19-58963106-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58963106
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58963106
    reference: chr 19
allele count: 1
allele frequency: 1.442543492686305e-5
allele num: 69322
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000472178
  ensembl transcript: ENST00000599194
  gene symbol: ZNF324B
  hgvsc: ENST00000599194.1:c.-11C>T
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000473115
  ensembl transcript: ENST00000599193
  gene symbol: ZNF324B
  hgvsc: ENST00000599193.1:c.-21C>T
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000375578
  ensembl transcript: ENST00000391696
  gene symbol: ZNF324B
  hgvsc: ENST00000391696.1:c.-875+35C>T
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471086
  ensembl transcript: ENST00000594214
  gene symbol: ZNF324B
  hgvsc: ENST00000594214.1:c.-7+35C>T
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471122
  ensembl transcript: ENST00000598244
  gene symbol: ZNF324B
  hgvsc: ENST00000598244.1:c.-662+35C>T
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000337473
  ensembl transcript: ENST00000336614
  gene symbol: ZNF324B
  hgvsc: ENST00000336614.4:c.-7+35C>T
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000438930
  ensembl transcript: ENST00000545523
  gene symbol: ZNF324B
  hgvsc: ENST00000545523.1:c.-87+35C>T
  variant of: http://identifiers.org/hgnc/33107
canonical: false
consequence: 5' UTR
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2844
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20554
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2796
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6065
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14440
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8104
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6150
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1522
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22312
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 196
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6820
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 146
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 662
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5397
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1847
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum

19-58963109-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58963109
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58963109
    reference: chr 19
allele count: 37
allele frequency: 5.507099693388503e-4
allele num: 67186
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000375578
  ensembl transcript: ENST00000391696
  gene symbol: ZNF324B
  hgvsc: ENST00000391696.1:c.-875+38C>G
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471122
  ensembl transcript: ENST00000598244
  gene symbol: ZNF324B
  hgvsc: ENST00000598244.1:c.-662+38C>G
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000472178
  ensembl transcript: ENST00000599194
  gene symbol: ZNF324B
  hgvsc: ENST00000599194.1:c.-8C>G
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000438930
  ensembl transcript: ENST00000545523
  gene symbol: ZNF324B
  hgvsc: ENST00000545523.1:c.-87+38C>G
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000473115
  ensembl transcript: ENST00000599193
  gene symbol: ZNF324B
  hgvsc: ENST00000599193.1:c.-18C>G
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471086
  ensembl transcript: ENST00000594214
  gene symbol: ZNF324B
  hgvsc: ENST00000594214.1:c.-7+38C>G
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000337473
  ensembl transcript: ENST00000336614
  gene symbol: ZNF324B
  hgvsc: ENST00000336614.4:c.-7+38C>G
  variant of: http://identifiers.org/hgnc/33107
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9121
  bin: 1.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19800
  bin: 1.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15230
  bin: 7.5e0
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 2126
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2419
  bin: 2.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6150
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 597
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3705
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2473
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 996
  bin: 4.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 6314
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20432
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2410
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5411
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 874
  bin: 2.5e0
  variant carriers: 0
hgvs: c.-8C>G
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD

19-58963110-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58963110
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58963110
    reference: chr 19
allele count: 0
allele frequency: 0.0e0
allele num: 66986
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000438930
  ensembl transcript: ENST00000545523
  gene symbol: ZNF324B
  hgvsc: ENST00000545523.1:c.-87+39G>A
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471122
  ensembl transcript: ENST00000598244
  gene symbol: ZNF324B
  hgvsc: ENST00000598244.1:c.-662+39G>A
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000472178
  ensembl transcript: ENST00000599194
  gene symbol: ZNF324B
  hgvsc: ENST00000599194.1:c.-7G>A
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000375578
  ensembl transcript: ENST00000391696
  gene symbol: ZNF324B
  hgvsc: ENST00000391696.1:c.-875+39G>A
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000473115
  ensembl transcript: ENST00000599193
  gene symbol: ZNF324B
  hgvsc: ENST00000599193.1:c.-17G>A
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000337473
  ensembl transcript: ENST00000336614
  gene symbol: ZNF324B
  hgvsc: ENST00000336614.4:c.-7+39G>A
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471086
  ensembl transcript: ENST00000594214
  gene symbol: ZNF324B
  hgvsc: ENST00000594214.1:c.-7+39G>A
  variant of: http://identifiers.org/hgnc/33107
canonical: false
consequence: splice region
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 2454
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6187
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9050
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19806
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15303
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2093
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2103
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 915
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5369
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 245
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 591
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3686
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 7.25e1
  variant carriers: 0
hgvs: c.-7G>A
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: VQSLOD

19-58963118-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58963118
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58963118
    reference: chr 19
allele count: 1
allele frequency: 1.630523398010761e-5
allele num: 61330
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471122
  ensembl transcript: ENST00000598244
  gene symbol: ZNF324B
  hgvsc: ENST00000598244.1:c.-662+47C>T
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000375578
  ensembl transcript: ENST00000391696
  gene symbol: ZNF324B
  hgvsc: ENST00000391696.1:c.-875+47C>T
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471086
  ensembl transcript: ENST00000594214
  gene symbol: ZNF324B
  hgvsc: ENST00000594214.1:c.-7+47C>T
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000337473
  ensembl transcript: ENST00000336614
  gene symbol: ZNF324B
  hgvsc: ENST00000336614.4:c.-7+47C>T
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000472178
  ensembl transcript: ENST00000599194
  gene symbol: ZNF324B
  hgvsc: ENST00000599194.1:c.-7+8C>T
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000438930
  ensembl transcript: ENST00000545523
  gene symbol: ZNF324B
  hgvsc: ENST00000545523.1:c.-87+47C>T
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000473115
  ensembl transcript: ENST00000599193
  gene symbol: ZNF324B
  hgvsc: ENST00000599193.1:c.-9C>T
  variant of: http://identifiers.org/hgnc/33107
canonical: false
consequence: splice region
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17927
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17506
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8813
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6173
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3419
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1137
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3714
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7280
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3926
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1532
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6238
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5129
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15985
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 311
  bin: 6.75e1
  variant carriers: 0
hgvs: c.-7+8C>T
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
reference allele: C
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: MQ

19-58963119-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58963119
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58963119
    reference: chr 19
allele count: 0
allele frequency: 0.0e0
allele num: 61536
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000473115
  ensembl transcript: ENST00000599193
  gene symbol: ZNF324B
  hgvsc: ENST00000599193.1:c.-8G>C
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000375578
  ensembl transcript: ENST00000391696
  gene symbol: ZNF324B
  hgvsc: ENST00000391696.1:c.-875+48G>C
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000472178
  ensembl transcript: ENST00000599194
  gene symbol: ZNF324B
  hgvsc: ENST00000599194.1:c.-7+9G>C
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000337473
  ensembl transcript: ENST00000336614
  gene symbol: ZNF324B
  hgvsc: ENST00000336614.4:c.-7+48G>C
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471086
  ensembl transcript: ENST00000594214
  gene symbol: ZNF324B
  hgvsc: ENST00000594214.1:c.-7+48G>C
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000438930
  ensembl transcript: ENST00000545523
  gene symbol: ZNF324B
  hgvsc: ENST00000545523.1:c.-87+48G>C
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471122
  ensembl transcript: ENST00000598244
  gene symbol: ZNF324B
  hgvsc: ENST00000598244.1:c.-662+48G>C
  variant of: http://identifiers.org/hgnc/33107
canonical: false
consequence: splice region
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17961
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8790
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6190
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3414
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17499
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3747
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5345
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3936
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1413
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 776
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1837
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5131
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 16240
  bin: 2.25e1
  variant carriers: 0
hgvs: c.-8G>C
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum

19-58965023-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58965023
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58965023
    reference: chr 19
allele count: 28
allele frequency: 2.306843085237852e-4
allele num: 121378
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471086
  ensembl transcript: ENST00000594214
  gene symbol: ZNF324B
  hgvsc: ENST00000594214.1:c.-6-40A>G
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000438930
  ensembl transcript: ENST00000545523
  gene symbol: ZNF324B
  hgvsc: ENST00000545523.1:c.-6-40A>G
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000473115
  ensembl transcript: ENST00000599193
  gene symbol: ZNF324B
  hgvsc: ENST00000599193.1:c.-6-40A>G
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000337473
  ensembl transcript: ENST00000336614
  gene symbol: ZNF324B
  hgvsc: ENST00000336614.4:c.-6-40A>G
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000375578
  ensembl transcript: ENST00000391696
  gene symbol: ZNF324B
  hgvsc: ENST00000391696.1:c.-874-40A>G
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000472178
  ensembl transcript: ENST00000599194
  gene symbol: ZNF324B
  hgvsc: ENST00000599194.1:c.-6-40A>G
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471122
  ensembl transcript: ENST00000598244
  gene symbol: ZNF324B
  hgvsc: ENST00000598244.1:c.-6-40A>G
  variant of: http://identifiers.org/hgnc/33107
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 6.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 27358
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1279
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 13617
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7863
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4419
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2217
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3996
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31716
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6889
  bin: 9.75e1
  variant carriers: 28
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1147
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: MQ

19-58965027-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58965027
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58965027
    reference: chr 19
allele count: 1
allele frequency: 8.2387253044209e-6
allele num: 121378
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000472178
  ensembl transcript: ENST00000599194
  gene symbol: ZNF324B
  hgvsc: ENST00000599194.1:c.-6-36T>C
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471086
  ensembl transcript: ENST00000594214
  gene symbol: ZNF324B
  hgvsc: ENST00000594214.1:c.-6-36T>C
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000438930
  ensembl transcript: ENST00000545523
  gene symbol: ZNF324B
  hgvsc: ENST00000545523.1:c.-6-36T>C
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000473115
  ensembl transcript: ENST00000599193
  gene symbol: ZNF324B
  hgvsc: ENST00000599193.1:c.-6-36T>C
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471122
  ensembl transcript: ENST00000598244
  gene symbol: ZNF324B
  hgvsc: ENST00000598244.1:c.-6-36T>C
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000375578
  ensembl transcript: ENST00000391696
  gene symbol: ZNF324B
  hgvsc: ENST00000391696.1:c.-874-36T>C
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000337473
  ensembl transcript: ENST00000336614
  gene symbol: ZNF324B
  hgvsc: ENST00000336614.4:c.-6-36T>C
  variant of: http://identifiers.org/hgnc/33107
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13624
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27385
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7895
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4413
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2215
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1143
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2792
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3216
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31800
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP

19-58965028-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58965028
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58965028
    reference: chr 19
allele count: 2
allele frequency: 1.647772211969417e-5
allele num: 121376
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000337473
  ensembl transcript: ENST00000336614
  gene symbol: ZNF324B
  hgvsc: ENST00000336614.4:c.-6-35A>T
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000473115
  ensembl transcript: ENST00000599193
  gene symbol: ZNF324B
  hgvsc: ENST00000599193.1:c.-6-35A>T
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000375578
  ensembl transcript: ENST00000391696
  gene symbol: ZNF324B
  hgvsc: ENST00000391696.1:c.-874-35A>T
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471086
  ensembl transcript: ENST00000594214
  gene symbol: ZNF324B
  hgvsc: ENST00000594214.1:c.-6-35A>T
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471122
  ensembl transcript: ENST00000598244
  gene symbol: ZNF324B
  hgvsc: ENST00000598244.1:c.-6-35A>T
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000438930
  ensembl transcript: ENST00000545523
  gene symbol: ZNF324B
  hgvsc: ENST00000545523.1:c.-6-35A>T
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000472178
  ensembl transcript: ENST00000599194
  gene symbol: ZNF324B
  hgvsc: ENST00000599194.1:c.-6-35A>T
  variant of: http://identifiers.org/hgnc/33107
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4413
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27390
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13624
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2215
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7899
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6855
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3214
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31814
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD

19-58965037-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58965037
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58965037
    reference: chr 19
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000375578
  ensembl transcript: ENST00000391696
  gene symbol: ZNF324B
  hgvsc: ENST00000391696.1:c.-874-26C>G
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000473115
  ensembl transcript: ENST00000599193
  gene symbol: ZNF324B
  hgvsc: ENST00000599193.1:c.-6-26C>G
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000337473
  ensembl transcript: ENST00000336614
  gene symbol: ZNF324B
  hgvsc: ENST00000336614.4:c.-6-26C>G
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471122
  ensembl transcript: ENST00000598244
  gene symbol: ZNF324B
  hgvsc: ENST00000598244.1:c.-6-26C>G
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471086
  ensembl transcript: ENST00000594214
  gene symbol: ZNF324B
  hgvsc: ENST00000594214.1:c.-6-26C>G
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000438930
  ensembl transcript: ENST00000545523
  gene symbol: ZNF324B
  hgvsc: ENST00000545523.1:c.-6-26C>G
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000472178
  ensembl transcript: ENST00000599194
  gene symbol: ZNF324B
  hgvsc: ENST00000599194.1:c.-6-26C>G
  variant of: http://identifiers.org/hgnc/33107
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4406
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13620
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2215
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7911
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1274
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27423
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3998
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2789
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum

19-58965037-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58965037
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58965037
    reference: chr 19
allele count: 2
allele frequency: 1.647636465490254e-5
allele num: 121386
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000472178
  ensembl transcript: ENST00000599194
  gene symbol: ZNF324B
  hgvsc: ENST00000599194.1:c.-6-26C>T
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471086
  ensembl transcript: ENST00000594214
  gene symbol: ZNF324B
  hgvsc: ENST00000594214.1:c.-6-26C>T
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000375578
  ensembl transcript: ENST00000391696
  gene symbol: ZNF324B
  hgvsc: ENST00000391696.1:c.-874-26C>T
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000337473
  ensembl transcript: ENST00000336614
  gene symbol: ZNF324B
  hgvsc: ENST00000336614.4:c.-6-26C>T
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000473115
  ensembl transcript: ENST00000599193
  gene symbol: ZNF324B
  hgvsc: ENST00000599193.1:c.-6-26C>T
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471122
  ensembl transcript: ENST00000598244
  gene symbol: ZNF324B
  hgvsc: ENST00000598244.1:c.-6-26C>T
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000438930
  ensembl transcript: ENST00000545523
  gene symbol: ZNF324B
  hgvsc: ENST00000545523.1:c.-6-26C>T
  variant of: http://identifiers.org/hgnc/33107
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7911
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13620
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4406
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27423
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1274
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2215
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31859
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1142
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9230
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQ

http://identifiers.org/exac.variant/19-58965046-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58965046
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58965046
    reference: chr 19
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000337473
  ensembl transcript: ENST00000336614
  gene symbol: ZNF324B
  hgvsc: ENST00000336614.4:c.-6-17C>A
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000473115
  ensembl transcript: ENST00000599193
  gene symbol: ZNF324B
  hgvsc: ENST00000599193.1:c.-6-17C>A
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471122
  ensembl transcript: ENST00000598244
  gene symbol: ZNF324B
  hgvsc: ENST00000598244.1:c.-6-17C>A
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000375578
  ensembl transcript: ENST00000391696
  gene symbol: ZNF324B
  hgvsc: ENST00000391696.1:c.-874-17C>A
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000472178
  ensembl transcript: ENST00000599194
  gene symbol: ZNF324B
  hgvsc: ENST00000599194.1:c.-6-17C>A
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471086
  ensembl transcript: ENST00000594214
  gene symbol: ZNF324B
  hgvsc: ENST00000594214.1:c.-6-17C>A
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000438930
  ensembl transcript: ENST00000545523
  gene symbol: ZNF324B
  hgvsc: ENST00000545523.1:c.-6-17C>A
  variant of: http://identifiers.org/hgnc/33107
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2216
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13621
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27449
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7910
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4404
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 31913
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3997
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1142
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3215
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2789
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum

19-58965065-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58965065
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58965065
    reference: chr 19
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471122
  ensembl transcript: ENST00000598244
  gene symbol: ZNF324B
  hgvsc: ENST00000598244.1:c.-4C>T
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000438930
  ensembl transcript: ENST00000545523
  gene symbol: ZNF324B
  hgvsc: ENST00000545523.1:c.-4C>T
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000337473
  ensembl transcript: ENST00000336614
  gene symbol: ZNF324B
  hgvsc: ENST00000336614.4:c.-4C>T
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000375578
  ensembl transcript: ENST00000391696
  gene symbol: ZNF324B
  hgvsc: ENST00000391696.1:c.-872C>T
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000472178
  ensembl transcript: ENST00000599194
  gene symbol: ZNF324B
  hgvsc: ENST00000599194.1:c.-4C>T
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000473115
  ensembl transcript: ENST00000599193
  gene symbol: ZNF324B
  hgvsc: ENST00000599193.1:c.-4C>T
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471086
  ensembl transcript: ENST00000594214
  gene symbol: ZNF324B
  hgvsc: ENST00000594214.1:c.-4C>T
  variant of: http://identifiers.org/hgnc/33107
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7921
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2219
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27456
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4406
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13624
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9239
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2791
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
hgvs: c.-4C>T
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum

19-58965070-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58965070
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58965070
    reference: chr 19
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000375578
  ensembl transcript: ENST00000391696
  gene symbol: ZNF324B
  hgvsc: ENST00000391696.1:c.-867T>A
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: true
  consequence: start_lost
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000337473
  ensembl transcript: ENST00000336614
  gene symbol: ZNF324B
  hgvsc: ENST00000336614.4:c.2T>A
  hgvsp: ENSP00000337473.3:p.Met1?
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000473115
  ensembl transcript: ENST00000599193
  gene symbol: ZNF324B
  hgvsc: ENST00000599193.1:c.2T>A
  hgvsp: ENSP00000473115.1:p.Met1?
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471086
  ensembl transcript: ENST00000594214
  gene symbol: ZNF324B
  hgvsc: ENST00000594214.1:c.2T>A
  hgvsp: ENSP00000471086.1:p.Met1?
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000472178
  ensembl transcript: ENST00000599194
  gene symbol: ZNF324B
  hgvsc: ENST00000599194.1:c.2T>A
  hgvsp: ENSP00000472178.1:p.Met1?
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000438930
  ensembl transcript: ENST00000545523
  gene symbol: ZNF324B
  hgvsc: ENST00000545523.1:c.2T>A
  hgvsp: ENSP00000438930.1:p.Met1?
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471122
  ensembl transcript: ENST00000598244
  gene symbol: ZNF324B
  hgvsc: ENST00000598244.1:c.2T>A
  hgvsp: ENSP00000471122.1:p.Met1?
  variant of: http://identifiers.org/hgnc/33107
canonical: true
consequence: start lost
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7919
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4406
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13625
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27459
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2219
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3996
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3213
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Met1?
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ

19-58965075-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58965075
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58965075
    reference: chr 19
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471086
  ensembl transcript: ENST00000594214
  gene symbol: ZNF324B
  hgvsc: ENST00000594214.1:c.7T>G
  hgvsp: ENSP00000471086.1:p.Phe3Val
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000473115
  ensembl transcript: ENST00000599193
  gene symbol: ZNF324B
  hgvsc: ENST00000599193.1:c.7T>G
  hgvsp: ENSP00000473115.1:p.Phe3Val
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000375578
  ensembl transcript: ENST00000391696
  gene symbol: ZNF324B
  hgvsc: ENST00000391696.1:c.-862T>G
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000337473
  ensembl transcript: ENST00000336614
  gene symbol: ZNF324B
  hgvsc: ENST00000336614.4:c.7T>G
  hgvsp: ENSP00000337473.3:p.Phe3Val
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000438930
  ensembl transcript: ENST00000545523
  gene symbol: ZNF324B
  hgvsc: ENST00000545523.1:c.7T>G
  hgvsp: ENSP00000438930.1:p.Phe3Val
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000472178
  ensembl transcript: ENST00000599194
  gene symbol: ZNF324B
  hgvsc: ENST00000599194.1:c.7T>G
  hgvsp: ENSP00000472178.1:p.Phe3Val
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471122
  ensembl transcript: ENST00000598244
  gene symbol: ZNF324B
  hgvsc: ENST00000598244.1:c.7T>G
  hgvsp: ENSP00000471122.1:p.Phe3Val
  variant of: http://identifiers.org/hgnc/33107
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2219
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13621
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4407
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7922
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27461
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6845
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9239
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3994
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Phe3Val
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: European (Finnish)
reference allele: T
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD

19-58965076-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58965076
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58965076
    reference: chr 19
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000473115
  ensembl transcript: ENST00000599193
  gene symbol: ZNF324B
  hgvsc: ENST00000599193.1:c.8T>C
  hgvsp: ENSP00000473115.1:p.Phe3Ser
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000472178
  ensembl transcript: ENST00000599194
  gene symbol: ZNF324B
  hgvsc: ENST00000599194.1:c.8T>C
  hgvsp: ENSP00000472178.1:p.Phe3Ser
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000438930
  ensembl transcript: ENST00000545523
  gene symbol: ZNF324B
  hgvsc: ENST00000545523.1:c.8T>C
  hgvsp: ENSP00000438930.1:p.Phe3Ser
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000337473
  ensembl transcript: ENST00000336614
  gene symbol: ZNF324B
  hgvsc: ENST00000336614.4:c.8T>C
  hgvsp: ENSP00000337473.3:p.Phe3Ser
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471122
  ensembl transcript: ENST00000598244
  gene symbol: ZNF324B
  hgvsc: ENST00000598244.1:c.8T>C
  hgvsp: ENSP00000471122.1:p.Phe3Ser
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000375578
  ensembl transcript: ENST00000391696
  gene symbol: ZNF324B
  hgvsc: ENST00000391696.1:c.-861T>C
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471086
  ensembl transcript: ENST00000594214
  gene symbol: ZNF324B
  hgvsc: ENST00000594214.1:c.8T>C
  hgvsp: ENSP00000471086.1:p.Phe3Ser
  variant of: http://identifiers.org/hgnc/33107
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7922
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27461
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2219
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13621
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4407
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1142
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3212
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2789
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3994
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Phe3Ser
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

19-58965077-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58965077
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58965077
    reference: chr 19
allele count: 5
allele frequency: 4.118412599047823e-5
allele num: 121406
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471122
  ensembl transcript: ENST00000598244
  gene symbol: ZNF324B
  hgvsc: ENST00000598244.1:c.9C>T
  hgvsp: ENST00000598244.1:c.9C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000473115
  ensembl transcript: ENST00000599193
  gene symbol: ZNF324B
  hgvsc: ENST00000599193.1:c.9C>T
  hgvsp: ENST00000599193.1:c.9C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000472178
  ensembl transcript: ENST00000599194
  gene symbol: ZNF324B
  hgvsc: ENST00000599194.1:c.9C>T
  hgvsp: ENST00000599194.1:c.9C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471086
  ensembl transcript: ENST00000594214
  gene symbol: ZNF324B
  hgvsc: ENST00000594214.1:c.9C>T
  hgvsp: ENST00000594214.1:c.9C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000438930
  ensembl transcript: ENST00000545523
  gene symbol: ZNF324B
  hgvsc: ENST00000545523.1:c.9C>T
  hgvsp: ENST00000545523.1:c.9C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000375578
  ensembl transcript: ENST00000391696
  gene symbol: ZNF324B
  hgvsc: ENST00000391696.1:c.-860C>T
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000337473
  ensembl transcript: ENST00000336614
  gene symbol: ZNF324B
  hgvsc: ENST00000336614.4:c.9C>T
  hgvsp: ENST00000336614.4:c.9C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33107
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7924
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27461
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4408
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13620
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2219
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31945
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2788
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Phe3Phe
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

19-58965081-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58965081
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58965081
    reference: chr 19
allele count: 2
allele frequency: 1.647337901950448e-5
allele num: 121408
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471086
  ensembl transcript: ENST00000594214
  gene symbol: ZNF324B
  hgvsc: ENST00000594214.1:c.13G>A
  hgvsp: ENSP00000471086.1:p.Asp5Asn
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000337473
  ensembl transcript: ENST00000336614
  gene symbol: ZNF324B
  hgvsc: ENST00000336614.4:c.13G>A
  hgvsp: ENSP00000337473.3:p.Asp5Asn
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000473115
  ensembl transcript: ENST00000599193
  gene symbol: ZNF324B
  hgvsc: ENST00000599193.1:c.13G>A
  hgvsp: ENSP00000473115.1:p.Asp5Asn
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000438930
  ensembl transcript: ENST00000545523
  gene symbol: ZNF324B
  hgvsc: ENST00000545523.1:c.13G>A
  hgvsp: ENSP00000438930.1:p.Asp5Asn
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471122
  ensembl transcript: ENST00000598244
  gene symbol: ZNF324B
  hgvsc: ENST00000598244.1:c.13G>A
  hgvsp: ENSP00000471122.1:p.Asp5Asn
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000375578
  ensembl transcript: ENST00000391696
  gene symbol: ZNF324B
  hgvsc: ENST00000391696.1:c.-856G>A
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000472178
  ensembl transcript: ENST00000599194
  gene symbol: ZNF324B
  hgvsc: ENST00000599194.1:c.13G>A
  hgvsp: ENSP00000472178.1:p.Asp5Asn
  variant of: http://identifiers.org/hgnc/33107
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13621
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2219
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4409
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27465
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7920
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3993
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6841
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3213
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Asp5Asn
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ

19-58965088-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58965088
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58965088
    reference: chr 19
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000473115
  ensembl transcript: ENST00000599193
  gene symbol: ZNF324B
  hgvsc: ENST00000599193.1:c.20C>T
  hgvsp: ENSP00000473115.1:p.Ala7Val
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000438930
  ensembl transcript: ENST00000545523
  gene symbol: ZNF324B
  hgvsc: ENST00000545523.1:c.20C>T
  hgvsp: ENSP00000438930.1:p.Ala7Val
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471122
  ensembl transcript: ENST00000598244
  gene symbol: ZNF324B
  hgvsc: ENST00000598244.1:c.20C>T
  hgvsp: ENSP00000471122.1:p.Ala7Val
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471086
  ensembl transcript: ENST00000594214
  gene symbol: ZNF324B
  hgvsc: ENST00000594214.1:c.20C>T
  hgvsp: ENSP00000471086.1:p.Ala7Val
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000337473
  ensembl transcript: ENST00000336614
  gene symbol: ZNF324B
  hgvsc: ENST00000336614.4:c.20C>T
  hgvsp: ENSP00000337473.3:p.Ala7Val
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000472178
  ensembl transcript: ENST00000599194
  gene symbol: ZNF324B
  hgvsc: ENST00000599194.1:c.20C>T
  hgvsp: ENSP00000472178.1:p.Ala7Val
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000375578
  ensembl transcript: ENST00000391696
  gene symbol: ZNF324B
  hgvsc: ENST00000391696.1:c.-849C>T
  variant of: http://identifiers.org/hgnc/33107
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13622
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27464
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7920
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2219
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4410
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3215
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31952
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1520
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ala7Val
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP

19-58965089-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58965089
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58965089
    reference: chr 19
allele count: 2
allele frequency: 1.647337901950448e-5
allele num: 121408
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000438930
  ensembl transcript: ENST00000545523
  gene symbol: ZNF324B
  hgvsc: ENST00000545523.1:c.21C>T
  hgvsp: ENST00000545523.1:c.21C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000473115
  ensembl transcript: ENST00000599193
  gene symbol: ZNF324B
  hgvsc: ENST00000599193.1:c.21C>T
  hgvsp: ENST00000599193.1:c.21C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471122
  ensembl transcript: ENST00000598244
  gene symbol: ZNF324B
  hgvsc: ENST00000598244.1:c.21C>T
  hgvsp: ENST00000598244.1:c.21C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000337473
  ensembl transcript: ENST00000336614
  gene symbol: ZNF324B
  hgvsc: ENST00000336614.4:c.21C>T
  hgvsp: ENST00000336614.4:c.21C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000472178
  ensembl transcript: ENST00000599194
  gene symbol: ZNF324B
  hgvsc: ENST00000599194.1:c.21C>T
  hgvsp: ENST00000599194.1:c.21C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471086
  ensembl transcript: ENST00000594214
  gene symbol: ZNF324B
  hgvsc: ENST00000594214.1:c.21C>T
  hgvsp: ENST00000594214.1:c.21C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000375578
  ensembl transcript: ENST00000391696
  gene symbol: ZNF324B
  hgvsc: ENST00000391696.1:c.-848C>T
  variant of: http://identifiers.org/hgnc/33107
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2219
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27463
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13623
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4411
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7920
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31953
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1520
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ala7Ala
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum

19-58965090-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58965090
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58965090
    reference: chr 19
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000337473
  ensembl transcript: ENST00000336614
  gene symbol: ZNF324B
  hgvsc: ENST00000336614.4:c.22G>A
  hgvsp: ENSP00000337473.3:p.Val8Met
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000473115
  ensembl transcript: ENST00000599193
  gene symbol: ZNF324B
  hgvsc: ENST00000599193.1:c.22G>A
  hgvsp: ENSP00000473115.1:p.Val8Met
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471122
  ensembl transcript: ENST00000598244
  gene symbol: ZNF324B
  hgvsc: ENST00000598244.1:c.22G>A
  hgvsp: ENSP00000471122.1:p.Val8Met
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000472178
  ensembl transcript: ENST00000599194
  gene symbol: ZNF324B
  hgvsc: ENST00000599194.1:c.22G>A
  hgvsp: ENSP00000472178.1:p.Val8Met
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471086
  ensembl transcript: ENST00000594214
  gene symbol: ZNF324B
  hgvsc: ENST00000594214.1:c.22G>A
  hgvsp: ENSP00000471086.1:p.Val8Met
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000375578
  ensembl transcript: ENST00000391696
  gene symbol: ZNF324B
  hgvsc: ENST00000391696.1:c.-847G>A
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000438930
  ensembl transcript: ENST00000545523
  gene symbol: ZNF324B
  hgvsc: ENST00000545523.1:c.22G>A
  hgvsp: ENSP00000438930.1:p.Val8Met
  variant of: http://identifiers.org/hgnc/33107
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13622
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1274
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27465
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2220
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4410
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7920
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3213
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3993
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6836
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Val8Met
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: QD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff

19-58965092-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58965092
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58965092
    reference: chr 19
allele count: 2
allele frequency: 1.647337901950448e-5
allele num: 121408
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471122
  ensembl transcript: ENST00000598244
  gene symbol: ZNF324B
  hgvsc: ENST00000598244.1:c.24G>A
  hgvsp: ENST00000598244.1:c.24G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000438930
  ensembl transcript: ENST00000545523
  gene symbol: ZNF324B
  hgvsc: ENST00000545523.1:c.24G>A
  hgvsp: ENST00000545523.1:c.24G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000473115
  ensembl transcript: ENST00000599193
  gene symbol: ZNF324B
  hgvsc: ENST00000599193.1:c.24G>A
  hgvsp: ENST00000599193.1:c.24G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000337473
  ensembl transcript: ENST00000336614
  gene symbol: ZNF324B
  hgvsc: ENST00000336614.4:c.24G>A
  hgvsp: ENST00000336614.4:c.24G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000472178
  ensembl transcript: ENST00000599194
  gene symbol: ZNF324B
  hgvsc: ENST00000599194.1:c.24G>A
  hgvsp: ENST00000599194.1:c.24G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000375578
  ensembl transcript: ENST00000391696
  gene symbol: ZNF324B
  hgvsc: ENST00000391696.1:c.-845G>A
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471086
  ensembl transcript: ENST00000594214
  gene symbol: ZNF324B
  hgvsc: ENST00000594214.1:c.24G>A
  hgvsp: ENST00000594214.1:c.24G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33107
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7918
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27468
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13622
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4411
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2219
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1519
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3214
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9237
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Val8Val
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD

19-58965105-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58965105
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58965105
    reference: chr 19
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000472178
  ensembl transcript: ENST00000599194
  gene symbol: ZNF324B
  hgvsc: ENST00000599194.1:c.37G>A
  hgvsp: ENSP00000472178.1:p.Glu13Lys
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000473115
  ensembl transcript: ENST00000599193
  gene symbol: ZNF324B
  hgvsc: ENST00000599193.1:c.37G>A
  hgvsp: ENSP00000473115.1:p.Glu13Lys
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471122
  ensembl transcript: ENST00000598244
  gene symbol: ZNF324B
  hgvsc: ENST00000598244.1:c.37G>A
  hgvsp: ENSP00000471122.1:p.Glu13Lys
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000337473
  ensembl transcript: ENST00000336614
  gene symbol: ZNF324B
  hgvsc: ENST00000336614.4:c.37G>A
  hgvsp: ENSP00000337473.3:p.Glu13Lys
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471086
  ensembl transcript: ENST00000594214
  gene symbol: ZNF324B
  hgvsc: ENST00000594214.1:c.37G>A
  hgvsp: ENSP00000471086.1:p.Glu13Lys
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000438930
  ensembl transcript: ENST00000545523
  gene symbol: ZNF324B
  hgvsc: ENST00000545523.1:c.37G>A
  hgvsp: ENSP00000438930.1:p.Glu13Lys
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000375578
  ensembl transcript: ENST00000391696
  gene symbol: ZNF324B
  hgvsc: ENST00000391696.1:c.-832G>A
  variant of: http://identifiers.org/hgnc/33107
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27468
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7906
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13623
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4412
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2219
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1519
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1142
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Glu13Lys
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Other
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum

19-58965110-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58965110
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58965110
    reference: chr 19
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000375578
  ensembl transcript: ENST00000391696
  gene symbol: ZNF324B
  hgvsc: ENST00000391696.1:c.-827G>C
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000438930
  ensembl transcript: ENST00000545523
  gene symbol: ZNF324B
  hgvsc: ENST00000545523.1:c.42G>C
  hgvsp: ENSP00000438930.1:p.Glu14Asp
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000337473
  ensembl transcript: ENST00000336614
  gene symbol: ZNF324B
  hgvsc: ENST00000336614.4:c.42G>C
  hgvsp: ENSP00000337473.3:p.Glu14Asp
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471086
  ensembl transcript: ENST00000594214
  gene symbol: ZNF324B
  hgvsc: ENST00000594214.1:c.42G>C
  hgvsp: ENSP00000471086.1:p.Glu14Asp
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000473115
  ensembl transcript: ENST00000599193
  gene symbol: ZNF324B
  hgvsc: ENST00000599193.1:c.42G>C
  hgvsp: ENSP00000473115.1:p.Glu14Asp
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000472178
  ensembl transcript: ENST00000599194
  gene symbol: ZNF324B
  hgvsc: ENST00000599194.1:c.42G>C
  hgvsp: ENSP00000472178.1:p.Glu14Asp
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471122
  ensembl transcript: ENST00000598244
  gene symbol: ZNF324B
  hgvsc: ENST00000598244.1:c.42G>C
  hgvsp: ENSP00000471122.1:p.Glu14Asp
  variant of: http://identifiers.org/hgnc/33107
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7902
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13623
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27470
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2218
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4411
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6834
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1141
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Glu14Asp
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

19-58965110-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58965110
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58965110
    reference: chr 19
allele count: 3
allele frequency: 2.471128976458378e-5
allele num: 121402
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000375578
  ensembl transcript: ENST00000391696
  gene symbol: ZNF324B
  hgvsc: ENST00000391696.1:c.-827G>T
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471086
  ensembl transcript: ENST00000594214
  gene symbol: ZNF324B
  hgvsc: ENST00000594214.1:c.42G>T
  hgvsp: ENSP00000471086.1:p.Glu14Asp
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000473115
  ensembl transcript: ENST00000599193
  gene symbol: ZNF324B
  hgvsc: ENST00000599193.1:c.42G>T
  hgvsp: ENSP00000473115.1:p.Glu14Asp
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000438930
  ensembl transcript: ENST00000545523
  gene symbol: ZNF324B
  hgvsc: ENST00000545523.1:c.42G>T
  hgvsp: ENSP00000438930.1:p.Glu14Asp
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000337473
  ensembl transcript: ENST00000336614
  gene symbol: ZNF324B
  hgvsc: ENST00000336614.4:c.42G>T
  hgvsp: ENSP00000337473.3:p.Glu14Asp
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471122
  ensembl transcript: ENST00000598244
  gene symbol: ZNF324B
  hgvsc: ENST00000598244.1:c.42G>T
  hgvsp: ENSP00000471122.1:p.Glu14Asp
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000472178
  ensembl transcript: ENST00000599194
  gene symbol: ZNF324B
  hgvsc: ENST00000599194.1:c.42G>T
  hgvsp: ENSP00000472178.1:p.Glu14Asp
  variant of: http://identifiers.org/hgnc/33107
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4411
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13623
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7902
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27470
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2218
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9236
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3210
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1141
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Glu14Asp
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff

19-58965116-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58965116
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58965116
    reference: chr 19
allele count: 76
allele frequency: 6.260193407027891e-4
allele num: 121402
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000438930
  ensembl transcript: ENST00000545523
  gene symbol: ZNF324B
  hgvsc: ENST00000545523.1:c.48G>C
  hgvsp: ENST00000545523.1:c.48G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471122
  ensembl transcript: ENST00000598244
  gene symbol: ZNF324B
  hgvsc: ENST00000598244.1:c.48G>C
  hgvsp: ENST00000598244.1:c.48G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000337473
  ensembl transcript: ENST00000336614
  gene symbol: ZNF324B
  hgvsc: ENST00000336614.4:c.48G>C
  hgvsp: ENST00000336614.4:c.48G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000473115
  ensembl transcript: ENST00000599193
  gene symbol: ZNF324B
  hgvsc: ENST00000599193.1:c.48G>C
  hgvsp: ENST00000599193.1:c.48G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000375578
  ensembl transcript: ENST00000391696
  gene symbol: ZNF324B
  hgvsc: ENST00000391696.1:c.-821G>C
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471086
  ensembl transcript: ENST00000594214
  gene symbol: ZNF324B
  hgvsc: ENST00000594214.1:c.48G>C
  hgvsp: ENST00000594214.1:c.48G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000472178
  ensembl transcript: ENST00000599194
  gene symbol: ZNF324B
  hgvsc: ENST00000599194.1:c.48G>C
  hgvsp: ENST00000599194.1:c.48G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/33107
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13619
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2220
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 7910
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4407
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 8.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 9.75e1
  variant carriers: 43
genotype depth: GenotypeDepth
  all individuals: 27464
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2783
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9232
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Gly16Gly
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: QD

19-58965123-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58965123
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58965123
    reference: chr 19
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471122
  ensembl transcript: ENST00000598244
  gene symbol: ZNF324B
  hgvsc: ENST00000598244.1:c.55G>A
  hgvsp: ENSP00000471122.1:p.Asp19Asn
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000375578
  ensembl transcript: ENST00000391696
  gene symbol: ZNF324B
  hgvsc: ENST00000391696.1:c.-814G>A
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000472178
  ensembl transcript: ENST00000599194
  gene symbol: ZNF324B
  hgvsc: ENST00000599194.1:c.55G>A
  hgvsp: ENSP00000472178.1:p.Asp19Asn
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000337473
  ensembl transcript: ENST00000336614
  gene symbol: ZNF324B
  hgvsc: ENST00000336614.4:c.55G>A
  hgvsp: ENSP00000337473.3:p.Asp19Asn
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000473115
  ensembl transcript: ENST00000599193
  gene symbol: ZNF324B
  hgvsc: ENST00000599193.1:c.55G>A
  hgvsp: ENSP00000473115.1:p.Asp19Asn
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471086
  ensembl transcript: ENST00000594214
  gene symbol: ZNF324B
  hgvsc: ENST00000594214.1:c.55G>A
  hgvsp: ENSP00000471086.1:p.Asp19Asn
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000438930
  ensembl transcript: ENST00000545523
  gene symbol: ZNF324B
  hgvsc: ENST00000545523.1:c.55G>A
  hgvsp: ENSP00000438930.1:p.Asp19Asn
  variant of: http://identifiers.org/hgnc/33107
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2219
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7915
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13629
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4409
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27507
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1515
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6762
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2783
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9244
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Asp19Asn
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: QD

19-58965127-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58965127
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58965127
    reference: chr 19
allele count: 2
allele frequency: 1.647527884409444e-5
allele num: 121394
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471122
  ensembl transcript: ENST00000598244
  gene symbol: ZNF324B
  hgvsc: ENST00000598244.1:c.59C>G
  hgvsp: ENSP00000471122.1:p.Thr20Arg
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000438930
  ensembl transcript: ENST00000545523
  gene symbol: ZNF324B
  hgvsc: ENST00000545523.1:c.59C>G
  hgvsp: ENSP00000438930.1:p.Thr20Arg
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471086
  ensembl transcript: ENST00000594214
  gene symbol: ZNF324B
  hgvsc: ENST00000594214.1:c.59C>G
  hgvsp: ENSP00000471086.1:p.Thr20Arg
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000375578
  ensembl transcript: ENST00000391696
  gene symbol: ZNF324B
  hgvsc: ENST00000391696.1:c.-810C>G
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000473115
  ensembl transcript: ENST00000599193
  gene symbol: ZNF324B
  hgvsc: ENST00000599193.1:c.59C>G
  hgvsp: ENSP00000473115.1:p.Thr20Arg
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000337473
  ensembl transcript: ENST00000336614
  gene symbol: ZNF324B
  hgvsc: ENST00000336614.4:c.59C>G
  hgvsp: ENSP00000337473.3:p.Thr20Arg
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000472178
  ensembl transcript: ENST00000599194
  gene symbol: ZNF324B
  hgvsc: ENST00000599194.1:c.59C>G
  hgvsp: ENSP00000472178.1:p.Thr20Arg
  variant of: http://identifiers.org/hgnc/33107
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4409
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13629
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7917
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27505
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2219
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31993
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2784
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Thr20Arg
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/19-58965128-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58965128
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58965128
    reference: chr 19
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000473115
  ensembl transcript: ENST00000599193
  gene symbol: ZNF324B
  hgvsc: ENST00000599193.1:c.60A>C
  hgvsp: ENST00000599193.1:c.60A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000337473
  ensembl transcript: ENST00000336614
  gene symbol: ZNF324B
  hgvsc: ENST00000336614.4:c.60A>C
  hgvsp: ENST00000336614.4:c.60A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471122
  ensembl transcript: ENST00000598244
  gene symbol: ZNF324B
  hgvsc: ENST00000598244.1:c.60A>C
  hgvsp: ENST00000598244.1:c.60A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471086
  ensembl transcript: ENST00000594214
  gene symbol: ZNF324B
  hgvsc: ENST00000594214.1:c.60A>C
  hgvsp: ENST00000594214.1:c.60A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000472178
  ensembl transcript: ENST00000599194
  gene symbol: ZNF324B
  hgvsc: ENST00000599194.1:c.60A>C
  hgvsp: ENST00000599194.1:c.60A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000438930
  ensembl transcript: ENST00000545523
  gene symbol: ZNF324B
  hgvsc: ENST00000545523.1:c.60A>C
  hgvsp: ENST00000545523.1:c.60A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000375578
  ensembl transcript: ENST00000391696
  gene symbol: ZNF324B
  hgvsc: ENST00000391696.1:c.-809A>C
  variant of: http://identifiers.org/hgnc/33107
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7920
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4409
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27502
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2219
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1268
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13630
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9247
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1515
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4001
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3207
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Thr20Thr
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

19-58965130-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58965130
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58965130
    reference: chr 19
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471122
  ensembl transcript: ENST00000598244
  gene symbol: ZNF324B
  hgvsc: ENST00000598244.1:c.62C>T
  hgvsp: ENSP00000471122.1:p.Ala21Val
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000472178
  ensembl transcript: ENST00000599194
  gene symbol: ZNF324B
  hgvsc: ENST00000599194.1:c.62C>T
  hgvsp: ENSP00000472178.1:p.Ala21Val
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000438930
  ensembl transcript: ENST00000545523
  gene symbol: ZNF324B
  hgvsc: ENST00000545523.1:c.62C>T
  hgvsp: ENSP00000438930.1:p.Ala21Val
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000337473
  ensembl transcript: ENST00000336614
  gene symbol: ZNF324B
  hgvsc: ENST00000336614.4:c.62C>T
  hgvsp: ENSP00000337473.3:p.Ala21Val
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000473115
  ensembl transcript: ENST00000599193
  gene symbol: ZNF324B
  hgvsc: ENST00000599193.1:c.62C>T
  hgvsp: ENSP00000473115.1:p.Ala21Val
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000375578
  ensembl transcript: ENST00000391696
  gene symbol: ZNF324B
  hgvsc: ENST00000391696.1:c.-807C>T
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471086
  ensembl transcript: ENST00000594214
  gene symbol: ZNF324B
  hgvsc: ENST00000594214.1:c.62C>T
  hgvsp: ENSP00000471086.1:p.Ala21Val
  variant of: http://identifiers.org/hgnc/33107
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27499
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13628
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2222
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7920
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4409
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3206
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2783
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31982
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9241
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Ala21Val
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: C
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum

19-58965131-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58965131
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58965131
    reference: chr 19
allele count: 3
allele frequency: 2.47137325974133e-5
allele num: 121390
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000375578
  ensembl transcript: ENST00000391696
  gene symbol: ZNF324B
  hgvsc: ENST00000391696.1:c.-806G>A
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471122
  ensembl transcript: ENST00000598244
  gene symbol: ZNF324B
  hgvsc: ENST00000598244.1:c.63G>A
  hgvsp: ENST00000598244.1:c.63G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000473115
  ensembl transcript: ENST00000599193
  gene symbol: ZNF324B
  hgvsc: ENST00000599193.1:c.63G>A
  hgvsp: ENST00000599193.1:c.63G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471086
  ensembl transcript: ENST00000594214
  gene symbol: ZNF324B
  hgvsc: ENST00000594214.1:c.63G>A
  hgvsp: ENST00000594214.1:c.63G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000438930
  ensembl transcript: ENST00000545523
  gene symbol: ZNF324B
  hgvsc: ENST00000545523.1:c.63G>A
  hgvsp: ENST00000545523.1:c.63G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000337473
  ensembl transcript: ENST00000336614
  gene symbol: ZNF324B
  hgvsc: ENST00000336614.4:c.63G>A
  hgvsp: ENST00000336614.4:c.63G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000472178
  ensembl transcript: ENST00000599194
  gene symbol: ZNF324B
  hgvsc: ENST00000599194.1:c.63G>A
  hgvsp: ENST00000599194.1:c.63G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33107
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7927
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13623
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4407
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2221
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1268
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27502
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3207
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1140
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31997
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1513
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ala21Ala
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum

19-58965147-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58965147
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58965147
    reference: chr 19
allele count: 7
allele frequency: 5.771101620855113e-5
allele num: 121294
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000375578
  ensembl transcript: ENST00000391696
  gene symbol: ZNF324B
  hgvsc: ENST00000391696.1:c.-790C>T
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471086
  ensembl transcript: ENST00000594214
  gene symbol: ZNF324B
  hgvsc: ENST00000594214.1:c.79C>T
  hgvsp: ENSP00000471086.1:p.Arg27Cys
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000438930
  ensembl transcript: ENST00000545523
  gene symbol: ZNF324B
  hgvsc: ENST00000545523.1:c.79C>T
  hgvsp: ENSP00000438930.1:p.Arg27Cys
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000337473
  ensembl transcript: ENST00000336614
  gene symbol: ZNF324B
  hgvsc: ENST00000336614.4:c.79C>T
  hgvsp: ENSP00000337473.3:p.Arg27Cys
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000472178
  ensembl transcript: ENST00000599194
  gene symbol: ZNF324B
  hgvsc: ENST00000599194.1:c.79C>T
  hgvsp: ENSP00000472178.1:p.Arg27Cys
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000473115
  ensembl transcript: ENST00000599193
  gene symbol: ZNF324B
  hgvsc: ENST00000599193.1:c.79C>T
  hgvsp: ENSP00000473115.1:p.Arg27Cys
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471122
  ensembl transcript: ENST00000598244
  gene symbol: ZNF324B
  hgvsc: ENST00000598244.1:c.79C>T
  hgvsp: ENSP00000471122.1:p.Arg27Cys
  variant of: http://identifiers.org/hgnc/33107
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4385
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1268
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2211
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7919
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13585
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27454
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1135
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31932
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3190
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Arg27Cys
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

19-58965152-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58965152
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58965152
    reference: chr 19
allele count: 2
allele frequency: 1.649811096629436e-5
allele num: 121226
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000438930
  ensembl transcript: ENST00000545523
  gene symbol: ZNF324B
  hgvsc: ENST00000545523.1:c.84C>T
  hgvsp: ENST00000545523.1:c.84C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000375578
  ensembl transcript: ENST00000391696
  gene symbol: ZNF324B
  hgvsc: ENST00000391696.1:c.-785C>T
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471086
  ensembl transcript: ENST00000594214
  gene symbol: ZNF324B
  hgvsc: ENST00000594214.1:c.84C>T
  hgvsp: ENST00000594214.1:c.84C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000472178
  ensembl transcript: ENST00000599194
  gene symbol: ZNF324B
  hgvsc: ENST00000599194.1:c.84C>T
  hgvsp: ENST00000599194.1:c.84C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471122
  ensembl transcript: ENST00000598244
  gene symbol: ZNF324B
  hgvsc: ENST00000598244.1:c.84C>T
  hgvsp: ENST00000598244.1:c.84C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000337473
  ensembl transcript: ENST00000336614
  gene symbol: ZNF324B
  hgvsc: ENST00000336614.4:c.84C>T
  hgvsp: ENST00000336614.4:c.84C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000473115
  ensembl transcript: ENST00000599193
  gene symbol: ZNF324B
  hgvsc: ENST00000599193.1:c.84C>T
  hgvsp: ENST00000599193.1:c.84C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33107
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27455
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7933
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1261
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13531
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4368
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2202
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1132
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6729
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 31918
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1504
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
hgvs: p.His28His
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: QD
site quality: DP

19-58965153-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58965153
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58965153
    reference: chr 19
allele count: 1
allele frequency: 8.25000825000825e-6
allele num: 121212
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471122
  ensembl transcript: ENST00000598244
  gene symbol: ZNF324B
  hgvsc: ENST00000598244.1:c.85G>A
  hgvsp: ENSP00000471122.1:p.Val29Met
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000375578
  ensembl transcript: ENST00000391696
  gene symbol: ZNF324B
  hgvsc: ENST00000391696.1:c.-784G>A
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000473115
  ensembl transcript: ENST00000599193
  gene symbol: ZNF324B
  hgvsc: ENST00000599193.1:c.85G>A
  hgvsp: ENSP00000473115.1:p.Val29Met
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471086
  ensembl transcript: ENST00000594214
  gene symbol: ZNF324B
  hgvsc: ENST00000594214.1:c.85G>A
  hgvsp: ENSP00000471086.1:p.Val29Met
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000472178
  ensembl transcript: ENST00000599194
  gene symbol: ZNF324B
  hgvsc: ENST00000599194.1:c.85G>A
  hgvsp: ENSP00000472178.1:p.Val29Met
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000438930
  ensembl transcript: ENST00000545523
  gene symbol: ZNF324B
  hgvsc: ENST00000545523.1:c.85G>A
  hgvsp: ENSP00000438930.1:p.Val29Met
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000337473
  ensembl transcript: ENST00000336614
  gene symbol: ZNF324B
  hgvsc: ENST00000336614.4:c.85G>A
  hgvsp: ENSP00000337473.3:p.Val29Met
  variant of: http://identifiers.org/hgnc/33107
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4361
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13516
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7948
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27444
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1261
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2202
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 9172
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 184
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3176
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31898
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Val29Met
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP

19-58965169-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58965169
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58965169
    reference: chr 19
allele count: 69
allele frequency: 5.710880468788797e-4
allele num: 120822
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000473115
  ensembl transcript: ENST00000599193
  gene symbol: ZNF324B
  hgvsc: ENST00000599193.1:c.101T>C
  hgvsp: ENSP00000473115.1:p.Phe34Ser
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000438930
  ensembl transcript: ENST00000545523
  gene symbol: ZNF324B
  hgvsc: ENST00000545523.1:c.101T>C
  hgvsp: ENSP00000438930.1:p.Phe34Ser
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000375578
  ensembl transcript: ENST00000391696
  gene symbol: ZNF324B
  hgvsc: ENST00000391696.1:c.-768T>C
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000472178
  ensembl transcript: ENST00000599194
  gene symbol: ZNF324B
  hgvsc: ENST00000599194.1:c.101T>C
  hgvsp: ENSP00000472178.1:p.Phe34Ser
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471086
  ensembl transcript: ENST00000594214
  gene symbol: ZNF324B
  hgvsc: ENST00000594214.1:c.101T>C
  hgvsp: ENSP00000471086.1:p.Phe34Ser
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000337473
  ensembl transcript: ENST00000336614
  gene symbol: ZNF324B
  hgvsc: ENST00000336614.4:c.101T>C
  hgvsp: ENSP00000337473.3:p.Phe34Ser
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471122
  ensembl transcript: ENST00000598244
  gene symbol: ZNF324B
  hgvsc: ENST00000598244.1:c.101T>C
  hgvsp: ENSP00000471122.1:p.Phe34Ser
  variant of: http://identifiers.org/hgnc/33107
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27130
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 6.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1251
  bin: 4.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 13286
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2168
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4327
  bin: 3.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8017
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 6.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 5.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 3141
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1493
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9036
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Phe34Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: African
population: East Asian
reference allele: T
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum

19-58965173-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58965173
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58965173
    reference: chr 19
allele count: 1
allele frequency: 8.28953694646617e-6
allele num: 120634
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471086
  ensembl transcript: ENST00000594214
  gene symbol: ZNF324B
  hgvsc: ENST00000594214.1:c.105A>G
  hgvsp: ENST00000594214.1:c.105A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000472178
  ensembl transcript: ENST00000599194
  gene symbol: ZNF324B
  hgvsc: ENST00000599194.1:c.105A>G
  hgvsp: ENST00000599194.1:c.105A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000438930
  ensembl transcript: ENST00000545523
  gene symbol: ZNF324B
  hgvsc: ENST00000545523.1:c.105A>G
  hgvsp: ENST00000545523.1:c.105A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000473115
  ensembl transcript: ENST00000599193
  gene symbol: ZNF324B
  hgvsc: ENST00000599193.1:c.105A>G
  hgvsp: ENST00000599193.1:c.105A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000375578
  ensembl transcript: ENST00000391696
  gene symbol: ZNF324B
  hgvsc: ENST00000391696.1:c.-764A>G
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000337473
  ensembl transcript: ENST00000336614
  gene symbol: ZNF324B
  hgvsc: ENST00000336614.4:c.105A>G
  hgvsp: ENST00000336614.4:c.105A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471122
  ensembl transcript: ENST00000598244
  gene symbol: ZNF324B
  hgvsc: ENST00000598244.1:c.105A>G
  hgvsp: ENST00000598244.1:c.105A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/33107
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8038
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27032
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13177
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2155
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1243
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4297
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9001
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3124
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6654
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 779
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31422
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Thr35Thr
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/19-58965174-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58965174
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58965174
    reference: chr 19
allele count: 1
allele frequency: 8.297515723792297e-6
allele num: 120518
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471086
  ensembl transcript: ENST00000594214
  gene symbol: ZNF324B
  hgvsc: ENST00000594214.1:c.106C>A
  hgvsp: ENSP00000471086.1:p.Leu36Ile
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000438930
  ensembl transcript: ENST00000545523
  gene symbol: ZNF324B
  hgvsc: ENST00000545523.1:c.106C>A
  hgvsp: ENSP00000438930.1:p.Leu36Ile
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000472178
  ensembl transcript: ENST00000599194
  gene symbol: ZNF324B
  hgvsc: ENST00000599194.1:c.106C>A
  hgvsp: ENSP00000472178.1:p.Leu36Ile
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471122
  ensembl transcript: ENST00000598244
  gene symbol: ZNF324B
  hgvsc: ENST00000598244.1:c.106C>A
  hgvsp: ENSP00000471122.1:p.Leu36Ile
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000473115
  ensembl transcript: ENST00000599193
  gene symbol: ZNF324B
  hgvsc: ENST00000599193.1:c.106C>A
  hgvsp: ENSP00000473115.1:p.Leu36Ile
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000337473
  ensembl transcript: ENST00000336614
  gene symbol: ZNF324B
  hgvsc: ENST00000336614.4:c.106C>A
  hgvsp: ENSP00000337473.3:p.Leu36Ile
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000375578
  ensembl transcript: ENST00000391696
  gene symbol: ZNF324B
  hgvsc: ENST00000391696.1:c.-763C>A
  variant of: http://identifiers.org/hgnc/33107
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13142
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1243
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8027
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2153
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4287
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26928
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6650
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3116
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8954
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 899
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Leu36Ile
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

19-58965180-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58965180
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58965180
    reference: chr 19
allele count: 2
allele frequency: 1.664447403462051e-5
allele num: 120160
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000438930
  ensembl transcript: ENST00000545523
  gene symbol: ZNF324B
  hgvsc: ENST00000545523.1:c.112A>G
  hgvsp: ENSP00000438930.1:p.Thr38Ala
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000337473
  ensembl transcript: ENST00000336614
  gene symbol: ZNF324B
  hgvsc: ENST00000336614.4:c.112A>G
  hgvsp: ENSP00000337473.3:p.Thr38Ala
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471086
  ensembl transcript: ENST00000594214
  gene symbol: ZNF324B
  hgvsc: ENST00000594214.1:c.112A>G
  hgvsp: ENSP00000471086.1:p.Thr38Ala
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000473115
  ensembl transcript: ENST00000599193
  gene symbol: ZNF324B
  hgvsc: ENST00000599193.1:c.112A>G
  hgvsp: ENSP00000473115.1:p.Thr38Ala
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471122
  ensembl transcript: ENST00000598244
  gene symbol: ZNF324B
  hgvsc: ENST00000598244.1:c.112A>G
  hgvsp: ENSP00000471122.1:p.Thr38Ala
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000472178
  ensembl transcript: ENST00000599194
  gene symbol: ZNF324B
  hgvsc: ENST00000599194.1:c.112A>G
  hgvsp: ENSP00000472178.1:p.Thr38Ala
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000375578
  ensembl transcript: ENST00000391696
  gene symbol: ZNF324B
  hgvsc: ENST00000391696.1:c.-757A>G
  variant of: http://identifiers.org/hgnc/33107
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8091
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26569
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4253
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12929
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2137
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1096
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1275
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30892
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Thr38Ala
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum

19-58965182-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58965182
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58965182
    reference: chr 19
allele count: 2
allele frequency: 1.666833350001667e-5
allele num: 119988
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000473115
  ensembl transcript: ENST00000599193
  gene symbol: ZNF324B
  hgvsc: ENST00000599193.1:c.114C>G
  hgvsp: ENST00000599193.1:c.114C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000375578
  ensembl transcript: ENST00000391696
  gene symbol: ZNF324B
  hgvsc: ENST00000391696.1:c.-755C>G
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471086
  ensembl transcript: ENST00000594214
  gene symbol: ZNF324B
  hgvsc: ENST00000594214.1:c.114C>G
  hgvsp: ENST00000594214.1:c.114C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000472178
  ensembl transcript: ENST00000599194
  gene symbol: ZNF324B
  hgvsc: ENST00000599194.1:c.114C>G
  hgvsp: ENST00000599194.1:c.114C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471122
  ensembl transcript: ENST00000598244
  gene symbol: ZNF324B
  hgvsc: ENST00000598244.1:c.114C>G
  hgvsp: ENST00000598244.1:c.114C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000337473
  ensembl transcript: ENST00000336614
  gene symbol: ZNF324B
  hgvsc: ENST00000336614.4:c.114C>G
  hgvsp: ENST00000336614.4:c.114C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000438930
  ensembl transcript: ENST00000545523
  gene symbol: ZNF324B
  hgvsc: ENST00000545523.1:c.114C>G
  hgvsp: ENST00000545523.1:c.114C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/33107
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12864
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1239
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1053
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8094
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4245
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2128
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26426
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8743
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6634
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2705
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1466
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1438
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1096
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3054
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Thr38Thr
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: African
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum

19-58965196-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58965196
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58965196
    reference: chr 19
allele count: 12
allele frequency: 1.013581998783702e-4
allele num: 118392
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000472178
  ensembl transcript: ENST00000599194
  gene symbol: ZNF324B
  hgvsc: ENST00000599194.1:c.121+7C>T
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471086
  ensembl transcript: ENST00000594214
  gene symbol: ZNF324B
  hgvsc: ENST00000594214.1:c.121+7C>T
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000438930
  ensembl transcript: ENST00000545523
  gene symbol: ZNF324B
  hgvsc: ENST00000545523.1:c.121+7C>T
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000375578
  ensembl transcript: ENST00000391696
  gene symbol: ZNF324B
  hgvsc: ENST00000391696.1:c.-748+7C>T
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000337473
  ensembl transcript: ENST00000336614
  gene symbol: ZNF324B
  hgvsc: ENST00000336614.4:c.121+7C>T
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471122
  ensembl transcript: ENST00000598244
  gene symbol: ZNF324B
  hgvsc: ENST00000598244.1:c.121+7C>T
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000473115
  ensembl transcript: ENST00000599193
  gene symbol: ZNF324B
  hgvsc: ENST00000599193.1:c.121+7C>T
  variant of: http://identifiers.org/hgnc/33107
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12029
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7826
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1369
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2828
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2094
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1225
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24709
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4122
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 687
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 188
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1073
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3648
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8215
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 1.75e1
  variant carriers: 0
hgvs: c.121+7C>T
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ClippingRankSum

19-58965197-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58965197
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58965197
    reference: chr 19
allele count: 1
allele frequency: 8.462098261885017e-6
allele num: 118174
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000337473
  ensembl transcript: ENST00000336614
  gene symbol: ZNF324B
  hgvsc: ENST00000336614.4:c.121+8C>G
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000472178
  ensembl transcript: ENST00000599194
  gene symbol: ZNF324B
  hgvsc: ENST00000599194.1:c.121+8C>G
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471086
  ensembl transcript: ENST00000594214
  gene symbol: ZNF324B
  hgvsc: ENST00000594214.1:c.121+8C>G
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000473115
  ensembl transcript: ENST00000599193
  gene symbol: ZNF324B
  hgvsc: ENST00000599193.1:c.121+8C>G
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000375578
  ensembl transcript: ENST00000391696
  gene symbol: ZNF324B
  hgvsc: ENST00000391696.1:c.-748+8C>G
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471122
  ensembl transcript: ENST00000598244
  gene symbol: ZNF324B
  hgvsc: ENST00000598244.1:c.121+8C>G
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000438930
  ensembl transcript: ENST00000545523
  gene symbol: ZNF324B
  hgvsc: ENST00000545523.1:c.121+8C>G
  variant of: http://identifiers.org/hgnc/33107
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1490
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7805
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24263
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11850
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4103
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3229
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2090
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1221
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27768
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2896
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 751
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 416
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1442
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 340
  bin: 5.75e1
  variant carriers: 0
hgvs: c.121+8C>G
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: African
population: Latino
reference allele: C
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum

19-58965197-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58965197
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58965197
    reference: chr 19
allele count: 5
allele frequency: 4.231049130942508e-5
allele num: 118174
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471086
  ensembl transcript: ENST00000594214
  gene symbol: ZNF324B
  hgvsc: ENST00000594214.1:c.121+8C>T
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000472178
  ensembl transcript: ENST00000599194
  gene symbol: ZNF324B
  hgvsc: ENST00000599194.1:c.121+8C>T
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000337473
  ensembl transcript: ENST00000336614
  gene symbol: ZNF324B
  hgvsc: ENST00000336614.4:c.121+8C>T
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000438930
  ensembl transcript: ENST00000545523
  gene symbol: ZNF324B
  hgvsc: ENST00000545523.1:c.121+8C>T
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000375578
  ensembl transcript: ENST00000391696
  gene symbol: ZNF324B
  hgvsc: ENST00000391696.1:c.-748+8C>T
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471122
  ensembl transcript: ENST00000598244
  gene symbol: ZNF324B
  hgvsc: ENST00000598244.1:c.121+8C>T
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000473115
  ensembl transcript: ENST00000599193
  gene symbol: ZNF324B
  hgvsc: ENST00000599193.1:c.121+8C>T
  variant of: http://identifiers.org/hgnc/33107
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7805
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11850
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24263
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1490
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3229
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4103
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1221
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2090
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1070
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2896
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6600
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8059
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2629
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 416
  bin: 3.75e1
  variant carriers: 0
hgvs: c.121+8C>T
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum

19-58965200-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58965200
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58965200
    reference: chr 19
allele count: 1
allele frequency: 8.474145382438182e-6
allele num: 118006
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000473115
  ensembl transcript: ENST00000599193
  gene symbol: ZNF324B
  hgvsc: ENST00000599193.1:c.121+11G>A
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000375578
  ensembl transcript: ENST00000391696
  gene symbol: ZNF324B
  hgvsc: ENST00000391696.1:c.-748+11G>A
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471122
  ensembl transcript: ENST00000598244
  gene symbol: ZNF324B
  hgvsc: ENST00000598244.1:c.121+11G>A
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000472178
  ensembl transcript: ENST00000599194
  gene symbol: ZNF324B
  hgvsc: ENST00000599194.1:c.121+11G>A
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000337473
  ensembl transcript: ENST00000336614
  gene symbol: ZNF324B
  hgvsc: ENST00000336614.4:c.121+11G>A
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000438930
  ensembl transcript: ENST00000545523
  gene symbol: ZNF324B
  hgvsc: ENST00000545523.1:c.121+11G>A
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471086
  ensembl transcript: ENST00000594214
  gene symbol: ZNF324B
  hgvsc: ENST00000594214.1:c.121+11G>A
  variant of: http://identifiers.org/hgnc/33107
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24078
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2076
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7910
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1559
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3411
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4076
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1214
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11664
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 455
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3624
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6582
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 796
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1063
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: Other
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

19-58965200-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58965200
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58965200
    reference: chr 19
allele count: 2
allele frequency: 1.694829076487636e-5
allele num: 118006
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000472178
  ensembl transcript: ENST00000599194
  gene symbol: ZNF324B
  hgvsc: ENST00000599194.1:c.121+11G>C
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000337473
  ensembl transcript: ENST00000336614
  gene symbol: ZNF324B
  hgvsc: ENST00000336614.4:c.121+11G>C
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471086
  ensembl transcript: ENST00000594214
  gene symbol: ZNF324B
  hgvsc: ENST00000594214.1:c.121+11G>C
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000375578
  ensembl transcript: ENST00000391696
  gene symbol: ZNF324B
  hgvsc: ENST00000391696.1:c.-748+11G>C
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000438930
  ensembl transcript: ENST00000545523
  gene symbol: ZNF324B
  hgvsc: ENST00000545523.1:c.121+11G>C
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471122
  ensembl transcript: ENST00000598244
  gene symbol: ZNF324B
  hgvsc: ENST00000598244.1:c.121+11G>C
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000473115
  ensembl transcript: ENST00000599193
  gene symbol: ZNF324B
  hgvsc: ENST00000599193.1:c.121+11G>C
  variant of: http://identifiers.org/hgnc/33107
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11664
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1559
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4076
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24078
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2076
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7910
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3411
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1214
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27867
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1434
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3576
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 247
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 455
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2608
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

19-58965209-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58965209
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58965209
    reference: chr 19
allele count: 2
allele frequency: 1.707912759816228e-5
allele num: 117102
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000375578
  ensembl transcript: ENST00000391696
  gene symbol: ZNF324B
  hgvsc: ENST00000391696.1:c.-748+20A>G
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000337473
  ensembl transcript: ENST00000336614
  gene symbol: ZNF324B
  hgvsc: ENST00000336614.4:c.121+20A>G
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471086
  ensembl transcript: ENST00000594214
  gene symbol: ZNF324B
  hgvsc: ENST00000594214.1:c.121+20A>G
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000438930
  ensembl transcript: ENST00000545523
  gene symbol: ZNF324B
  hgvsc: ENST00000545523.1:c.121+20A>G
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000472178
  ensembl transcript: ENST00000599194
  gene symbol: ZNF324B
  hgvsc: ENST00000599194.1:c.121+20A>G
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000473115
  ensembl transcript: ENST00000599193
  gene symbol: ZNF324B
  hgvsc: ENST00000599193.1:c.121+20A>G
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471122
  ensembl transcript: ENST00000598244
  gene symbol: ZNF324B
  hgvsc: ENST00000598244.1:c.121+20A>G
  variant of: http://identifiers.org/hgnc/33107
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4913
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1198
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8055
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3944
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1909
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22427
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1662
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10777
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2028
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 237
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7507
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4497
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 326
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 817
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26026
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1509
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD

19-58965217-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58965217
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58965217
    reference: chr 19
allele count: 1
allele frequency: 8.59697386519945e-6
allele num: 116320
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000473115
  ensembl transcript: ENST00000599193
  gene symbol: ZNF324B
  hgvsc: ENST00000599193.1:c.121+28T>A
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471122
  ensembl transcript: ENST00000598244
  gene symbol: ZNF324B
  hgvsc: ENST00000598244.1:c.121+28T>A
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471086
  ensembl transcript: ENST00000594214
  gene symbol: ZNF324B
  hgvsc: ENST00000594214.1:c.121+28T>A
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000337473
  ensembl transcript: ENST00000336614
  gene symbol: ZNF324B
  hgvsc: ENST00000336614.4:c.121+28T>A
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000375578
  ensembl transcript: ENST00000391696
  gene symbol: ZNF324B
  hgvsc: ENST00000391696.1:c.-748+28T>A
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000438930
  ensembl transcript: ENST00000545523
  gene symbol: ZNF324B
  hgvsc: ENST00000545523.1:c.121+28T>A
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000472178
  ensembl transcript: ENST00000599194
  gene symbol: ZNF324B
  hgvsc: ENST00000599194.1:c.121+28T>A
  variant of: http://identifiers.org/hgnc/33107
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7217
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19966
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2108
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2007
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3849
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3855
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6517
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10060
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1197
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4951
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22412
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 584
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1724
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 550
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1016
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 603
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2431
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: Other
population: East Asian
reference allele: T
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

19-58965220-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58965220
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58965220
    reference: chr 19
allele count: 1
allele frequency: 8.626936747299768e-6
allele num: 115916
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000472178
  ensembl transcript: ENST00000599194
  gene symbol: ZNF324B
  hgvsc: ENST00000599194.1:c.121+31A>T
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000337473
  ensembl transcript: ENST00000336614
  gene symbol: ZNF324B
  hgvsc: ENST00000336614.4:c.121+31A>T
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000375578
  ensembl transcript: ENST00000391696
  gene symbol: ZNF324B
  hgvsc: ENST00000391696.1:c.-748+31A>T
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000438930
  ensembl transcript: ENST00000545523
  gene symbol: ZNF324B
  hgvsc: ENST00000545523.1:c.121+31A>T
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471086
  ensembl transcript: ENST00000594214
  gene symbol: ZNF324B
  hgvsc: ENST00000594214.1:c.121+31A>T
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471122
  ensembl transcript: ENST00000598244
  gene symbol: ZNF324B
  hgvsc: ENST00000598244.1:c.121+31A>T
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000473115
  ensembl transcript: ENST00000599193
  gene symbol: ZNF324B
  hgvsc: ENST00000599193.1:c.121+31A>T
  variant of: http://identifiers.org/hgnc/33107
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18976
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1195
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3806
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9540
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2002
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6863
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2231
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7007
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5099
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21277
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1383
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3162
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 910
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 222
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1856
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6301
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2351
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5075
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: A
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

19-58965238-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58965238
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58965238
    reference: chr 19
allele count: 1
allele frequency: 8.84830466482622e-6
allele num: 113016
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471122
  ensembl transcript: ENST00000598244
  gene symbol: ZNF324B
  hgvsc: ENST00000598244.1:c.121+49C>T
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000473115
  ensembl transcript: ENST00000599193
  gene symbol: ZNF324B
  hgvsc: ENST00000599193.1:c.121+49C>T
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000472178
  ensembl transcript: ENST00000599194
  gene symbol: ZNF324B
  hgvsc: ENST00000599194.1:c.121+49C>T
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000375578
  ensembl transcript: ENST00000391696
  gene symbol: ZNF324B
  hgvsc: ENST00000391696.1:c.-748+49C>T
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471086
  ensembl transcript: ENST00000594214
  gene symbol: ZNF324B
  hgvsc: ENST00000594214.1:c.121+49C>T
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000438930
  ensembl transcript: ENST00000545523
  gene symbol: ZNF324B
  hgvsc: ENST00000545523.1:c.121+49C>T
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000337473
  ensembl transcript: ENST00000336614
  gene symbol: ZNF324B
  hgvsc: ENST00000336614.4:c.121+49C>T
  variant of: http://identifiers.org/hgnc/33107
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10663
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10853
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6469
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3328
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6641
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11888
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3574
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1963
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 748
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2296
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2115
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9471
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2267
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3935
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4628
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 648
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5129
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum

19-58965545-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58965545
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58965545
    reference: chr 19
allele count: 3
allele frequency: 2.894467707388611e-5
allele num: 103646
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000473115
  ensembl transcript: ENST00000599193
  gene symbol: ZNF324B
  hgvsc: ENST00000599193.1:c.122-50G>A
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000438930
  ensembl transcript: ENST00000545523
  gene symbol: ZNF324B
  hgvsc: ENST00000545523.1:c.122-50G>A
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471122
  ensembl transcript: ENST00000598244
  gene symbol: ZNF324B
  hgvsc: ENST00000598244.1:c.122-50G>A
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000472178
  ensembl transcript: ENST00000599194
  gene symbol: ZNF324B
  hgvsc: ENST00000599194.1:c.122-50G>A
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000375578
  ensembl transcript: ENST00000391696
  gene symbol: ZNF324B
  hgvsc: ENST00000391696.1:c.-747-50G>A
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000337473
  ensembl transcript: ENST00000336614
  gene symbol: ZNF324B
  hgvsc: ENST00000336614.4:c.122-50G>A
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471086
  ensembl transcript: ENST00000594214
  gene symbol: ZNF324B
  hgvsc: ENST00000594214.1:c.122-50G>A
  variant of: http://identifiers.org/hgnc/33107
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 995
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1882
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15171
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16464
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7313
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11413
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7024
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 345
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6963
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6775
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2745
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 713
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 4516
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1060
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 201
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1640
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: QD

19-58965558-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58965558
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58965558
    reference: chr 19
allele count: 1
allele frequency: 9.559498317528296e-6
allele num: 104608
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000438930
  ensembl transcript: ENST00000545523
  gene symbol: ZNF324B
  hgvsc: ENST00000545523.1:c.122-37G>T
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000337473
  ensembl transcript: ENST00000336614
  gene symbol: ZNF324B
  hgvsc: ENST00000336614.4:c.122-37G>T
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471086
  ensembl transcript: ENST00000594214
  gene symbol: ZNF324B
  hgvsc: ENST00000594214.1:c.122-37G>T
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000472178
  ensembl transcript: ENST00000599194
  gene symbol: ZNF324B
  hgvsc: ENST00000599194.1:c.122-37G>T
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471122
  ensembl transcript: ENST00000598244
  gene symbol: ZNF324B
  hgvsc: ENST00000598244.1:c.122-37G>T
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000473115
  ensembl transcript: ENST00000599193
  gene symbol: ZNF324B
  hgvsc: ENST00000599193.1:c.122-37G>T
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000375578
  ensembl transcript: ENST00000391696
  gene symbol: ZNF324B
  hgvsc: ENST00000391696.1:c.-747-37G>T
  variant of: http://identifiers.org/hgnc/33107
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15249
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8405
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18903
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7188
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7870
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1970
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 654
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 197
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4190
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 523
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6436
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5877
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2549
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 472
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8350
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQ

19-58965562-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58965562
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58965562
    reference: chr 19
allele count: 1
allele frequency: 9.498841141380751e-6
allele num: 105276
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471086
  ensembl transcript: ENST00000594214
  gene symbol: ZNF324B
  hgvsc: ENST00000594214.1:c.122-33T>C
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471122
  ensembl transcript: ENST00000598244
  gene symbol: ZNF324B
  hgvsc: ENST00000598244.1:c.122-33T>C
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000337473
  ensembl transcript: ENST00000336614
  gene symbol: ZNF324B
  hgvsc: ENST00000336614.4:c.122-33T>C
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000472178
  ensembl transcript: ENST00000599194
  gene symbol: ZNF324B
  hgvsc: ENST00000599194.1:c.122-33T>C
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000375578
  ensembl transcript: ENST00000391696
  gene symbol: ZNF324B
  hgvsc: ENST00000391696.1:c.-747-33T>C
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000473115
  ensembl transcript: ENST00000599193
  gene symbol: ZNF324B
  hgvsc: ENST00000599193.1:c.122-33T>C
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000438930
  ensembl transcript: ENST00000545523
  gene symbol: ZNF324B
  hgvsc: ENST00000545523.1:c.122-33T>C
  variant of: http://identifiers.org/hgnc/33107
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7076
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2105
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13600
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6226
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8502
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22261
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 303
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1910
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 466
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 319
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5835
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4859
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3869
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2618
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1872
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Other
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ

19-58965562-TG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58965562
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58965561
    reference: chr 19
allele count: 229
allele frequency: 2.175234621376192e-3
allele num: 105276
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000472178
  ensembl transcript: ENST00000599194
  gene symbol: ZNF324B
  hgvsc: ENST00000599194.1:c.122-29delG
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471086
  ensembl transcript: ENST00000594214
  gene symbol: ZNF324B
  hgvsc: ENST00000594214.1:c.122-29delG
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000375578
  ensembl transcript: ENST00000391696
  gene symbol: ZNF324B
  hgvsc: ENST00000391696.1:c.-747-29delG
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000337473
  ensembl transcript: ENST00000336614
  gene symbol: ZNF324B
  hgvsc: ENST00000336614.4:c.122-29delG
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000473115
  ensembl transcript: ENST00000599193
  gene symbol: ZNF324B
  hgvsc: ENST00000599193.1:c.122-29delG
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000438930
  ensembl transcript: ENST00000545523
  gene symbol: ZNF324B
  hgvsc: ENST00000545523.1:c.122-29delG
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471122
  ensembl transcript: ENST00000598244
  gene symbol: ZNF324B
  hgvsc: ENST00000598244.1:c.122-29delG
  variant of: http://identifiers.org/hgnc/33107
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6226
  bin: 1.75e1
  variant carriers: 49
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 3.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 8502
  bin: 2.75e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 7076
  bin: 7.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 4.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 13600
  bin: 1.25e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 22261
  bin: 2.25e1
  variant carriers: 46
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2105
  bin: 3.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 4.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 1910
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 451
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27450
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 2.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 518
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3869
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 932
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 303
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 9.25e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 319
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 2
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: TG
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum

19-58965569-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58965569
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58965569
    reference: chr 19
allele count: 1
allele frequency: 9.340207726219832e-6
allele num: 107064
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000337473
  ensembl transcript: ENST00000336614
  gene symbol: ZNF324B
  hgvsc: ENST00000336614.4:c.122-26G>A
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471122
  ensembl transcript: ENST00000598244
  gene symbol: ZNF324B
  hgvsc: ENST00000598244.1:c.122-26G>A
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000375578
  ensembl transcript: ENST00000391696
  gene symbol: ZNF324B
  hgvsc: ENST00000391696.1:c.-747-26G>A
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000473115
  ensembl transcript: ENST00000599193
  gene symbol: ZNF324B
  hgvsc: ENST00000599193.1:c.122-26G>A
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000438930
  ensembl transcript: ENST00000545523
  gene symbol: ZNF324B
  hgvsc: ENST00000545523.1:c.122-26G>A
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000472178
  ensembl transcript: ENST00000599194
  gene symbol: ZNF324B
  hgvsc: ENST00000599194.1:c.122-26G>A
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471086
  ensembl transcript: ENST00000594214
  gene symbol: ZNF324B
  hgvsc: ENST00000594214.1:c.122-26G>A
  variant of: http://identifiers.org/hgnc/33107
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3913
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6490
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9782
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27563
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9990
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2287
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33974
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1224
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 391
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 844
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 336
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1164
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4426
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

19-58965571-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58965571
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58965571
    reference: chr 19
allele count: 59
allele frequency: 5.476349595307046e-4
allele num: 107736
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000438930
  ensembl transcript: ENST00000545523
  gene symbol: ZNF324B
  hgvsc: ENST00000545523.1:c.122-24G>C
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000472178
  ensembl transcript: ENST00000599194
  gene symbol: ZNF324B
  hgvsc: ENST00000599194.1:c.122-24G>C
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471122
  ensembl transcript: ENST00000598244
  gene symbol: ZNF324B
  hgvsc: ENST00000598244.1:c.122-24G>C
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000473115
  ensembl transcript: ENST00000599193
  gene symbol: ZNF324B
  hgvsc: ENST00000599193.1:c.122-24G>C
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000375578
  ensembl transcript: ENST00000391696
  gene symbol: ZNF324B
  hgvsc: ENST00000391696.1:c.-747-24G>C
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000337473
  ensembl transcript: ENST00000336614
  gene symbol: ZNF324B
  hgvsc: ENST00000336614.4:c.122-24G>C
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471086
  ensembl transcript: ENST00000594214
  gene symbol: ZNF324B
  hgvsc: ENST00000594214.1:c.122-24G>C
  variant of: http://identifiers.org/hgnc/33107
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28087
  bin: 2.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 6280
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3816
  bin: 1.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 10176
  bin: 2.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 9380
  bin: 1.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2328
  bin: 3.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4222
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1100
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 212
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1256
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 302
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 384
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2960
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: East Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP

19-58965583-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58965583
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58965583
    reference: chr 19
allele count: 2
allele frequency: 1.755679623582289e-5
allele num: 113916
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000375578
  ensembl transcript: ENST00000391696
  gene symbol: ZNF324B
  hgvsc: ENST00000391696.1:c.-747-12T>C
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000472178
  ensembl transcript: ENST00000599194
  gene symbol: ZNF324B
  hgvsc: ENST00000599194.1:c.122-12T>C
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000337473
  ensembl transcript: ENST00000336614
  gene symbol: ZNF324B
  hgvsc: ENST00000336614.4:c.122-12T>C
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471086
  ensembl transcript: ENST00000594214
  gene symbol: ZNF324B
  hgvsc: ENST00000594214.1:c.122-12T>C
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000473115
  ensembl transcript: ENST00000599193
  gene symbol: ZNF324B
  hgvsc: ENST00000599193.1:c.122-12T>C
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471122
  ensembl transcript: ENST00000598244
  gene symbol: ZNF324B
  hgvsc: ENST00000598244.1:c.122-12T>C
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000438930
  ensembl transcript: ENST00000545523
  gene symbol: ZNF324B
  hgvsc: ENST00000545523.1:c.122-12T>C
  variant of: http://identifiers.org/hgnc/33107
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3794
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1408
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3586
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12923
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2685
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35828
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45984
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 500
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 480
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 376
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1344
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1013
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: T
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ

19-58965584-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58965584
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58965584
    reference: chr 19
allele count: 1
allele frequency: 8.751662815935028e-6
allele num: 114264
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000438930
  ensembl transcript: ENST00000545523
  gene symbol: ZNF324B
  hgvsc: ENST00000545523.1:c.122-11C>T
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471086
  ensembl transcript: ENST00000594214
  gene symbol: ZNF324B
  hgvsc: ENST00000594214.1:c.122-11C>T
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000472178
  ensembl transcript: ENST00000599194
  gene symbol: ZNF324B
  hgvsc: ENST00000599194.1:c.122-11C>T
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000473115
  ensembl transcript: ENST00000599193
  gene symbol: ZNF324B
  hgvsc: ENST00000599193.1:c.122-11C>T
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000337473
  ensembl transcript: ENST00000336614
  gene symbol: ZNF324B
  hgvsc: ENST00000336614.4:c.122-11C>T
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000375578
  ensembl transcript: ENST00000391696
  gene symbol: ZNF324B
  hgvsc: ENST00000391696.1:c.-747-11C>T
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471122
  ensembl transcript: ENST00000598244
  gene symbol: ZNF324B
  hgvsc: ENST00000598244.1:c.122-11C>T
  variant of: http://identifiers.org/hgnc/33107
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13115
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36143
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3532
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2733
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3386
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1307
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3912
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 525
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 417
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 976
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 516
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum

19-58965587-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58965587
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58965587
    reference: chr 19
allele count: 1
allele frequency: 8.659508139937652e-6
allele num: 115480
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000375578
  ensembl transcript: ENST00000391696
  gene symbol: ZNF324B
  hgvsc: ENST00000391696.1:c.-747-8C>T
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471086
  ensembl transcript: ENST00000594214
  gene symbol: ZNF324B
  hgvsc: ENST00000594214.1:c.122-8C>T
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000337473
  ensembl transcript: ENST00000336614
  gene symbol: ZNF324B
  hgvsc: ENST00000336614.4:c.122-8C>T
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000472178
  ensembl transcript: ENST00000599194
  gene symbol: ZNF324B
  hgvsc: ENST00000599194.1:c.122-8C>T
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471122
  ensembl transcript: ENST00000598244
  gene symbol: ZNF324B
  hgvsc: ENST00000598244.1:c.122-8C>T
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000473115
  ensembl transcript: ENST00000599193
  gene symbol: ZNF324B
  hgvsc: ENST00000599193.1:c.122-8C>T
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000438930
  ensembl transcript: ENST00000545523
  gene symbol: ZNF324B
  hgvsc: ENST00000545523.1:c.122-8C>T
  variant of: http://identifiers.org/hgnc/33107
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2813
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13604
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37104
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2816
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2805
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 425
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1048
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3261
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 325
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 570
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 9.75e1
  variant carriers: 1
hgvs: c.122-8C>T
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: European (Finnish)
population: East Asian
population: Latino
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD

19-58965604-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58965604
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58965604
    reference: chr 19
allele count: 8
allele frequency: 6.687397599224261e-5
allele num: 119628
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000438930
  ensembl transcript: ENST00000545523
  gene symbol: ZNF324B
  hgvsc: ENST00000545523.1:c.131C>T
  hgvsp: ENSP00000438930.1:p.Thr44Ile
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471086
  ensembl transcript: ENST00000594214
  gene symbol: ZNF324B
  hgvsc: ENST00000594214.1:c.131C>T
  hgvsp: ENSP00000471086.1:p.Thr44Ile
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000472178
  ensembl transcript: ENST00000599194
  gene symbol: ZNF324B
  hgvsc: ENST00000599194.1:c.131C>T
  hgvsp: ENSP00000472178.1:p.Thr44Ile
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000473115
  ensembl transcript: ENST00000599193
  gene symbol: ZNF324B
  hgvsc: ENST00000599193.1:c.131C>T
  hgvsp: ENSP00000473115.1:p.Thr44Ile
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000337473
  ensembl transcript: ENST00000336614
  gene symbol: ZNF324B
  hgvsc: ENST00000336614.4:c.131C>T
  hgvsp: ENSP00000337473.3:p.Thr44Ile
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471122
  ensembl transcript: ENST00000598244
  gene symbol: ZNF324B
  hgvsc: ENST00000598244.1:c.131C>T
  hgvsp: ENSP00000471122.1:p.Thr44Ile
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000375578
  ensembl transcript: ENST00000391696
  gene symbol: ZNF324B
  hgvsc: ENST00000391696.1:c.-738C>T
  variant of: http://identifiers.org/hgnc/33107
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39365
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3253
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15703
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 295
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 609
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1018
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 431
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 146
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 230
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Thr44Ile
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: FS
site quality: BaseQRankSum

http://identifiers.org/exac.variant/19-58965609-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58965609
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58965609
    reference: chr 19
allele count: 1
allele frequency: 8.323206765102459e-6
allele num: 120146
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000438930
  ensembl transcript: ENST00000545523
  gene symbol: ZNF324B
  hgvsc: ENST00000545523.1:c.136C>A
  hgvsp: ENST00000545523.1:c.136C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000473115
  ensembl transcript: ENST00000599193
  gene symbol: ZNF324B
  hgvsc: ENST00000599193.1:c.136C>A
  hgvsp: ENST00000599193.1:c.136C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000375578
  ensembl transcript: ENST00000391696
  gene symbol: ZNF324B
  hgvsc: ENST00000391696.1:c.-733C>A
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471086
  ensembl transcript: ENST00000594214
  gene symbol: ZNF324B
  hgvsc: ENST00000594214.1:c.136C>A
  hgvsp: ENST00000594214.1:c.136C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000337473
  ensembl transcript: ENST00000336614
  gene symbol: ZNF324B
  hgvsc: ENST00000336614.4:c.136C>A
  hgvsp: ENST00000336614.4:c.136C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000472178
  ensembl transcript: ENST00000599194
  gene symbol: ZNF324B
  hgvsc: ENST00000599194.1:c.136C>A
  hgvsp: ENST00000599194.1:c.136C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471122
  ensembl transcript: ENST00000598244
  gene symbol: ZNF324B
  hgvsc: ENST00000598244.1:c.136C>A
  hgvsp: ENST00000598244.1:c.136C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33107
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39528
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3388
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16037
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 601
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 435
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 699
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Arg46Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: African
population: Latino
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

19-58965616-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58965616
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58965616
    reference: chr 19
allele count: 3
allele frequency: 2.484718978283556e-5
allele num: 120738
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000337473
  ensembl transcript: ENST00000336614
  gene symbol: ZNF324B
  hgvsc: ENST00000336614.4:c.143G>C
  hgvsp: ENSP00000337473.3:p.Arg48Pro
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471086
  ensembl transcript: ENST00000594214
  gene symbol: ZNF324B
  hgvsc: ENST00000594214.1:c.143G>C
  hgvsp: ENSP00000471086.1:p.Arg48Pro
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000472178
  ensembl transcript: ENST00000599194
  gene symbol: ZNF324B
  hgvsc: ENST00000599194.1:c.143G>C
  hgvsp: ENSP00000472178.1:p.Arg48Pro
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471122
  ensembl transcript: ENST00000598244
  gene symbol: ZNF324B
  hgvsc: ENST00000598244.1:c.143G>C
  hgvsp: ENSP00000471122.1:p.Arg48Pro
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000438930
  ensembl transcript: ENST00000545523
  gene symbol: ZNF324B
  hgvsc: ENST00000545523.1:c.143G>C
  hgvsp: ENSP00000438930.1:p.Arg48Pro
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000473115
  ensembl transcript: ENST00000599193
  gene symbol: ZNF324B
  hgvsc: ENST00000599193.1:c.143G>C
  hgvsp: ENSP00000473115.1:p.Arg48Pro
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000375578
  ensembl transcript: ENST00000391696
  gene symbol: ZNF324B
  hgvsc: ENST00000391696.1:c.-726G>C
  variant of: http://identifiers.org/hgnc/33107
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3457
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16348
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39832
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54729
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Arg48Pro
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

19-58965619-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58965619
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58965619
    reference: chr 19
allele count: 1
allele frequency: 8.274583788435442e-6
allele num: 120852
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000438930
  ensembl transcript: ENST00000545523
  gene symbol: ZNF324B
  hgvsc: ENST00000545523.1:c.146T>C
  hgvsp: ENSP00000438930.1:p.Val49Ala
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471122
  ensembl transcript: ENST00000598244
  gene symbol: ZNF324B
  hgvsc: ENST00000598244.1:c.146T>C
  hgvsp: ENSP00000471122.1:p.Val49Ala
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471086
  ensembl transcript: ENST00000594214
  gene symbol: ZNF324B
  hgvsc: ENST00000594214.1:c.146T>C
  hgvsp: ENSP00000471086.1:p.Val49Ala
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000472178
  ensembl transcript: ENST00000599194
  gene symbol: ZNF324B
  hgvsc: ENST00000599194.1:c.146T>C
  hgvsp: ENSP00000472178.1:p.Val49Ala
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000473115
  ensembl transcript: ENST00000599193
  gene symbol: ZNF324B
  hgvsc: ENST00000599193.1:c.146T>C
  hgvsp: ENSP00000473115.1:p.Val49Ala
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000375578
  ensembl transcript: ENST00000391696
  gene symbol: ZNF324B
  hgvsc: ENST00000391696.1:c.-723T>C
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000337473
  ensembl transcript: ENST00000336614
  gene symbol: ZNF324B
  hgvsc: ENST00000336614.4:c.146T>C
  hgvsp: ENSP00000337473.3:p.Val49Ala
  variant of: http://identifiers.org/hgnc/33107
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39930
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16404
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3447
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 315
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3881
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54911
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Val49Ala
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
reference allele: T
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum

19-58965623-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58965623
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58965623
    reference: chr 19
allele count: 2
allele frequency: 1.653575857792476e-5
allele num: 120950
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000375578
  ensembl transcript: ENST00000391696
  gene symbol: ZNF324B
  hgvsc: ENST00000391696.1:c.-719C>T
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000337473
  ensembl transcript: ENST00000336614
  gene symbol: ZNF324B
  hgvsc: ENST00000336614.4:c.150C>T
  hgvsp: ENST00000336614.4:c.150C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000438930
  ensembl transcript: ENST00000545523
  gene symbol: ZNF324B
  hgvsc: ENST00000545523.1:c.150C>T
  hgvsp: ENST00000545523.1:c.150C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000472178
  ensembl transcript: ENST00000599194
  gene symbol: ZNF324B
  hgvsc: ENST00000599194.1:c.150C>T
  hgvsp: ENST00000599194.1:c.150C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000473115
  ensembl transcript: ENST00000599193
  gene symbol: ZNF324B
  hgvsc: ENST00000599193.1:c.150C>T
  hgvsp: ENST00000599193.1:c.150C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471122
  ensembl transcript: ENST00000598244
  gene symbol: ZNF324B
  hgvsc: ENST00000598244.1:c.150C>T
  hgvsp: ENST00000598244.1:c.150C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471086
  ensembl transcript: ENST00000594214
  gene symbol: ZNF324B
  hgvsc: ENST00000594214.1:c.150C>T
  hgvsp: ENST00000594214.1:c.150C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/33107
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16448
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3463
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39977
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55024
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 263
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Val50Val
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS

19-58965624-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58965624
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58965624
    reference: chr 19
allele count: 1
allele frequency: 8.266512358435975e-6
allele num: 120970
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471122
  ensembl transcript: ENST00000598244
  gene symbol: ZNF324B
  hgvsc: ENST00000598244.1:c.151A>G
  hgvsp: ENSP00000471122.1:p.Ile51Val
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000472178
  ensembl transcript: ENST00000599194
  gene symbol: ZNF324B
  hgvsc: ENST00000599194.1:c.151A>G
  hgvsp: ENSP00000472178.1:p.Ile51Val
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000438930
  ensembl transcript: ENST00000545523
  gene symbol: ZNF324B
  hgvsc: ENST00000545523.1:c.151A>G
  hgvsp: ENSP00000438930.1:p.Ile51Val
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471086
  ensembl transcript: ENST00000594214
  gene symbol: ZNF324B
  hgvsc: ENST00000594214.1:c.151A>G
  hgvsp: ENSP00000471086.1:p.Ile51Val
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000473115
  ensembl transcript: ENST00000599193
  gene symbol: ZNF324B
  hgvsc: ENST00000599193.1:c.151A>G
  hgvsp: ENSP00000473115.1:p.Ile51Val
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000375578
  ensembl transcript: ENST00000391696
  gene symbol: ZNF324B
  hgvsc: ENST00000391696.1:c.-718A>G
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000337473
  ensembl transcript: ENST00000336614
  gene symbol: ZNF324B
  hgvsc: ENST00000336614.4:c.151A>G
  hgvsp: ENSP00000337473.3:p.Ile51Val
  variant of: http://identifiers.org/hgnc/33107
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16461
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3465
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39971
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55034
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 616
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3886
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 260
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ile51Val
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum

http://identifiers.org/exac.variant/19-58965629-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58965629
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58965629
    reference: chr 19
allele count: 1
allele frequency: 8.260639703938672e-6
allele num: 121056
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471086
  ensembl transcript: ENST00000594214
  gene symbol: ZNF324B
  hgvsc: ENST00000594214.1:c.156A>C
  hgvsp: ENSP00000471086.1:p.Gln52His
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000438930
  ensembl transcript: ENST00000545523
  gene symbol: ZNF324B
  hgvsc: ENST00000545523.1:c.156A>C
  hgvsp: ENSP00000438930.1:p.Gln52His
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000472178
  ensembl transcript: ENST00000599194
  gene symbol: ZNF324B
  hgvsc: ENST00000599194.1:c.156A>C
  hgvsp: ENSP00000472178.1:p.Gln52His
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000473115
  ensembl transcript: ENST00000599193
  gene symbol: ZNF324B
  hgvsc: ENST00000599193.1:c.156A>C
  hgvsp: ENSP00000473115.1:p.Gln52His
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000375578
  ensembl transcript: ENST00000391696
  gene symbol: ZNF324B
  hgvsc: ENST00000391696.1:c.-713A>C
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000337473
  ensembl transcript: ENST00000336614
  gene symbol: ZNF324B
  hgvsc: ENST00000336614.4:c.156A>C
  hgvsp: ENSP00000337473.3:p.Gln52His
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471122
  ensembl transcript: ENST00000598244
  gene symbol: ZNF324B
  hgvsc: ENST00000598244.1:c.156A>C
  hgvsp: ENSP00000471122.1:p.Gln52His
  variant of: http://identifiers.org/hgnc/33107
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3459
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40024
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16487
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55109
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 428
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 146
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 614
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Gln52His
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ

19-58965629-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58965629
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58965629
    reference: chr 19
allele count: 1
allele frequency: 8.260639703938672e-6
allele num: 121056
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000473115
  ensembl transcript: ENST00000599193
  gene symbol: ZNF324B
  hgvsc: ENST00000599193.1:c.156A>G
  hgvsp: ENST00000599193.1:c.156A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000472178
  ensembl transcript: ENST00000599194
  gene symbol: ZNF324B
  hgvsc: ENST00000599194.1:c.156A>G
  hgvsp: ENST00000599194.1:c.156A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000337473
  ensembl transcript: ENST00000336614
  gene symbol: ZNF324B
  hgvsc: ENST00000336614.4:c.156A>G
  hgvsp: ENST00000336614.4:c.156A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471086
  ensembl transcript: ENST00000594214
  gene symbol: ZNF324B
  hgvsc: ENST00000594214.1:c.156A>G
  hgvsp: ENST00000594214.1:c.156A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000375578
  ensembl transcript: ENST00000391696
  gene symbol: ZNF324B
  hgvsc: ENST00000391696.1:c.-713A>G
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471122
  ensembl transcript: ENST00000598244
  gene symbol: ZNF324B
  hgvsc: ENST00000598244.1:c.156A>G
  hgvsp: ENST00000598244.1:c.156A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000438930
  ensembl transcript: ENST00000545523
  gene symbol: ZNF324B
  hgvsc: ENST00000545523.1:c.156A>G
  hgvsp: ENST00000545523.1:c.156A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/33107
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3459
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16487
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40024
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3887
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 215
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 614
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 428
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Gln52Gln
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: African
reference allele: A
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: DP

19-58965630-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58965630
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58965630
    reference: chr 19
allele count: 1
allele frequency: 8.259957378619926e-6
allele num: 121066
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000438930
  ensembl transcript: ENST00000545523
  gene symbol: ZNF324B
  hgvsc: ENST00000545523.1:c.157C>T
  hgvsp: ENSP00000438930.1:p.Leu53Phe
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000337473
  ensembl transcript: ENST00000336614
  gene symbol: ZNF324B
  hgvsc: ENST00000336614.4:c.157C>T
  hgvsp: ENSP00000337473.3:p.Leu53Phe
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000375578
  ensembl transcript: ENST00000391696
  gene symbol: ZNF324B
  hgvsc: ENST00000391696.1:c.-712C>T
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471122
  ensembl transcript: ENST00000598244
  gene symbol: ZNF324B
  hgvsc: ENST00000598244.1:c.157C>T
  hgvsp: ENSP00000471122.1:p.Leu53Phe
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000473115
  ensembl transcript: ENST00000599193
  gene symbol: ZNF324B
  hgvsc: ENST00000599193.1:c.157C>T
  hgvsp: ENSP00000473115.1:p.Leu53Phe
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471086
  ensembl transcript: ENST00000594214
  gene symbol: ZNF324B
  hgvsc: ENST00000594214.1:c.157C>T
  hgvsp: ENSP00000471086.1:p.Leu53Phe
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000472178
  ensembl transcript: ENST00000599194
  gene symbol: ZNF324B
  hgvsc: ENST00000599194.1:c.157C>T
  hgvsp: ENSP00000472178.1:p.Leu53Phe
  variant of: http://identifiers.org/hgnc/33107
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40023
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16494
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3465
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 615
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Leu53Phe
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: Other
population: European (Finnish)
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum

19-58965633-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58965633
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58965633
    reference: chr 19
allele count: 2
allele frequency: 1.651827747402501e-5
allele num: 121078
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471086
  ensembl transcript: ENST00000594214
  gene symbol: ZNF324B
  hgvsc: ENST00000594214.1:c.160G>A
  hgvsp: ENSP00000471086.1:p.Glu54Lys
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000473115
  ensembl transcript: ENST00000599193
  gene symbol: ZNF324B
  hgvsc: ENST00000599193.1:c.160G>A
  hgvsp: ENSP00000473115.1:p.Glu54Lys
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000472178
  ensembl transcript: ENST00000599194
  gene symbol: ZNF324B
  hgvsc: ENST00000599194.1:c.160G>A
  hgvsp: ENSP00000472178.1:p.Glu54Lys
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000375578
  ensembl transcript: ENST00000391696
  gene symbol: ZNF324B
  hgvsc: ENST00000391696.1:c.-709G>A
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000337473
  ensembl transcript: ENST00000336614
  gene symbol: ZNF324B
  hgvsc: ENST00000336614.4:c.160G>A
  hgvsp: ENSP00000337473.3:p.Glu54Lys
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471122
  ensembl transcript: ENST00000598244
  gene symbol: ZNF324B
  hgvsc: ENST00000598244.1:c.160G>A
  hgvsp: ENSP00000471122.1:p.Glu54Lys
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000438930
  ensembl transcript: ENST00000545523
  gene symbol: ZNF324B
  hgvsc: ENST00000545523.1:c.160G>A
  hgvsp: ENSP00000438930.1:p.Glu54Lys
  variant of: http://identifiers.org/hgnc/33107
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3466
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40017
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16510
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3896
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Glu54Lys
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: East Asian
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

19-58965635-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58965635
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58965635
    reference: chr 19
allele count: 1
allele frequency: 8.257774694875225e-6
allele num: 121098
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471086
  ensembl transcript: ENST00000594214
  gene symbol: ZNF324B
  hgvsc: ENST00000594214.1:c.162G>A
  hgvsp: ENST00000594214.1:c.162G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000337473
  ensembl transcript: ENST00000336614
  gene symbol: ZNF324B
  hgvsc: ENST00000336614.4:c.162G>A
  hgvsp: ENST00000336614.4:c.162G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000438930
  ensembl transcript: ENST00000545523
  gene symbol: ZNF324B
  hgvsc: ENST00000545523.1:c.162G>A
  hgvsp: ENST00000545523.1:c.162G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000473115
  ensembl transcript: ENST00000599193
  gene symbol: ZNF324B
  hgvsc: ENST00000599193.1:c.162G>A
  hgvsp: ENST00000599193.1:c.162G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471122
  ensembl transcript: ENST00000598244
  gene symbol: ZNF324B
  hgvsc: ENST00000598244.1:c.162G>A
  hgvsp: ENST00000598244.1:c.162G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000375578
  ensembl transcript: ENST00000391696
  gene symbol: ZNF324B
  hgvsc: ENST00000391696.1:c.-707G>A
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000472178
  ensembl transcript: ENST00000599194
  gene symbol: ZNF324B
  hgvsc: ENST00000599194.1:c.162G>A
  hgvsp: ENST00000599194.1:c.162G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/33107
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16518
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40026
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3468
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55139
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 616
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Glu54Glu
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum

19-58965637-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58965637
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58965637
    reference: chr 19
allele count: 5
allele frequency: 4.128137384412153e-5
allele num: 121120
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000472178
  ensembl transcript: ENST00000599194
  gene symbol: ZNF324B
  hgvsc: ENST00000599194.1:c.164G>A
  hgvsp: ENSP00000472178.1:p.Arg55His
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000337473
  ensembl transcript: ENST00000336614
  gene symbol: ZNF324B
  hgvsc: ENST00000336614.4:c.164G>A
  hgvsp: ENSP00000337473.3:p.Arg55His
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000438930
  ensembl transcript: ENST00000545523
  gene symbol: ZNF324B
  hgvsc: ENST00000545523.1:c.164G>A
  hgvsp: ENSP00000438930.1:p.Arg55His
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000473115
  ensembl transcript: ENST00000599193
  gene symbol: ZNF324B
  hgvsc: ENST00000599193.1:c.164G>A
  hgvsp: ENSP00000473115.1:p.Arg55His
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471086
  ensembl transcript: ENST00000594214
  gene symbol: ZNF324B
  hgvsc: ENST00000594214.1:c.164G>A
  hgvsp: ENSP00000471086.1:p.Arg55His
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000375578
  ensembl transcript: ENST00000391696
  gene symbol: ZNF324B
  hgvsc: ENST00000391696.1:c.-705G>A
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471122
  ensembl transcript: ENST00000598244
  gene symbol: ZNF324B
  hgvsc: ENST00000598244.1:c.164G>A
  hgvsp: ENSP00000471122.1:p.Arg55His
  variant of: http://identifiers.org/hgnc/33107
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16536
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40022
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3465
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 615
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3905
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Arg55His
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS

19-58965638-TG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58965638
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58965637
    reference: chr 19
allele count: 4
allele frequency: 3.302455375571737e-5
allele num: 121122
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471086
  ensembl transcript: ENST00000594214
  gene symbol: ZNF324B
  hgvsc: ENST00000594214.1:c.167delG
  hgvsp: ENSP00000471086.1:p.Gly56AlafsTer12
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000375578
  ensembl transcript: ENST00000391696
  gene symbol: ZNF324B
  hgvsc: ENST00000391696.1:c.-702delG
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000438930
  ensembl transcript: ENST00000545523
  gene symbol: ZNF324B
  hgvsc: ENST00000545523.1:c.167delG
  hgvsp: ENSP00000438930.1:p.Gly56AlafsTer12
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000472178
  ensembl transcript: ENST00000599194
  gene symbol: ZNF324B
  hgvsc: ENST00000599194.1:c.167delG
  hgvsp: ENSP00000472178.1:p.Gly56AlafsTer12
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000473115
  ensembl transcript: ENST00000599193
  gene symbol: ZNF324B
  hgvsc: ENST00000599193.1:c.167delG
  hgvsp: ENSP00000473115.1:p.Gly56AlafsTer12
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000337473
  ensembl transcript: ENST00000336614
  gene symbol: ZNF324B
  hgvsc: ENST00000336614.4:c.167delG
  hgvsp: ENSP00000337473.3:p.Gly56AlafsTer12
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471122
  ensembl transcript: ENST00000598244
  gene symbol: ZNF324B
  hgvsc: ENST00000598244.1:c.167delG
  hgvsp: ENSP00000471122.1:p.Gly56AlafsTer12
  variant of: http://identifiers.org/hgnc/33107
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16545
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3469
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 40022
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 616
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3908
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 428
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Gly56AlafsTer12
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: TG
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum

19-58965642-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58965642
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58965642
    reference: chr 19
allele count: 4
allele frequency: 3.30169211721007e-5
allele num: 121150
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000472178
  ensembl transcript: ENST00000599194
  gene symbol: ZNF324B
  hgvsc: ENST00000599194.1:c.169G>A
  hgvsp: ENSP00000472178.1:p.Glu57Lys
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000438930
  ensembl transcript: ENST00000545523
  gene symbol: ZNF324B
  hgvsc: ENST00000545523.1:c.169G>A
  hgvsp: ENSP00000438930.1:p.Glu57Lys
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471086
  ensembl transcript: ENST00000594214
  gene symbol: ZNF324B
  hgvsc: ENST00000594214.1:c.169G>A
  hgvsp: ENSP00000471086.1:p.Glu57Lys
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000473115
  ensembl transcript: ENST00000599193
  gene symbol: ZNF324B
  hgvsc: ENST00000599193.1:c.169G>A
  hgvsp: ENSP00000473115.1:p.Glu57Lys
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471122
  ensembl transcript: ENST00000598244
  gene symbol: ZNF324B
  hgvsc: ENST00000598244.1:c.169G>A
  hgvsp: ENSP00000471122.1:p.Glu57Lys
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000337473
  ensembl transcript: ENST00000336614
  gene symbol: ZNF324B
  hgvsc: ENST00000336614.4:c.169G>A
  hgvsp: ENSP00000337473.3:p.Glu57Lys
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000375578
  ensembl transcript: ENST00000391696
  gene symbol: ZNF324B
  hgvsc: ENST00000391696.1:c.-700G>A
  variant of: http://identifiers.org/hgnc/33107
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3471
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16561
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40022
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 620
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3911
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Glu57Lys
num of homozygotes: 0
population: Other
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: QD

19-58965643-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58965643
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58965643
    reference: chr 19
allele count: 2
allele frequency: 1.650737054094653e-5
allele num: 121158
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000473115
  ensembl transcript: ENST00000599193
  gene symbol: ZNF324B
  hgvsc: ENST00000599193.1:c.170A>G
  hgvsp: ENSP00000473115.1:p.Glu57Gly
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471086
  ensembl transcript: ENST00000594214
  gene symbol: ZNF324B
  hgvsc: ENST00000594214.1:c.170A>G
  hgvsp: ENSP00000471086.1:p.Glu57Gly
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000337473
  ensembl transcript: ENST00000336614
  gene symbol: ZNF324B
  hgvsc: ENST00000336614.4:c.170A>G
  hgvsp: ENSP00000337473.3:p.Glu57Gly
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000375578
  ensembl transcript: ENST00000391696
  gene symbol: ZNF324B
  hgvsc: ENST00000391696.1:c.-699A>G
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000438930
  ensembl transcript: ENST00000545523
  gene symbol: ZNF324B
  hgvsc: ENST00000545523.1:c.170A>G
  hgvsp: ENSP00000438930.1:p.Glu57Gly
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471122
  ensembl transcript: ENST00000598244
  gene symbol: ZNF324B
  hgvsc: ENST00000598244.1:c.170A>G
  hgvsp: ENSP00000471122.1:p.Glu57Gly
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000472178
  ensembl transcript: ENST00000599194
  gene symbol: ZNF324B
  hgvsc: ENST00000599194.1:c.170A>G
  hgvsp: ENSP00000472178.1:p.Glu57Gly
  variant of: http://identifiers.org/hgnc/33107
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3475
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40030
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16562
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3915
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Glu57Gly
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQ

19-58965647-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58965647
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 58965647
    reference: chr 19
allele count: 1
allele frequency: 8.252050634582693e-6
allele num: 121182
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000375578
  ensembl transcript: ENST00000391696
  gene symbol: ZNF324B
  hgvsc: ENST00000391696.1:c.-695G>T
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471086
  ensembl transcript: ENST00000594214
  gene symbol: ZNF324B
  hgvsc: ENST00000594214.1:c.174G>T
  hgvsp: ENSP00000471086.1:p.Glu58Asp
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000471122
  ensembl transcript: ENST00000598244
  gene symbol: ZNF324B
  hgvsc: ENST00000598244.1:c.174G>T
  hgvsp: ENSP00000471122.1:p.Glu58Asp
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000337473
  ensembl transcript: ENST00000336614
  gene symbol: ZNF324B
  hgvsc: ENST00000336614.4:c.174G>T
  hgvsp: ENSP00000337473.3:p.Glu58Asp
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000472178
  ensembl transcript: ENST00000599194
  gene symbol: ZNF324B
  hgvsc: ENST00000599194.1:c.174G>T
  hgvsp: ENSP00000472178.1:p.Glu58Asp
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000438930
  ensembl transcript: ENST00000545523
  gene symbol: ZNF324B
  hgvsc: ENST00000545523.1:c.174G>T
  hgvsp: ENSP00000438930.1:p.Glu58Asp
  variant of: http://identifiers.org/hgnc/33107
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000249471
  ensembl protein: ENSP00000473115
  ensembl transcript: ENST00000599193
  gene symbol: ZNF324B
  hgvsc: ENST00000599193.1:c.174G>T
  hgvsp: ENSP00000473115.1:p.Glu58Asp
  variant of: http://identifiers.org/hgnc/33107
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3476
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40039
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16567
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Glu58Asp
num of homozygotes: 0
reference allele: G

GenotypeQuality
all individuals: 140
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3285
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4567
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 657
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 748
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 22
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 805
bin: 4.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10860
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5578
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 460
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3318
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4542
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.581577860388269e-5
allele num: 38736
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5828
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.355e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.55e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.591e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.711e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.77e-1

DP
type: SiteQuality
SIO_000300: 6.6533e5

QD
type: SiteQuality
SIO_000300: 5.03e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.66e-1

GenotypeQuality
all individuals: 1056
bin: 4.25e1
variant carriers: 2

GenotypeQuality
all individuals: 7207
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 135
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 15
bin: 8.75e1
variant carriers: 2

GenotypeQuality
all individuals: 300
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3091
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 115
bin: 9.75e1
variant carriers: 36

GenotypeQuality
all individuals: 176
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 24
bin: 9.25e1
variant carriers: 3

South Asian
type: Population
allele count: 23
allele frequency: 2.175146585965576e-3
allele num: 10574
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4394
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 448
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.795332136445242e-4
allele num: 5570
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5394
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 13
allele frequency: 3.456527519276788e-4
allele num: 37610
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3196
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.65e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.69e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.48e-1

DP
type: SiteQuality
SIO_000300: 6.47267e5

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.15e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.44e-1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.223e1

GenotypeQuality
all individuals: 7318
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 1052
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20772
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2480
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 996
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3281
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6275
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10540
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 37484
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5566
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3188
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5386
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4376
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 446
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.71e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.85e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.93e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.817e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.85e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.89e-1

QD
type: SiteQuality
SIO_000300: 3.01e0

DP
type: SiteQuality
SIO_000300: 6.46296e5

VQSLOD
type: SiteQuality
SIO_000300: -2.599e0

GenotypeQuality
all individuals: 150
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1832
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1383
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1253
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 794
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5564
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4930
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4026
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9630
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.901241731461065e-5
allele num: 34468
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2910
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4964
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 6.25579e5

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -8.110000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.78e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.78e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.777e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.01e-2

QD
type: SiteQuality
SIO_000300: 9.42e0

VQSLOD
type: SiteQuality
SIO_000300: -3.689e0

MQ
type: SiteQuality
SIO_000300: 5.855e1

GenotypeQuality
all individuals: 7320
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1317
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6249
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 316
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1380
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 34544
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4956
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4050
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4956
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9688
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 406
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.4065e1

DP
type: SiteQuality
SIO_000300: 6.25415e5

VQSLOD
type: SiteQuality
SIO_000300: -1.867e0

QD
type: SiteQuality
SIO_000300: 1.528e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.97e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.12e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.31e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.31e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.59e-1

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

GenotypeQuality
all individuals: 9229
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2797
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3213
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1526
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 8
allele frequency: 1.209555488358028e-3
allele num: 6614
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 18
allele frequency: 2.698327037236913e-4
allele num: 66708
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.727414061150458e-4
allele num: 11578
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.68e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.0e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.16e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.84e-1

DP
type: SiteQuality
SIO_000300: 1.950122e6

QD
type: SiteQuality
SIO_000300: 1.499e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.56e0

MQ
type: SiteQuality
SIO_000300: 5.969e1

GenotypeQuality
all individuals: 8
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6856
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 9
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9230
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1525
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 22
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3994
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499115521842113e-5
allele num: 66706
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.1e-2

MQ
type: SiteQuality
SIO_000300: 5.864e1

FS
type: SiteQuality
SIO_000300: 2.067e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.67e-1

QD
type: SiteQuality
SIO_000300: 9.800000000000001e0

VQSLOD
type: SiteQuality
SIO_000300: -1.519e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.9e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -7.92e-1

DP
type: SiteQuality
SIO_000300: 1.948713e6

GenotypeQuality
all individuals: 24
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1144
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9227
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1525
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2794
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
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variant carriers: 0

GenotypeQuality
all individuals: 3995
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.211240310077519e-4
allele num: 16512
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66708
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.71e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.55e0

FS
type: SiteQuality
SIO_000300: 2.102e0

DP
type: SiteQuality
SIO_000300: 1.948684e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 8.0e-2

VQSLOD
type: SiteQuality
SIO_000300: 7.25e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.4e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 1.311e1

GenotypeQuality
all individuals: 31859
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1522
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1142
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3212
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6851
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 9230
bin: 6.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66714
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.21e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.39e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.983e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.61e-1

DP
type: SiteQuality
SIO_000300: 1.948921e6

VQSLOD
type: SiteQuality
SIO_000300: 4.61e0

MQRankSum
type: SiteQuality
SIO_000300: 2.54e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.51e-1

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

GenotypeQuality
all individuals: 3212
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 17
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2789
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1522
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3998
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6851
bin: 9.75e1
variant carriers: 2

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.997871511227029e-5
allele num: 66714
num of homozygotes: 0

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

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

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

Other
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
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South Asian
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allele num: 16512
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East Asian
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Latino
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allele frequency: 0.0e0
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African
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European (Finnish)
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allele frequency: 0.0e0
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MQ
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ReadPosRankSum
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VQSLOD
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DP
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QD
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FS
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BaseQRankSum
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InbreedingCoeff
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ClippingRankSum
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Finnish)
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allele frequency: 0.0e0
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African
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Latino
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allele frequency: 0.0e0
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Other
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European (Non-Finnish)
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allele frequency: 1.498576352465158e-5
allele num: 66730
num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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East Asian
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Other
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South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.498531439189594e-5
allele num: 66732
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

ReadPosRankSum
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DP
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InbreedingCoeff
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BaseQRankSum
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FS
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MQRankSum
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ClippingRankSum
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VQSLOD
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QD
type: SiteQuality
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MQ
type: SiteQuality
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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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South Asian
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East Asian
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allele num: 8654
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European (Non-Finnish)
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Latino
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Other
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African
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

MQ
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ReadPosRankSum
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VQSLOD
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BaseQRankSum
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InbreedingCoeff
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FS
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MQRankSum
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DP
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ClippingRankSum
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QD
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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
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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Latino
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European (Non-Finnish)
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allele num: 66732
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South Asian
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East Asian
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Other
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BaseQRankSum
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MQ
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DP
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VQSLOD
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FS
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MQRankSum
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QD
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InbreedingCoeff
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ClippingRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11578
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European (Non-Finnish)
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allele count: 4
allele frequency: 5.993946114424431e-5
allele num: 66734
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South Asian
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allele frequency: 6.056201550387597e-5
allele num: 16512
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European (Finnish)
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allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele num: 908
num of homozygotes: 0

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

East Asian
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allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498441620714457e-5
allele num: 66736
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

QD
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MQ
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FS
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ReadPosRankSum
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BaseQRankSum
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ClippingRankSum
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DP
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SIO_000300: 1.948953e6

VQSLOD
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MQRankSum
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SIO_000300: 9.67e-1

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

South Asian
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allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.498441620714457e-5
allele num: 66736
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

BaseQRankSum
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FS
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MQ
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ClippingRankSum
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ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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DP
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QD
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VQSLOD
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SIO_000300: 9.66e-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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variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498531439189594e-5
allele num: 66732
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: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

FS
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ClippingRankSum
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BaseQRankSum
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SIO_000300: -2.754e0

InbreedingCoeff
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MQRankSum
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DP
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QD
type: SiteQuality
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VQSLOD
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MQ
type: SiteQuality
SIO_000300: 5.876e1

ReadPosRankSum
type: SiteQuality
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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
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allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.498576352465158e-5
allele num: 66730
num of homozygotes: 0

Other
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num of homozygotes: 0

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

Latino
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num of homozygotes: 0

MQRankSum
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SIO_000300: -1.35e-1

InbreedingCoeff
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DP
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FS
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BaseQRankSum
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SIO_000300: -1.184e0

ReadPosRankSum
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MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.6e-2

VQSLOD
type: SiteQuality
SIO_000300: 8.400000000000001e-2

QD
type: SiteQuality
SIO_000300: 9.1e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele count: 0
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num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.591121091725686e-4
allele num: 11578
num of homozygotes: 0

African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

Other
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num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.6e-2

DP
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MQ
type: SiteQuality
SIO_000300: 6.0e1

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

Latino
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allele count: 2
allele frequency: 1.727414061150458e-4
allele num: 11578
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 3
allele frequency: 4.535833081342606e-4
allele num: 6614
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 71
allele frequency: 1.063989210250262e-3
allele num: 66730
num of homozygotes: 0

East Asian
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num of homozygotes: 0

South Asian
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Other
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DP
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ClippingRankSum
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VQSLOD
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ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
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MQRankSum
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FS
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MQ
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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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Latino
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num of homozygotes: 0

European (Non-Finnish)
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allele num: 66722
num of homozygotes: 0

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

European (Finnish)
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num of homozygotes: 0

Latino
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East Asian
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African
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Other
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South Asian
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European (Non-Finnish)
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FS
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InbreedingCoeff
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MQ
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DP
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MQRankSum
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ClippingRankSum
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QD
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ReadPosRankSum
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BaseQRankSum
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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African
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East Asian
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Other
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European (Non-Finnish)
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Latino
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South Asian
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BaseQRankSum
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ClippingRankSum
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DP
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MQ
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MQRankSum
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FS
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InbreedingCoeff
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VQSLOD
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QD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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African
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East Asian
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South Asian
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European (Non-Finnish)
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allele frequency: 1.498845888665727e-5
allele num: 66718
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 6.51e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.6e-1

FS
type: SiteQuality
SIO_000300: 2.734e0

MQRankSum
type: SiteQuality
SIO_000300: 1.04e0

InbreedingCoeff
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SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.944754e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.51e-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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Latino
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allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

South Asian
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allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

African
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allele count: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498800959232614e-5
allele num: 66720
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 8654
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
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InbreedingCoeff
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QD
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MQRankSum
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FS
type: SiteQuality
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DP
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MQ
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VQSLOD
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ReadPosRankSum
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 9.611687812379854e-5
allele num: 10404
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66654
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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East Asian
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allele count: 6
allele frequency: 6.933210076265311e-4
allele num: 8654
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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BaseQRankSum
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InbreedingCoeff
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VQSLOD
type: SiteQuality
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MQRankSum
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DP
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ClippingRankSum
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FS
type: SiteQuality
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ReadPosRankSum
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MQ
type: SiteQuality
SIO_000300: 5.982e1

QD
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Latino
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allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.500645277469312e-5
allele num: 66638
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16440
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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Other
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allele frequency: 1.101321585903084e-3
allele num: 908
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.965e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.346e1

DP
type: SiteQuality
SIO_000300: 1.939727e6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 8.644536652835408e-5
allele num: 11568
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
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66634
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East Asian
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allele frequency: 0.0e0
allele num: 8654
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 1.56e0

QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -1.587e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.914e0

MQRankSum
type: SiteQuality
SIO_000300: 3.79e-1

FS
type: SiteQuality
SIO_000300: 1.49e0

VQSLOD
type: SiteQuality
SIO_000300: -3.321e-1

DP
type: SiteQuality
SIO_000300: 1.939054e6

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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variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66524
num of homozygotes: 0

South Asian
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allele count: 68
allele frequency: 4.199604743083004e-3
allele num: 16192
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11552
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.106194690265487e-3
allele num: 904
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African
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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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ClippingRankSum
type: SiteQuality
SIO_000300: -1.43e-1

FS
type: SiteQuality
SIO_000300: 7.14e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.43e0

ReadPosRankSum
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DP
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SIO_000300: 1.927907e6

MQ
type: SiteQuality
SIO_000300: 5.97e1

BaseQRankSum
type: SiteQuality
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InbreedingCoeff
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QD
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MQRankSum
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11548
num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6610
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African
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.504573904670197e-5
allele num: 66464
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South Asian
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East Asian
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InbreedingCoeff
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MQ
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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FS
type: SiteQuality
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MQRankSum
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BaseQRankSum
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DP
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QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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South Asian
type: Population
allele count: 0
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African
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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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European (Non-Finnish)
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allele count: 1
allele frequency: 1.505479947007106e-5
allele num: 66424
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East Asian
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European (Finnish)
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ClippingRankSum
type: SiteQuality
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FS
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DP
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MQRankSum
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VQSLOD
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BaseQRankSum
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InbreedingCoeff
type: SiteQuality
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MQ
type: SiteQuality
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QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 2.16e-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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East Asian
type: Population
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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Other
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allele frequency: 0.0e0
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European (Finnish)
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South Asian
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African
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European (Non-Finnish)
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allele count: 2
allele frequency: 3.016409266409266e-5
allele num: 66304
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VQSLOD
type: SiteQuality
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MQRankSum
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InbreedingCoeff
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MQ
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FS
type: SiteQuality
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DP
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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QD
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ClippingRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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European (Finnish)
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South Asian
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East Asian
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Latino
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allele num: 11522
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African
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BaseQRankSum
type: SiteQuality
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ClippingRankSum
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FS
type: SiteQuality
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QD
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InbreedingCoeff
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DP
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MQ
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ReadPosRankSum
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VQSLOD
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MQRankSum
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 12

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1445
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 4.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14844
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8582
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65754
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6590
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10316
num of homozygotes: 0

Latino
type: Population
allele count: 12
allele frequency: 1.049501486793773e-3
allele num: 11434
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.14e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.042e0

DP
type: SiteQuality
SIO_000300: 1.850792e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

MQRankSum
type: SiteQuality
SIO_000300: 5.86e-1

FS
type: SiteQuality
SIO_000300: 5.995e0

VQSLOD
type: SiteQuality
SIO_000300: -7.619e-1

MQ
type: SiteQuality
SIO_000300: 5.881e1

QD
type: SiteQuality
SIO_000300: 1.28e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.17e-1

GenotypeQuality
all individuals: 3448
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 6600
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 842
bin: 3.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.522718966987453e-5
allele num: 65672
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8574
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6586
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14742
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10310
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11420
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.156e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 5.2e0

MQRankSum
type: SiteQuality
SIO_000300: -2.01e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

DP
type: SiteQuality
SIO_000300: 1.839329e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.097e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.9e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.38e-1

GenotypeQuality
all individuals: 751
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14742
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6586
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11420
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 2.909796314258002e-4
allele num: 10310
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8574
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.045437933974906e-5
allele num: 65672
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 5.2e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.097e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.38e-1

DP
type: SiteQuality
SIO_000300: 1.839329e6

QD
type: SiteQuality
SIO_000300: 1.156e1

MQRankSum
type: SiteQuality
SIO_000300: -2.01e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.9e-1

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2608
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 899
bin: 3.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65606
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11412
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.810133478616181e-5
allele num: 14684
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10306
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8550
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 866
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.832234e6

VQSLOD
type: SiteQuality
SIO_000300: 2.27e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.87e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.398e0

MQRankSum
type: SiteQuality
SIO_000300: 1.98e-1

MQ
type: SiteQuality
SIO_000300: 5.901e1

FS
type: SiteQuality
SIO_000300: 2.865e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.7e-1

QD
type: SiteQuality
SIO_000300: 1.185e1

GenotypeQuality
all individuals: 6582
bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2869
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 899
bin: 3.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8550
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11412
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.048501661433405e-5
allele num: 65606
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 866
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10306
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14684
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.27e-1

FS
type: SiteQuality
SIO_000300: 2.865e0

MQ
type: SiteQuality
SIO_000300: 5.901e1

DP
type: SiteQuality
SIO_000300: 1.832234e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.398e0

MQRankSum
type: SiteQuality
SIO_000300: 1.98e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -8.87e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.7e-1

QD
type: SiteQuality
SIO_000300: 1.185e1

GenotypeQuality
all individuals: 1033
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 314
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2499
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 2
allele frequency: 1.758705592683785e-4
allele num: 11372
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8538
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 856
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10268
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14166
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65324
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.889e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.31e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.06e-1

FS
type: SiteQuality
SIO_000300: 3.087e0

QD
type: SiteQuality
SIO_000300: 9.52e0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.86e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.46e-1

DP
type: SiteQuality
SIO_000300: 1.786316e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.99e0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65094
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.769441187964049e-5
allele num: 10236
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6560
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13738
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11330
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 844
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8518
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.456e-1

QD
type: SiteQuality
SIO_000300: 1.055e1

MQRankSum
type: SiteQuality
SIO_000300: -1.26e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 4.06e0

FS
type: SiteQuality
SIO_000300: 8.715e0

MQ
type: SiteQuality
SIO_000300: 5.97e1

DP
type: SiteQuality
SIO_000300: 1.732203e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.88e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.23e0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6552
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10234
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13514
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.837044892188053e-5
allele num: 11316
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64966
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8492
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 842
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.721e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.84e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 8.609999999999999e0

MQRankSum
type: SiteQuality
SIO_000300: -7.84e-1

MQ
type: SiteQuality
SIO_000300: 5.878e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.06e-1

DP
type: SiteQuality
SIO_000300: 1.708676e6

ClippingRankSum
type: SiteQuality
SIO_000300: 9.5e-1

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
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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
all individuals: 1364
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variant carriers: 0

GenotypeQuality
all individuals: 2658
bin: 4.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11164
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11944
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6502
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 812
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8400
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10148
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.56137775973519e-5
allele num: 64046
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.932e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 7.38e0

VQSLOD
type: SiteQuality
SIO_000300: -8.192e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.03e0

MQRankSum
type: SiteQuality
SIO_000300: 7.9e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.590152e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.51e-1

GenotypeQuality
all individuals: 527
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 48
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GenotypeQuality
all individuals: 57
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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9220
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9088
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6970
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14862
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5262
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 5.218661935079846e-5
allele num: 57486
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 758
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.17e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.219e0

VQSLOD
type: SiteQuality
SIO_000300: -1.464e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.8e-1

DP
type: SiteQuality
SIO_000300: 1.027236e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.5e-3

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 1.7778e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.466e1

GenotypeQuality
all individuals: 23463
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 443
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 387
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 467
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1107
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2566
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2729
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 57964
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7054
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9260
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14978
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5328
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.078981441519206e-4
allele num: 9268
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -6.76e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.51e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.36e-1

QD
type: SiteQuality
SIO_000300: 8.859999999999999e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.7e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.51e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.081022e6

VQSLOD
type: SiteQuality
SIO_000300: 2.23e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 169
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 451
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 518
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8227
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27450
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 932
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 264
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 135
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 402
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9336
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58250
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.402918069584736e-4
allele num: 7128
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9408
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5356
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 762
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15036
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.69e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.61e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.17e-2

QD
type: SiteQuality
SIO_000300: 1.347e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.81e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.29e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.64e-1

DP
type: SiteQuality
SIO_000300: 1.117834e6

MQ
type: SiteQuality
SIO_000300: 6.018e1

GenotypeQuality
all individuals: 1872
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4859
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 264
bin: 9.75e1
variant carriers: 220

GenotypeQuality
all individuals: 2618
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8227
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 402
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 466
bin: 7.25e1
variant carriers: 2

GenotypeQuality
all individuals: 135
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 47
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5835
bin: 3.25e1
variant carriers: 0

African
type: Population
allele count: 219
allele frequency: 2.32780612244898e-2
allele num: 9408
num of homozygotes: 2

Latino
type: Population
allele count: 10
allele frequency: 1.071122536418166e-3
allele num: 9336
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7128
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5356
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58250
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15036
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 762
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.64e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.17e-2

VQSLOD
type: SiteQuality
SIO_000300: 6.61e0

DP
type: SiteQuality
SIO_000300: 1.117834e6

MQRankSum
type: SiteQuality
SIO_000300: 3.69e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.347e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.81e-1

MQ
type: SiteQuality
SIO_000300: 6.018e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.29e-1

GenotypeQuality
all individuals: 2838
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3091
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7569
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 195
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 491
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 437
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3159
bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.050640890943476e-4
allele num: 9518
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5424
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7272
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15196
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9630
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59250
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 774
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.932e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.42e1

MQRankSum
type: SiteQuality
SIO_000300: 1.52e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.36e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.094e0

VQSLOD
type: SiteQuality
SIO_000300: 2.66e-1

DP
type: SiteQuality
SIO_000300: 1.18187e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.57e-1

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

GenotypeQuality
all individuals: 2975
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33191
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1493
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7270
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1425
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2869
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 500
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 9.75e1
variant carriers: 60

European (Non-Finnish)
type: Population
allele count: 27
allele frequency: 4.528529737345275e-4
allele num: 59622
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15248
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.295336787564767e-3
allele num: 772
num of homozygotes: 0

African
type: Population
allele count: 4
allele frequency: 4.170141784820684e-4
allele num: 9592
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7316
num of homozygotes: 0

Latino
type: Population
allele count: 27
allele frequency: 2.775493421052632e-3
allele num: 9728
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5458
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.187e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.9e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.76e-1

QD
type: SiteQuality
SIO_000300: 1.44e1

VQSLOD
type: SiteQuality
SIO_000300: 1.86e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -1.43e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.72e-1

DP
type: SiteQuality
SIO_000300: 1.195401e6

GenotypeQuality
all individuals: 38
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3399
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 580
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4143
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1716
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 432
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 263
bin: 5.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5700
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9964
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 822
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8012
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.176216490916021e-5
allele num: 62968
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15778
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10672
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.75e0

QD
type: SiteQuality
SIO_000300: 1.709e1

DP
type: SiteQuality
SIO_000300: 1.322354e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.76e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

FS
type: SiteQuality
SIO_000300: 1.0112e1

MQRankSum
type: SiteQuality
SIO_000300: 5.02e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.11e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.04e0

MQ
type: SiteQuality
SIO_000300: 5.938e1

GenotypeQuality
all individuals: 41
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1590
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1260
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46291
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 565
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 386
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 391
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3391
bin: 6.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 836
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.002204850671477e-4
allele num: 9978
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8056
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63160
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10728
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5710
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15796
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.330174e6

MQRankSum
type: SiteQuality
SIO_000300: 6.46e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.24e-1

QD
type: SiteQuality
SIO_000300: 1.46e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.46e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.67e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.45e-1

GenotypeQuality
all individuals: 3464
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 503
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47498
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 772
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 477
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1294
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 612
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63794
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15898
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.942334460131238e-5
allele num: 10058
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 840
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5772
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8224
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10894
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 6.18e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.2e-1

FS
type: SiteQuality
SIO_000300: 3.129e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.350609e6

ClippingRankSum
type: SiteQuality
SIO_000300: 4.98e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.01e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.235e0

QD
type: SiteQuality
SIO_000300: 1.336e1

GenotypeQuality
all individuals: 53044
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 3761
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 187
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 227
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 323
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16332
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8618
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10302
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.212819502137594e-4
allele num: 65962
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11460
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6078
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.83e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.35e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -2.89e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.52e-1

QD
type: SiteQuality
SIO_000300: 1.311e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.421018e6

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.357e0

GenotypeQuality
all individuals: 194
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3784
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 207
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53837
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66214
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6178
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 878
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16416
num of homozygotes: 0

African
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allele count: 1
allele frequency: 9.688044952528579e-5
allele num: 10322
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11512
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 4.58e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

DP
type: SiteQuality
SIO_000300: 1.431933e6

FS
type: SiteQuality
SIO_000300: 2.324e0

QD
type: SiteQuality
SIO_000300: 1.422e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.888e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.98e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.3e-2

GenotypeQuality
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bin: 7.5e0
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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variant carriers: 3

GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

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

African
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allele frequency: 2.898550724637681e-4
allele num: 10350
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6348
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 892
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16492
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66460
num of homozygotes: 0

MQRankSum
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MQ
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InbreedingCoeff
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SIO_000300: -3.0e-4

FS
type: SiteQuality
SIO_000300: 1.8448e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.7e-2

ClippingRankSum
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SIO_000300: -4.0e-1

BaseQRankSum
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SIO_000300: 3.46e0

VQSLOD
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SIO_000300: -2.687e0

DP
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SIO_000300: 1.440659e6

QD
type: SiteQuality
SIO_000300: 1.114e1

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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Other
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allele frequency: 0.0e0
allele num: 892
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66512
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6384
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16500
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10360
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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East Asian
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allele count: 1
allele frequency: 1.15606936416185e-4
allele num: 8650
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InbreedingCoeff
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SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.29e-1

VQSLOD
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SIO_000300: 1.08e0

BaseQRankSum
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SIO_000300: 2.55e0

FS
type: SiteQuality
SIO_000300: 1.173e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.442164e6

QD
type: SiteQuality
SIO_000300: 1.267e1

MQRankSum
type: SiteQuality
SIO_000300: -2.58e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.18e-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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Latino
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allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66536
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Other
type: Population
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allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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African
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allele count: 2
allele frequency: 1.929384526336099e-4
allele num: 10366
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6440
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 9.869999999999999e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
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SIO_000300: 8.44e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.45e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.19e0

DP
type: SiteQuality
SIO_000300: 1.443909e6

VQSLOD
type: SiteQuality
SIO_000300: 7.42e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.276e0

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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bin: 4.75e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6452
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16506
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African
type: Population
allele count: 1
allele frequency: 9.646922631680494e-5
allele num: 10366
num of homozygotes: 0

Other
type: Population
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: 66542
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -6.534e-1

FS
type: SiteQuality
SIO_000300: 3.18e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.34e-1

QD
type: SiteQuality
SIO_000300: 1.018e1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.53e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.163e0

DP
type: SiteQuality
SIO_000300: 1.443913e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.56e-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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variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6494
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
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South Asian
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allele count: 1
allele frequency: 6.058403004967891e-5
allele num: 16506
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66580
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.0e-3

MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 7.11e-1

InbreedingCoeff
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FS
type: SiteQuality
SIO_000300: 1.328e0

QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.444921e6

VQSLOD
type: SiteQuality
SIO_000300: 7.0e-1

BaseQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.938e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66580
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6494
num of homozygotes: 0

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

Other
type: Population
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allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

African
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allele count: 1
allele frequency: 9.63948332369385e-5
allele num: 10374
num of homozygotes: 0

QD
type: SiteQuality
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FS
type: SiteQuality
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MQRankSum
type: SiteQuality
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BaseQRankSum
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ReadPosRankSum
type: SiteQuality
SIO_000300: 7.11e-1

InbreedingCoeff
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VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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MQ
type: SiteQuality
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DP
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

South Asian
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allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66582
num of homozygotes: 0

Latino
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num of homozygotes: 0

East Asian
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allele frequency: 1.156336725254394e-4
allele num: 8648
num of homozygotes: 0

African
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Other
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European (Finnish)
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allele frequency: 0.0e0
allele num: 6500
num of homozygotes: 0

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

European (Finnish)
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allele frequency: 0.0e0
allele num: 6504
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.003724618526973e-5
allele num: 66584
num of homozygotes: 0

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

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

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 frequency: 0.0e0
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Other
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East Asian
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.501636784094663e-5
allele num: 66594
num of homozygotes: 0

DP
type: SiteQuality
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MQ
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MQRankSum
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FS
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SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.354e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.4e-2

QD
type: SiteQuality
SIO_000300: 1.099e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.84e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.22e-1

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 40
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 428
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 16
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55162
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 43
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10378
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.422774076317383e-4
allele num: 16510
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6522
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501411326647048e-5
allele num: 66604
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 3.4e-1

MQ
type: SiteQuality
SIO_000300: 5.959e1

DP
type: SiteQuality
SIO_000300: 1.446291e6

QD
type: SiteQuality
SIO_000300: 9.69e0

VQSLOD
type: SiteQuality
SIO_000300: 6.38e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.03e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.29e0

FS
type: SiteQuality
SIO_000300: 1.273e0

GenotypeQuality
all individuals: 40
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 28
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 28
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55172
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6524
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10378
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66604
num of homozygotes: 0

East Asian
type: Population
allele count: 4
allele frequency: 4.624277456647399e-4
allele num: 8650
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 6.76e-1

DP
type: SiteQuality
SIO_000300: 1.446405e6

QD
type: SiteQuality
SIO_000300: 1.413e1

VQSLOD
type: SiteQuality
SIO_000300: 2.7e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.91e-1

FS
type: SiteQuality
SIO_000300: 5.33e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.102e0

MQ
type: SiteQuality
SIO_000300: 6.012e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.09e-1

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

GenotypeQuality
all individuals: 425
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55189
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 22
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 9.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10380
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.646031471554557e-5
allele num: 11566
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66612
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6538
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.817080557238038e-4
allele num: 16510
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.79e0

DP
type: SiteQuality
SIO_000300: 1.446751e6

ClippingRankSum
type: SiteQuality
SIO_000300: -6.36e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.24e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.965e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.42e-1

FS
type: SiteQuality
SIO_000300: 2.021e0

VQSLOD
type: SiteQuality
SIO_000300: -2.642e0

QD
type: SiteQuality
SIO_000300: 2.964e1

GenotypeQuality
all individuals: 55211
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 618
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 425
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10380
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66612
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6542
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.729206294310911e-4
allele num: 11566
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.12e0

QD
type: SiteQuality
SIO_000300: 1.275e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.09e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.14e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.83e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.65e0

DP
type: SiteQuality
SIO_000300: 1.446766e6

MQ
type: SiteQuality
SIO_000300: 6.0e1