriers: 30
genotype quality: GenotypeQuality
  all individuals: 2338
  bin: 2.75e1
  variant carriers: 68
genotype quality: GenotypeQuality
  all individuals: 1498
  bin: 7.25e1
  variant carriers: 40
genotype quality: GenotypeQuality
  all individuals: 17039
  bin: 2.5e0
  variant carriers: 147
genotype quality: GenotypeQuality
  all individuals: 2691
  bin: 4.25e1
  variant carriers: 46
genotype quality: GenotypeQuality
  all individuals: 2573
  bin: 3.75e1
  variant carriers: 44
genotype quality: GenotypeQuality
  all individuals: 976
  bin: 8.75e1
  variant carriers: 37
genotype quality: GenotypeQuality
  all individuals: 2751
  bin: 1.25e1
  variant carriers: 89
genotype quality: GenotypeQuality
  all individuals: 2375
  bin: 5.25e1
  variant carriers: 35
genotype quality: GenotypeQuality
  all individuals: 1801
  bin: 6.75e1
  variant carriers: 25
genotype quality: GenotypeQuality
  all individuals: 2411
  bin: 1.75e1
  variant carriers: 105
genotype quality: GenotypeQuality
  all individuals: 1859
  bin: 6.25e1
  variant carriers: 28
genotype quality: GenotypeQuality
  all individuals: 4981
  bin: 9.75e1
  variant carriers: 209
genotype quality: GenotypeQuality
  all individuals: 846
  bin: 9.25e1
  variant carriers: 39
genotype quality: GenotypeQuality
  all individuals: 2488
  bin: 3.25e1
  variant carriers: 58
num of homozygotes: 0
population: African
  type: Population
  allele count: 48
  allele frequency: 1.045979516234474e-2
  allele num: 4589
  num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 26
  allele frequency: 7.575757575757576e-3
  allele num: 3432
  num of homozygotes: 0
population: Latino
  type: Population
  allele count: 57
  allele frequency: 1.085300837776085e-2
  allele num: 5252
  num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 203
  allele frequency: 7.626991283438534e-3
  allele num: 26616
  num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
reference allele: ATTT
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum

X-19037667-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24019037667
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24019037667
    reference: chr 0
allele count: 1
allele frequency: 2.325581395348837e-2
allele num: 43
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000346845
  ensembl transcript: ENST00000354791
  gene symbol: GPR64
  hgvsc: ENST00000354791.3:c.662+50A>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369207
  ensembl transcript: ENST00000379878
  gene symbol: GPR64
  hgvsc: ENST00000379878.3:c.662+50A>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000353421
  ensembl transcript: ENST00000360279
  gene symbol: GPR64
  hgvsc: ENST00000360279.4:c.644+50A>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000344972
  ensembl transcript: ENST00000340581
  gene symbol: GPR64
  hgvsc: ENST00000340581.3:c.620+50A>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000349015
  ensembl transcript: ENST00000356606
  gene symbol: GPR64
  hgvsc: ENST00000356606.4:c.668+50A>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350680
  ensembl transcript: ENST00000357991
  gene symbol: GPR64
  hgvsc: ENST00000357991.3:c.701+50A>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369198
  ensembl transcript: ENST00000379869
  gene symbol: GPR64
  hgvsc: ENST00000379869.3:c.710+50A>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369205
  ensembl transcript: ENST00000379876
  gene symbol: GPR64
  hgvsc: ENST00000379876.1:c.638+50A>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350152
  ensembl transcript: ENST00000357544
  gene symbol: GPR64
  hgvsc: ENST00000357544.3:c.620+50A>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369202
  ensembl transcript: ENST00000379873
  gene symbol: GPR64
  hgvsc: ENST00000379873.2:c.710+50A>C
  variant of: http://identifiers.org/hgnc/4516
canonical: true
consequence: intron
filter: InbreedingCoeff_Filter
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3087
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1579
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1499
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5005
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4227
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum

X-19037687-AG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24019037687
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24019037686
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 80661
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000344972
  ensembl transcript: ENST00000340581
  gene symbol: GPR64
  hgvsc: ENST00000340581.3:c.620+29delC
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173698
  ensembl transcript: ENST00000479496
  gene symbol: GPR64
  hgvsc: ENST00000479496.1:n.5786delC
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369205
  ensembl transcript: ENST00000379876
  gene symbol: GPR64
  hgvsc: ENST00000379876.1:c.638+29delC
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369207
  ensembl transcript: ENST00000379878
  gene symbol: GPR64
  hgvsc: ENST00000379878.3:c.662+29delC
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000349015
  ensembl transcript: ENST00000356606
  gene symbol: GPR64
  hgvsc: ENST00000356606.4:c.668+29delC
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350152
  ensembl transcript: ENST00000357544
  gene symbol: GPR64
  hgvsc: ENST00000357544.3:c.620+29delC
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369198
  ensembl transcript: ENST00000379869
  gene symbol: GPR64
  hgvsc: ENST00000379869.3:c.710+29delC
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369202
  ensembl transcript: ENST00000379873
  gene symbol: GPR64
  hgvsc: ENST00000379873.2:c.710+29delC
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350680
  ensembl transcript: ENST00000357991
  gene symbol: GPR64
  hgvsc: ENST00000357991.3:c.701+29delC
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000353421
  ensembl transcript: ENST00000360279
  gene symbol: GPR64
  hgvsc: ENST00000360279.4:c.644+29delC
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000346845
  ensembl transcript: ENST00000354791
  gene symbol: GPR64
  hgvsc: ENST00000354791.3:c.662+29delC
  variant of: http://identifiers.org/hgnc/4516
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 2038
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5356
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9546
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7647
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4114
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6076
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1242
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2996
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8743
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1972
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7146
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1085
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: AG
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

X-19037694-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24019037694
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24019037694
    reference: chr 0
allele count: 12
allele frequency: 1.400413121870952e-4
allele num: 85689
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350152
  ensembl transcript: ENST00000357544
  gene symbol: GPR64
  hgvsc: ENST00000357544.3:c.620+23C>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000344972
  ensembl transcript: ENST00000340581
  gene symbol: GPR64
  hgvsc: ENST00000340581.3:c.620+23C>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000346845
  ensembl transcript: ENST00000354791
  gene symbol: GPR64
  hgvsc: ENST00000354791.3:c.662+23C>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369198
  ensembl transcript: ENST00000379869
  gene symbol: GPR64
  hgvsc: ENST00000379869.3:c.710+23C>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000349015
  ensembl transcript: ENST00000356606
  gene symbol: GPR64
  hgvsc: ENST00000356606.4:c.668+23C>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000353421
  ensembl transcript: ENST00000360279
  gene symbol: GPR64
  hgvsc: ENST00000360279.4:c.644+23C>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173698
  ensembl transcript: ENST00000479496
  gene symbol: GPR64
  hgvsc: ENST00000479496.1:n.5780C>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350680
  ensembl transcript: ENST00000357991
  gene symbol: GPR64
  hgvsc: ENST00000357991.3:c.701+23C>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369207
  ensembl transcript: ENST00000379878
  gene symbol: GPR64
  hgvsc: ENST00000379878.3:c.662+23C>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369205
  ensembl transcript: ENST00000379876
  gene symbol: GPR64
  hgvsc: ENST00000379876.1:c.638+23C>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369202
  ensembl transcript: ENST00000379873
  gene symbol: GPR64
  hgvsc: ENST00000379873.2:c.710+23C>T
  variant of: http://identifiers.org/hgnc/4516
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1925
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1236
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2122
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11156
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14771
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7480
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4308
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2935
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1817
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4017
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5273
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1956
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: Other
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: QD

X-19037694-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24019037694
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24019037694
    reference: chr 0
allele count: 1
allele frequency: 1.16701093489246e-5
allele num: 85689
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350680
  ensembl transcript: ENST00000357991
  gene symbol: GPR64
  hgvsc: ENST00000357991.3:c.701+23C>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173698
  ensembl transcript: ENST00000479496
  gene symbol: GPR64
  hgvsc: ENST00000479496.1:n.5780C>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369205
  ensembl transcript: ENST00000379876
  gene symbol: GPR64
  hgvsc: ENST00000379876.1:c.638+23C>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369207
  ensembl transcript: ENST00000379878
  gene symbol: GPR64
  hgvsc: ENST00000379878.3:c.662+23C>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369202
  ensembl transcript: ENST00000379873
  gene symbol: GPR64
  hgvsc: ENST00000379873.2:c.710+23C>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350152
  ensembl transcript: ENST00000357544
  gene symbol: GPR64
  hgvsc: ENST00000357544.3:c.620+23C>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000344972
  ensembl transcript: ENST00000340581
  gene symbol: GPR64
  hgvsc: ENST00000340581.3:c.620+23C>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369198
  ensembl transcript: ENST00000379869
  gene symbol: GPR64
  hgvsc: ENST00000379869.3:c.710+23C>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000346845
  ensembl transcript: ENST00000354791
  gene symbol: GPR64
  hgvsc: ENST00000354791.3:c.662+23C>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000353421
  ensembl transcript: ENST00000360279
  gene symbol: GPR64
  hgvsc: ENST00000360279.4:c.644+23C>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000349015
  ensembl transcript: ENST00000356606
  gene symbol: GPR64
  hgvsc: ENST00000356606.4:c.668+23C>G
  variant of: http://identifiers.org/hgnc/4516
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4017
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14771
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2122
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1817
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7480
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1925
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4308
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11156
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1236
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2935
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5273
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: DP
site quality: FS
site quality: ClippingRankSum

X-19037712-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24019037712
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24019037712
    reference: chr 0
allele count: 1
allele frequency: 1.154587754442276e-5
allele num: 86611
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000344972
  ensembl transcript: ENST00000340581
  gene symbol: GPR64
  hgvsc: ENST00000340581.3:c.620+5G>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000353421
  ensembl transcript: ENST00000360279
  gene symbol: GPR64
  hgvsc: ENST00000360279.4:c.644+5G>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000349015
  ensembl transcript: ENST00000356606
  gene symbol: GPR64
  hgvsc: ENST00000356606.4:c.668+5G>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000346845
  ensembl transcript: ENST00000354791
  gene symbol: GPR64
  hgvsc: ENST00000354791.3:c.662+5G>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350680
  ensembl transcript: ENST00000357991
  gene symbol: GPR64
  hgvsc: ENST00000357991.3:c.701+5G>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350152
  ensembl transcript: ENST00000357544
  gene symbol: GPR64
  hgvsc: ENST00000357544.3:c.620+5G>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369198
  ensembl transcript: ENST00000379869
  gene symbol: GPR64
  hgvsc: ENST00000379869.3:c.710+5G>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369205
  ensembl transcript: ENST00000379876
  gene symbol: GPR64
  hgvsc: ENST00000379876.1:c.638+5G>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369202
  ensembl transcript: ENST00000379873
  gene symbol: GPR64
  hgvsc: ENST00000379873.2:c.710+5G>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369207
  ensembl transcript: ENST00000379878
  gene symbol: GPR64
  hgvsc: ENST00000379878.3:c.662+5G>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173698
  ensembl transcript: ENST00000479496
  gene symbol: GPR64
  hgvsc: ENST00000479496.1:n.5762G>A
  variant of: http://identifiers.org/hgnc/4516
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7758
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19061
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12711
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4043
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2931
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5295
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1210
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1916
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.710+5G>A
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

X-19037713-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24019037713
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24019037713
    reference: chr 0
allele count: 752
allele frequency: 8.66668971637336e-3
allele num: 86769
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000346845
  ensembl transcript: ENST00000354791
  gene symbol: GPR64
  hgvsc: ENST00000354791.3:c.662+4T>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369198
  ensembl transcript: ENST00000379869
  gene symbol: GPR64
  hgvsc: ENST00000379869.3:c.710+4T>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000344972
  ensembl transcript: ENST00000340581
  gene symbol: GPR64
  hgvsc: ENST00000340581.3:c.620+4T>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350152
  ensembl transcript: ENST00000357544
  gene symbol: GPR64
  hgvsc: ENST00000357544.3:c.620+4T>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000353421
  ensembl transcript: ENST00000360279
  gene symbol: GPR64
  hgvsc: ENST00000360279.4:c.644+4T>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369207
  ensembl transcript: ENST00000379878
  gene symbol: GPR64
  hgvsc: ENST00000379878.3:c.662+4T>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369202
  ensembl transcript: ENST00000379873
  gene symbol: GPR64
  hgvsc: ENST00000379873.2:c.710+4T>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350680
  ensembl transcript: ENST00000357991
  gene symbol: GPR64
  hgvsc: ENST00000357991.3:c.701+4T>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369205
  ensembl transcript: ENST00000379876
  gene symbol: GPR64
  hgvsc: ENST00000379876.1:c.638+4T>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173698
  ensembl transcript: ENST00000479496
  gene symbol: GPR64
  hgvsc: ENST00000479496.1:n.5761T>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000349015
  ensembl transcript: ENST00000356606
  gene symbol: GPR64
  hgvsc: ENST00000356606.4:c.668+4T>C
  variant of: http://identifiers.org/hgnc/4516
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 6.25e1
  variant carriers: 45
genotype depth: GenotypeDepth
  all individuals: 7712
  bin: 3.25e1
  variant carriers: 59
genotype depth: GenotypeDepth
  all individuals: 2937
  bin: 4.75e1
  variant carriers: 47
genotype depth: GenotypeDepth
  all individuals: 4046
  bin: 4.25e1
  variant carriers: 56
genotype depth: GenotypeDepth
  all individuals: 12750
  bin: 2.75e1
  variant carriers: 45
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 9.75e1
  variant carriers: 132
genotype depth: GenotypeDepth
  all individuals: 1217
  bin: 5.75e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 5271
  bin: 3.75e1
  variant carriers: 58
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 1.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 940
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1930
  bin: 5.25e1
  variant carriers: 49
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.25e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 9.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.75e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 6.75e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 7.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 7.25e1
  variant carriers: 32
genotype quality: GenotypeQuality
hgvs: c.710+4T>C
num of homozygotes: 2
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: A
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: BaseQRankSum

X-19037733-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24019037733
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24019037733
    reference: chr 0
allele count: 2
allele frequency: 2.285139736294874e-5
allele num: 87522
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369202
  ensembl transcript: ENST00000379873
  gene symbol: GPR64
  hgvsc: ENST00000379873.2:c.694T>C
  hgvsp: ENST00000379873.2:c.694T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350680
  ensembl transcript: ENST00000357991
  gene symbol: GPR64
  hgvsc: ENST00000357991.3:c.685T>C
  hgvsp: ENST00000357991.3:c.685T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369207
  ensembl transcript: ENST00000379878
  gene symbol: GPR64
  hgvsc: ENST00000379878.3:c.646T>C
  hgvsp: ENST00000379878.3:c.646T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173698
  ensembl transcript: ENST00000479496
  gene symbol: GPR64
  hgvsc: ENST00000479496.1:n.5741T>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369198
  ensembl transcript: ENST00000379869
  gene symbol: GPR64
  hgvsc: ENST00000379869.3:c.694T>C
  hgvsp: ENST00000379869.3:c.694T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000346845
  ensembl transcript: ENST00000354791
  gene symbol: GPR64
  hgvsc: ENST00000354791.3:c.646T>C
  hgvsp: ENST00000354791.3:c.646T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000349015
  ensembl transcript: ENST00000356606
  gene symbol: GPR64
  hgvsc: ENST00000356606.4:c.652T>C
  hgvsp: ENST00000356606.4:c.652T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350152
  ensembl transcript: ENST00000357544
  gene symbol: GPR64
  hgvsc: ENST00000357544.3:c.604T>C
  hgvsp: ENST00000357544.3:c.604T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000353421
  ensembl transcript: ENST00000360279
  gene symbol: GPR64
  hgvsc: ENST00000360279.4:c.628T>C
  hgvsp: ENST00000360279.4:c.628T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000344972
  ensembl transcript: ENST00000340581
  gene symbol: GPR64
  hgvsc: ENST00000340581.3:c.604T>C
  hgvsp: ENST00000340581.3:c.604T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369205
  ensembl transcript: ENST00000379876
  gene symbol: GPR64
  hgvsc: ENST00000379876.1:c.622T>C
  hgvsp: ENST00000379876.1:c.622T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4516
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13583
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5251
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7864
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1911
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20009
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4036
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2911
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu232Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: African
population: Latino
reference allele: A
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum

X-19037757-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24019037757
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24019037757
    reference: chr 0
allele count: 96
allele frequency: 1.095577746077033e-3
allele num: 87625
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369202
  ensembl transcript: ENST00000379873
  gene symbol: GPR64
  hgvsc: ENST00000379873.2:c.670C>T
  hgvsp: ENSP00000369202.2:p.Pro224Ser
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000344972
  ensembl transcript: ENST00000340581
  gene symbol: GPR64
  hgvsc: ENST00000340581.3:c.580C>T
  hgvsp: ENSP00000344972.3:p.Pro194Ser
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369207
  ensembl transcript: ENST00000379878
  gene symbol: GPR64
  hgvsc: ENST00000379878.3:c.622C>T
  hgvsp: ENSP00000369207.3:p.Pro208Ser
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173698
  ensembl transcript: ENST00000479496
  gene symbol: GPR64
  hgvsc: ENST00000479496.1:n.5717C>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350680
  ensembl transcript: ENST00000357991
  gene symbol: GPR64
  hgvsc: ENST00000357991.3:c.661C>T
  hgvsp: ENSP00000350680.3:p.Pro221Ser
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000346845
  ensembl transcript: ENST00000354791
  gene symbol: GPR64
  hgvsc: ENST00000354791.3:c.622C>T
  hgvsp: ENSP00000346845.3:p.Pro208Ser
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369205
  ensembl transcript: ENST00000379876
  gene symbol: GPR64
  hgvsc: ENST00000379876.1:c.598C>T
  hgvsp: ENSP00000369205.1:p.Pro200Ser
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350152
  ensembl transcript: ENST00000357544
  gene symbol: GPR64
  hgvsc: ENST00000357544.3:c.580C>T
  hgvsp: ENSP00000350152.3:p.Pro194Ser
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369198
  ensembl transcript: ENST00000379869
  gene symbol: GPR64
  hgvsc: ENST00000379869.3:c.670C>T
  hgvsp: ENSP00000369198.3:p.Pro224Ser
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000353421
  ensembl transcript: ENST00000360279
  gene symbol: GPR64
  hgvsc: ENST00000360279.4:c.604C>T
  hgvsp: ENSP00000353421.4:p.Pro202Ser
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000349015
  ensembl transcript: ENST00000356606
  gene symbol: GPR64
  hgvsc: ENST00000356606.4:c.628C>T
  hgvsp: ENSP00000349015.4:p.Pro210Ser
  variant of: http://identifiers.org/hgnc/4516
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19799
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4026
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13755
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7884
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 7.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 8.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 9.75e1
  variant carriers: 57
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2901
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5242
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1216
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 9.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
hgvs: p.Pro224Ser
num of homozygotes: 2
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: Other
population: Latino
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum

X-19037764-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24019037764
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24019037764
    reference: chr 0
allele count: 1
allele frequency: 1.141552511415525e-5
allele num: 87600
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369207
  ensembl transcript: ENST00000379878
  gene symbol: GPR64
  hgvsc: ENST00000379878.3:c.615C>G
  hgvsp: ENST00000379878.3:c.615C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000349015
  ensembl transcript: ENST00000356606
  gene symbol: GPR64
  hgvsc: ENST00000356606.4:c.621C>G
  hgvsp: ENST00000356606.4:c.621C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000346845
  ensembl transcript: ENST00000354791
  gene symbol: GPR64
  hgvsc: ENST00000354791.3:c.615C>G
  hgvsp: ENST00000354791.3:c.615C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350680
  ensembl transcript: ENST00000357991
  gene symbol: GPR64
  hgvsc: ENST00000357991.3:c.654C>G
  hgvsp: ENST00000357991.3:c.654C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350152
  ensembl transcript: ENST00000357544
  gene symbol: GPR64
  hgvsc: ENST00000357544.3:c.573C>G
  hgvsp: ENST00000357544.3:c.573C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369198
  ensembl transcript: ENST00000379869
  gene symbol: GPR64
  hgvsc: ENST00000379869.3:c.663C>G
  hgvsp: ENST00000379869.3:c.663C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369202
  ensembl transcript: ENST00000379873
  gene symbol: GPR64
  hgvsc: ENST00000379873.2:c.663C>G
  hgvsp: ENST00000379873.2:c.663C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369205
  ensembl transcript: ENST00000379876
  gene symbol: GPR64
  hgvsc: ENST00000379876.1:c.591C>G
  hgvsp: ENST00000379876.1:c.591C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173698
  ensembl transcript: ENST00000479496
  gene symbol: GPR64
  hgvsc: ENST00000479496.1:n.5710C>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000353421
  ensembl transcript: ENST00000360279
  gene symbol: GPR64
  hgvsc: ENST00000360279.4:c.597C>G
  hgvsp: ENST00000360279.4:c.597C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000344972
  ensembl transcript: ENST00000340581
  gene symbol: GPR64
  hgvsc: ENST00000340581.3:c.573C>G
  hgvsp: ENST00000340581.3:c.573C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4516
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2910
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19682
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1910
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5257
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7895
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1221
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 842
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4029
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13786
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val221Val
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: Latino
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: QD

X-19037778-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24019037778
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24019037778
    reference: chr 0
allele count: 1
allele frequency: 1.142739603926453e-5
allele num: 87509
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369202
  ensembl transcript: ENST00000379873
  gene symbol: GPR64
  hgvsc: ENST00000379873.2:c.649T>G
  hgvsp: ENSP00000369202.2:p.Cys217Gly
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000349015
  ensembl transcript: ENST00000356606
  gene symbol: GPR64
  hgvsc: ENST00000356606.4:c.607T>G
  hgvsp: ENSP00000349015.4:p.Cys203Gly
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350680
  ensembl transcript: ENST00000357991
  gene symbol: GPR64
  hgvsc: ENST00000357991.3:c.640T>G
  hgvsp: ENSP00000350680.3:p.Cys214Gly
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350152
  ensembl transcript: ENST00000357544
  gene symbol: GPR64
  hgvsc: ENST00000357544.3:c.559T>G
  hgvsp: ENSP00000350152.3:p.Cys187Gly
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369207
  ensembl transcript: ENST00000379878
  gene symbol: GPR64
  hgvsc: ENST00000379878.3:c.601T>G
  hgvsp: ENSP00000369207.3:p.Cys201Gly
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369205
  ensembl transcript: ENST00000379876
  gene symbol: GPR64
  hgvsc: ENST00000379876.1:c.577T>G
  hgvsp: ENSP00000369205.1:p.Cys193Gly
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000344972
  ensembl transcript: ENST00000340581
  gene symbol: GPR64
  hgvsc: ENST00000340581.3:c.559T>G
  hgvsp: ENSP00000344972.3:p.Cys187Gly
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369198
  ensembl transcript: ENST00000379869
  gene symbol: GPR64
  hgvsc: ENST00000379869.3:c.649T>G
  hgvsp: ENSP00000369198.3:p.Cys217Gly
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173698
  ensembl transcript: ENST00000479496
  gene symbol: GPR64
  hgvsc: ENST00000479496.1:n.5696T>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000346845
  ensembl transcript: ENST00000354791
  gene symbol: GPR64
  hgvsc: ENST00000354791.3:c.601T>G
  hgvsp: ENSP00000346845.3:p.Cys201Gly
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000353421
  ensembl transcript: ENST00000360279
  gene symbol: GPR64
  hgvsc: ENST00000360279.4:c.583T>G
  hgvsp: ENSP00000353421.4:p.Cys195Gly
  variant of: http://identifiers.org/hgnc/4516
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2910
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4027
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13867
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19229
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1910
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5253
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7886
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 842
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1222
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys217Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum

X-19037778-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24019037778
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24019037778
    reference: chr 0
allele count: 1
allele frequency: 1.142739603926453e-5
allele num: 87509
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369207
  ensembl transcript: ENST00000379878
  gene symbol: GPR64
  hgvsc: ENST00000379878.3:c.601T>C
  hgvsp: ENSP00000369207.3:p.Cys201Arg
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000344972
  ensembl transcript: ENST00000340581
  gene symbol: GPR64
  hgvsc: ENST00000340581.3:c.559T>C
  hgvsp: ENSP00000344972.3:p.Cys187Arg
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000349015
  ensembl transcript: ENST00000356606
  gene symbol: GPR64
  hgvsc: ENST00000356606.4:c.607T>C
  hgvsp: ENSP00000349015.4:p.Cys203Arg
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369205
  ensembl transcript: ENST00000379876
  gene symbol: GPR64
  hgvsc: ENST00000379876.1:c.577T>C
  hgvsp: ENSP00000369205.1:p.Cys193Arg
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000353421
  ensembl transcript: ENST00000360279
  gene symbol: GPR64
  hgvsc: ENST00000360279.4:c.583T>C
  hgvsp: ENSP00000353421.4:p.Cys195Arg
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173698
  ensembl transcript: ENST00000479496
  gene symbol: GPR64
  hgvsc: ENST00000479496.1:n.5696T>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369198
  ensembl transcript: ENST00000379869
  gene symbol: GPR64
  hgvsc: ENST00000379869.3:c.649T>C
  hgvsp: ENSP00000369198.3:p.Cys217Arg
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000346845
  ensembl transcript: ENST00000354791
  gene symbol: GPR64
  hgvsc: ENST00000354791.3:c.601T>C
  hgvsp: ENSP00000346845.3:p.Cys201Arg
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350152
  ensembl transcript: ENST00000357544
  gene symbol: GPR64
  hgvsc: ENST00000357544.3:c.559T>C
  hgvsp: ENSP00000350152.3:p.Cys187Arg
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350680
  ensembl transcript: ENST00000357991
  gene symbol: GPR64
  hgvsc: ENST00000357991.3:c.640T>C
  hgvsp: ENSP00000350680.3:p.Cys214Arg
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369202
  ensembl transcript: ENST00000379873
  gene symbol: GPR64
  hgvsc: ENST00000379873.2:c.649T>C
  hgvsp: ENSP00000369202.2:p.Cys217Arg
  variant of: http://identifiers.org/hgnc/4516
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19229
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1910
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5253
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2910
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1222
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13867
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7886
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4027
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Cys217Arg
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
reference allele: A
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD

X-19037779-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24019037779
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24019037779
    reference: chr 0
allele count: 2
allele frequency: 2.285949411939514e-5
allele num: 87491
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000353421
  ensembl transcript: ENST00000360279
  gene symbol: GPR64
  hgvsc: ENST00000360279.4:c.582C>T
  hgvsp: ENST00000360279.4:c.582C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000349015
  ensembl transcript: ENST00000356606
  gene symbol: GPR64
  hgvsc: ENST00000356606.4:c.606C>T
  hgvsp: ENST00000356606.4:c.606C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000346845
  ensembl transcript: ENST00000354791
  gene symbol: GPR64
  hgvsc: ENST00000354791.3:c.600C>T
  hgvsp: ENST00000354791.3:c.600C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000344972
  ensembl transcript: ENST00000340581
  gene symbol: GPR64
  hgvsc: ENST00000340581.3:c.558C>T
  hgvsp: ENST00000340581.3:c.558C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173698
  ensembl transcript: ENST00000479496
  gene symbol: GPR64
  hgvsc: ENST00000479496.1:n.5695C>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369205
  ensembl transcript: ENST00000379876
  gene symbol: GPR64
  hgvsc: ENST00000379876.1:c.576C>T
  hgvsp: ENST00000379876.1:c.576C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369198
  ensembl transcript: ENST00000379869
  gene symbol: GPR64
  hgvsc: ENST00000379869.3:c.648C>T
  hgvsp: ENST00000379869.3:c.648C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350680
  ensembl transcript: ENST00000357991
  gene symbol: GPR64
  hgvsc: ENST00000357991.3:c.639C>T
  hgvsp: ENST00000357991.3:c.639C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369207
  ensembl transcript: ENST00000379878
  gene symbol: GPR64
  hgvsc: ENST00000379878.3:c.600C>T
  hgvsp: ENST00000379878.3:c.600C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369202
  ensembl transcript: ENST00000379873
  gene symbol: GPR64
  hgvsc: ENST00000379873.2:c.648C>T
  hgvsp: ENST00000379873.2:c.648C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350152
  ensembl transcript: ENST00000357544
  gene symbol: GPR64
  hgvsc: ENST00000357544.3:c.558C>T
  hgvsp: ENST00000357544.3:c.558C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4516
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5249
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19168
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 842
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13857
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7892
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4027
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1910
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2910
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1222
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His216His
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQ

X-19037791-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24019037791
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24019037791
    reference: chr 0
allele count: 2
allele frequency: 2.291081963457243e-5
allele num: 87295
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000349015
  ensembl transcript: ENST00000356606
  gene symbol: GPR64
  hgvsc: ENST00000356606.4:c.602-8T>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369198
  ensembl transcript: ENST00000379869
  gene symbol: GPR64
  hgvsc: ENST00000379869.3:c.644-8T>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369205
  ensembl transcript: ENST00000379876
  gene symbol: GPR64
  hgvsc: ENST00000379876.1:c.572-8T>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369202
  ensembl transcript: ENST00000379873
  gene symbol: GPR64
  hgvsc: ENST00000379873.2:c.644-8T>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000344972
  ensembl transcript: ENST00000340581
  gene symbol: GPR64
  hgvsc: ENST00000340581.3:c.554-8T>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000346845
  ensembl transcript: ENST00000354791
  gene symbol: GPR64
  hgvsc: ENST00000354791.3:c.596-8T>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350152
  ensembl transcript: ENST00000357544
  gene symbol: GPR64
  hgvsc: ENST00000357544.3:c.554-8T>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350680
  ensembl transcript: ENST00000357991
  gene symbol: GPR64
  hgvsc: ENST00000357991.3:c.635-8T>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000353421
  ensembl transcript: ENST00000360279
  gene symbol: GPR64
  hgvsc: ENST00000360279.4:c.578-8T>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369207
  ensembl transcript: ENST00000379878
  gene symbol: GPR64
  hgvsc: ENST00000379878.3:c.596-8T>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl transcript: ENST00000479496
  gene symbol: GPR64
  hgvsc: ENST00000479496.1:n.5691-8T>A
  variant of: http://identifiers.org/hgnc/4516
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17880
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 842
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4028
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1285
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1911
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13810
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5250
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1221
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7892
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2910
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.644-8T>A
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
population: African
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

X-19037793-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24019037793
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24019037793
    reference: chr 0
allele count: 1
allele frequency: 1.146079262841818e-5
allele num: 87254
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369205
  ensembl transcript: ENST00000379876
  gene symbol: GPR64
  hgvsc: ENST00000379876.1:c.572-10T>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000353421
  ensembl transcript: ENST00000360279
  gene symbol: GPR64
  hgvsc: ENST00000360279.4:c.578-10T>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000346845
  ensembl transcript: ENST00000354791
  gene symbol: GPR64
  hgvsc: ENST00000354791.3:c.596-10T>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369202
  ensembl transcript: ENST00000379873
  gene symbol: GPR64
  hgvsc: ENST00000379873.2:c.644-10T>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000344972
  ensembl transcript: ENST00000340581
  gene symbol: GPR64
  hgvsc: ENST00000340581.3:c.554-10T>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350152
  ensembl transcript: ENST00000357544
  gene symbol: GPR64
  hgvsc: ENST00000357544.3:c.554-10T>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350680
  ensembl transcript: ENST00000357991
  gene symbol: GPR64
  hgvsc: ENST00000357991.3:c.635-10T>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl transcript: ENST00000479496
  gene symbol: GPR64
  hgvsc: ENST00000479496.1:n.5691-10T>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369207
  ensembl transcript: ENST00000379878
  gene symbol: GPR64
  hgvsc: ENST00000379878.3:c.596-10T>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369198
  ensembl transcript: ENST00000379869
  gene symbol: GPR64
  hgvsc: ENST00000379869.3:c.644-10T>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000349015
  ensembl transcript: ENST00000356606
  gene symbol: GPR64
  hgvsc: ENST00000356606.4:c.602-10T>C
  variant of: http://identifiers.org/hgnc/4516
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1221
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4029
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5250
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 842
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1488
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13762
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2910
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17609
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1912
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7898
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
reference allele: A
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: DP
site quality: FS

X-19037822-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24019037822
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24019037822
    reference: chr 0
allele count: 1
allele frequency: 1.160617912976869e-5
allele num: 86161
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000346845
  ensembl transcript: ENST00000354791
  gene symbol: GPR64
  hgvsc: ENST00000354791.3:c.596-39G>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000344972
  ensembl transcript: ENST00000340581
  gene symbol: GPR64
  hgvsc: ENST00000340581.3:c.554-39G>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl transcript: ENST00000479496
  gene symbol: GPR64
  hgvsc: ENST00000479496.1:n.5691-39G>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000353421
  ensembl transcript: ENST00000360279
  gene symbol: GPR64
  hgvsc: ENST00000360279.4:c.578-39G>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350152
  ensembl transcript: ENST00000357544
  gene symbol: GPR64
  hgvsc: ENST00000357544.3:c.554-39G>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369205
  ensembl transcript: ENST00000379876
  gene symbol: GPR64
  hgvsc: ENST00000379876.1:c.572-39G>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369207
  ensembl transcript: ENST00000379878
  gene symbol: GPR64
  hgvsc: ENST00000379878.3:c.596-39G>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350680
  ensembl transcript: ENST00000357991
  gene symbol: GPR64
  hgvsc: ENST00000357991.3:c.635-39G>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000349015
  ensembl transcript: ENST00000356606
  gene symbol: GPR64
  hgvsc: ENST00000356606.4:c.602-39G>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369202
  ensembl transcript: ENST00000379873
  gene symbol: GPR64
  hgvsc: ENST00000379873.2:c.644-39G>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369198
  ensembl transcript: ENST00000379869
  gene symbol: GPR64
  hgvsc: ENST00000379869.3:c.644-39G>C
  variant of: http://identifiers.org/hgnc/4516
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1053
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8691
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7353
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9136
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4046
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5262
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10222
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1221
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5235
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2916
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1915
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1666
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
population: African
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum

X-19037822-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24019037822
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24019037822
    reference: chr 0
allele count: 7
allele frequency: 8.124325390838082e-5
allele num: 86161
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369205
  ensembl transcript: ENST00000379876
  gene symbol: GPR64
  hgvsc: ENST00000379876.1:c.572-39G>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369202
  ensembl transcript: ENST00000379873
  gene symbol: GPR64
  hgvsc: ENST00000379873.2:c.644-39G>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000346845
  ensembl transcript: ENST00000354791
  gene symbol: GPR64
  hgvsc: ENST00000354791.3:c.596-39G>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000344972
  ensembl transcript: ENST00000340581
  gene symbol: GPR64
  hgvsc: ENST00000340581.3:c.554-39G>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000349015
  ensembl transcript: ENST00000356606
  gene symbol: GPR64
  hgvsc: ENST00000356606.4:c.602-39G>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000353421
  ensembl transcript: ENST00000360279
  gene symbol: GPR64
  hgvsc: ENST00000360279.4:c.578-39G>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369207
  ensembl transcript: ENST00000379878
  gene symbol: GPR64
  hgvsc: ENST00000379878.3:c.596-39G>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350680
  ensembl transcript: ENST00000357991
  gene symbol: GPR64
  hgvsc: ENST00000357991.3:c.635-39G>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369198
  ensembl transcript: ENST00000379869
  gene symbol: GPR64
  hgvsc: ENST00000379869.3:c.644-39G>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350152
  ensembl transcript: ENST00000357544
  gene symbol: GPR64
  hgvsc: ENST00000357544.3:c.554-39G>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl transcript: ENST00000479496
  gene symbol: GPR64
  hgvsc: ENST00000479496.1:n.5691-39G>A
  variant of: http://identifiers.org/hgnc/4516
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10222
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2916
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7353
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1053
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4046
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1915
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5235
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9136
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5262
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8691
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1221
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2564
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: African
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: MQ

X-19037823-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24019037823
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24019037823
    reference: chr 0
allele count: 9
allele frequency: 1.045964320994828e-4
allele num: 86045
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000353421
  ensembl transcript: ENST00000360279
  gene symbol: GPR64
  hgvsc: ENST00000360279.4:c.578-40C>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369207
  ensembl transcript: ENST00000379878
  gene symbol: GPR64
  hgvsc: ENST00000379878.3:c.596-40C>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369198
  ensembl transcript: ENST00000379869
  gene symbol: GPR64
  hgvsc: ENST00000379869.3:c.644-40C>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000344972
  ensembl transcript: ENST00000340581
  gene symbol: GPR64
  hgvsc: ENST00000340581.3:c.554-40C>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350680
  ensembl transcript: ENST00000357991
  gene symbol: GPR64
  hgvsc: ENST00000357991.3:c.635-40C>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000346845
  ensembl transcript: ENST00000354791
  gene symbol: GPR64
  hgvsc: ENST00000354791.3:c.596-40C>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000349015
  ensembl transcript: ENST00000356606
  gene symbol: GPR64
  hgvsc: ENST00000356606.4:c.602-40C>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350152
  ensembl transcript: ENST00000357544
  gene symbol: GPR64
  hgvsc: ENST00000357544.3:c.554-40C>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369202
  ensembl transcript: ENST00000379873
  gene symbol: GPR64
  hgvsc: ENST00000379873.2:c.644-40C>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl transcript: ENST00000479496
  gene symbol: GPR64
  hgvsc: ENST00000479496.1:n.5691-40C>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369205
  ensembl transcript: ENST00000379876
  gene symbol: GPR64
  hgvsc: ENST00000379876.1:c.572-40C>T
  variant of: http://identifiers.org/hgnc/4516
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1078
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2915
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4036
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10247
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1218
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1913
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5339
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9197
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7238
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5234
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8633
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 843
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1969
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

X-19039177-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24019039177
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24019039177
    reference: chr 0
allele count: 1
allele frequency: 1.241696156950394e-5
allele num: 80535
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369207
  ensembl transcript: ENST00000379878
  gene symbol: GPR64
  hgvsc: ENST00000379878.3:c.595+45A>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350680
  ensembl transcript: ENST00000357991
  gene symbol: GPR64
  hgvsc: ENST00000357991.3:c.634+45A>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000344972
  ensembl transcript: ENST00000340581
  gene symbol: GPR64
  hgvsc: ENST00000340581.3:c.553+45A>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369202
  ensembl transcript: ENST00000379873
  gene symbol: GPR64
  hgvsc: ENST00000379873.2:c.643+45A>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369198
  ensembl transcript: ENST00000379869
  gene symbol: GPR64
  hgvsc: ENST00000379869.3:c.643+45A>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350152
  ensembl transcript: ENST00000357544
  gene symbol: GPR64
  hgvsc: ENST00000357544.3:c.553+45A>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369205
  ensembl transcript: ENST00000379876
  gene symbol: GPR64
  hgvsc: ENST00000379876.1:c.571+45A>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000353421
  ensembl transcript: ENST00000360279
  gene symbol: GPR64
  hgvsc: ENST00000360279.4:c.577+45A>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000346845
  ensembl transcript: ENST00000354791
  gene symbol: GPR64
  hgvsc: ENST00000354791.3:c.595+45A>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000349015
  ensembl transcript: ENST00000356606
  gene symbol: GPR64
  hgvsc: ENST00000356606.4:c.601+45A>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl transcript: ENST00000479496
  gene symbol: GPR64
  hgvsc: ENST00000479496.1:n.5690+45A>T
  variant of: http://identifiers.org/hgnc/4516
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4629
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14071
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9344
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13920
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6437
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5750
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1317
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1276
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25494
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: Other
reference allele: T
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: DP

X-19039196-TAATGCAGC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24019039196
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24019039188
    reference: chr 0
allele count: 8
allele frequency: 9.77803852547179e-5
allele num: 81816
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350152
  ensembl transcript: ENST00000357544
  gene symbol: GPR64
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369198
  ensembl transcript: ENST00000379869
  gene symbol: GPR64
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000344972
  ensembl transcript: ENST00000340581
  gene symbol: GPR64
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000353421
  ensembl transcript: ENST00000360279
  gene symbol: GPR64
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369207
  ensembl transcript: ENST00000379878
  gene symbol: GPR64
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350680
  ensembl transcript: ENST00000357991
  gene symbol: GPR64
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000346845
  ensembl transcript: ENST00000354791
  gene symbol: GPR64
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369205
  ensembl transcript: ENST00000379876
  gene symbol: GPR64
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369202
  ensembl transcript: ENST00000379873
  gene symbol: GPR64
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000349015
  ensembl transcript: ENST00000356606
  gene symbol: GPR64
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl transcript: ENST00000479496
  gene symbol: GPR64
  variant of: http://identifiers.org/hgnc/4516
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 4784
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1317
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15303
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24343
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5231
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4094
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1276
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1132
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 304
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: TAATGCAGC
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: MQ

X-19039210-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24019039210
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24019039210
    reference: chr 0
allele count: 1
allele frequency: 1.198968886757389e-5
allele num: 83405
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350680
  ensembl transcript: ENST00000357991
  gene symbol: GPR64
  hgvsc: ENST00000357991.3:c.634+12A>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369205
  ensembl transcript: ENST00000379876
  gene symbol: GPR64
  hgvsc: ENST00000379876.1:c.571+12A>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350152
  ensembl transcript: ENST00000357544
  gene symbol: GPR64
  hgvsc: ENST00000357544.3:c.553+12A>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000349015
  ensembl transcript: ENST00000356606
  gene symbol: GPR64
  hgvsc: ENST00000356606.4:c.601+12A>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000346845
  ensembl transcript: ENST00000354791
  gene symbol: GPR64
  hgvsc: ENST00000354791.3:c.595+12A>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369207
  ensembl transcript: ENST00000379878
  gene symbol: GPR64
  hgvsc: ENST00000379878.3:c.595+12A>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369198
  ensembl transcript: ENST00000379869
  gene symbol: GPR64
  hgvsc: ENST00000379869.3:c.643+12A>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000344972
  ensembl transcript: ENST00000340581
  gene symbol: GPR64
  hgvsc: ENST00000340581.3:c.553+12A>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000353421
  ensembl transcript: ENST00000360279
  gene symbol: GPR64
  hgvsc: ENST00000360279.4:c.577+12A>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369202
  ensembl transcript: ENST00000379873
  gene symbol: GPR64
  hgvsc: ENST00000379873.2:c.643+12A>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl transcript: ENST00000479496
  gene symbol: GPR64
  hgvsc: ENST00000479496.1:n.5690+12A>G
  variant of: http://identifiers.org/hgnc/4516
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1697
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3969
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27576
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4886
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1322
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16282
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1276
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41076
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: MQ
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum

X-19039230-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24019039230
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24019039230
    reference: chr 0
allele count: 2
allele frequency: 2.360745523436301e-5
allele num: 84719
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369202
  ensembl transcript: ENST00000379873
  gene symbol: GPR64
  hgvsc: ENST00000379873.2:c.635G>A
  hgvsp: ENSP00000369202.2:p.Arg212Gln
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000344972
  ensembl transcript: ENST00000340581
  gene symbol: GPR64
  hgvsc: ENST00000340581.3:c.545G>A
  hgvsp: ENSP00000344972.3:p.Arg182Gln
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350152
  ensembl transcript: ENST00000357544
  gene symbol: GPR64
  hgvsc: ENST00000357544.3:c.545G>A
  hgvsp: ENSP00000350152.3:p.Arg182Gln
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369207
  ensembl transcript: ENST00000379878
  gene symbol: GPR64
  hgvsc: ENST00000379878.3:c.587G>A
  hgvsp: ENSP00000369207.3:p.Arg196Gln
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000349015
  ensembl transcript: ENST00000356606
  gene symbol: GPR64
  hgvsc: ENST00000356606.4:c.593G>A
  hgvsp: ENSP00000349015.4:p.Arg198Gln
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000346845
  ensembl transcript: ENST00000354791
  gene symbol: GPR64
  hgvsc: ENST00000354791.3:c.587G>A
  hgvsp: ENSP00000346845.3:p.Arg196Gln
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000353421
  ensembl transcript: ENST00000360279
  gene symbol: GPR64
  hgvsc: ENST00000360279.4:c.569G>A
  hgvsp: ENSP00000353421.4:p.Arg190Gln
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350680
  ensembl transcript: ENST00000357991
  gene symbol: GPR64
  hgvsc: ENST00000357991.3:c.626G>A
  hgvsp: ENSP00000350680.3:p.Arg209Gln
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369198
  ensembl transcript: ENST00000379869
  gene symbol: GPR64
  hgvsc: ENST00000379869.3:c.635G>A
  hgvsp: ENSP00000369198.3:p.Arg212Gln
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173698
  ensembl transcript: ENST00000479496
  gene symbol: GPR64
  hgvsc: ENST00000479496.1:n.5682G>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369205
  ensembl transcript: ENST00000379876
  gene symbol: GPR64
  hgvsc: ENST00000379876.1:c.563G>A
  hgvsp: ENSP00000369205.1:p.Arg188Gln
  variant of: http://identifiers.org/hgnc/4516
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16931
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1330
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29130
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4947
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1276
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2805
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg212Gln
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: South Asian
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum

X-19039244-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24019039244
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24019039244
    reference: chr 0
allele count: 1
allele frequency: 1.17609700448093e-5
allele num: 85027
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369207
  ensembl transcript: ENST00000379878
  gene symbol: GPR64
  hgvsc: ENST00000379878.3:c.573A>G
  hgvsp: ENST00000379878.3:c.573A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369205
  ensembl transcript: ENST00000379876
  gene symbol: GPR64
  hgvsc: ENST00000379876.1:c.549A>G
  hgvsp: ENST00000379876.1:c.549A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000346845
  ensembl transcript: ENST00000354791
  gene symbol: GPR64
  hgvsc: ENST00000354791.3:c.573A>G
  hgvsp: ENST00000354791.3:c.573A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173698
  ensembl transcript: ENST00000479496
  gene symbol: GPR64
  hgvsc: ENST00000479496.1:n.5668A>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350152
  ensembl transcript: ENST00000357544
  gene symbol: GPR64
  hgvsc: ENST00000357544.3:c.531A>G
  hgvsp: ENST00000357544.3:c.531A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350680
  ensembl transcript: ENST00000357991
  gene symbol: GPR64
  hgvsc: ENST00000357991.3:c.612A>G
  hgvsp: ENST00000357991.3:c.612A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000344972
  ensembl transcript: ENST00000340581
  gene symbol: GPR64
  hgvsc: ENST00000340581.3:c.531A>G
  hgvsp: ENST00000340581.3:c.531A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369198
  ensembl transcript: ENST00000379869
  gene symbol: GPR64
  hgvsc: ENST00000379869.3:c.621A>G
  hgvsp: ENST00000379869.3:c.621A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369202
  ensembl transcript: ENST00000379873
  gene symbol: GPR64
  hgvsc: ENST00000379873.2:c.621A>G
  hgvsp: ENST00000379873.2:c.621A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000353421
  ensembl transcript: ENST00000360279
  gene symbol: GPR64
  hgvsc: ENST00000360279.4:c.555A>G
  hgvsp: ENST00000360279.4:c.555A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000349015
  ensembl transcript: ENST00000356606
  gene symbol: GPR64
  hgvsc: ENST00000356606.4:c.579A>G
  hgvsp: ENST00000356606.4:c.579A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4516
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1332
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1277
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2543
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17173
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29269
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4957
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu207Glu
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

X-19039276-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24019039276
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24019039276
    reference: chr 0
allele count: 1
allele frequency: 1.199918405548423e-5
allele num: 83339
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369198
  ensembl transcript: ENST00000379869
  gene symbol: GPR64
  hgvsc: ENST00000379869.3:c.589A>G
  hgvsp: ENSP00000369198.3:p.Met197Val
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000346845
  ensembl transcript: ENST00000354791
  gene symbol: GPR64
  hgvsc: ENST00000354791.3:c.541A>G
  hgvsp: ENSP00000346845.3:p.Met181Val
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000344972
  ensembl transcript: ENST00000340581
  gene symbol: GPR64
  hgvsc: ENST00000340581.3:c.499A>G
  hgvsp: ENSP00000344972.3:p.Met167Val
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369207
  ensembl transcript: ENST00000379878
  gene symbol: GPR64
  hgvsc: ENST00000379878.3:c.541A>G
  hgvsp: ENSP00000369207.3:p.Met181Val
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369202
  ensembl transcript: ENST00000379873
  gene symbol: GPR64
  hgvsc: ENST00000379873.2:c.589A>G
  hgvsp: ENSP00000369202.2:p.Met197Val
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350680
  ensembl transcript: ENST00000357991
  gene symbol: GPR64
  hgvsc: ENST00000357991.3:c.580A>G
  hgvsp: ENSP00000350680.3:p.Met194Val
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369205
  ensembl transcript: ENST00000379876
  gene symbol: GPR64
  hgvsc: ENST00000379876.1:c.517A>G
  hgvsp: ENSP00000369205.1:p.Met173Val
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350152
  ensembl transcript: ENST00000357544
  gene symbol: GPR64
  hgvsc: ENST00000357544.3:c.499A>G
  hgvsp: ENSP00000350152.3:p.Met167Val
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000353421
  ensembl transcript: ENST00000360279
  gene symbol: GPR64
  hgvsc: ENST00000360279.4:c.523A>G
  hgvsp: ENSP00000353421.4:p.Met175Val
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000349015
  ensembl transcript: ENST00000356606
  gene symbol: GPR64
  hgvsc: ENST00000356606.4:c.547A>G
  hgvsp: ENSP00000349015.4:p.Met183Val
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173698
  ensembl transcript: ENST00000479496
  gene symbol: GPR64
  hgvsc: ENST00000479496.1:n.5636A>G
  variant of: http://identifiers.org/hgnc/4516
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25860
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4935
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3940
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17327
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2200
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1324
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1277
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met197Val
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

X-19039283-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24019039283
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24019039283
    reference: chr 0
allele count: 3
allele frequency: 3.657287755400595e-5
allele num: 82028
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000346845
  ensembl transcript: ENST00000354791
  gene symbol: GPR64
  hgvsc: ENST00000354791.3:c.534T>C
  hgvsp: ENST00000354791.3:c.534T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173698
  ensembl transcript: ENST00000479496
  gene symbol: GPR64
  hgvsc: ENST00000479496.1:n.5629T>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000353421
  ensembl transcript: ENST00000360279
  gene symbol: GPR64
  hgvsc: ENST00000360279.4:c.516T>C
  hgvsp: ENST00000360279.4:c.516T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369198
  ensembl transcript: ENST00000379869
  gene symbol: GPR64
  hgvsc: ENST00000379869.3:c.582T>C
  hgvsp: ENST00000379869.3:c.582T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000349015
  ensembl transcript: ENST00000356606
  gene symbol: GPR64
  hgvsc: ENST00000356606.4:c.540T>C
  hgvsp: ENST00000356606.4:c.540T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369207
  ensembl transcript: ENST00000379878
  gene symbol: GPR64
  hgvsc: ENST00000379878.3:c.534T>C
  hgvsp: ENST00000379878.3:c.534T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000344972
  ensembl transcript: ENST00000340581
  gene symbol: GPR64
  hgvsc: ENST00000340581.3:c.492T>C
  hgvsp: ENST00000340581.3:c.492T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369205
  ensembl transcript: ENST00000379876
  gene symbol: GPR64
  hgvsc: ENST00000379876.1:c.510T>C
  hgvsp: ENST00000379876.1:c.510T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350680
  ensembl transcript: ENST00000357991
  gene symbol: GPR64
  hgvsc: ENST00000357991.3:c.573T>C
  hgvsp: ENST00000357991.3:c.573T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350152
  ensembl transcript: ENST00000357544
  gene symbol: GPR64
  hgvsc: ENST00000357544.3:c.492T>C
  hgvsp: ENST00000357544.3:c.492T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369202
  ensembl transcript: ENST00000379873
  gene symbol: GPR64
  hgvsc: ENST00000379873.2:c.582T>C
  hgvsp: ENST00000379873.2:c.582T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4516
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4928
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3304
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1326
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1277
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17097
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4955
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23613
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn194Asn
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: Other
population: East Asian
reference allele: A
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum

X-19039294-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24019039294
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24019039294
    reference: chr 0
allele count: 1
allele frequency: 1.240417772705847e-5
allele num: 80618
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350152
  ensembl transcript: ENST00000357544
  gene symbol: GPR64
  hgvsc: ENST00000357544.3:c.481A>G
  hgvsp: ENSP00000350152.3:p.Ile161Val
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000344972
  ensembl transcript: ENST00000340581
  gene symbol: GPR64
  hgvsc: ENST00000340581.3:c.481A>G
  hgvsp: ENSP00000344972.3:p.Ile161Val
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369198
  ensembl transcript: ENST00000379869
  gene symbol: GPR64
  hgvsc: ENST00000379869.3:c.571A>G
  hgvsp: ENSP00000369198.3:p.Ile191Val
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369207
  ensembl transcript: ENST00000379878
  gene symbol: GPR64
  hgvsc: ENST00000379878.3:c.523A>G
  hgvsp: ENSP00000369207.3:p.Ile175Val
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000349015
  ensembl transcript: ENST00000356606
  gene symbol: GPR64
  hgvsc: ENST00000356606.4:c.529A>G
  hgvsp: ENSP00000349015.4:p.Ile177Val
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000353421
  ensembl transcript: ENST00000360279
  gene symbol: GPR64
  hgvsc: ENST00000360279.4:c.505A>G
  hgvsp: ENSP00000353421.4:p.Ile169Val
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369205
  ensembl transcript: ENST00000379876
  gene symbol: GPR64
  hgvsc: ENST00000379876.1:c.499A>G
  hgvsp: ENSP00000369205.1:p.Ile167Val
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173698
  ensembl transcript: ENST00000479496
  gene symbol: GPR64
  hgvsc: ENST00000479496.1:n.5618A>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000346845
  ensembl transcript: ENST00000354791
  gene symbol: GPR64
  hgvsc: ENST00000354791.3:c.523A>G
  hgvsp: ENSP00000346845.3:p.Ile175Val
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369202
  ensembl transcript: ENST00000379873
  gene symbol: GPR64
  hgvsc: ENST00000379873.2:c.571A>G
  hgvsp: ENSP00000369202.2:p.Ile191Val
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350680
  ensembl transcript: ENST00000357991
  gene symbol: GPR64
  hgvsc: ENST00000357991.3:c.562A>G
  hgvsp: ENSP00000350680.3:p.Ile188Val
  variant of: http://identifiers.org/hgnc/4516
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 4565
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1276
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21810
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6039
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 906
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1314
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4824
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16401
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile191Val
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Other
population: Latino
reference allele: T
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

X-19039303-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24019039303
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24019039303
    reference: chr 0
allele count: 1
allele frequency: 1.275054827357576e-5
allele num: 78428
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000344972
  ensembl transcript: ENST00000340581
  gene symbol: GPR64
  hgvsc: ENST00000340581.3:c.472A>G
  hgvsp: ENSP00000344972.3:p.Thr158Ala
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350152
  ensembl transcript: ENST00000357544
  gene symbol: GPR64
  hgvsc: ENST00000357544.3:c.472A>G
  hgvsp: ENSP00000350152.3:p.Thr158Ala
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000346845
  ensembl transcript: ENST00000354791
  gene symbol: GPR64
  hgvsc: ENST00000354791.3:c.514A>G
  hgvsp: ENSP00000346845.3:p.Thr172Ala
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350680
  ensembl transcript: ENST00000357991
  gene symbol: GPR64
  hgvsc: ENST00000357991.3:c.553A>G
  hgvsp: ENSP00000350680.3:p.Thr185Ala
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369205
  ensembl transcript: ENST00000379876
  gene symbol: GPR64
  hgvsc: ENST00000379876.1:c.490A>G
  hgvsp: ENSP00000369205.1:p.Thr164Ala
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000353421
  ensembl transcript: ENST00000360279
  gene symbol: GPR64
  hgvsc: ENST00000360279.4:c.496A>G
  hgvsp: ENSP00000353421.4:p.Thr166Ala
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173698
  ensembl transcript: ENST00000479496
  gene symbol: GPR64
  hgvsc: ENST00000479496.1:n.5609A>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000349015
  ensembl transcript: ENST00000356606
  gene symbol: GPR64
  hgvsc: ENST00000356606.4:c.520A>G
  hgvsp: ENSP00000349015.4:p.Thr174Ala
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369198
  ensembl transcript: ENST00000379869
  gene symbol: GPR64
  hgvsc: ENST00000379869.3:c.562A>G
  hgvsp: ENSP00000369198.3:p.Thr188Ala
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369207
  ensembl transcript: ENST00000379878
  gene symbol: GPR64
  hgvsc: ENST00000379878.3:c.514A>G
  hgvsp: ENSP00000369207.3:p.Thr172Ala
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369202
  ensembl transcript: ENST00000379873
  gene symbol: GPR64
  hgvsc: ENST00000379873.2:c.562A>G
  hgvsp: ENSP00000369202.2:p.Thr188Ala
  variant of: http://identifiers.org/hgnc/4516
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6558
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1197
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18365
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7591
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1311
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4759
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15792
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1276
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr188Ala
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: DP
site quality: FS
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD

X-19039314-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24019039314
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24019039314
    reference: chr 0
allele count: 2
allele frequency: 2.661343978709248e-5
allele num: 75150
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369202
  ensembl transcript: ENST00000379873
  gene symbol: GPR64
  hgvsc: ENST00000379873.2:c.551C>T
  hgvsp: ENSP00000369202.2:p.Thr184Ile
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350680
  ensembl transcript: ENST00000357991
  gene symbol: GPR64
  hgvsc: ENST00000357991.3:c.542C>T
  hgvsp: ENSP00000350680.3:p.Thr181Ile
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000173698
  ensembl transcript: ENST00000479496
  gene symbol: GPR64
  hgvsc: ENST00000479496.1:n.5598C>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000346845
  ensembl transcript: ENST00000354791
  gene symbol: GPR64
  hgvsc: ENST00000354791.3:c.503C>T
  hgvsp: ENSP00000346845.3:p.Thr168Ile
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000344972
  ensembl transcript: ENST00000340581
  gene symbol: GPR64
  hgvsc: ENST00000340581.3:c.461C>T
  hgvsp: ENSP00000344972.3:p.Thr154Ile
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000353421
  ensembl transcript: ENST00000360279
  gene symbol: GPR64
  hgvsc: ENST00000360279.4:c.485C>T
  hgvsp: ENSP00000353421.4:p.Thr162Ile
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369198
  ensembl transcript: ENST00000379869
  gene symbol: GPR64
  hgvsc: ENST00000379869.3:c.551C>T
  hgvsp: ENSP00000369198.3:p.Thr184Ile
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000349015
  ensembl transcript: ENST00000356606
  gene symbol: GPR64
  hgvsc: ENST00000356606.4:c.509C>T
  hgvsp: ENSP00000349015.4:p.Thr170Ile
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350152
  ensembl transcript: ENST00000357544
  gene symbol: GPR64
  hgvsc: ENST00000357544.3:c.461C>T
  hgvsp: ENSP00000350152.3:p.Thr154Ile
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369207
  ensembl transcript: ENST00000379878
  gene symbol: GPR64
  hgvsc: ENST00000379878.3:c.503C>T
  hgvsp: ENSP00000369207.3:p.Thr168Ile
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369205
  ensembl transcript: ENST00000379876
  gene symbol: GPR64
  hgvsc: ENST00000379876.1:c.479C>T
  hgvsp: ENSP00000369205.1:p.Thr160Ile
  variant of: http://identifiers.org/hgnc/4516
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4529
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14365
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10041
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9619
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13451
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1289
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1316
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1643
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr184Ile
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum

X-19039319-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24019039319
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24019039319
    reference: chr 0
allele count: 1
allele frequency: 1.352265043948614e-5
allele num: 73950
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000346845
  ensembl transcript: ENST00000354791
  gene symbol: GPR64
  hgvsc: ENST00000354791.3:c.501-3C>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369202
  ensembl transcript: ENST00000379873
  gene symbol: GPR64
  hgvsc: ENST00000379873.2:c.549-3C>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369207
  ensembl transcript: ENST00000379878
  gene symbol: GPR64
  hgvsc: ENST00000379878.3:c.501-3C>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000344972
  ensembl transcript: ENST00000340581
  gene symbol: GPR64
  hgvsc: ENST00000340581.3:c.459-3C>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl transcript: ENST00000479496
  gene symbol: GPR64
  hgvsc: ENST00000479496.1:n.5596-3C>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000349015
  ensembl transcript: ENST00000356606
  gene symbol: GPR64
  hgvsc: ENST00000356606.4:c.507-3C>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350152
  ensembl transcript: ENST00000357544
  gene symbol: GPR64
  hgvsc: ENST00000357544.3:c.459-3C>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000353421
  ensembl transcript: ENST00000360279
  gene symbol: GPR64
  hgvsc: ENST00000360279.4:c.483-3C>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369198
  ensembl transcript: ENST00000379869
  gene symbol: GPR64
  hgvsc: ENST00000379869.3:c.549-3C>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369205
  ensembl transcript: ENST00000379876
  gene symbol: GPR64
  hgvsc: ENST00000379876.1:c.477-3C>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350680
  ensembl transcript: ENST00000357991
  gene symbol: GPR64
  hgvsc: ENST00000357991.3:c.540-3C>T
  variant of: http://identifiers.org/hgnc/4516
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10263
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11141
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1592
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4317
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13758
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1647
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12259
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.549-3C>T
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff

X-19039329-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24019039329
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24019039329
    reference: chr 0
allele count: 1
allele frequency: 1.394680687856515e-5
allele num: 71701
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369205
  ensembl transcript: ENST00000379876
  gene symbol: GPR64
  hgvsc: ENST00000379876.1:c.477-13T>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369198
  ensembl transcript: ENST00000379869
  gene symbol: GPR64
  hgvsc: ENST00000379869.3:c.549-13T>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369207
  ensembl transcript: ENST00000379878
  gene symbol: GPR64
  hgvsc: ENST00000379878.3:c.501-13T>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000353421
  ensembl transcript: ENST00000360279
  gene symbol: GPR64
  hgvsc: ENST00000360279.4:c.483-13T>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350152
  ensembl transcript: ENST00000357544
  gene symbol: GPR64
  hgvsc: ENST00000357544.3:c.459-13T>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000346845
  ensembl transcript: ENST00000354791
  gene symbol: GPR64
  hgvsc: ENST00000354791.3:c.501-13T>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369202
  ensembl transcript: ENST00000379873
  gene symbol: GPR64
  hgvsc: ENST00000379873.2:c.549-13T>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350680
  ensembl transcript: ENST00000357991
  gene symbol: GPR64
  hgvsc: ENST00000357991.3:c.540-13T>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000344972
  ensembl transcript: ENST00000340581
  gene symbol: GPR64
  hgvsc: ENST00000340581.3:c.459-13T>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000349015
  ensembl transcript: ENST00000356606
  gene symbol: GPR64
  hgvsc: ENST00000356606.4:c.507-13T>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl transcript: ENST00000479496
  gene symbol: GPR64
  hgvsc: ENST00000479496.1:n.5596-13T>G
  variant of: http://identifiers.org/hgnc/4516
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3892
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2013
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1243
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12007
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2483
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11348
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13942
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9313
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 222
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

X-19039332-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24019039332
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24019039332
    reference: chr 0
allele count: 7
allele frequency: 9.876403860262994e-5
allele num: 70876
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000346845
  ensembl transcript: ENST00000354791
  gene symbol: GPR64
  hgvsc: ENST00000354791.3:c.501-16A>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369207
  ensembl transcript: ENST00000379878
  gene symbol: GPR64
  hgvsc: ENST00000379878.3:c.501-16A>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369198
  ensembl transcript: ENST00000379869
  gene symbol: GPR64
  hgvsc: ENST00000379869.3:c.549-16A>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369205
  ensembl transcript: ENST00000379876
  gene symbol: GPR64
  hgvsc: ENST00000379876.1:c.477-16A>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000344972
  ensembl transcript: ENST00000340581
  gene symbol: GPR64
  hgvsc: ENST00000340581.3:c.459-16A>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000353421
  ensembl transcript: ENST00000360279
  gene symbol: GPR64
  hgvsc: ENST00000360279.4:c.483-16A>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000349015
  ensembl transcript: ENST00000356606
  gene symbol: GPR64
  hgvsc: ENST00000356606.4:c.507-16A>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl transcript: ENST00000479496
  gene symbol: GPR64
  hgvsc: ENST00000479496.1:n.5596-16A>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350152
  ensembl transcript: ENST00000357544
  gene symbol: GPR64
  hgvsc: ENST00000357544.3:c.459-16A>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369202
  ensembl transcript: ENST00000379873
  gene symbol: GPR64
  hgvsc: ENST00000379873.2:c.549-16A>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350680
  ensembl transcript: ENST00000357991
  gene symbol: GPR64
  hgvsc: ENST00000357991.3:c.540-16A>G
  variant of: http://identifiers.org/hgnc/4516
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11537
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11287
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8261
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3810
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2904
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1236
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14916
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2283
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 551
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: T
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

X-19039340-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24019039340
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24019039340
    reference: chr 0
allele count: 2
allele frequency: 2.927486167627858e-5
allele num: 68318
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000344972
  ensembl transcript: ENST00000340581
  gene symbol: GPR64
  hgvsc: ENST00000340581.3:c.459-24G>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369205
  ensembl transcript: ENST00000379876
  gene symbol: GPR64
  hgvsc: ENST00000379876.1:c.477-24G>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl transcript: ENST00000479496
  gene symbol: GPR64
  hgvsc: ENST00000479496.1:n.5596-24G>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369198
  ensembl transcript: ENST00000379869
  gene symbol: GPR64
  hgvsc: ENST00000379869.3:c.549-24G>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350152
  ensembl transcript: ENST00000357544
  gene symbol: GPR64
  hgvsc: ENST00000357544.3:c.459-24G>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000346845
  ensembl transcript: ENST00000354791
  gene symbol: GPR64
  hgvsc: ENST00000354791.3:c.501-24G>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350680
  ensembl transcript: ENST00000357991
  gene symbol: GPR64
  hgvsc: ENST00000357991.3:c.540-24G>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000349015
  ensembl transcript: ENST00000356606
  gene symbol: GPR64
  hgvsc: ENST00000356606.4:c.507-24G>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369202
  ensembl transcript: ENST00000379873
  gene symbol: GPR64
  hgvsc: ENST00000379873.2:c.549-24G>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000353421
  ensembl transcript: ENST00000360279
  gene symbol: GPR64
  hgvsc: ENST00000360279.4:c.483-24G>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369207
  ensembl transcript: ENST00000379878
  gene symbol: GPR64
  hgvsc: ENST00000379878.3:c.501-24G>T
  variant of: http://identifiers.org/hgnc/4516
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5580
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4286
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1213
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3419
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11865
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17326
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3534
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8950
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1477
  bin: 3.75e1
  variant carriers: 1
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum

X-19039346-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24019039346
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24019039346
    reference: chr 0
allele count: 2
allele frequency: 3.008604609182261e-5
allele num: 66476
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000346845
  ensembl transcript: ENST00000354791
  gene symbol: GPR64
  hgvsc: ENST00000354791.3:c.501-30C>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl transcript: ENST00000479496
  gene symbol: GPR64
  hgvsc: ENST00000479496.1:n.5596-30C>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350152
  ensembl transcript: ENST00000357544
  gene symbol: GPR64
  hgvsc: ENST00000357544.3:c.459-30C>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000344972
  ensembl transcript: ENST00000340581
  gene symbol: GPR64
  hgvsc: ENST00000340581.3:c.459-30C>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369202
  ensembl transcript: ENST00000379873
  gene symbol: GPR64
  hgvsc: ENST00000379873.2:c.549-30C>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369205
  ensembl transcript: ENST00000379876
  gene symbol: GPR64
  hgvsc: ENST00000379876.1:c.477-30C>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000353421
  ensembl transcript: ENST00000360279
  gene symbol: GPR64
  hgvsc: ENST00000360279.4:c.483-30C>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000349015
  ensembl transcript: ENST00000356606
  gene symbol: GPR64
  hgvsc: ENST00000356606.4:c.507-30C>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369207
  ensembl transcript: ENST00000379878
  gene symbol: GPR64
  hgvsc: ENST00000379878.3:c.501-30C>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369198
  ensembl transcript: ENST00000379869
  gene symbol: GPR64
  hgvsc: ENST00000379869.3:c.549-30C>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350680
  ensembl transcript: ENST00000357991
  gene symbol: GPR64
  hgvsc: ENST00000357991.3:c.540-30C>T
  variant of: http://identifiers.org/hgnc/4516
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17760
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12482
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5072
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5217
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1176
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7159
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2774
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4463
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2111
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

X-19039446-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24019039446
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24019039446
    reference: chr 0
allele count: 1
allele frequency: 6.455361177457879e-5
allele num: 15491
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000349015
  ensembl transcript: ENST00000356606
  gene symbol: GPR64
  hgvsc: ENST00000356606.4:c.507-130T>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000346845
  ensembl transcript: ENST00000354791
  gene symbol: GPR64
  hgvsc: ENST00000354791.3:c.501-130T>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350152
  ensembl transcript: ENST00000357544
  gene symbol: GPR64
  hgvsc: ENST00000357544.3:c.459-130T>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369198
  ensembl transcript: ENST00000379869
  gene symbol: GPR64
  hgvsc: ENST00000379869.3:c.549-130T>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369202
  ensembl transcript: ENST00000379873
  gene symbol: GPR64
  hgvsc: ENST00000379873.2:c.549-130T>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000344972
  ensembl transcript: ENST00000340581
  gene symbol: GPR64
  hgvsc: ENST00000340581.3:c.459-130T>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000353421
  ensembl transcript: ENST00000360279
  gene symbol: GPR64
  hgvsc: ENST00000360279.4:c.483-130T>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350680
  ensembl transcript: ENST00000357991
  gene symbol: GPR64
  hgvsc: ENST00000357991.3:c.540-130T>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369205
  ensembl transcript: ENST00000379876
  gene symbol: GPR64
  hgvsc: ENST00000379876.1:c.477-130T>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl transcript: ENST00000479496
  gene symbol: GPR64
  hgvsc: ENST00000479496.1:n.5596-130T>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369207
  ensembl transcript: ENST00000379878
  gene symbol: GPR64
  hgvsc: ENST00000379878.3:c.501-130T>C
  variant of: http://identifiers.org/hgnc/4516
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4487
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2061
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2853
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1077
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23600
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2058
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 809
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: Other
population: East Asian
population: European (Finnish)
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD

X-19039449-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24019039449
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24019039449
    reference: chr 0
allele count: 3
allele frequency: 1.950078003120125e-4
allele num: 15384
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369205
  ensembl transcript: ENST00000379876
  gene symbol: GPR64
  hgvsc: ENST00000379876.1:c.477-133T>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000346845
  ensembl transcript: ENST00000354791
  gene symbol: GPR64
  hgvsc: ENST00000354791.3:c.501-133T>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000344972
  ensembl transcript: ENST00000340581
  gene symbol: GPR64
  hgvsc: ENST00000340581.3:c.459-133T>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000353421
  ensembl transcript: ENST00000360279
  gene symbol: GPR64
  hgvsc: ENST00000360279.4:c.483-133T>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369202
  ensembl transcript: ENST00000379873
  gene symbol: GPR64
  hgvsc: ENST00000379873.2:c.549-133T>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350680
  ensembl transcript: ENST00000357991
  gene symbol: GPR64
  hgvsc: ENST00000357991.3:c.540-133T>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl transcript: ENST00000479496
  gene symbol: GPR64
  hgvsc: ENST00000479496.1:n.5596-133T>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369207
  ensembl transcript: ENST00000379878
  gene symbol: GPR64
  hgvsc: ENST00000379878.3:c.501-133T>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000349015
  ensembl transcript: ENST00000356606
  gene symbol: GPR64
  hgvsc: ENST00000356606.4:c.507-133T>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350152
  ensembl transcript: ENST00000357544
  gene symbol: GPR64
  hgvsc: ENST00000357544.3:c.459-133T>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369198
  ensembl transcript: ENST00000379869
  gene symbol: GPR64
  hgvsc: ENST00000379869.3:c.549-133T>C
  variant of: http://identifiers.org/hgnc/4516
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 939
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2196
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23196
  bin: 2.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4358
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2059
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2788
  bin: 1.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 391
  bin: 1.25e1
  variant carriers: 2
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum

X-19039455-TA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24019039455
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24019039454
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 14861
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369198
  ensembl transcript: ENST00000379869
  gene symbol: GPR64
  hgvsc: ENST00000379869.3:c.549-140delT
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369207
  ensembl transcript: ENST00000379878
  gene symbol: GPR64
  hgvsc: ENST00000379878.3:c.501-140delT
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000346845
  ensembl transcript: ENST00000354791
  gene symbol: GPR64
  hgvsc: ENST00000354791.3:c.501-140delT
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350680
  ensembl transcript: ENST00000357991
  gene symbol: GPR64
  hgvsc: ENST00000357991.3:c.540-140delT
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369202
  ensembl transcript: ENST00000379873
  gene symbol: GPR64
  hgvsc: ENST00000379873.2:c.549-140delT
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000344972
  ensembl transcript: ENST00000340581
  gene symbol: GPR64
  hgvsc: ENST00000340581.3:c.459-140delT
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369205
  ensembl transcript: ENST00000379876
  gene symbol: GPR64
  hgvsc: ENST00000379876.1:c.477-140delT
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000349015
  ensembl transcript: ENST00000356606
  gene symbol: GPR64
  hgvsc: ENST00000356606.4:c.507-140delT
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350152
  ensembl transcript: ENST00000357544
  gene symbol: GPR64
  hgvsc: ENST00000357544.3:c.459-140delT
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000353421
  ensembl transcript: ENST00000360279
  gene symbol: GPR64
  hgvsc: ENST00000360279.4:c.483-140delT
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl transcript: ENST00000479496
  gene symbol: GPR64
  hgvsc: ENST00000479496.1:n.5596-140delT
  variant of: http://identifiers.org/hgnc/4516
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2314
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21300
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1944
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3904
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2707
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: East Asian
reference allele: TA
site quality: FS
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

X-19039466-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24019039466
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24019039466
    reference: chr 0
allele count: 1
allele frequency: 7.198387561186294e-5
allele num: 13892
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350680
  ensembl transcript: ENST00000357991
  gene symbol: GPR64
  hgvsc: ENST00000357991.3:c.540-150A>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000344972
  ensembl transcript: ENST00000340581
  gene symbol: GPR64
  hgvsc: ENST00000340581.3:c.459-150A>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350152
  ensembl transcript: ENST00000357544
  gene symbol: GPR64
  hgvsc: ENST00000357544.3:c.459-150A>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000349015
  ensembl transcript: ENST00000356606
  gene symbol: GPR64
  hgvsc: ENST00000356606.4:c.507-150A>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369202
  ensembl transcript: ENST00000379873
  gene symbol: GPR64
  hgvsc: ENST00000379873.2:c.549-150A>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369205
  ensembl transcript: ENST00000379876
  gene symbol: GPR64
  hgvsc: ENST00000379876.1:c.477-150A>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000346845
  ensembl transcript: ENST00000354791
  gene symbol: GPR64
  hgvsc: ENST00000354791.3:c.501-150A>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369207
  ensembl transcript: ENST00000379878
  gene symbol: GPR64
  hgvsc: ENST00000379878.3:c.501-150A>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl transcript: ENST00000479496
  gene symbol: GPR64
  hgvsc: ENST00000479496.1:n.5596-150A>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369198
  ensembl transcript: ENST00000379869
  gene symbol: GPR64
  hgvsc: ENST00000379869.3:c.549-150A>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000353421
  ensembl transcript: ENST00000360279
  gene symbol: GPR64
  hgvsc: ENST00000360279.4:c.483-150A>G
  variant of: http://identifiers.org/hgnc/4516
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2482
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2518
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3303
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17694
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1836
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
reference allele: T
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum

X-19039472-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24019039472
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24019039472
    reference: chr 0
allele count: 9
allele frequency: 6.76335763132186e-4
allele num: 13307
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369202
  ensembl transcript: ENST00000379873
  gene symbol: GPR64
  hgvsc: ENST00000379873.2:c.549-156G>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000344972
  ensembl transcript: ENST00000340581
  gene symbol: GPR64
  hgvsc: ENST00000340581.3:c.459-156G>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000346845
  ensembl transcript: ENST00000354791
  gene symbol: GPR64
  hgvsc: ENST00000354791.3:c.501-156G>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350680
  ensembl transcript: ENST00000357991
  gene symbol: GPR64
  hgvsc: ENST00000357991.3:c.540-156G>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369198
  ensembl transcript: ENST00000379869
  gene symbol: GPR64
  hgvsc: ENST00000379869.3:c.549-156G>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369205
  ensembl transcript: ENST00000379876
  gene symbol: GPR64
  hgvsc: ENST00000379876.1:c.477-156G>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369207
  ensembl transcript: ENST00000379878
  gene symbol: GPR64
  hgvsc: ENST00000379878.3:c.501-156G>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350152
  ensembl transcript: ENST00000357544
  gene symbol: GPR64
  hgvsc: ENST00000357544.3:c.459-156G>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000349015
  ensembl transcript: ENST00000356606
  gene symbol: GPR64
  hgvsc: ENST00000356606.4:c.507-156G>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000353421
  ensembl transcript: ENST00000360279
  gene symbol: GPR64
  hgvsc: ENST00000360279.4:c.483-156G>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl transcript: ENST00000479496
  gene symbol: GPR64
  hgvsc: ENST00000479496.1:n.5596-156G>A
  variant of: http://identifiers.org/hgnc/4516
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3071
  bin: 7.5e0
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 2503
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15427
  bin: 2.5e0
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2379
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1753
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

X-19039487-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24019039487
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24019039487
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 12290
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369198
  ensembl transcript: ENST00000379869
  gene symbol: GPR64
  hgvsc: ENST00000379869.3:c.549-171G>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl transcript: ENST00000479496
  gene symbol: GPR64
  hgvsc: ENST00000479496.1:n.5596-171G>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369202
  ensembl transcript: ENST00000379873
  gene symbol: GPR64
  hgvsc: ENST00000379873.2:c.549-171G>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369205
  ensembl transcript: ENST00000379876
  gene symbol: GPR64
  hgvsc: ENST00000379876.1:c.477-171G>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000346845
  ensembl transcript: ENST00000354791
  gene symbol: GPR64
  hgvsc: ENST00000354791.3:c.501-171G>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369207
  ensembl transcript: ENST00000379878
  gene symbol: GPR64
  hgvsc: ENST00000379878.3:c.501-171G>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000344972
  ensembl transcript: ENST00000340581
  gene symbol: GPR64
  hgvsc: ENST00000340581.3:c.459-171G>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000349015
  ensembl transcript: ENST00000356606
  gene symbol: GPR64
  hgvsc: ENST00000356606.4:c.507-171G>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000353421
  ensembl transcript: ENST00000360279
  gene symbol: GPR64
  hgvsc: ENST00000360279.4:c.483-171G>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350680
  ensembl transcript: ENST00000357991
  gene symbol: GPR64
  hgvsc: ENST00000357991.3:c.540-171G>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350152
  ensembl transcript: ENST00000357544
  gene symbol: GPR64
  hgvsc: ENST00000357544.3:c.459-171G>A
  variant of: http://identifiers.org/hgnc/4516
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 2431
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2255
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2795
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11254
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1528
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

X-19041498-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24019041498
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24019041498
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 66241
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369202
  ensembl transcript: ENST00000379873
  gene symbol: GPR64
  hgvsc: ENST00000379873.2:c.548+36C>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl transcript: ENST00000479496
  gene symbol: GPR64
  hgvsc: ENST00000479496.1:n.5595+36C>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000344972
  ensembl transcript: ENST00000340581
  gene symbol: GPR64
  hgvsc: ENST00000340581.3:c.458+36C>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000349015
  ensembl transcript: ENST00000356606
  gene symbol: GPR64
  hgvsc: ENST00000356606.4:c.506+36C>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369198
  ensembl transcript: ENST00000379869
  gene symbol: GPR64
  hgvsc: ENST00000379869.3:c.548+36C>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350152
  ensembl transcript: ENST00000357544
  gene symbol: GPR64
  hgvsc: ENST00000357544.3:c.458+36C>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369207
  ensembl transcript: ENST00000379878
  gene symbol: GPR64
  hgvsc: ENST00000379878.3:c.500+36C>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000346845
  ensembl transcript: ENST00000354791
  gene symbol: GPR64
  hgvsc: ENST00000354791.3:c.500+36C>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369205
  ensembl transcript: ENST00000379876
  gene symbol: GPR64
  hgvsc: ENST00000379876.1:c.476+36C>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350680
  ensembl transcript: ENST00000357991
  gene symbol: GPR64
  hgvsc: ENST00000357991.3:c.539+36C>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000353421
  ensembl transcript: ENST00000360279
  gene symbol: GPR64
  hgvsc: ENST00000360279.4:c.482+36C>A
  variant of: http://identifiers.org/hgnc/4516
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2620
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1357
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12804
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14871
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15171
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3210
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2955
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4883
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 960
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: DP

X-19041501-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24019041501
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24019041501
    reference: chr 0
allele count: 1
allele frequency: 1.501749538212017e-5
allele num: 66589
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000344972
  ensembl transcript: ENST00000340581
  gene symbol: GPR64
  hgvsc: ENST00000340581.3:c.458+33T>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369207
  ensembl transcript: ENST00000379878
  gene symbol: GPR64
  hgvsc: ENST00000379878.3:c.500+33T>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl transcript: ENST00000479496
  gene symbol: GPR64
  hgvsc: ENST00000479496.1:n.5595+33T>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000349015
  ensembl transcript: ENST00000356606
  gene symbol: GPR64
  hgvsc: ENST00000356606.4:c.506+33T>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350680
  ensembl transcript: ENST00000357991
  gene symbol: GPR64
  hgvsc: ENST00000357991.3:c.539+33T>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369205
  ensembl transcript: ENST00000379876
  gene symbol: GPR64
  hgvsc: ENST00000379876.1:c.476+33T>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000353421
  ensembl transcript: ENST00000360279
  gene symbol: GPR64
  hgvsc: ENST00000360279.4:c.482+33T>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369202
  ensembl transcript: ENST00000379873
  gene symbol: GPR64
  hgvsc: ENST00000379873.2:c.548+33T>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350152
  ensembl transcript: ENST00000357544
  gene symbol: GPR64
  hgvsc: ENST00000357544.3:c.458+33T>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369198
  ensembl transcript: ENST00000379869
  gene symbol: GPR64
  hgvsc: ENST00000379869.3:c.548+33T>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000346845
  ensembl transcript: ENST00000354791
  gene symbol: GPR64
  hgvsc: ENST00000354791.3:c.500+33T>C
  variant of: http://identifiers.org/hgnc/4516
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15328
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2662
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5033
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11867
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2590
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2601
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16446
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1358
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 836
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
reference allele: A
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: QD

X-19041504-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24019041504
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24019041504
    reference: chr 0
allele count: 1
allele frequency: 1.490668415717608e-5
allele num: 67084
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000349015
  ensembl transcript: ENST00000356606
  gene symbol: GPR64
  hgvsc: ENST00000356606.4:c.506+30T>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl transcript: ENST00000479496
  gene symbol: GPR64
  hgvsc: ENST00000479496.1:n.5595+30T>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000344972
  ensembl transcript: ENST00000340581
  gene symbol: GPR64
  hgvsc: ENST00000340581.3:c.458+30T>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000346845
  ensembl transcript: ENST00000354791
  gene symbol: GPR64
  hgvsc: ENST00000354791.3:c.500+30T>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369207
  ensembl transcript: ENST00000379878
  gene symbol: GPR64
  hgvsc: ENST00000379878.3:c.500+30T>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350680
  ensembl transcript: ENST00000357991
  gene symbol: GPR64
  hgvsc: ENST00000357991.3:c.539+30T>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369202
  ensembl transcript: ENST00000379873
  gene symbol: GPR64
  hgvsc: ENST00000379873.2:c.548+30T>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369198
  ensembl transcript: ENST00000379869
  gene symbol: GPR64
  hgvsc: ENST00000379869.3:c.548+30T>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000353421
  ensembl transcript: ENST00000360279
  gene symbol: GPR64
  hgvsc: ENST00000360279.4:c.482+30T>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350152
  ensembl transcript: ENST00000357544
  gene symbol: GPR64
  hgvsc: ENST00000357544.3:c.458+30T>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369205
  ensembl transcript: ENST00000379876
  gene symbol: GPR64
  hgvsc: ENST00000379876.1:c.476+30T>G
  variant of: http://identifiers.org/hgnc/4516
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2087
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2267
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1362
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5167
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2699
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15316
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18220
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10774
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3460
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
reference allele: A
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

X-19041505-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24019041505
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24019041505
    reference: chr 0
allele count: 1
allele frequency: 1.487342713508047e-5
allele num: 67234
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000353421
  ensembl transcript: ENST00000360279
  gene symbol: GPR64
  hgvsc: ENST00000360279.4:c.482+29A>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000346845
  ensembl transcript: ENST00000354791
  gene symbol: GPR64
  hgvsc: ENST00000354791.3:c.500+29A>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369202
  ensembl transcript: ENST00000379873
  gene symbol: GPR64
  hgvsc: ENST00000379873.2:c.548+29A>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369198
  ensembl transcript: ENST00000379869
  gene symbol: GPR64
  hgvsc: ENST00000379869.3:c.548+29A>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350680
  ensembl transcript: ENST00000357991
  gene symbol: GPR64
  hgvsc: ENST00000357991.3:c.539+29A>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000344972
  ensembl transcript: ENST00000340581
  gene symbol: GPR64
  hgvsc: ENST00000340581.3:c.458+29A>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350152
  ensembl transcript: ENST00000357544
  gene symbol: GPR64
  hgvsc: ENST00000357544.3:c.458+29A>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369205
  ensembl transcript: ENST00000379876
  gene symbol: GPR64
  hgvsc: ENST00000379876.1:c.476+29A>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000349015
  ensembl transcript: ENST00000356606
  gene symbol: GPR64
  hgvsc: ENST00000356606.4:c.506+29A>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl transcript: ENST00000479496
  gene symbol: GPR64
  hgvsc: ENST00000479496.1:n.5595+29A>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369207
  ensembl transcript: ENST00000379878
  gene symbol: GPR64
  hgvsc: ENST00000379878.3:c.500+29A>G
  variant of: http://identifiers.org/hgnc/4516
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15276
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5214
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18835
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2706
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2171
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1928
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10401
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1364
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3119
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Finnish)
reference allele: T
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS

X-19041510-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24019041510
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24019041510
    reference: chr 0
allele count: 1
allele frequency: 1.461753226820248e-5
allele num: 68411
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000346845
  ensembl transcript: ENST00000354791
  gene symbol: GPR64
  hgvsc: ENST00000354791.3:c.500+24T>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350152
  ensembl transcript: ENST00000357544
  gene symbol: GPR64
  hgvsc: ENST00000357544.3:c.458+24T>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369202
  ensembl transcript: ENST00000379873
  gene symbol: GPR64
  hgvsc: ENST00000379873.2:c.548+24T>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350680
  ensembl transcript: ENST00000357991
  gene symbol: GPR64
  hgvsc: ENST00000357991.3:c.539+24T>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369205
  ensembl transcript: ENST00000379876
  gene symbol: GPR64
  hgvsc: ENST00000379876.1:c.476+24T>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369207
  ensembl transcript: ENST00000379878
  gene symbol: GPR64
  hgvsc: ENST00000379878.3:c.500+24T>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000353421
  ensembl transcript: ENST00000360279
  gene symbol: GPR64
  hgvsc: ENST00000360279.4:c.482+24T>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl transcript: ENST00000479496
  gene symbol: GPR64
  hgvsc: ENST00000479496.1:n.5595+24T>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369198
  ensembl transcript: ENST00000379869
  gene symbol: GPR64
  hgvsc: ENST00000379869.3:c.548+24T>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000349015
  ensembl transcript: ENST00000356606
  gene symbol: GPR64
  hgvsc: ENST00000356606.4:c.506+24T>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000344972
  ensembl transcript: ENST00000340581
  gene symbol: GPR64
  hgvsc: ENST00000340581.3:c.458+24T>C
  variant of: http://identifiers.org/hgnc/4516
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1676
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14928
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5541
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21691
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8549
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1370
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2761
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1395
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1127
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: DP

X-19041511-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24019041511
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24019041511
    reference: chr 0
allele count: 1
allele frequency: 1.455159267181793e-5
allele num: 68721
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000353421
  ensembl transcript: ENST00000360279
  gene symbol: GPR64
  hgvsc: ENST00000360279.4:c.482+23A>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000349015
  ensembl transcript: ENST00000356606
  gene symbol: GPR64
  hgvsc: ENST00000356606.4:c.506+23A>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl transcript: ENST00000479496
  gene symbol: GPR64
  hgvsc: ENST00000479496.1:n.5595+23A>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350680
  ensembl transcript: ENST00000357991
  gene symbol: GPR64
  hgvsc: ENST00000357991.3:c.539+23A>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000344972
  ensembl transcript: ENST00000340581
  gene symbol: GPR64
  hgvsc: ENST00000340581.3:c.458+23A>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369207
  ensembl transcript: ENST00000379878
  gene symbol: GPR64
  hgvsc: ENST00000379878.3:c.500+23A>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000346845
  ensembl transcript: ENST00000354791
  gene symbol: GPR64
  hgvsc: ENST00000354791.3:c.500+23A>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369198
  ensembl transcript: ENST00000379869
  gene symbol: GPR64
  hgvsc: ENST00000379869.3:c.548+23A>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350152
  ensembl transcript: ENST00000357544
  gene symbol: GPR64
  hgvsc: ENST00000357544.3:c.458+23A>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369205
  ensembl transcript: ENST00000379876
  gene symbol: GPR64
  hgvsc: ENST00000379876.1:c.476+23A>G
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369202
  ensembl transcript: ENST00000379873
  gene symbol: GPR64
  hgvsc: ENST00000379873.2:c.548+23A>G
  variant of: http://identifiers.org/hgnc/4516
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1576
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22348
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1320
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8118
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1374
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2767
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14812
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5601
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 824
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: FS

X-19041516-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24019041516
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24019041516
    reference: chr 0
allele count: 1
allele frequency: 1.422232335874389e-5
allele num: 70312
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000346845
  ensembl transcript: ENST00000354791
  gene symbol: GPR64
  hgvsc: ENST00000354791.3:c.500+18C>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350680
  ensembl transcript: ENST00000357991
  gene symbol: GPR64
  hgvsc: ENST00000357991.3:c.539+18C>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000349015
  ensembl transcript: ENST00000356606
  gene symbol: GPR64
  hgvsc: ENST00000356606.4:c.506+18C>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000344972
  ensembl transcript: ENST00000340581
  gene symbol: GPR64
  hgvsc: ENST00000340581.3:c.458+18C>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350152
  ensembl transcript: ENST00000357544
  gene symbol: GPR64
  hgvsc: ENST00000357544.3:c.458+18C>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369198
  ensembl transcript: ENST00000379869
  gene symbol: GPR64
  hgvsc: ENST00000379869.3:c.548+18C>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369202
  ensembl transcript: ENST00000379873
  gene symbol: GPR64
  hgvsc: ENST00000379873.2:c.548+18C>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl transcript: ENST00000479496
  gene symbol: GPR64
  hgvsc: ENST00000479496.1:n.5595+18C>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369205
  ensembl transcript: ENST00000379876
  gene symbol: GPR64
  hgvsc: ENST00000379876.1:c.476+18C>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369207
  ensembl transcript: ENST00000379878
  gene symbol: GPR64
  hgvsc: ENST00000379878.3:c.500+18C>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000353421
  ensembl transcript: ENST00000360279
  gene symbol: GPR64
  hgvsc: ENST00000360279.4:c.482+18C>T
  variant of: http://identifiers.org/hgnc/4516
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13976
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2894
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1110
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1190
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6626
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6035
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1393
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24715
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

X-19041525-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24019041525
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24019041525
    reference: chr 0
allele count: 2
allele frequency: 2.707642320449469e-5
allele num: 73865
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369205
  ensembl transcript: ENST00000379876
  gene symbol: GPR64
  hgvsc: ENST00000379876.1:c.476+9T>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000353421
  ensembl transcript: ENST00000360279
  gene symbol: GPR64
  hgvsc: ENST00000360279.4:c.482+9T>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000346845
  ensembl transcript: ENST00000354791
  gene symbol: GPR64
  hgvsc: ENST00000354791.3:c.500+9T>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369207
  ensembl transcript: ENST00000379878
  gene symbol: GPR64
  hgvsc: ENST00000379878.3:c.500+9T>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350152
  ensembl transcript: ENST00000357544
  gene symbol: GPR64
  hgvsc: ENST00000357544.3:c.458+9T>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000349015
  ensembl transcript: ENST00000356606
  gene symbol: GPR64
  hgvsc: ENST00000356606.4:c.506+9T>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350680
  ensembl transcript: ENST00000357991
  gene symbol: GPR64
  hgvsc: ENST00000357991.3:c.539+9T>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl transcript: ENST00000479496
  gene symbol: GPR64
  hgvsc: ENST00000479496.1:n.5595+9T>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000344972
  ensembl transcript: ENST00000340581
  gene symbol: GPR64
  hgvsc: ENST00000340581.3:c.458+9T>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369202
  ensembl transcript: ENST00000379873
  gene symbol: GPR64
  hgvsc: ENST00000379873.2:c.548+9T>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369198
  ensembl transcript: ENST00000379869
  gene symbol: GPR64
  hgvsc: ENST00000379869.3:c.548+9T>C
  variant of: http://identifiers.org/hgnc/4516
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29864
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3022
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11607
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6570
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1403
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4124
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 716
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum

X-19041527-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24019041527
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24019041527
    reference: chr 0
allele count: 76
allele frequency: 1.019641515509284e-3
allele num: 74536
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350680
  ensembl transcript: ENST00000357991
  gene symbol: GPR64
  hgvsc: ENST00000357991.3:c.539+7C>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369202
  ensembl transcript: ENST00000379873
  gene symbol: GPR64
  hgvsc: ENST00000379873.2:c.548+7C>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000344972
  ensembl transcript: ENST00000340581
  gene symbol: GPR64
  hgvsc: ENST00000340581.3:c.458+7C>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl transcript: ENST00000479496
  gene symbol: GPR64
  hgvsc: ENST00000479496.1:n.5595+7C>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369198
  ensembl transcript: ENST00000379869
  gene symbol: GPR64
  hgvsc: ENST00000379869.3:c.548+7C>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369205
  ensembl transcript: ENST00000379876
  gene symbol: GPR64
  hgvsc: ENST00000379876.1:c.476+7C>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000346845
  ensembl transcript: ENST00000354791
  gene symbol: GPR64
  hgvsc: ENST00000354791.3:c.500+7C>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350152
  ensembl transcript: ENST00000357544
  gene symbol: GPR64
  hgvsc: ENST00000357544.3:c.458+7C>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000349015
  ensembl transcript: ENST00000356606
  gene symbol: GPR64
  hgvsc: ENST00000356606.4:c.506+7C>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000353421
  ensembl transcript: ENST00000360279
  gene symbol: GPR64
  hgvsc: ENST00000360279.4:c.482+7C>T
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369207
  ensembl transcript: ENST00000379878
  gene symbol: GPR64
  hgvsc: ENST00000379878.3:c.500+7C>T
  variant of: http://identifiers.org/hgnc/4516
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 5.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 11058
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1408
  bin: 3.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 30575
  bin: 2.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 6725
  bin: 2.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 3768
  bin: 1.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 1.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3083
  bin: 3.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: c.548+7C>T
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

X-19041530-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24019041530
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24019041530
    reference: chr 0
allele count: 2
allele frequency: 2.646377770426728e-5
allele num: 75575
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000346845
  ensembl transcript: ENST00000354791
  gene symbol: GPR64
  hgvsc: ENST00000354791.3:c.500+4A>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000353421
  ensembl transcript: ENST00000360279
  gene symbol: GPR64
  hgvsc: ENST00000360279.4:c.482+4A>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000349015
  ensembl transcript: ENST00000356606
  gene symbol: GPR64
  hgvsc: ENST00000356606.4:c.506+4A>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369207
  ensembl transcript: ENST00000379878
  gene symbol: GPR64
  hgvsc: ENST00000379878.3:c.500+4A>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369198
  ensembl transcript: ENST00000379869
  gene symbol: GPR64
  hgvsc: ENST00000379869.3:c.548+4A>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl transcript: ENST00000479496
  gene symbol: GPR64
  hgvsc: ENST00000479496.1:n.5595+4A>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350680
  ensembl transcript: ENST00000357991
  gene symbol: GPR64
  hgvsc: ENST00000357991.3:c.539+4A>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000344972
  ensembl transcript: ENST00000340581
  gene symbol: GPR64
  hgvsc: ENST00000340581.3:c.458+4A>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369202
  ensembl transcript: ENST00000379873
  gene symbol: GPR64
  hgvsc: ENST00000379873.2:c.548+4A>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369205
  ensembl transcript: ENST00000379876
  gene symbol: GPR64
  hgvsc: ENST00000379876.1:c.476+4A>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350152
  ensembl transcript: ENST00000357544
  gene symbol: GPR64
  hgvsc: ENST00000357544.3:c.458+4A>C
  variant of: http://identifiers.org/hgnc/4516
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6898
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3369
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10276
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31672
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1407
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3101
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.548+4A>C
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff

X-19041548-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24019041548
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24019041548
    reference: chr 0
allele count: 1
allele frequency: 1.268182567562426e-5
allele num: 78853
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350680
  ensembl transcript: ENST00000357991
  gene symbol: GPR64
  hgvsc: ENST00000357991.3:c.525A>C
  hgvsp: ENST00000357991.3:c.525A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369198
  ensembl transcript: ENST00000379869
  gene symbol: GPR64
  hgvsc: ENST00000379869.3:c.534A>C
  hgvsp: ENST00000379869.3:c.534A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000344972
  ensembl transcript: ENST00000340581
  gene symbol: GPR64
  hgvsc: ENST00000340581.3:c.444A>C
  hgvsp: ENST00000340581.3:c.444A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000349015
  ensembl transcript: ENST00000356606
  gene symbol: GPR64
  hgvsc: ENST00000356606.4:c.492A>C
  hgvsp: ENST00000356606.4:c.492A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000353421
  ensembl transcript: ENST00000360279
  gene symbol: GPR64
  hgvsc: ENST00000360279.4:c.468A>C
  hgvsp: ENST00000360279.4:c.468A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369207
  ensembl transcript: ENST00000379878
  gene symbol: GPR64
  hgvsc: ENST00000379878.3:c.486A>C
  hgvsp: ENST00000379878.3:c.486A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350152
  ensembl transcript: ENST00000357544
  gene symbol: GPR64
  hgvsc: ENST00000357544.3:c.444A>C
  hgvsp: ENST00000357544.3:c.444A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369202
  ensembl transcript: ENST00000379873
  gene symbol: GPR64
  hgvsc: ENST00000379873.2:c.534A>C
  hgvsp: ENST00000379873.2:c.534A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369205
  ensembl transcript: ENST00000379876
  gene symbol: GPR64
  hgvsc: ENST00000379876.1:c.462A>C
  hgvsp: ENST00000379876.1:c.462A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000346845
  ensembl transcript: ENST00000354791
  gene symbol: GPR64
  hgvsc: ENST00000354791.3:c.486A>C
  hgvsp: ENST00000354791.3:c.486A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173698
  ensembl transcript: ENST00000479496
  gene symbol: GPR64
  hgvsc: ENST00000479496.1:n.5581A>C
  variant of: http://identifiers.org/hgnc/4516
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7528
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3226
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33521
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2968
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1415
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7854
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr178Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: South Asian
population: African
reference allele: T
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQ

X-19041549-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24019041549
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24019041549
    reference: chr 0
allele count: 52
allele frequency: 6.589117818495147e-4
allele num: 78918
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000346845
  ensembl transcript: ENST00000354791
  gene symbol: GPR64
  hgvsc: ENST00000354791.3:c.485C>A
  hgvsp: ENSP00000346845.3:p.Thr162Lys
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369207
  ensembl transcript: ENST00000379878
  gene symbol: GPR64
  hgvsc: ENST00000379878.3:c.485C>A
  hgvsp: ENSP00000369207.3:p.Thr162Lys
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369202
  ensembl transcript: ENST00000379873
  gene symbol: GPR64
  hgvsc: ENST00000379873.2:c.533C>A
  hgvsp: ENSP00000369202.2:p.Thr178Lys
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369198
  ensembl transcript: ENST00000379869
  gene symbol: GPR64
  hgvsc: ENST00000379869.3:c.533C>A
  hgvsp: ENSP00000369198.3:p.Thr178Lys
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173698
  ensembl transcript: ENST00000479496
  gene symbol: GPR64
  hgvsc: ENST00000479496.1:n.5580C>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350152
  ensembl transcript: ENST00000357544
  gene symbol: GPR64
  hgvsc: ENST00000357544.3:c.443C>A
  hgvsp: ENSP00000350152.3:p.Thr148Lys
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000353421
  ensembl transcript: ENST00000360279
  gene symbol: GPR64
  hgvsc: ENST00000360279.4:c.467C>A
  hgvsp: ENSP00000353421.4:p.Thr156Lys
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000349015
  ensembl transcript: ENST00000356606
  gene symbol: GPR64
  hgvsc: ENST00000356606.4:c.491C>A
  hgvsp: ENSP00000349015.4:p.Thr164Lys
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369205
  ensembl transcript: ENST00000379876
  gene symbol: GPR64
  hgvsc: ENST00000379876.1:c.461C>A
  hgvsp: ENSP00000369205.1:p.Thr154Lys
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000344972
  ensembl transcript: ENST00000340581
  gene symbol: GPR64
  hgvsc: ENST00000340581.3:c.443C>A
  hgvsp: ENSP00000344972.3:p.Thr148Lys
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350680
  ensembl transcript: ENST00000357991
  gene symbol: GPR64
  hgvsc: ENST00000357991.3:c.524C>A
  hgvsp: ENSP00000350680.3:p.Thr175Lys
  variant of: http://identifiers.org/hgnc/4516
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7940
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 7425
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1433
  bin: 3.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 3284
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3029
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 33315
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr178Lys
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: Other
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

X-19041551-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24019041551
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24019041551
    reference: chr 0
allele count: 52
allele frequency: 6.578115117014548e-4
allele num: 79050
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173698
  ensembl transcript: ENST00000479496
  gene symbol: GPR64
  hgvsc: ENST00000479496.1:n.5578T>C
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350680
  ensembl transcript: ENST00000357991
  gene symbol: GPR64
  hgvsc: ENST00000357991.3:c.522T>C
  hgvsp: ENST00000357991.3:c.522T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369202
  ensembl transcript: ENST00000379873
  gene symbol: GPR64
  hgvsc: ENST00000379873.2:c.531T>C
  hgvsp: ENST00000379873.2:c.531T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000346845
  ensembl transcript: ENST00000354791
  gene symbol: GPR64
  hgvsc: ENST00000354791.3:c.483T>C
  hgvsp: ENST00000354791.3:c.483T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000344972
  ensembl transcript: ENST00000340581
  gene symbol: GPR64
  hgvsc: ENST00000340581.3:c.441T>C
  hgvsp: ENST00000340581.3:c.441T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000349015
  ensembl transcript: ENST00000356606
  gene symbol: GPR64
  hgvsc: ENST00000356606.4:c.489T>C
  hgvsp: ENST00000356606.4:c.489T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350152
  ensembl transcript: ENST00000357544
  gene symbol: GPR64
  hgvsc: ENST00000357544.3:c.441T>C
  hgvsp: ENST00000357544.3:c.441T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369198
  ensembl transcript: ENST00000379869
  gene symbol: GPR64
  hgvsc: ENST00000379869.3:c.531T>C
  hgvsp: ENST00000379869.3:c.531T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000353421
  ensembl transcript: ENST00000360279
  gene symbol: GPR64
  hgvsc: ENST00000360279.4:c.465T>C
  hgvsp: ENST00000360279.4:c.465T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369205
  ensembl transcript: ENST00000379876
  gene symbol: GPR64
  hgvsc: ENST00000379876.1:c.459T>C
  hgvsp: ENST00000379876.1:c.459T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369207
  ensembl transcript: ENST00000379878
  gene symbol: GPR64
  hgvsc: ENST00000379878.3:c.483T>C
  hgvsp: ENST00000379878.3:c.483T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4516
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 5.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1423
  bin: 3.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 3226
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 32960
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3244
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8012
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7333
  bin: 7.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Ala177Ala
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: A
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD

X-19041557-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24019041557
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24019041557
    reference: chr 0
allele count: 1
allele frequency: 1.260875047282814e-5
allele num: 79310
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000349015
  ensembl transcript: ENST00000356606
  gene symbol: GPR64
  hgvsc: ENST00000356606.4:c.483G>A
  hgvsp: ENSP00000349015.4:p.Met161Ile
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350680
  ensembl transcript: ENST00000357991
  gene symbol: GPR64
  hgvsc: ENST00000357991.3:c.516G>A
  hgvsp: ENSP00000350680.3:p.Met172Ile
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000346845
  ensembl transcript: ENST00000354791
  gene symbol: GPR64
  hgvsc: ENST00000354791.3:c.477G>A
  hgvsp: ENSP00000346845.3:p.Met159Ile
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000350152
  ensembl transcript: ENST00000357544
  gene symbol: GPR64
  hgvsc: ENST00000357544.3:c.435G>A
  hgvsp: ENSP00000350152.3:p.Met145Ile
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000344972
  ensembl transcript: ENST00000340581
  gene symbol: GPR64
  hgvsc: ENST00000340581.3:c.435G>A
  hgvsp: ENSP00000344972.3:p.Met145Ile
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173698
  ensembl transcript: ENST00000479496
  gene symbol: GPR64
  hgvsc: ENST00000479496.1:n.5572G>A
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369198
  ensembl transcript: ENST00000379869
  gene symbol: GPR64
  hgvsc: ENST00000379869.3:c.525G>A
  hgvsp: ENSP00000369198.3:p.Met175Ile
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369207
  ensembl transcript: ENST00000379878
  gene symbol: GPR64
  hgvsc: ENST00000379878.3:c.477G>A
  hgvsp: ENSP00000369207.3:p.Met159Ile
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000353421
  ensembl transcript: ENST00000360279
  gene symbol: GPR64
  hgvsc: ENST00000360279.4:c.459G>A
  hgvsp: ENSP00000353421.4:p.Met153Ile
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369205
  ensembl transcript: ENST00000379876
  gene symbol: GPR64
  hgvsc: ENST00000379876.1:c.453G>A
  hgvsp: ENSP00000369205.1:p.Met151Ile
  variant of: http://identifiers.org/hgnc/4516
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173698
  ensembl protein: ENSP00000369202
  ensembl transcript: ENST00000379873
  gene symbol: GPR64
  hgvsc: ENST00000379873.2:c.525G>A
  hgvsp: ENSP00000369202.2:p.Met175Ile
  variant of: http://identifiers.org/hgnc/4516
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31954
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1779
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3708
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8257
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7035
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3289
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Met175Ile
num of homozygotes: 0
reference allele: C

GenotypeQuality
all individuals: 1711
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 289
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 24495
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 536
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 251
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 457
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 289
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 612
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1987
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 689
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 298
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21095
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2028
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 865
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 315
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3412
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 551
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6083
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3540
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 38188
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 477
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7181
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7490
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5346
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.51e-1

QD
type: SiteQuality
SIO_000300: 2.152e1

VQSLOD
type: SiteQuality
SIO_000300: -1.171e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.9e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -7.51e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.51e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.51e-1

MQ
type: SiteQuality
SIO_000300: 5.811e1

DP
type: SiteQuality
SIO_000300: 1.079757e6

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 278
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 256
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 3414
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 256
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 262
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 477
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 358
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1946
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 24798
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 845
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 687
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 270
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 566
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 553
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21572
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1718
bin: 3.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.869158878504673e-4
allele num: 5350
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6138
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3553
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7191
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 38258
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7508
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.9e-3

VQSLOD
type: SiteQuality
SIO_000300: 9.77e-1

DP
type: SiteQuality
SIO_000300: 1.07768e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 2.496e1

GenotypeQuality
all individuals: 2268
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 912
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 460
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2759
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16961
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 271
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3477
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1824
bin: 3.25e1
variant carriers: 2

GenotypeQuality
all individuals: 190
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 442
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 808
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 551
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 335
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 329
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27796
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 559
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 214
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6778
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 439
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3300
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 5.620345651257552e-5
allele num: 35585
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6889
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4935
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5343
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 9.72988e5

MQRankSum
type: SiteQuality
SIO_000300: 6.909999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.769e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.678e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.28e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.68e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.8e-3

QD
type: SiteQuality
SIO_000300: 2.522e1

GenotypeQuality
all individuals: 1801
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2315
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 277
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 843
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 235
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29196
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 552
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 918
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 193
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2332
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4450
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 525
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14980
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 360
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 386
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 472
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 34066
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3142
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4899
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 424
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6539
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.516070345664039e-4
allele num: 6596
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4762
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.87e0

MQRankSum
type: SiteQuality
SIO_000300: -4.86e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.02e-2

VQSLOD
type: SiteQuality
SIO_000300: 9.25e-1

DP
type: SiteQuality
SIO_000300: 9.18727e5

BaseQRankSum
type: SiteQuality
SIO_000300: -1.686e0

MQ
type: SiteQuality
SIO_000300: 5.915e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.38e-1

QD
type: SiteQuality
SIO_000300: 1.068e1

GenotypeQuality
all individuals: 372
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30259
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1804
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 566
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 218
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1070
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 550
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 904
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8845
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 239
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8384
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1078
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2652
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2178
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 263
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 227
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 475
bin: 5.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4053
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2653
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5483
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5916
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 2.707825616030328e-4
allele num: 3693
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 355
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 29349
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.65e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.73e-2

DP
type: SiteQuality
SIO_000300: 7.44985e5

QD
type: SiteQuality
SIO_000300: 2.44e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 152
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 230
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7167
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10530
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 909
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 205
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 508
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1479
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2773
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 549
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 205
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 202
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2337
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 80
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 234
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3370
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5702
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2527
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.554670837480449e-5
allele num: 28132
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3897
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5250
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 344
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -5.760999999999999e-1

DP
type: SiteQuality
SIO_000300: 6.97836e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.91e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 3.169e1

GenotypeQuality
all individuals: 1007
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 491
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 3043
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 15013
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2488
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3000
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 3589
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2165
bin: 1.75e1
variant carriers: 3

GenotypeQuality
all individuals: 25820
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 165
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 557
bin: 9.75e1
variant carriers: 11

African
type: Population
allele count: 14
allele frequency: 2.684049079754601e-3
allele num: 5216
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 25016
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2179
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 294
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3440
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4497
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2671
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.798e0

DP
type: SiteQuality
SIO_000300: 5.98644e5

ClippingRankSum
type: SiteQuality
SIO_000300: -3.46e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.46e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.49e-2

FS
type: SiteQuality
SIO_000300: 1.46e0

VQSLOD
type: SiteQuality
SIO_000300: 2.76e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.09e-1

MQ
type: SiteQuality
SIO_000300: 5.939e1

QD
type: SiteQuality
SIO_000300: 1.283e1

GenotypeQuality
all individuals: 4535
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2991
bin: 2.75e1
variant carriers: 3

GenotypeQuality
all individuals: 147
bin: 7.25e1
variant carriers: 2

GenotypeQuality
all individuals: 1636
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 568
bin: 9.75e1
variant carriers: 25

GenotypeQuality
all individuals: 48
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3110
bin: 1.75e1
variant carriers: 11

GenotypeQuality
all individuals: 1699
bin: 3.75e1
variant carriers: 2

GenotypeQuality
all individuals: 19984
bin: 2.25e1
variant carriers: 6

GenotypeQuality
all individuals: 79
bin: 8.75e1
variant carriers: 2

GenotypeQuality
all individuals: 97
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 330
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17844
bin: 7.5e0
variant carriers: 5

GenotypeQuality
all individuals: 1698
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1833
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2124
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 33
allele frequency: 1.523123788424259e-3
allele num: 21666
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 2.164970772894566e-4
allele num: 4619
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2906
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3695
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 5.28844e5

VQSLOD
type: SiteQuality
SIO_000300: 3.77e0

QD
type: SiteQuality
SIO_000300: 1.879e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.31e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.65e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.500000000000001e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.89e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 452
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 418
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3334
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19199
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 310
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1890
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1517
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4809
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 544
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18011
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3239
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 118
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 21256
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3556
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 233
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2853
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1786
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4508
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2046
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.59e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.403e-1

FS
type: SiteQuality
SIO_000300: 3.08e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.298e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.84e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.71e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.12e-1

QD
type: SiteQuality
SIO_000300: 1.188e1

DP
type: SiteQuality
SIO_000300: 5.22022e5

GenotypeQuality
all individuals: 79
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1834
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 574
bin: 4.25e1
variant carriers: 4

GenotypeQuality
all individuals: 135
bin: 7.25e1
variant carriers: 2

GenotypeQuality
all individuals: 11367
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 8340
bin: 1.75e1
variant carriers: 3

GenotypeQuality
all individuals: 3696
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 738
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6853
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 95
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 554
bin: 9.75e1
variant carriers: 12

GenotypeQuality
all individuals: 403
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 531
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1576
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 17544
num of homozygotes: 0

African
type: Population
allele count: 11
allele frequency: 2.883355176933158e-3
allele num: 3815
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 206
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2622
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1428
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2231
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.98e-1

FS
type: SiteQuality
SIO_000300: 6.16e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.73e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.3e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.61e-1

DP
type: SiteQuality
SIO_000300: 4.83131e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.72e-2

QD
type: SiteQuality
SIO_000300: 1.23e1

VQSLOD
type: SiteQuality
SIO_000300: 2.51e0

GenotypeQuality
all individuals: 443
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2801
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10191
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4225
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 745
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1836
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3252
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16332
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 139
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 239
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 429
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 542
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 17166
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3731
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1379
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 205
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1545
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2160
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2543
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 4.83418e5

VQSLOD
type: SiteQuality
SIO_000300: 4.54e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.221e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.06e-2

GenotypeQuality
all individuals: 976
bin: 8.75e1
variant carriers: 25

GenotypeQuality
all individuals: 1859
bin: 6.25e1
variant carriers: 156

GenotypeQuality
all individuals: 2573
bin: 3.75e1
variant carriers: 534

GenotypeQuality
all individuals: 2137
bin: 5.75e1
variant carriers: 224

GenotypeQuality
all individuals: 17039
bin: 2.5e0
variant carriers: 536

GenotypeQuality
all individuals: 1168
bin: 8.25e1
variant carriers: 64

GenotypeQuality
all individuals: 1498
bin: 7.25e1
variant carriers: 91

GenotypeQuality
all individuals: 4981
bin: 9.75e1
variant carriers: 136

GenotypeQuality
all individuals: 2488
bin: 3.25e1
variant carriers: 527

GenotypeQuality
all individuals: 2375
bin: 5.25e1
variant carriers: 283

GenotypeQuality
all individuals: 2707
bin: 2.25e1
variant carriers: 641

GenotypeQuality
all individuals: 2447
bin: 4.75e1
variant carriers: 292

GenotypeQuality
all individuals: 2411
bin: 1.75e1
variant carriers: 427

GenotypeQuality
all individuals: 2751
bin: 1.25e1
variant carriers: 520

GenotypeQuality
all individuals: 2691
bin: 4.25e1
variant carriers: 486

GenotypeQuality
all individuals: 846
bin: 9.25e1
variant carriers: 23

African
type: Population
allele count: 391
allele frequency: 8.52037480932665e-2
allele num: 4589
num of homozygotes: 1

European (Finnish)
type: Population
allele count: 66
allele frequency: 2.332155477031802e-2
allele num: 2830
num of homozygotes: 0

Other
type: Population
allele count: 15
allele frequency: 4.658385093167702e-2
allele num: 322
num of homozygotes: 0

Latino
type: Population
allele count: 255
allele frequency: 4.855293221629856e-2
allele num: 5252
num of homozygotes: 0

East Asian
type: Population
allele count: 201
allele frequency: 5.218068535825545e-2
allele num: 3852
num of homozygotes: 0

South Asian
type: Population
allele count: 196
allele frequency: 5.710955710955711e-2
allele num: 3432
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1079
allele frequency: 4.05395250976856e-2
allele num: 26616
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.41e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.12e-1

QD
type: SiteQuality
SIO_000300: 3.33e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.78e-1

DP
type: SiteQuality
SIO_000300: 1.085837e6

VQSLOD
type: SiteQuality
SIO_000300: 9.07e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.8e-2

FS
type: SiteQuality
SIO_000300: 4.006e0

MQ
type: SiteQuality
SIO_000300: 5.833e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.49e-1

GenotypeQuality
all individuals: 2573
bin: 3.75e1
variant carriers: 41

GenotypeQuality
all individuals: 1859
bin: 6.25e1
variant carriers: 23

GenotypeQuality
all individuals: 2707
bin: 2.25e1
variant carriers: 59

GenotypeQuality
all individuals: 2488
bin: 3.25e1
variant carriers: 37

GenotypeQuality
all individuals: 2411
bin: 1.75e1
variant carriers: 35

GenotypeQuality
all individuals: 2751
bin: 1.25e1
variant carriers: 42

GenotypeQuality
all individuals: 3123
bin: 7.5e0
variant carriers: 59

GenotypeQuality
all individuals: 1801
bin: 6.75e1
variant carriers: 16

GenotypeQuality
all individuals: 17039
bin: 2.5e0
variant carriers: 53

GenotypeQuality
all individuals: 1324
bin: 7.75e1
variant carriers: 19

GenotypeQuality
all individuals: 2137
bin: 5.75e1
variant carriers: 38

GenotypeQuality
all individuals: 1168
bin: 8.25e1
variant carriers: 6

GenotypeQuality
all individuals: 2691
bin: 4.25e1
variant carriers: 46

GenotypeQuality
all individuals: 2447
bin: 4.75e1
variant carriers: 44

GenotypeQuality
all individuals: 2338
bin: 2.75e1
variant carriers: 46

GenotypeQuality
all individuals: 846
bin: 9.25e1
variant carriers: 3

East Asian
type: Population
allele count: 19
allele frequency: 4.932502596053998e-3
allele num: 3852
num of homozygotes: 0

African
type: Population
allele count: 54
allele frequency: 1.176726955763783e-2
allele num: 4589
num of homozygotes: 0

Latino
type: Population
allele count: 32
allele frequency: 6.092916984006093e-3
allele num: 5252
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 97
allele frequency: 3.644424406372107e-3
allele num: 26616
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 3.105590062111801e-3
allele num: 322
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 7
allele frequency: 2.473498233215548e-3
allele num: 2830
num of homozygotes: 0

South Asian
type: Population
allele count: 20
allele frequency: 5.827505827505828e-3
allele num: 3432
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.12e-1

QD
type: SiteQuality
SIO_000300: 3.33e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.8e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.41e-2

DP
type: SiteQuality
SIO_000300: 1.085837e6

FS
type: SiteQuality
SIO_000300: 4.006e0

MQ
type: SiteQuality
SIO_000300: 5.833e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.78e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.07e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.49e-1

GenotypeQuality
all individuals: 1498
bin: 7.25e1
variant carriers: 5

GenotypeQuality
all individuals: 1168
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2411
bin: 1.75e1
variant carriers: 7

GenotypeQuality
all individuals: 3123
bin: 7.5e0
variant carriers: 9

GenotypeQuality
all individuals: 4981
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 1801
bin: 6.75e1
variant carriers: 4

GenotypeQuality
all individuals: 2338
bin: 2.75e1
variant carriers: 4

GenotypeQuality
all individuals: 2751
bin: 1.25e1
variant carriers: 7

GenotypeQuality
all individuals: 2707
bin: 2.25e1
variant carriers: 3

GenotypeQuality
all individuals: 2573
bin: 3.75e1
variant carriers: 3

GenotypeQuality
all individuals: 2488
bin: 3.25e1
variant carriers: 5

GenotypeQuality
all individuals: 2691
bin: 4.25e1
variant carriers: 5

GenotypeQuality
all individuals: 846
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2137
bin: 5.75e1
variant carriers: 4

GenotypeQuality
all individuals: 2375
bin: 5.25e1
variant carriers: 4

GenotypeQuality
all individuals: 976
bin: 8.75e1
variant carriers: 2

European (Finnish)
type: Population
allele count: 1
allele frequency: 3.533568904593639e-4
allele num: 2830
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 10
allele frequency: 3.757138563270213e-4
allele num: 26616
num of homozygotes: 0

Latino
type: Population
allele count: 5
allele frequency: 9.52018278750952e-4
allele num: 5252
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 4.358247984310307e-4
allele num: 4589
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 2.596053997923157e-4
allele num: 3852
num of homozygotes: 0

South Asian
type: Population
allele count: 5
allele frequency: 1.456876456876457e-3
allele num: 3432
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 322
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FS
type: SiteQuality
SIO_000300: 4.006e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.49e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.12e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.8e-2

DP
type: SiteQuality
SIO_000300: 1.085837e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.41e-2

VQSLOD
type: SiteQuality
SIO_000300: 9.07e-1

QD
type: SiteQuality
SIO_000300: 3.33e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.78e-1

MQ
type: SiteQuality
SIO_000300: 5.833e1

GenotypeQuality
all individuals: 2338
bin: 2.75e1
variant carriers: 1510

GenotypeQuality
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bin: 5.25e1
variant carriers: 1772

GenotypeQuality
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bin: 1.75e1
variant carriers: 1491

GenotypeQuality
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bin: 3.75e1
variant carriers: 1735

GenotypeQuality
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variant carriers: 1878

GenotypeQuality
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variant carriers: 1557

GenotypeQuality
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bin: 6.25e1
variant carriers: 1393

GenotypeQuality
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variant carriers: 1633

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 9.75e1
variant carriers: 3274

GenotypeQuality
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bin: 7.5e0
variant carriers: 1777

GenotypeQuality
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bin: 9.25e1
variant carriers: 549

GenotypeQuality
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variant carriers: 1277

GenotypeQuality
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variant carriers: 649

GenotypeQuality
all individuals: 2691
bin: 4.25e1
variant carriers: 2064

GenotypeQuality
all individuals: 1498
bin: 7.25e1
variant carriers: 1021

Other
type: Population
allele count: 101
allele frequency: 3.136645962732919e-1
allele num: 322
num of homozygotes: 0

African
type: Population
allele count: 1526
allele frequency: 3.325343212028765e-1
allele num: 4589
num of homozygotes: 0

Latino
type: Population
allele count: 1817
allele frequency: 3.45963442498096e-1
allele num: 5252
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1006
allele frequency: 3.554770318021201e-1
allele num: 2830
num of homozygotes: 0

South Asian
type: Population
allele count: 982
allele frequency: 2.861305361305361e-1
allele num: 3432
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 8882
allele frequency: 3.337090471896604e-1
allele num: 26616
num of homozygotes: 0

East Asian
type: Population
allele count: 1196
allele frequency: 3.104880581516096e-1
allele num: 3852
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.8e-2

FS
type: SiteQuality
SIO_000300: 4.006e0

MQRankSum
type: SiteQuality
SIO_000300: 1.12e-1

ClippingRankSum
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SIO_000300: -8.49e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.41e-2

QD
type: SiteQuality
SIO_000300: 3.33e0

MQ
type: SiteQuality
SIO_000300: 5.833e1

VQSLOD
type: SiteQuality
SIO_000300: 9.07e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.78e-1

DP
type: SiteQuality
SIO_000300: 1.085837e6

GenotypeQuality
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bin: 1.25e1
variant carriers: 859

GenotypeQuality
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bin: 1.75e1
variant carriers: 768

GenotypeQuality
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bin: 7.25e1
variant carriers: 404

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 253

GenotypeQuality
all individuals: 3123
bin: 7.5e0
variant carriers: 968

Latino
type: Population
allele count: 563
allele frequency: 1.071972581873572e-1
allele num: 5252
num of homozygotes: 0

East Asian
type: Population
allele count: 474
allele frequency: 1.230529595015576e-1
allele num: 3852
num of homozygotes: 0

Other
type: Population
allele count: 29
allele frequency: 9.006211180124224e-2
allele num: 322
num of homozygotes: 0

African
type: Population
allele count: 396
allele frequency: 8.629331008934409e-2
allele num: 4589
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 237
allele frequency: 8.374558303886925e-2
allele num: 2830
num of homozygotes: 0

South Asian
type: Population
allele count: 297
allele frequency: 8.653846153846154e-2
allele num: 3432
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2475
allele frequency: 9.298917944093778e-2
allele num: 26616
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.49e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.8e-2

QD
type: SiteQuality
SIO_000300: 3.33e0

VQSLOD
type: SiteQuality
SIO_000300: 9.07e-1

FS
type: SiteQuality
SIO_000300: 4.006e0

MQ
type: SiteQuality
SIO_000300: 5.833e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.41e-2

DP
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SIO_000300: 1.085837e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.78e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.12e-1

Other
type: Population
allele count: 2
allele frequency: 6.211180124223602e-3
allele num: 322
num of homozygotes: 0

East Asian
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allele count: 43
allele frequency: 1.116303219106957e-2
allele num: 3852
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 11
allele frequency: 3.886925795053004e-3
allele num: 2830
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.8e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.78e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.12e-1

VQSLOD
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SIO_000300: 9.07e-1

FS
type: SiteQuality
SIO_000300: 4.006e0

QD
type: SiteQuality
SIO_000300: 3.33e0

DP
type: SiteQuality
SIO_000300: 1.085837e6

MQ
type: SiteQuality
SIO_000300: 5.833e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.41e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -8.49e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.666666666666667e-1
allele num: 6
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ClippingRankSum
type: SiteQuality
SIO_000300: -4.91e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.23e0

DP
type: SiteQuality
SIO_000300: 3.24396e5

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.129e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.8e-2

MQ
type: SiteQuality
SIO_000300: 5.859e1

QD
type: SiteQuality
SIO_000300: 1.32e1

MQRankSum
type: SiteQuality
SIO_000300: -1.73e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.04e-1

GenotypeQuality
all individuals: 1022
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8870
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4165
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6284
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 573
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7937
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 44838
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.251e0

MQRankSum
type: SiteQuality
SIO_000300: -1.62e-1

MQ
type: SiteQuality
SIO_000300: 5.946e1

FS
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SIO_000300: 0.0e0

VQSLOD
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InbreedingCoeff
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SIO_000300: -1.12e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.353e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.55e-1

DP
type: SiteQuality
SIO_000300: 1.881419e6

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

GenotypeQuality
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variant carriers: 9

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7679
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47332
num of homozygotes: 0

East Asian
type: Population
allele count: 12
allele frequency: 1.824262693827911e-3
allele num: 6578
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4516
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8964
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 605
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DP
type: SiteQuality
SIO_000300: 1.927946e6

ClippingRankSum
type: SiteQuality
SIO_000300: 6.0e-2

ReadPosRankSum
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VQSLOD
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MQRankSum
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InbreedingCoeff
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FS
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MQ
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BaseQRankSum
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QD
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 0.0e0
allele num: 6578
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 605
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9249
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 2.112735570016057e-5
allele num: 47332
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4516
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.52e-2

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4504
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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East Asian
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allele count: 0
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South Asian
type: Population
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allele frequency: 1.062473438164046e-4
allele num: 9412
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Latino
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47664
num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.432e0

FS
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QD
type: SiteQuality
SIO_000300: 2.931e1

MQ
type: SiteQuality
SIO_000300: 5.892e1

VQSLOD
type: SiteQuality
SIO_000300: -7.186e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.48e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.121e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.24e-1

DP
type: SiteQuality
SIO_000300: 1.989926e6

GenotypeDepth
all individuals: 19099
bin: 2.25e1
variant carriers: 40

GenotypeQuality
all individuals: 12
bin: 1.25e1
variant carriers: 3

GenotypeQuality
all individuals: 20
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 3.75e1
variant carriers: 5

GenotypeQuality
all individuals: 81
bin: 4.75e1
variant carriers: 10

GenotypeQuality
all individuals: 34936
bin: 6.25e1
variant carriers: 13

GenotypeQuality
all individuals: 62
bin: 5.75e1
variant carriers: 7

GenotypeQuality
all individuals: 213
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1958
bin: 8.25e1
variant carriers: 9

GenotypeQuality
all individuals: 1171
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 7
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 75
bin: 5.25e1
variant carriers: 9

GenotypeQuality
all individuals: 1324
bin: 9.25e1
variant carriers: 23

GenotypeQuality
all individuals: 10
bin: 2.5e0
variant carriers: 1

GenotypeQuality
all individuals: 2978
bin: 7.75e1
variant carriers: 18

GenotypeQuality
all individuals: 2720
bin: 7.25e1
variant carriers: 11

GenotypeQuality
all individuals: 78
bin: 4.25e1
variant carriers: 7

GenotypeQuality
all individuals: 8048
bin: 6.75e1
variant carriers: 22

GenotypeQuality
all individuals: 259
bin: 3.25e1
variant carriers: 7

GenotypeQuality
all individuals: 5577
bin: 9.75e1
variant carriers: 587

GenotypeQuality
all individuals: 1017
bin: 8.75e1
variant carriers: 22

Other
type: Population
allele count: 4
allele frequency: 6.493506493506494e-3
allele num: 616
num of homozygotes: 0

African
type: Population
allele count: 11
allele frequency: 1.29366106080207e-3
allele num: 8503
num of homozygotes: 0

Latino
type: Population
allele count: 29
allele frequency: 3.121636167922497e-3
allele num: 9290
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 534
allele frequency: 1.11968464312673e-2
allele num: 47692
num of homozygotes: 2

European (Finnish)
type: Population
allele count: 6
allele frequency: 1.325381047051027e-3
allele num: 4527
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.508750754375377e-4
allele num: 6628
num of homozygotes: 0

South Asian
type: Population
allele count: 167
allele frequency: 1.755492483969305e-2
allele num: 9513
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.89e-1

DP
type: SiteQuality
SIO_000300: 2.015036e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.5e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.612e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.08e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.03e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.782e1

MQ
type: SiteQuality
SIO_000300: 5.895e1

QD
type: SiteQuality
SIO_000300: 1.761e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.675e0

GenotypeDepth
all individuals: 581
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1966
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2993
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8211
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36787
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variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
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variant carriers: 0

GenotypeQuality
all individuals: 261
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GenotypeQuality
all individuals: 1322
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variant carriers: 0

GenotypeQuality
all individuals: 29
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variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1002
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5218
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 25
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2750
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47909
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 3.013863773357444e-4
allele num: 6636
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4529
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9991
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 629
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8515
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9313
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.002e0

DP
type: SiteQuality
SIO_000300: 2.017201e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.64e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.43e-1

MQ
type: SiteQuality
SIO_000300: 5.898e1

MQRankSum
type: SiteQuality
SIO_000300: 3.8e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

QD
type: SiteQuality
SIO_000300: 1.147e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.121e0

GenotypeDepth
all individuals: 1910
bin: 5.25e1
variant carriers: 3

GenotypeQuality
all individuals: 998
bin: 8.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1961
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1321
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 36766
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2743
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8202
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 206
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5285
bin: 9.75e1
variant carriers: 91

GenotypeQuality
all individuals: 2990
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6637
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.085766727849157e-5
allele num: 47944
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10058
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4529
num of homozygotes: 0

African
type: Population
allele count: 89
allele frequency: 1.04533709184872e-2
allele num: 8514
num of homozygotes: 2

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 629
num of homozygotes: 0

Latino
type: Population
allele count: 6
allele frequency: 6.441915396177797e-4
allele num: 9314
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.66e-1

MQ
type: SiteQuality
SIO_000300: 5.919e1

QD
type: SiteQuality
SIO_000300: 1.46e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.355e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.477e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.48e-1

DP
type: SiteQuality
SIO_000300: 2.027053e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.9e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.1e-2

GenotypeDepth
all individuals: 244
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36691
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8196
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 997
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variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 270
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
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variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1963
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variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1323
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 2742
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5245
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2995
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 4.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 629
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10045
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.086245384182088e-5
allele num: 47933
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6636
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4529
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8515
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9313
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.43e0

DP
type: SiteQuality
SIO_000300: 2.020069e6

VQSLOD
type: SiteQuality
SIO_000300: -1.281e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.0e-3

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 1.32e0

MQ
type: SiteQuality
SIO_000300: 5.855e1

FS
type: SiteQuality
SIO_000300: 4.968e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.21e-1

QD
type: SiteQuality
SIO_000300: 1.548e1

GenotypeDepth
all individuals: 195
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8144
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 995
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 476
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2985
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36352
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1321
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2733
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5246
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 34
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1957
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47895
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4529
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.073767851390529e-4
allele num: 9313
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8512
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9998
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6632
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 630
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.69e-2

QD
type: SiteQuality
SIO_000300: 1.321e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.32e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.6e-1

FS
type: SiteQuality
SIO_000300: 1.89e0

MQ
type: SiteQuality
SIO_000300: 5.906e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.62e-1

VQSLOD
type: SiteQuality
SIO_000300: -9.5e-3

DP
type: SiteQuality
SIO_000300: 2.01691e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.04e0

GenotypeDepth
all individuals: 842
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1957
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 5.75e1
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GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 23
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variant carriers: 0

GenotypeQuality
all individuals: 34
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variant carriers: 0

GenotypeQuality
all individuals: 2985
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1321
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8144
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 111
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variant carriers: 0

GenotypeQuality
all individuals: 8
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GenotypeQuality
all individuals: 476
bin: 2.25e1
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GenotypeQuality
all individuals: 2
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GenotypeQuality
all individuals: 2733
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36352
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 2.75e1
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GenotypeQuality
all individuals: 71
bin: 5.25e1
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GenotypeQuality
all individuals: 5246
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 995
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9313
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4529
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9998
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6632
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47895
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 630
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.174812030075188e-4
allele num: 8512
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.04e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.62e-1

VQSLOD
type: SiteQuality
SIO_000300: -9.5e-3

MQ
type: SiteQuality
SIO_000300: 5.906e1

FS
type: SiteQuality
SIO_000300: 1.89e0

MQRankSum
type: SiteQuality
SIO_000300: 8.6e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.32e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.69e-2

DP
type: SiteQuality
SIO_000300: 2.01691e6

QD
type: SiteQuality
SIO_000300: 1.321e1

GenotypeDepth
all individuals: 451
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variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 1957
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 121
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variant carriers: 0

GenotypeQuality
all individuals: 8145
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
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GenotypeQuality
all individuals: 84
bin: 3.75e1
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GenotypeQuality
all individuals: 68
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GenotypeQuality
all individuals: 1321
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 513
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 4.25e1
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GenotypeQuality
all individuals: 36282
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2983
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 5245
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 56
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 995
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2726
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6630
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8512
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 630
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4529
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9312
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.176237210273544e-5
allele num: 47890
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9988
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.964e1

MQRankSum
type: SiteQuality
SIO_000300: 1.59e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.69e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.88e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.01e-2

VQSLOD
type: SiteQuality
SIO_000300: -2.219e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.93e-1

FS
type: SiteQuality
SIO_000300: 6.879999999999999e-1

DP
type: SiteQuality
SIO_000300: 2.016368e6

MQ
type: SiteQuality
SIO_000300: 5.912e1

GenotypeDepth
all individuals: 177
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1323
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8017
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1115
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 992
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 269
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1952
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 9
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 402
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5244
bin: 9.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2957
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2702
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 360
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 34819
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 185
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47839
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 3.019779556092405e-4
allele num: 6623
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 629
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9301
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9870
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8505
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4528
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.67e-2

FS
type: SiteQuality
SIO_000300: 4.759e0

MQ
type: SiteQuality
SIO_000300: 5.866e1

MQRankSum
type: SiteQuality
SIO_000300: 2.46e0

DP
type: SiteQuality
SIO_000300: 2.004353e6

QD
type: SiteQuality
SIO_000300: 1.844e1

VQSLOD
type: SiteQuality
SIO_000300: -9.724e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.84e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.982e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.816e0

GenotypeQuality
all individuals: 417
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 305
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 469
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2952
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1249
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1322
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1953
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2703
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5245
bin: 9.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9303
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6625
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9849
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 629
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4528
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.091350175673415e-5
allele num: 47816
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8504
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -7.074e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.79e-2

MQ
type: SiteQuality
SIO_000300: 5.836e1

QD
type: SiteQuality
SIO_000300: 3.217e1

DP
type: SiteQuality
SIO_000300: 2.001421e6

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 275
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 202
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21071
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2862
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 989
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3102
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2564
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2090
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 204
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1923
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3451
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3364
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6721
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 644
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1961
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 926
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5245
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1317
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47406
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.526251526251526e-4
allele num: 6552
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9242
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 617
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9359
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8471
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4514
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.64e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.035e0

FS
type: SiteQuality
SIO_000300: 8.307e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.9e0

MQRankSum
type: SiteQuality
SIO_000300: 5.05e-1

MQ
type: SiteQuality
SIO_000300: 5.897e1

DP
type: SiteQuality
SIO_000300: 1.896288e6

QD
type: SiteQuality
SIO_000300: 1.541e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.63e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.11e0

GenotypeQuality
all individuals: 6721
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 202
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 989
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1666
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1961
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3451
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 275
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2090
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5245
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 21071
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 204
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 926
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1923
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3364
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1317
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 644
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2862
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3102
bin: 2.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 617
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.476606336750622e-4
allele num: 47406
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9242
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6552
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9359
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4514
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8471
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.035e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.64e-2

MQRankSum
type: SiteQuality
SIO_000300: 5.05e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.11e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.63e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.9e0

QD
type: SiteQuality
SIO_000300: 1.541e1

DP
type: SiteQuality
SIO_000300: 1.896288e6

FS
type: SiteQuality
SIO_000300: 8.307e0

MQ
type: SiteQuality
SIO_000300: 5.897e1

GenotypeQuality
all individuals: 991
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3150
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 243
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2551
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 189
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5249
bin: 9.75e1
variant carriers: 9

GenotypeQuality
all individuals: 3367
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1909
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 810
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 379
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1312
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 246
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6661
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1654
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2105
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21394
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3473
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 208
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2844
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9329
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 617
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4511
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.112646300756327e-5
allele num: 47334
num of homozygotes: 0

African
type: Population
allele count: 7
allele frequency: 8.261536645816122e-4
allele num: 8473
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6550
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.083306250677066e-4
allele num: 9231
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.867e1

VQSLOD
type: SiteQuality
SIO_000300: 1.48e0

MQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

QD
type: SiteQuality
SIO_000300: 1.569e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.24e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.38e-2

FS
type: SiteQuality
SIO_000300: 1.459e0

DP
type: SiteQuality
SIO_000300: 1.894165e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.53e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.44e-1

GenotypeQuality
all individuals: 3717
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1932
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4143
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1057
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 422
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variant carriers: 0

GenotypeQuality
all individuals: 3970
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2942
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 698
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4801
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 581
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 816
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 182
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 522
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1999
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1117
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4461
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1404
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 303
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.261352169525732e-4
allele num: 7928
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6447
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 43151
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4293
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9294
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8843
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -1.44e0

MQRankSum
type: SiteQuality
SIO_000300: -5.26e-1

QD
type: SiteQuality
SIO_000300: 1.12e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.19e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.26e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.644e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.87e0

FS
type: SiteQuality
SIO_000300: 1.686e0

DP
type: SiteQuality
SIO_000300: 1.508366e6

GenotypeQuality
all individuals: 5172
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1844
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 699
bin: 8.25e1
variant carriers: 2

GenotypeQuality
all individuals: 37035
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 270
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1179
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4828
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4145
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 329
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 225
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 198
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1233
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1087
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 422
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 345
bin: 4.25e1
variant carriers: 2

South Asian
type: Population
allele count: 8
allele frequency: 8.52242462980718e-4
allele num: 9387
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8956
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8018
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6516
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 589
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44000
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4350
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.63e0

MQRankSum
type: SiteQuality
SIO_000300: -4.002e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.4e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.45e-2

FS
type: SiteQuality
SIO_000300: 3.857e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.27e0

VQSLOD
type: SiteQuality
SIO_000300: 9.2e-2

QD
type: SiteQuality
SIO_000300: 1.157e1

DP
type: SiteQuality
SIO_000300: 1.608133e6

MQ
type: SiteQuality
SIO_000300: 3.997e1

GenotypeQuality
all individuals: 30
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4098
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 222
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 303
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 667
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 396
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 702
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 238
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 570
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5080
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1143
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1132
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 419
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4142
bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9509
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.234263144902493e-4
allele num: 8102
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 601
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6561
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9060
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 45145
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4427
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.931e1

DP
type: SiteQuality
SIO_000300: 1.661648e6

QD
type: SiteQuality
SIO_000300: 1.097e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.7e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.7e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.424e0

VQSLOD
type: SiteQuality
SIO_000300: 1.47e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

FS
type: SiteQuality
SIO_000300: 3.009e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.15e-1

GenotypeDepth
all individuals: 206
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 19
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1153
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4143
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 64
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 229
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43098
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 418
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 219
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 709
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1172
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3055
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 5200
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 267
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 305
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 238
bin: 5.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.333882291756956e-5
allele num: 46148
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8168
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9135
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 609
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9611
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4460
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.47e-1

MQ
type: SiteQuality
SIO_000300: 5.915e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.74e-1

DP
type: SiteQuality
SIO_000300: 1.69373e6

VQSLOD
type: SiteQuality
SIO_000300: 3.89e-1

FS
type: SiteQuality
SIO_000300: 4.897e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.286e1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.6e-2

GenotypeDepth
all individuals: 709
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1164
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 304
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5252
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
all individuals: 4143
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
all individuals: 170
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
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GenotypeQuality
all individuals: 708
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 16
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 43682
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 1.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4466
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8195
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.155915833045878e-5
allele num: 46384
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9154
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6594
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9623
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 611
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.277e0

MQRankSum
type: SiteQuality
SIO_000300: 8.62e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.52e-1

MQ
type: SiteQuality
SIO_000300: 5.939e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.036e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

DP
type: SiteQuality
SIO_000300: 1.700315e6

VQSLOD
type: SiteQuality
SIO_000300: 6.98e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.74e-1

QD
type: SiteQuality
SIO_000300: 1.351e1

GenotypeDepth
all individuals: 686
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1134
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 355
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 335
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 254
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 301
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 688
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4142
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 62
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 219
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5485
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 164
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1116
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40437
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 413
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9425
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.522765341860819e-4
allele num: 6567
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8065
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9060
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 598
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4398
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 45226
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.981e1

VQSLOD
type: SiteQuality
SIO_000300: 5.98e-1

DP
type: SiteQuality
SIO_000300: 1.664694e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.57e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 4.98e0

MQRankSum
type: SiteQuality
SIO_000300: -9.09e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.24e-1

QD
type: SiteQuality
SIO_000300: 1.281e1

GenotypeDepth
all individuals: 134
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 413
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4143
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 235
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 276
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 636
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variant carriers: 0

GenotypeQuality
all individuals: 298
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 68
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variant carriers: 0

GenotypeQuality
all individuals: 540
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1095
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 684
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37549
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 372
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 426
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 515
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4847
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7215
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1072
bin: 7.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4337
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 6.770939129257228e-5
allele num: 44307
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9300
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8962
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7998
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 587
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6537
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.2e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.3e-1

DP
type: SiteQuality
SIO_000300: 1.635714e6

VQSLOD
type: SiteQuality
SIO_000300: -1.313e0

FS
type: SiteQuality
SIO_000300: 9.109e0

QD
type: SiteQuality
SIO_000300: 2.371e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.11e0

MQRankSum
type: SiteQuality
SIO_000300: -7.92e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.55e-1

GenotypeDepth
all individuals: 210
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 413
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 321
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variant carriers: 0

GenotypeQuality
all individuals: 398
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variant carriers: 0

GenotypeQuality
all individuals: 435
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variant carriers: 0

GenotypeQuality
all individuals: 684
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variant carriers: 0

GenotypeQuality
all individuals: 677
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 2.5e0
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GenotypeQuality
all individuals: 726
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variant carriers: 0

GenotypeQuality
all individuals: 138
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variant carriers: 0

GenotypeQuality
all individuals: 1057
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9213
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35637
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1081
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4731
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4143
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 276
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 298
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 43345
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.541782300339192e-4
allele num: 6486
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7916
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4273
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9170
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8847
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.6e-3

QD
type: SiteQuality
SIO_000300: 2.682e1

MQRankSum
type: SiteQuality
SIO_000300: 7.13e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.45e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.26e0

VQSLOD
type: SiteQuality
SIO_000300: -2.655e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.13e-1

DP
type: SiteQuality
SIO_000300: 1.600314e6

GenotypeDepth
all individuals: 210
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 366
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 41
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 669
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GenotypeQuality
all individuals: 1060
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 413
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GenotypeQuality
all individuals: 243
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GenotypeQuality
all individuals: 1053
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 993
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variant carriers: 0

GenotypeQuality
all individuals: 720
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variant carriers: 0

GenotypeQuality
all individuals: 4141
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12082
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 128
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GenotypeQuality
all individuals: 547
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variant carriers: 0

GenotypeQuality
all individuals: 185
bin: 4.25e1
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GenotypeQuality
all individuals: 31487
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1024
bin: 7.25e1
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GenotypeQuality
all individuals: 4593
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 296
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 228
bin: 4.75e1
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: 4150
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7803
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6381
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8986
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.386691806487028e-5
allele num: 41899
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.548426e6

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 3.318e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.634e-1

GenotypeDepth
all individuals: 1276
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 134
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 137
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GenotypeDepth
all individuals: 210
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GenotypeQuality
all individuals: 943
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GenotypeQuality
all individuals: 1647
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variant carriers: 0

GenotypeQuality
all individuals: 434
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GenotypeQuality
all individuals: 59
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GenotypeQuality
all individuals: 1007
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GenotypeQuality
all individuals: 232
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variant carriers: 0

GenotypeQuality
all individuals: 533
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GenotypeQuality
all individuals: 437
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16312
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 302
bin: 4.75e1
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GenotypeQuality
all individuals: 295
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GenotypeQuality
all individuals: 1412
bin: 7.5e0
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GenotypeQuality
all individuals: 25367
bin: 6.25e1
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GenotypeQuality
all individuals: 721
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 245
bin: 4.25e1
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GenotypeQuality
all individuals: 657
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4141
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1507
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 411
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4013
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8377
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.311131506490101e-4
allele num: 7627
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.150086256469235e-4
allele num: 8695
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 39723
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3983
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6200
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 545
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.865e0

MQRankSum
type: SiteQuality
SIO_000300: 7.25e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.24e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQ
type: SiteQuality
SIO_000300: 5.981e1

FS
type: SiteQuality
SIO_000300: 2.371e0

QD
type: SiteQuality
SIO_000300: 1.208e1

VQSLOD
type: SiteQuality
SIO_000300: 1.11e0

DP
type: SiteQuality
SIO_000300: 1.461545e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.92e-1

GenotypeDepth
all individuals: 677
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23794
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 535
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3921
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 2.567591855598634e-5
allele num: 38947
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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allele count: 0
allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

VQSLOD
type: SiteQuality
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DP
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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
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.2e-3

GenotypeQuality
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variant carriers: 0

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

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

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 37439
num of homozygotes: 0

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

South Asian
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allele frequency: 1.193887297039159e-4
allele num: 8376
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VQSLOD
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MQRankSum
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InbreedingCoeff
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ClippingRankSum
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BaseQRankSum
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FS
type: SiteQuality
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DP
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MQ
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ReadPosRankSum
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QD
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SIO_000300: 1.845e1

GenotypeQuality
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variant carriers: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 520
num of homozygotes: 0

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

South Asian
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allele frequency: 8.417508417508417e-4
allele num: 8316
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 36909
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3809
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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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InbreedingCoeff
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MQRankSum
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ClippingRankSum
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VQSLOD
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DP
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MQ
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SIO_000300: 6.0e1

BaseQRankSum
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SIO_000300: 4.44e0

QD
type: SiteQuality
SIO_000300: 2.74e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.7e-1

GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 2
allele frequency: 2.757479663587481e-4
allele num: 7253
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 7758
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5707
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 35278
num of homozygotes: 0

European (Finnish)
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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: 501
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South Asian
type: Population
allele count: 0
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ReadPosRankSum
type: SiteQuality
SIO_000300: 3.49e-1

DP
type: SiteQuality
SIO_000300: 1.247564e6

QD
type: SiteQuality
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FS
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VQSLOD
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InbreedingCoeff
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SIO_000300: -1.0e-2

MQ
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SIO_000300: 5.656e1

BaseQRankSum
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SIO_000300: -2.725e0

MQRankSum
type: SiteQuality
SIO_000300: 1.33e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.62e-1

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 7129
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 3.579738679076428e-4
allele num: 5587
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 34154
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3632
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 7563
num of homozygotes: 0

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

Other
type: Population
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allele frequency: 0.0e0
allele num: 490
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VQSLOD
type: SiteQuality
SIO_000300: -1.135e0

FS
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ReadPosRankSum
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DP
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InbreedingCoeff
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SIO_000300: 1.16e-2

MQ
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BaseQRankSum
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MQRankSum
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ClippingRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.354096140825999e-4
allele num: 7385
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
allele num: 311
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African
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allele frequency: 0.0e0
allele num: 1882
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
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East Asian
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1301
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

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

East Asian
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allele count: 0
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 4011
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele count: 0
allele frequency: 0.0e0
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1876
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European (Non-Finnish)
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allele count: 3
allele frequency: 4.105090311986864e-4
allele num: 7308
num of homozygotes: 0

Other
type: Population
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FS
type: SiteQuality
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InbreedingCoeff
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VQSLOD
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DP
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BaseQRankSum
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QD
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MQRankSum
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ReadPosRankSum
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MQ
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6992
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Other
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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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num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 1775
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 284
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1287
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 374
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 3.17113e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -3.58e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.41e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.23e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.06e-1

QD
type: SiteQuality
SIO_000300: 1.414e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.33e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.06e-1

GenotypeQuality
all individuals: 211
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 808
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1535
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.572079861656972e-4
allele num: 6361
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1276
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3937
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 345
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 271
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 167
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.9e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.2e0

FS
type: SiteQuality
SIO_000300: 1.987e0

DP
type: SiteQuality
SIO_000300: 2.92761e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.71e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 7.56e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.464e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.3e-2

MQRankSum
type: SiteQuality
SIO_000300: -3.8e-1

GenotypeQuality
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variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1275
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 9.230769230769232e-3
allele num: 325
num of homozygotes: 0

South Asian
type: Population
allele count: 5
allele frequency: 1.283367556468172e-3
allele num: 3896
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1422
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5979
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 251
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 6.289308176100629e-3
allele num: 159
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 6.51e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.08e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.4e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.23e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.78252e5

FS
type: SiteQuality
SIO_000300: 2.905e0

QD
type: SiteQuality
SIO_000300: 1.743e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.45e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.58e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 131
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1213
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 291
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 227
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3849
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5296
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1265
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 149
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.21e-1

DP
type: SiteQuality
SIO_000300: 2.50749e5

BaseQRankSum
type: SiteQuality
SIO_000300: 1.01e0

MQRankSum
type: SiteQuality
SIO_000300: -2.41e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.71e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.238e0

FS
type: SiteQuality
SIO_000300: 3.153e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.74e-1

QD
type: SiteQuality
SIO_000300: 1.538e1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8696
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 485
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 35959
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5241
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3698
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5792
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.1e-3

VQSLOD
type: SiteQuality
SIO_000300: -2.678e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 2.437e1

DP
type: SiteQuality
SIO_000300: 1.071663e6

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5289
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 2.053388090349076e-3
allele num: 487
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8704
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3718
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 36150
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5843
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6398
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -5.913e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.7e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.08983e6

QD
type: SiteQuality
SIO_000300: 2.943e1

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5341
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 487
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6442
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 36412
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8731
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3742
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.68662506324844e-4
allele num: 5929
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.96e1

MQRankSum
type: SiteQuality
SIO_000300: 1.65e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.51e0

FS
type: SiteQuality
SIO_000300: 1.242e0

QD
type: SiteQuality
SIO_000300: 1.758e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.5e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.8e-3

VQSLOD
type: SiteQuality
SIO_000300: -8.621e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.7e-2

DP
type: SiteQuality
SIO_000300: 1.110501e6

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 36500
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 489
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.864628006712661e-4
allele num: 5363
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6454
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3749
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.701e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.643e0

InbreedingCoeff
type: SiteQuality
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VQSLOD
type: SiteQuality
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DP
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SIO_000300: 1.117663e6

QD
type: SiteQuality
SIO_000300: 2.065e1

ClippingRankSum
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SIO_000300: 1.18e0

BaseQRankSum
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SIO_000300: -3.08e-1

MQRankSum
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SIO_000300: -1.746e0

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 522
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GenotypeQuality
all individuals: 456
bin: 4.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 497
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8794
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 5497
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3817
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6571
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.692804825506247e-5
allele num: 37136
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6099
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.9e-2

InbreedingCoeff
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BaseQRankSum
type: SiteQuality
SIO_000300: 3.35e0

MQRankSum
type: SiteQuality
SIO_000300: -9.1e-2

FS
type: SiteQuality
SIO_000300: 4.046e0

VQSLOD
type: SiteQuality
SIO_000300: 8.84e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.754e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.56e-1

DP
type: SiteQuality
SIO_000300: 1.15525e6

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6143
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3833
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 6603
num of homozygotes: 0

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

East Asian
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allele frequency: 1.804728388377549e-4
allele num: 5541
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 37302
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.163859e6

VQSLOD
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SIO_000300: 1.8e-1

MQ
type: SiteQuality
SIO_000300: 5.901e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

QD
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SIO_000300: 3.044e1

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 6775
num of homozygotes: 0

Other
type: Population
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allele frequency: 1.988071570576541e-3
allele num: 503
num of homozygotes: 0

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6386
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 38161
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.523e1

BaseQRankSum
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SIO_000300: -3.19e-1

DP
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SIO_000300: 1.203231e6

VQSLOD
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MQ
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SIO_000300: 5.828e1

FS
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InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-3

MQRankSum
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SIO_000300: -2.89e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.02e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.36e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 525
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6009
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4072
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9001
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6983
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 4.978344202718176e-5
allele num: 40174
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.275828e6

FS
type: SiteQuality
SIO_000300: 1.152e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.48e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.7e-3

QD
type: SiteQuality
SIO_000300: 1.34e1

BaseQRankSum
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SIO_000300: 2.98e0

VQSLOD
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SIO_000300: -1.632e0

MQ
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SIO_000300: 5.898e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.28e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.5e-1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 11710
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GenotypeQuality
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GenotypeQuality
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variant carriers: 4

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
all individuals: 843
bin: 9.25e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 40545
num of homozygotes: 0

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

African
type: Population
allele count: 70
allele frequency: 9.792949076664802e-3
allele num: 7148
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4105
num of homozygotes: 0

Latino
type: Population
allele count: 6
allele frequency: 6.649673057741328e-4
allele num: 9023
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7114
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 532
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ReadPosRankSum
type: SiteQuality
SIO_000300: 4.67e-1

VQSLOD
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DP
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SIO_000300: 1.290416e6

FS
type: SiteQuality
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MQRankSum
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QD
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MQ
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ClippingRankSum
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SIO_000300: -3.01e-1

InbreedingCoeff
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SIO_000300: 7.770000000000001e-2

BaseQRankSum
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SIO_000300: -2.136e0

GenotypeDepth
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variant carriers: 0

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

Latino
type: Population
allele count: 1
allele frequency: 1.104240282685512e-4
allele num: 9056
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7223
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4151
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6133
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.429956503778582e-5
allele num: 41153
num of homozygotes: 0

Other
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BaseQRankSum
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VQSLOD
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ReadPosRankSum
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FS
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MQRankSum
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MQ
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QD
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DP
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SIO_000300: 1.307664e6

ClippingRankSum
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SIO_000300: 3.85e-1

InbreedingCoeff
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SIO_000300: 2.4e-3

GenotypeDepth
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 43068
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Other
type: Population
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allele num: 573
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.581777918380259e-4
allele num: 6322
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele count: 0
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African
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ClippingRankSum
type: SiteQuality
SIO_000300: 4.97e-1

InbreedingCoeff
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ReadPosRankSum
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FS
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MQRankSum
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QD
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VQSLOD
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DP
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BaseQRankSum
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MQ
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GenotypeDepth
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variant carriers: 5

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
variant carriers: 2

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6324
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9152
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 51
allele frequency: 1.183184855233853e-3
allele num: 43104
num of homozygotes: 0

European (Finnish)
type: Population
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allele frequency: 2.334812047630166e-4
allele num: 4283
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African
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South Asian
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Other
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MQ
type: SiteQuality
SIO_000300: 5.963e1

VQSLOD
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QD
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InbreedingCoeff
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DP
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BaseQRankSum
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FS
type: SiteQuality
SIO_000300: 1.13e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.05e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.43e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.6e-1

GenotypeDepth
all individuals: 502
bin: 4.75e1
variant carriers: 5

GenotypeQuality
all individuals: 1318
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 248
bin: 4.75e1
variant carriers: 3

GenotypeQuality
all individuals: 405
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4088
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1062
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 960
bin: 3.25e1
variant carriers: 2

GenotypeQuality
all individuals: 21
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8834
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 64
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1316
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 486
bin: 5.25e1
variant carriers: 2

GenotypeQuality
all individuals: 3526
bin: 9.75e1
variant carriers: 40

GenotypeQuality
all individuals: 1766
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 479
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 541
bin: 8.75e1
variant carriers: 2

GenotypeQuality
all individuals: 34054
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 135
bin: 4.25e1
variant carriers: 2

GenotypeQuality
all individuals: 391
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 848
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7412
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8100
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9154
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6335
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 51
allele frequency: 1.180883578771881e-3
allele num: 43188
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 2.332089552238806e-4
allele num: 4288
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 573
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 2.113e1

MQRankSum
type: SiteQuality
SIO_000300: 8.0e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.113e-1

MQ
type: SiteQuality
SIO_000300: 5.967e1

DP
type: SiteQuality
SIO_000300: 1.359642e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.47e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.9e-2

FS
type: SiteQuality
SIO_000300: 1.111e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.29e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.0e0