20-25187696-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25187696
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 25187696
    reference: chr 20
allele count: 2
allele frequency: 1.817520901490367e-5
allele num: 110040
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390646
  ensembl transcript: ENST00000425813
  gene symbol: ENTPD6
  hgvsc: ENST00000425813.1:c.55-16C>T
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000365840
  ensembl transcript: ENST00000376652
  gene symbol: ENTPD6
  hgvsc: ENST00000376652.4:c.55-16C>T
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390511
  ensembl transcript: ENST00000418890
  gene symbol: ENTPD6
  hgvsc: ENST00000418890.1:c.4-16C>T
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000353131
  ensembl transcript: ENST00000360031
  gene symbol: ENTPD6
  hgvsc: ENST00000360031.2:c.55-19C>T
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000347084
  ensembl transcript: ENST00000354989
  gene symbol: ENTPD6
  hgvsc: ENST00000354989.5:c.4-16C>T
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000408098
  ensembl transcript: ENST00000439162
  gene symbol: ENTPD6
  hgvsc: ENST00000439162.1:c.4-19C>T
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000395064
  ensembl transcript: ENST00000417467
  gene symbol: ENTPD6
  hgvsc: ENST00000417467.1:c.4-19C>T
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401573
  ensembl transcript: ENST00000427553
  gene symbol: ENTPD6
  hgvsc: ENST00000427553.1:c.94-2789C>T
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401895
  ensembl transcript: ENST00000433259
  gene symbol: ENTPD6
  hgvsc: ENST00000433259.2:c.55-16C>T
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390095
  ensembl transcript: ENST00000433417
  gene symbol: ENTPD6
  hgvsc: ENST00000433417.1:c.139-2789C>T
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000398844
  ensembl transcript: ENST00000435520
  gene symbol: ENTPD6
  hgvsc: ENST00000435520.1:c.55-19C>T
  variant of: http://identifiers.org/hgnc/3368
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14976
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4334
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2051
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4884
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5252
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2091
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14822
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8962
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 627
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: QD
site quality: VQSLOD

20-25187697-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25187697
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 25187697
    reference: chr 20
allele count: 2
allele frequency: 1.814322259919807e-5
allele num: 110234
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000353131
  ensembl transcript: ENST00000360031
  gene symbol: ENTPD6
  hgvsc: ENST00000360031.2:c.55-18C>G
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390095
  ensembl transcript: ENST00000433417
  gene symbol: ENTPD6
  hgvsc: ENST00000433417.1:c.139-2788C>G
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390646
  ensembl transcript: ENST00000425813
  gene symbol: ENTPD6
  hgvsc: ENST00000425813.1:c.55-15C>G
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000398844
  ensembl transcript: ENST00000435520
  gene symbol: ENTPD6
  hgvsc: ENST00000435520.1:c.55-18C>G
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401573
  ensembl transcript: ENST00000427553
  gene symbol: ENTPD6
  hgvsc: ENST00000427553.1:c.94-2788C>G
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000395064
  ensembl transcript: ENST00000417467
  gene symbol: ENTPD6
  hgvsc: ENST00000417467.1:c.4-18C>G
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401895
  ensembl transcript: ENST00000433259
  gene symbol: ENTPD6
  hgvsc: ENST00000433259.2:c.55-15C>G
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000408098
  ensembl transcript: ENST00000439162
  gene symbol: ENTPD6
  hgvsc: ENST00000439162.1:c.4-18C>G
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000347084
  ensembl transcript: ENST00000354989
  gene symbol: ENTPD6
  hgvsc: ENST00000354989.5:c.4-15C>G
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390511
  ensembl transcript: ENST00000418890
  gene symbol: ENTPD6
  hgvsc: ENST00000418890.1:c.4-15C>G
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000365840
  ensembl transcript: ENST00000376652
  gene symbol: ENTPD6
  hgvsc: ENST00000376652.4:c.55-15C>G
  variant of: http://identifiers.org/hgnc/3368
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4331
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2049
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2079
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8954
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5342
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4844
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15003
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14830
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/20-25187699-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25187699
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 25187699
    reference: chr 20
allele count: 1
allele frequency: 9.037669004410382e-6
allele num: 110648
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000408098
  ensembl transcript: ENST00000439162
  gene symbol: ENTPD6
  hgvsc: ENST00000439162.1:c.4-16C>A
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000365840
  ensembl transcript: ENST00000376652
  gene symbol: ENTPD6
  hgvsc: ENST00000376652.4:c.55-13C>A
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401895
  ensembl transcript: ENST00000433259
  gene symbol: ENTPD6
  hgvsc: ENST00000433259.2:c.55-13C>A
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000395064
  ensembl transcript: ENST00000417467
  gene symbol: ENTPD6
  hgvsc: ENST00000417467.1:c.4-16C>A
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390646
  ensembl transcript: ENST00000425813
  gene symbol: ENTPD6
  hgvsc: ENST00000425813.1:c.55-13C>A
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390095
  ensembl transcript: ENST00000433417
  gene symbol: ENTPD6
  hgvsc: ENST00000433417.1:c.139-2786C>A
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390511
  ensembl transcript: ENST00000418890
  gene symbol: ENTPD6
  hgvsc: ENST00000418890.1:c.4-13C>A
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401573
  ensembl transcript: ENST00000427553
  gene symbol: ENTPD6
  hgvsc: ENST00000427553.1:c.94-2786C>A
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000347084
  ensembl transcript: ENST00000354989
  gene symbol: ENTPD6
  hgvsc: ENST00000354989.5:c.4-13C>A
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000353131
  ensembl transcript: ENST00000360031
  gene symbol: ENTPD6
  hgvsc: ENST00000360031.2:c.55-16C>A
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000398844
  ensembl transcript: ENST00000435520
  gene symbol: ENTPD6
  hgvsc: ENST00000435520.1:c.55-16C>A
  variant of: http://identifiers.org/hgnc/3368
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5448
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2051
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4331
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4746
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15014
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2075
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14834
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8955
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: MQRankSum

http://identifiers.org/exac.variant/20-25187700-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25187700
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 25187700
    reference: chr 20
allele count: 13
allele frequency: 1.172671345324649e-4
allele num: 110858
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401573
  ensembl transcript: ENST00000427553
  gene symbol: ENTPD6
  hgvsc: ENST00000427553.1:c.94-2785C>A
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000398844
  ensembl transcript: ENST00000435520
  gene symbol: ENTPD6
  hgvsc: ENST00000435520.1:c.55-15C>A
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000408098
  ensembl transcript: ENST00000439162
  gene symbol: ENTPD6
  hgvsc: ENST00000439162.1:c.4-15C>A
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000365840
  ensembl transcript: ENST00000376652
  gene symbol: ENTPD6
  hgvsc: ENST00000376652.4:c.55-12C>A
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390095
  ensembl transcript: ENST00000433417
  gene symbol: ENTPD6
  hgvsc: ENST00000433417.1:c.139-2785C>A
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000347084
  ensembl transcript: ENST00000354989
  gene symbol: ENTPD6
  hgvsc: ENST00000354989.5:c.4-12C>A
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000353131
  ensembl transcript: ENST00000360031
  gene symbol: ENTPD6
  hgvsc: ENST00000360031.2:c.55-15C>A
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390511
  ensembl transcript: ENST00000418890
  gene symbol: ENTPD6
  hgvsc: ENST00000418890.1:c.4-12C>A
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401895
  ensembl transcript: ENST00000433259
  gene symbol: ENTPD6
  hgvsc: ENST00000433259.2:c.55-12C>A
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390646
  ensembl transcript: ENST00000425813
  gene symbol: ENTPD6
  hgvsc: ENST00000425813.1:c.55-12C>A
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000395064
  ensembl transcript: ENST00000417467
  gene symbol: ENTPD6
  hgvsc: ENST00000417467.1:c.4-15C>A
  variant of: http://identifiers.org/hgnc/3368
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8922
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5501
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4302
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2074
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15029
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4683
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1025
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2027
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14814
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2456
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff

20-25187700-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25187700
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 25187700
    reference: chr 20
allele count: 12
allele frequency: 1.082465857222753e-4
allele num: 110858
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390095
  ensembl transcript: ENST00000433417
  gene symbol: ENTPD6
  hgvsc: ENST00000433417.1:c.139-2785C>G
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390646
  ensembl transcript: ENST00000425813
  gene symbol: ENTPD6
  hgvsc: ENST00000425813.1:c.55-12C>G
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000395064
  ensembl transcript: ENST00000417467
  gene symbol: ENTPD6
  hgvsc: ENST00000417467.1:c.4-15C>G
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000408098
  ensembl transcript: ENST00000439162
  gene symbol: ENTPD6
  hgvsc: ENST00000439162.1:c.4-15C>G
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000365840
  ensembl transcript: ENST00000376652
  gene symbol: ENTPD6
  hgvsc: ENST00000376652.4:c.55-12C>G
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000347084
  ensembl transcript: ENST00000354989
  gene symbol: ENTPD6
  hgvsc: ENST00000354989.5:c.4-12C>G
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000398844
  ensembl transcript: ENST00000435520
  gene symbol: ENTPD6
  hgvsc: ENST00000435520.1:c.55-15C>G
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401895
  ensembl transcript: ENST00000433259
  gene symbol: ENTPD6
  hgvsc: ENST00000433259.2:c.55-12C>G
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000353131
  ensembl transcript: ENST00000360031
  gene symbol: ENTPD6
  hgvsc: ENST00000360031.2:c.55-15C>G
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401573
  ensembl transcript: ENST00000427553
  gene symbol: ENTPD6
  hgvsc: ENST00000427553.1:c.94-2785C>G
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390511
  ensembl transcript: ENST00000418890
  gene symbol: ENTPD6
  hgvsc: ENST00000418890.1:c.4-12C>G
  variant of: http://identifiers.org/hgnc/3368
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4302
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14814
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1025
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5501
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2027
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8922
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4683
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2074
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15029
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ

20-25187700-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25187700
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 25187700
    reference: chr 20
allele count: 270
allele frequency: 2.435548178751195e-3
allele num: 110858
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000398844
  ensembl transcript: ENST00000435520
  gene symbol: ENTPD6
  hgvsc: ENST00000435520.1:c.55-15C>T
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000365840
  ensembl transcript: ENST00000376652
  gene symbol: ENTPD6
  hgvsc: ENST00000376652.4:c.55-12C>T
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390511
  ensembl transcript: ENST00000418890
  gene symbol: ENTPD6
  hgvsc: ENST00000418890.1:c.4-12C>T
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401573
  ensembl transcript: ENST00000427553
  gene symbol: ENTPD6
  hgvsc: ENST00000427553.1:c.94-2785C>T
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390646
  ensembl transcript: ENST00000425813
  gene symbol: ENTPD6
  hgvsc: ENST00000425813.1:c.55-12C>T
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401895
  ensembl transcript: ENST00000433259
  gene symbol: ENTPD6
  hgvsc: ENST00000433259.2:c.55-12C>T
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000408098
  ensembl transcript: ENST00000439162
  gene symbol: ENTPD6
  hgvsc: ENST00000439162.1:c.4-15C>T
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000395064
  ensembl transcript: ENST00000417467
  gene symbol: ENTPD6
  hgvsc: ENST00000417467.1:c.4-15C>T
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000353131
  ensembl transcript: ENST00000360031
  gene symbol: ENTPD6
  hgvsc: ENST00000360031.2:c.55-15C>T
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390095
  ensembl transcript: ENST00000433417
  gene symbol: ENTPD6
  hgvsc: ENST00000433417.1:c.139-2785C>T
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000347084
  ensembl transcript: ENST00000354989
  gene symbol: ENTPD6
  hgvsc: ENST00000354989.5:c.4-12C>T
  variant of: http://identifiers.org/hgnc/3368
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 1.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 2027
  bin: 4.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.75e1
  variant carriers: 63
genotype depth: GenotypeDepth
  all individuals: 15029
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 8922
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4683
  bin: 7.5e0
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 5501
  bin: 2.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 4302
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 6.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 2074
  bin: 1.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 14814
  bin: 3.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 5.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 6.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.25e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 1025
  bin: 5.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 14
genotype quality: GenotypeQuality
  all individuals: 3112
  bin: 7.25e1
  variant carriers: 1
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum

20-25187701-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25187701
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 25187701
    reference: chr 20
allele count: 2
allele frequency: 1.801217623113225e-5
allele num: 111036
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000365840
  ensembl transcript: ENST00000376652
  gene symbol: ENTPD6
  hgvsc: ENST00000376652.4:c.55-11C>G
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390511
  ensembl transcript: ENST00000418890
  gene symbol: ENTPD6
  hgvsc: ENST00000418890.1:c.4-11C>G
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401895
  ensembl transcript: ENST00000433259
  gene symbol: ENTPD6
  hgvsc: ENST00000433259.2:c.55-11C>G
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000353131
  ensembl transcript: ENST00000360031
  gene symbol: ENTPD6
  hgvsc: ENST00000360031.2:c.55-14C>G
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000395064
  ensembl transcript: ENST00000417467
  gene symbol: ENTPD6
  hgvsc: ENST00000417467.1:c.4-14C>G
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390095
  ensembl transcript: ENST00000433417
  gene symbol: ENTPD6
  hgvsc: ENST00000433417.1:c.139-2784C>G
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390646
  ensembl transcript: ENST00000425813
  gene symbol: ENTPD6
  hgvsc: ENST00000425813.1:c.55-11C>G
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000398844
  ensembl transcript: ENST00000435520
  gene symbol: ENTPD6
  hgvsc: ENST00000435520.1:c.55-14C>G
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000347084
  ensembl transcript: ENST00000354989
  gene symbol: ENTPD6
  hgvsc: ENST00000354989.5:c.4-11C>G
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401573
  ensembl transcript: ENST00000427553
  gene symbol: ENTPD6
  hgvsc: ENST00000427553.1:c.94-2784C>G
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000408098
  ensembl transcript: ENST00000439162
  gene symbol: ENTPD6
  hgvsc: ENST00000439162.1:c.4-14C>G
  variant of: http://identifiers.org/hgnc/3368
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2033
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2053
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8957
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5593
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15104
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14878
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4618
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4328
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 210
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: Latino
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

20-25187701-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25187701
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 25187701
    reference: chr 20
allele count: 1
allele frequency: 9.006088115566123e-6
allele num: 111036
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390646
  ensembl transcript: ENST00000425813
  gene symbol: ENTPD6
  hgvsc: ENST00000425813.1:c.55-11C>T
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401895
  ensembl transcript: ENST00000433259
  gene symbol: ENTPD6
  hgvsc: ENST00000433259.2:c.55-11C>T
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401573
  ensembl transcript: ENST00000427553
  gene symbol: ENTPD6
  hgvsc: ENST00000427553.1:c.94-2784C>T
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390095
  ensembl transcript: ENST00000433417
  gene symbol: ENTPD6
  hgvsc: ENST00000433417.1:c.139-2784C>T
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000398844
  ensembl transcript: ENST00000435520
  gene symbol: ENTPD6
  hgvsc: ENST00000435520.1:c.55-14C>T
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390511
  ensembl transcript: ENST00000418890
  gene symbol: ENTPD6
  hgvsc: ENST00000418890.1:c.4-11C>T
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000395064
  ensembl transcript: ENST00000417467
  gene symbol: ENTPD6
  hgvsc: ENST00000417467.1:c.4-14C>T
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000353131
  ensembl transcript: ENST00000360031
  gene symbol: ENTPD6
  hgvsc: ENST00000360031.2:c.55-14C>T
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000365840
  ensembl transcript: ENST00000376652
  gene symbol: ENTPD6
  hgvsc: ENST00000376652.4:c.55-11C>T
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000408098
  ensembl transcript: ENST00000439162
  gene symbol: ENTPD6
  hgvsc: ENST00000439162.1:c.4-14C>T
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000347084
  ensembl transcript: ENST00000354989
  gene symbol: ENTPD6
  hgvsc: ENST00000354989.5:c.4-11C>T
  variant of: http://identifiers.org/hgnc/3368
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2053
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4328
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5593
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15104
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2033
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4618
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8957
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14878
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 389
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff

20-25187702-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25187702
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 25187702
    reference: chr 20
allele count: 7
allele frequency: 6.292587332122759e-5
allele num: 111242
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000395064
  ensembl transcript: ENST00000417467
  gene symbol: ENTPD6
  hgvsc: ENST00000417467.1:c.4-13T>C
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000398844
  ensembl transcript: ENST00000435520
  gene symbol: ENTPD6
  hgvsc: ENST00000435520.1:c.55-13T>C
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401895
  ensembl transcript: ENST00000433259
  gene symbol: ENTPD6
  hgvsc: ENST00000433259.2:c.55-10T>C
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401573
  ensembl transcript: ENST00000427553
  gene symbol: ENTPD6
  hgvsc: ENST00000427553.1:c.94-2783T>C
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390095
  ensembl transcript: ENST00000433417
  gene symbol: ENTPD6
  hgvsc: ENST00000433417.1:c.139-2783T>C
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000365840
  ensembl transcript: ENST00000376652
  gene symbol: ENTPD6
  hgvsc: ENST00000376652.4:c.55-10T>C
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390646
  ensembl transcript: ENST00000425813
  gene symbol: ENTPD6
  hgvsc: ENST00000425813.1:c.55-10T>C
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000408098
  ensembl transcript: ENST00000439162
  gene symbol: ENTPD6
  hgvsc: ENST00000439162.1:c.4-13T>C
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000353131
  ensembl transcript: ENST00000360031
  gene symbol: ENTPD6
  hgvsc: ENST00000360031.2:c.55-13T>C
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390511
  ensembl transcript: ENST00000418890
  gene symbol: ENTPD6
  hgvsc: ENST00000418890.1:c.4-10T>C
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000347084
  ensembl transcript: ENST00000354989
  gene symbol: ENTPD6
  hgvsc: ENST00000354989.5:c.4-10T>C
  variant of: http://identifiers.org/hgnc/3368
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5669
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4588
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2017
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14882
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1022
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2029
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4325
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8953
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15109
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 4655
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum

20-25187702-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25187702
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 25187702
    reference: chr 20
allele count: 1
allele frequency: 8.989410474461085e-6
allele num: 111242
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401573
  ensembl transcript: ENST00000427553
  gene symbol: ENTPD6
  hgvsc: ENST00000427553.1:c.94-2783T>G
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390646
  ensembl transcript: ENST00000425813
  gene symbol: ENTPD6
  hgvsc: ENST00000425813.1:c.55-10T>G
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000347084
  ensembl transcript: ENST00000354989
  gene symbol: ENTPD6
  hgvsc: ENST00000354989.5:c.4-10T>G
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000408098
  ensembl transcript: ENST00000439162
  gene symbol: ENTPD6
  hgvsc: ENST00000439162.1:c.4-13T>G
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000365840
  ensembl transcript: ENST00000376652
  gene symbol: ENTPD6
  hgvsc: ENST00000376652.4:c.55-10T>G
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000353131
  ensembl transcript: ENST00000360031
  gene symbol: ENTPD6
  hgvsc: ENST00000360031.2:c.55-13T>G
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401895
  ensembl transcript: ENST00000433259
  gene symbol: ENTPD6
  hgvsc: ENST00000433259.2:c.55-10T>G
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390095
  ensembl transcript: ENST00000433417
  gene symbol: ENTPD6
  hgvsc: ENST00000433417.1:c.139-2783T>G
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000395064
  ensembl transcript: ENST00000417467
  gene symbol: ENTPD6
  hgvsc: ENST00000417467.1:c.4-13T>G
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000398844
  ensembl transcript: ENST00000435520
  gene symbol: ENTPD6
  hgvsc: ENST00000435520.1:c.55-13T>G
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390511
  ensembl transcript: ENST00000418890
  gene symbol: ENTPD6
  hgvsc: ENST00000418890.1:c.4-10T>G
  variant of: http://identifiers.org/hgnc/3368
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2017
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2029
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1022
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14882
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4325
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5669
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15109
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4588
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8953
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum

20-25187705-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25187705
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 25187705
    reference: chr 20
allele count: 1
allele frequency: 8.960734063334468e-6
allele num: 111598
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401895
  ensembl transcript: ENST00000433259
  gene symbol: ENTPD6
  hgvsc: ENST00000433259.2:c.55-7C>G
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000398844
  ensembl transcript: ENST00000435520
  gene symbol: ENTPD6
  hgvsc: ENST00000435520.1:c.55-10C>G
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390646
  ensembl transcript: ENST00000425813
  gene symbol: ENTPD6
  hgvsc: ENST00000425813.1:c.55-7C>G
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000365840
  ensembl transcript: ENST00000376652
  gene symbol: ENTPD6
  hgvsc: ENST00000376652.4:c.55-7C>G
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401573
  ensembl transcript: ENST00000427553
  gene symbol: ENTPD6
  hgvsc: ENST00000427553.1:c.94-2780C>G
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000395064
  ensembl transcript: ENST00000417467
  gene symbol: ENTPD6
  hgvsc: ENST00000417467.1:c.4-10C>G
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000347084
  ensembl transcript: ENST00000354989
  gene symbol: ENTPD6
  hgvsc: ENST00000354989.5:c.4-7C>G
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390511
  ensembl transcript: ENST00000418890
  gene symbol: ENTPD6
  hgvsc: ENST00000418890.1:c.4-7C>G
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000353131
  ensembl transcript: ENST00000360031
  gene symbol: ENTPD6
  hgvsc: ENST00000360031.2:c.55-10C>G
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390095
  ensembl transcript: ENST00000433417
  gene symbol: ENTPD6
  hgvsc: ENST00000433417.1:c.139-2780C>G
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000408098
  ensembl transcript: ENST00000439162
  gene symbol: ENTPD6
  hgvsc: ENST00000439162.1:c.4-10C>G
  variant of: http://identifiers.org/hgnc/3368
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5860
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14889
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8953
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1022
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4418
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1961
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4323
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2028
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15173
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: c.55-7C>G
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: QD

20-25187716-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25187716
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 25187716
    reference: chr 20
allele count: 6
allele frequency: 5.267038870746866e-5
allele num: 113916
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000365840
  ensembl transcript: ENST00000376652
  gene symbol: ENTPD6
  hgvsc: ENST00000376652.4:c.59C>T
  hgvsp: ENSP00000365840.4:p.Pro20Leu
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000353131
  ensembl transcript: ENST00000360031
  gene symbol: ENTPD6
  hgvsc: ENST00000360031.2:c.56C>T
  hgvsp: ENSP00000353131.2:p.Pro19Leu
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390646
  ensembl transcript: ENST00000425813
  gene symbol: ENTPD6
  hgvsc: ENST00000425813.1:c.59C>T
  hgvsp: ENSP00000390646.1:p.Pro20Leu
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000398844
  ensembl transcript: ENST00000435520
  gene symbol: ENTPD6
  hgvsc: ENST00000435520.1:c.56C>T
  hgvsp: ENSP00000398844.1:p.Pro19Leu
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000347084
  ensembl transcript: ENST00000354989
  gene symbol: ENTPD6
  hgvsc: ENST00000354989.5:c.8C>T
  hgvsp: ENSP00000347084.5:p.Pro3Leu
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000408098
  ensembl transcript: ENST00000439162
  gene symbol: ENTPD6
  hgvsc: ENST00000439162.1:c.5C>T
  hgvsp: ENSP00000408098.1:p.Pro2Leu
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401573
  ensembl transcript: ENST00000427553
  gene symbol: ENTPD6
  hgvsc: ENST00000427553.1:c.94-2769C>T
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390511
  ensembl transcript: ENST00000418890
  gene symbol: ENTPD6
  hgvsc: ENST00000418890.1:c.8C>T
  hgvsp: ENSP00000390511.1:p.Pro3Leu
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000395064
  ensembl transcript: ENST00000417467
  gene symbol: ENTPD6
  hgvsc: ENST00000417467.1:c.5C>T
  hgvsp: ENSP00000395064.1:p.Pro2Leu
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401895
  ensembl transcript: ENST00000433259
  gene symbol: ENTPD6
  hgvsc: ENST00000433259.2:c.59C>T
  hgvsp: ENSP00000401895.2:p.Pro20Leu
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390095
  ensembl transcript: ENST00000433417
  gene symbol: ENTPD6
  hgvsc: ENST00000433417.1:c.139-2769C>T
  variant of: http://identifiers.org/hgnc/3368
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4320
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3474
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1711
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8952
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6932
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2027
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14933
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Pro20Leu
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ

20-25187717-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25187717
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 25187717
    reference: chr 20
allele count: 6
allele frequency: 5.251549207016069e-5
allele num: 114252
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000365840
  ensembl transcript: ENST00000376652
  gene symbol: ENTPD6
  hgvsc: ENST00000376652.4:c.60G>A
  hgvsp: ENST00000376652.4:c.60G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390646
  ensembl transcript: ENST00000425813
  gene symbol: ENTPD6
  hgvsc: ENST00000425813.1:c.60G>A
  hgvsp: ENST00000425813.1:c.60G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000395064
  ensembl transcript: ENST00000417467
  gene symbol: ENTPD6
  hgvsc: ENST00000417467.1:c.6G>A
  hgvsp: ENST00000417467.1:c.6G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000398844
  ensembl transcript: ENST00000435520
  gene symbol: ENTPD6
  hgvsc: ENST00000435520.1:c.57G>A
  hgvsp: ENST00000435520.1:c.57G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390511
  ensembl transcript: ENST00000418890
  gene symbol: ENTPD6
  hgvsc: ENST00000418890.1:c.9G>A
  hgvsp: ENST00000418890.1:c.9G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390095
  ensembl transcript: ENST00000433417
  gene symbol: ENTPD6
  hgvsc: ENST00000433417.1:c.139-2768G>A
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000347084
  ensembl transcript: ENST00000354989
  gene symbol: ENTPD6
  hgvsc: ENST00000354989.5:c.9G>A
  hgvsp: ENST00000354989.5:c.9G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000353131
  ensembl transcript: ENST00000360031
  gene symbol: ENTPD6
  hgvsc: ENST00000360031.2:c.57G>A
  hgvsp: ENST00000360031.2:c.57G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401895
  ensembl transcript: ENST00000433259
  gene symbol: ENTPD6
  hgvsc: ENST00000433259.2:c.60G>A
  hgvsp: ENST00000433259.2:c.60G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000408098
  ensembl transcript: ENST00000439162
  gene symbol: ENTPD6
  hgvsc: ENST00000439162.1:c.6G>A
  hgvsp: ENST00000439162.1:c.6G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401573
  ensembl transcript: ENST00000427553
  gene symbol: ENTPD6
  hgvsc: ENST00000427553.1:c.94-2768G>A
  variant of: http://identifiers.org/hgnc/3368
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14940
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8951
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1636
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2025
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4320
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7116
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15523
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3338
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1022
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: c.57G>A
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD

20-25187723-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25187723
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 25187723
    reference: chr 20
allele count: 51
allele frequency: 4.402320281748498e-4
allele num: 115848
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401573
  ensembl transcript: ENST00000427553
  gene symbol: ENTPD6
  hgvsc: ENST00000427553.1:c.94-2762C>T
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000353131
  ensembl transcript: ENST00000360031
  gene symbol: ENTPD6
  hgvsc: ENST00000360031.2:c.63C>T
  hgvsp: ENST00000360031.2:c.63C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000365840
  ensembl transcript: ENST00000376652
  gene symbol: ENTPD6
  hgvsc: ENST00000376652.4:c.66C>T
  hgvsp: ENST00000376652.4:c.66C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390646
  ensembl transcript: ENST00000425813
  gene symbol: ENTPD6
  hgvsc: ENST00000425813.1:c.66C>T
  hgvsp: ENST00000425813.1:c.66C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401895
  ensembl transcript: ENST00000433259
  gene symbol: ENTPD6
  hgvsc: ENST00000433259.2:c.66C>T
  hgvsp: ENST00000433259.2:c.66C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000398844
  ensembl transcript: ENST00000435520
  gene symbol: ENTPD6
  hgvsc: ENST00000435520.1:c.63C>T
  hgvsp: ENST00000435520.1:c.63C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000395064
  ensembl transcript: ENST00000417467
  gene symbol: ENTPD6
  hgvsc: ENST00000417467.1:c.12C>T
  hgvsp: ENST00000417467.1:c.12C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000347084
  ensembl transcript: ENST00000354989
  gene symbol: ENTPD6
  hgvsc: ENST00000354989.5:c.15C>T
  hgvsp: ENST00000354989.5:c.15C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390095
  ensembl transcript: ENST00000433417
  gene symbol: ENTPD6
  hgvsc: ENST00000433417.1:c.139-2762C>T
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000408098
  ensembl transcript: ENST00000439162
  gene symbol: ENTPD6
  hgvsc: ENST00000439162.1:c.12C>T
  hgvsp: ENST00000439162.1:c.12C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390511
  ensembl transcript: ENST00000418890
  gene symbol: ENTPD6
  hgvsc: ENST00000418890.1:c.15C>T
  hgvsp: ENST00000418890.1:c.15C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 6.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8953
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2613
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2021
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8027
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 4310
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14974
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15761
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1018
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1318
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.His22His
num of homozygotes: 1
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
population: African
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP

20-25187724-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25187724
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 25187724
    reference: chr 20
allele count: 1553
allele frequency: 1.335270751294e-2
allele num: 116306
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000395064
  ensembl transcript: ENST00000417467
  gene symbol: ENTPD6
  hgvsc: ENST00000417467.1:c.13G>A
  hgvsp: ENSP00000395064.1:p.Gly5Ser
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000353131
  ensembl transcript: ENST00000360031
  gene symbol: ENTPD6
  hgvsc: ENST00000360031.2:c.64G>A
  hgvsp: ENSP00000353131.2:p.Gly22Ser
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000408098
  ensembl transcript: ENST00000439162
  gene symbol: ENTPD6
  hgvsc: ENST00000439162.1:c.13G>A
  hgvsp: ENSP00000408098.1:p.Gly5Ser
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000398844
  ensembl transcript: ENST00000435520
  gene symbol: ENTPD6
  hgvsc: ENST00000435520.1:c.64G>A
  hgvsp: ENSP00000398844.1:p.Gly22Ser
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401895
  ensembl transcript: ENST00000433259
  gene symbol: ENTPD6
  hgvsc: ENST00000433259.2:c.67G>A
  hgvsp: ENSP00000401895.2:p.Gly23Ser
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390095
  ensembl transcript: ENST00000433417
  gene symbol: ENTPD6
  hgvsc: ENST00000433417.1:c.139-2761G>A
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401573
  ensembl transcript: ENST00000427553
  gene symbol: ENTPD6
  hgvsc: ENST00000427553.1:c.94-2761G>A
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390511
  ensembl transcript: ENST00000418890
  gene symbol: ENTPD6
  hgvsc: ENST00000418890.1:c.16G>A
  hgvsp: ENSP00000390511.1:p.Gly6Ser
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000365840
  ensembl transcript: ENST00000376652
  gene symbol: ENTPD6
  hgvsc: ENST00000376652.4:c.67G>A
  hgvsp: ENSP00000365840.4:p.Gly23Ser
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000347084
  ensembl transcript: ENST00000354989
  gene symbol: ENTPD6
  hgvsc: ENST00000354989.5:c.16G>A
  hgvsp: ENSP00000347084.5:p.Gly6Ser
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390646
  ensembl transcript: ENST00000425813
  gene symbol: ENTPD6
  hgvsc: ENST00000425813.1:c.67G>A
  hgvsp: ENSP00000390646.1:p.Gly23Ser
  variant of: http://identifiers.org/hgnc/3368
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.75e1
  variant carriers: 91
genotype depth: GenotypeDepth
  all individuals: 1227
  bin: 1.25e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.75e1
  variant carriers: 96
genotype depth: GenotypeDepth
  all individuals: 15761
  bin: 2.75e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 9.75e1
  variant carriers: 656
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.25e1
  variant carriers: 111
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 1.75e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 5.25e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 8207
  bin: 2.25e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 5.75e1
  variant carriers: 40
genotype depth: GenotypeDepth
  all individuals: 2414
  bin: 7.5e0
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 14870
  bin: 3.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.25e1
  variant carriers: 91
genotype depth: GenotypeDepth
  all individuals: 8775
  bin: 3.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.25e1
  variant carriers: 52
genotype depth: GenotypeDepth
  all individuals: 4131
  bin: 4.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 6.75e1
  variant carriers: 60
genotype depth: GenotypeDepth
  all individuals: 1853
  bin: 4.75e1
  variant carriers: 20
genotype quality: GenotypeQuality
hgvs: p.Gly23Ser
num of homozygotes: 16
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum

20-25187724-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25187724
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 25187724
    reference: chr 20
allele count: 1
allele frequency: 8.598008701184805e-6
allele num: 116306
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000408098
  ensembl transcript: ENST00000439162
  gene symbol: ENTPD6
  hgvsc: ENST00000439162.1:c.13G>T
  hgvsp: ENSP00000408098.1:p.Gly5Cys
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390646
  ensembl transcript: ENST00000425813
  gene symbol: ENTPD6
  hgvsc: ENST00000425813.1:c.67G>T
  hgvsp: ENSP00000390646.1:p.Gly23Cys
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000347084
  ensembl transcript: ENST00000354989
  gene symbol: ENTPD6
  hgvsc: ENST00000354989.5:c.16G>T
  hgvsp: ENSP00000347084.5:p.Gly6Cys
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401895
  ensembl transcript: ENST00000433259
  gene symbol: ENTPD6
  hgvsc: ENST00000433259.2:c.67G>T
  hgvsp: ENSP00000401895.2:p.Gly23Cys
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390095
  ensembl transcript: ENST00000433417
  gene symbol: ENTPD6
  hgvsc: ENST00000433417.1:c.139-2761G>T
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000365840
  ensembl transcript: ENST00000376652
  gene symbol: ENTPD6
  hgvsc: ENST00000376652.4:c.67G>T
  hgvsp: ENSP00000365840.4:p.Gly23Cys
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000398844
  ensembl transcript: ENST00000435520
  gene symbol: ENTPD6
  hgvsc: ENST00000435520.1:c.64G>T
  hgvsp: ENSP00000398844.1:p.Gly22Cys
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401573
  ensembl transcript: ENST00000427553
  gene symbol: ENTPD6
  hgvsc: ENST00000427553.1:c.94-2761G>T
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000395064
  ensembl transcript: ENST00000417467
  gene symbol: ENTPD6
  hgvsc: ENST00000417467.1:c.13G>T
  hgvsp: ENSP00000395064.1:p.Gly5Cys
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000353131
  ensembl transcript: ENST00000360031
  gene symbol: ENTPD6
  hgvsc: ENST00000360031.2:c.64G>T
  hgvsp: ENSP00000353131.2:p.Gly22Cys
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390511
  ensembl transcript: ENST00000418890
  gene symbol: ENTPD6
  hgvsc: ENST00000418890.1:c.16G>T
  hgvsp: ENSP00000390511.1:p.Gly6Cys
  variant of: http://identifiers.org/hgnc/3368
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4131
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1227
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1853
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8207
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14870
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8775
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2414
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15761
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly23Cys
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: African
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: DP

20-25187726-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25187726
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 25187726
    reference: chr 20
allele count: 2
allele frequency: 1.712211492363537e-5
allele num: 116808
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000395064
  ensembl transcript: ENST00000417467
  gene symbol: ENTPD6
  hgvsc: ENST00000417467.1:c.15T>A
  hgvsp: ENST00000417467.1:c.15T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000347084
  ensembl transcript: ENST00000354989
  gene symbol: ENTPD6
  hgvsc: ENST00000354989.5:c.18T>A
  hgvsp: ENST00000354989.5:c.18T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000365840
  ensembl transcript: ENST00000376652
  gene symbol: ENTPD6
  hgvsc: ENST00000376652.4:c.69T>A
  hgvsp: ENST00000376652.4:c.69T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000408098
  ensembl transcript: ENST00000439162
  gene symbol: ENTPD6
  hgvsc: ENST00000439162.1:c.15T>A
  hgvsp: ENST00000439162.1:c.15T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390646
  ensembl transcript: ENST00000425813
  gene symbol: ENTPD6
  hgvsc: ENST00000425813.1:c.69T>A
  hgvsp: ENST00000425813.1:c.69T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401895
  ensembl transcript: ENST00000433259
  gene symbol: ENTPD6
  hgvsc: ENST00000433259.2:c.69T>A
  hgvsp: ENST00000433259.2:c.69T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000353131
  ensembl transcript: ENST00000360031
  gene symbol: ENTPD6
  hgvsc: ENST00000360031.2:c.66T>A
  hgvsp: ENST00000360031.2:c.66T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401573
  ensembl transcript: ENST00000427553
  gene symbol: ENTPD6
  hgvsc: ENST00000427553.1:c.94-2759T>A
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000398844
  ensembl transcript: ENST00000435520
  gene symbol: ENTPD6
  hgvsc: ENST00000435520.1:c.66T>A
  hgvsp: ENST00000435520.1:c.66T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390095
  ensembl transcript: ENST00000433417
  gene symbol: ENTPD6
  hgvsc: ENST00000433417.1:c.139-2759T>A
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390511
  ensembl transcript: ENST00000418890
  gene symbol: ENTPD6
  hgvsc: ENST00000418890.1:c.18T>A
  hgvsp: ENST00000418890.1:c.18T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15304
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4236
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8612
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1878
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2191
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16226
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9025
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly23Gly
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: African
population: South Asian
reference allele: T
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

20-25187726-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25187726
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 25187726
    reference: chr 20
allele count: 1
allele frequency: 8.561057461817683e-6
allele num: 116808
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390511
  ensembl transcript: ENST00000418890
  gene symbol: ENTPD6
  hgvsc: ENST00000418890.1:c.18T>C
  hgvsp: ENST00000418890.1:c.18T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000398844
  ensembl transcript: ENST00000435520
  gene symbol: ENTPD6
  hgvsc: ENST00000435520.1:c.66T>C
  hgvsp: ENST00000435520.1:c.66T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000395064
  ensembl transcript: ENST00000417467
  gene symbol: ENTPD6
  hgvsc: ENST00000417467.1:c.15T>C
  hgvsp: ENST00000417467.1:c.15T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000353131
  ensembl transcript: ENST00000360031
  gene symbol: ENTPD6
  hgvsc: ENST00000360031.2:c.66T>C
  hgvsp: ENST00000360031.2:c.66T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401573
  ensembl transcript: ENST00000427553
  gene symbol: ENTPD6
  hgvsc: ENST00000427553.1:c.94-2759T>C
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390646
  ensembl transcript: ENST00000425813
  gene symbol: ENTPD6
  hgvsc: ENST00000425813.1:c.69T>C
  hgvsp: ENST00000425813.1:c.69T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000347084
  ensembl transcript: ENST00000354989
  gene symbol: ENTPD6
  hgvsc: ENST00000354989.5:c.18T>C
  hgvsp: ENST00000354989.5:c.18T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000408098
  ensembl transcript: ENST00000439162
  gene symbol: ENTPD6
  hgvsc: ENST00000439162.1:c.15T>C
  hgvsp: ENST00000439162.1:c.15T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000365840
  ensembl transcript: ENST00000376652
  gene symbol: ENTPD6
  hgvsc: ENST00000376652.4:c.69T>C
  hgvsp: ENST00000376652.4:c.69T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401895
  ensembl transcript: ENST00000433259
  gene symbol: ENTPD6
  hgvsc: ENST00000433259.2:c.69T>C
  hgvsp: ENST00000433259.2:c.69T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390095
  ensembl transcript: ENST00000433417
  gene symbol: ENTPD6
  hgvsc: ENST00000433417.1:c.139-2759T>C
  variant of: http://identifiers.org/hgnc/3368
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1878
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9025
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15304
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8612
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2191
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4236
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly23Gly
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
reference allele: T
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

20-25187762-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25187762
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 25187762
    reference: chr 20
allele count: 4
allele frequency: 3.334222459322486e-5
allele num: 119968
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401895
  ensembl transcript: ENST00000433259
  gene symbol: ENTPD6
  hgvsc: ENST00000433259.2:c.105C>T
  hgvsp: ENST00000433259.2:c.105C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000408098
  ensembl transcript: ENST00000439162
  gene symbol: ENTPD6
  hgvsc: ENST00000439162.1:c.51C>T
  hgvsp: ENST00000439162.1:c.51C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000353131
  ensembl transcript: ENST00000360031
  gene symbol: ENTPD6
  hgvsc: ENST00000360031.2:c.102C>T
  hgvsp: ENST00000360031.2:c.102C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390511
  ensembl transcript: ENST00000418890
  gene symbol: ENTPD6
  hgvsc: ENST00000418890.1:c.54C>T
  hgvsp: ENST00000418890.1:c.54C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390095
  ensembl transcript: ENST00000433417
  gene symbol: ENTPD6
  hgvsc: ENST00000433417.1:c.139-2723C>T
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000365840
  ensembl transcript: ENST00000376652
  gene symbol: ENTPD6
  hgvsc: ENST00000376652.4:c.105C>T
  hgvsp: ENST00000376652.4:c.105C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000347084
  ensembl transcript: ENST00000354989
  gene symbol: ENTPD6
  hgvsc: ENST00000354989.5:c.54C>T
  hgvsp: ENST00000354989.5:c.54C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401573
  ensembl transcript: ENST00000427553
  gene symbol: ENTPD6
  hgvsc: ENST00000427553.1:c.94-2723C>T
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000398844
  ensembl transcript: ENST00000435520
  gene symbol: ENTPD6
  hgvsc: ENST00000435520.1:c.102C>T
  hgvsp: ENST00000435520.1:c.102C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000395064
  ensembl transcript: ENST00000417467
  gene symbol: ENTPD6
  hgvsc: ENST00000417467.1:c.51C>T
  hgvsp: ENST00000417467.1:c.51C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390646
  ensembl transcript: ENST00000425813
  gene symbol: ENTPD6
  hgvsc: ENST00000425813.1:c.105C>T
  hgvsp: ENST00000425813.1:c.105C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1879
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9865
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17161
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9049
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15493
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4244
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His35His
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: DP
site quality: QD
site quality: ClippingRankSum

20-25187769-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25187769
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 25187769
    reference: chr 20
allele count: 1
allele frequency: 8.315178526882972e-6
allele num: 120262
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390511
  ensembl transcript: ENST00000418890
  gene symbol: ENTPD6
  hgvsc: ENST00000418890.1:c.61C>T
  hgvsp: ENST00000418890.1:c.61C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000408098
  ensembl transcript: ENST00000439162
  gene symbol: ENTPD6
  hgvsc: ENST00000439162.1:c.58C>T
  hgvsp: ENST00000439162.1:c.58C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000353131
  ensembl transcript: ENST00000360031
  gene symbol: ENTPD6
  hgvsc: ENST00000360031.2:c.109C>T
  hgvsp: ENST00000360031.2:c.109C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401573
  ensembl transcript: ENST00000427553
  gene symbol: ENTPD6
  hgvsc: ENST00000427553.1:c.94-2716C>T
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390095
  ensembl transcript: ENST00000433417
  gene symbol: ENTPD6
  hgvsc: ENST00000433417.1:c.139-2716C>T
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000347084
  ensembl transcript: ENST00000354989
  gene symbol: ENTPD6
  hgvsc: ENST00000354989.5:c.61C>T
  hgvsp: ENST00000354989.5:c.61C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000365840
  ensembl transcript: ENST00000376652
  gene symbol: ENTPD6
  hgvsc: ENST00000376652.4:c.112C>T
  hgvsp: ENST00000376652.4:c.112C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401895
  ensembl transcript: ENST00000433259
  gene symbol: ENTPD6
  hgvsc: ENST00000433259.2:c.112C>T
  hgvsp: ENST00000433259.2:c.112C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000398844
  ensembl transcript: ENST00000435520
  gene symbol: ENTPD6
  hgvsc: ENST00000435520.1:c.109C>T
  hgvsp: ENST00000435520.1:c.109C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000395064
  ensembl transcript: ENST00000417467
  gene symbol: ENTPD6
  hgvsc: ENST00000417467.1:c.58C>T
  hgvsp: ENST00000417467.1:c.58C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390646
  ensembl transcript: ENST00000425813
  gene symbol: ENTPD6
  hgvsc: ENST00000425813.1:c.112C>T
  hgvsp: ENST00000425813.1:c.112C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4236
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17263
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15494
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9040
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9947
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Leu38Leu
num of homozygotes: 0
population: Other
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

20-25187771-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25187771
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 25187771
    reference: chr 20
allele count: 3
allele frequency: 2.493765586034913e-5
allele num: 120300
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000353131
  ensembl transcript: ENST00000360031
  gene symbol: ENTPD6
  hgvsc: ENST00000360031.2:c.111G>T
  hgvsp: ENST00000360031.2:c.111G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000347084
  ensembl transcript: ENST00000354989
  gene symbol: ENTPD6
  hgvsc: ENST00000354989.5:c.63G>T
  hgvsp: ENST00000354989.5:c.63G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000408098
  ensembl transcript: ENST00000439162
  gene symbol: ENTPD6
  hgvsc: ENST00000439162.1:c.60G>T
  hgvsp: ENST00000439162.1:c.60G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000395064
  ensembl transcript: ENST00000417467
  gene symbol: ENTPD6
  hgvsc: ENST00000417467.1:c.60G>T
  hgvsp: ENST00000417467.1:c.60G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401895
  ensembl transcript: ENST00000433259
  gene symbol: ENTPD6
  hgvsc: ENST00000433259.2:c.114G>T
  hgvsp: ENST00000433259.2:c.114G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390646
  ensembl transcript: ENST00000425813
  gene symbol: ENTPD6
  hgvsc: ENST00000425813.1:c.114G>T
  hgvsp: ENST00000425813.1:c.114G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000398844
  ensembl transcript: ENST00000435520
  gene symbol: ENTPD6
  hgvsc: ENST00000435520.1:c.111G>T
  hgvsp: ENST00000435520.1:c.111G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390511
  ensembl transcript: ENST00000418890
  gene symbol: ENTPD6
  hgvsc: ENST00000418890.1:c.63G>T
  hgvsp: ENST00000418890.1:c.63G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000365840
  ensembl transcript: ENST00000376652
  gene symbol: ENTPD6
  hgvsc: ENST00000376652.4:c.114G>T
  hgvsp: ENST00000376652.4:c.114G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390095
  ensembl transcript: ENST00000433417
  gene symbol: ENTPD6
  hgvsc: ENST00000433417.1:c.139-2714G>T
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401573
  ensembl transcript: ENST00000427553
  gene symbol: ENTPD6
  hgvsc: ENST00000427553.1:c.94-2714G>T
  variant of: http://identifiers.org/hgnc/3368
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1879
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15493
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4237
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9967
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17277
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9038
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu38Leu
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: African
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ClippingRankSum

20-25187772-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25187772
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 25187772
    reference: chr 20
allele count: 1
allele frequency: 8.312137383006666e-6
allele num: 120306
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000347084
  ensembl transcript: ENST00000354989
  gene symbol: ENTPD6
  hgvsc: ENST00000354989.5:c.64C>T
  hgvsp: ENSP00000347084.5:p.Arg22Trp
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000398844
  ensembl transcript: ENST00000435520
  gene symbol: ENTPD6
  hgvsc: ENST00000435520.1:c.112C>T
  hgvsp: ENSP00000398844.1:p.Arg38Trp
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401895
  ensembl transcript: ENST00000433259
  gene symbol: ENTPD6
  hgvsc: ENST00000433259.2:c.115C>T
  hgvsp: ENSP00000401895.2:p.Arg39Trp
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390511
  ensembl transcript: ENST00000418890
  gene symbol: ENTPD6
  hgvsc: ENST00000418890.1:c.64C>T
  hgvsp: ENSP00000390511.1:p.Arg22Trp
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390646
  ensembl transcript: ENST00000425813
  gene symbol: ENTPD6
  hgvsc: ENST00000425813.1:c.115C>T
  hgvsp: ENSP00000390646.1:p.Arg39Trp
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000395064
  ensembl transcript: ENST00000417467
  gene symbol: ENTPD6
  hgvsc: ENST00000417467.1:c.61C>T
  hgvsp: ENSP00000395064.1:p.Arg21Trp
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401573
  ensembl transcript: ENST00000427553
  gene symbol: ENTPD6
  hgvsc: ENST00000427553.1:c.94-2713C>T
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390095
  ensembl transcript: ENST00000433417
  gene symbol: ENTPD6
  hgvsc: ENST00000433417.1:c.139-2713C>T
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000365840
  ensembl transcript: ENST00000376652
  gene symbol: ENTPD6
  hgvsc: ENST00000376652.4:c.115C>T
  hgvsp: ENSP00000365840.4:p.Arg39Trp
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000408098
  ensembl transcript: ENST00000439162
  gene symbol: ENTPD6
  hgvsc: ENST00000439162.1:c.61C>T
  hgvsp: ENSP00000408098.1:p.Arg21Trp
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000353131
  ensembl transcript: ENST00000360031
  gene symbol: ENTPD6
  hgvsc: ENST00000360031.2:c.112C>T
  hgvsp: ENSP00000353131.2:p.Arg38Trp
  variant of: http://identifiers.org/hgnc/3368
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9946
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17299
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4237
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1882
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15498
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9043
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg39Trp
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: C
site quality: MQ
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

20-25187773-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25187773
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 25187773
    reference: chr 20
allele count: 3
allele frequency: 2.492646692257839e-5
allele num: 120354
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401895
  ensembl transcript: ENST00000433259
  gene symbol: ENTPD6
  hgvsc: ENST00000433259.2:c.116G>A
  hgvsp: ENSP00000401895.2:p.Arg39Gln
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000353131
  ensembl transcript: ENST00000360031
  gene symbol: ENTPD6
  hgvsc: ENST00000360031.2:c.113G>A
  hgvsp: ENSP00000353131.2:p.Arg38Gln
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000408098
  ensembl transcript: ENST00000439162
  gene symbol: ENTPD6
  hgvsc: ENST00000439162.1:c.62G>A
  hgvsp: ENSP00000408098.1:p.Arg21Gln
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000398844
  ensembl transcript: ENST00000435520
  gene symbol: ENTPD6
  hgvsc: ENST00000435520.1:c.113G>A
  hgvsp: ENSP00000398844.1:p.Arg38Gln
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000395064
  ensembl transcript: ENST00000417467
  gene symbol: ENTPD6
  hgvsc: ENST00000417467.1:c.62G>A
  hgvsp: ENSP00000395064.1:p.Arg21Gln
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000347084
  ensembl transcript: ENST00000354989
  gene symbol: ENTPD6
  hgvsc: ENST00000354989.5:c.65G>A
  hgvsp: ENSP00000347084.5:p.Arg22Gln
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390095
  ensembl transcript: ENST00000433417
  gene symbol: ENTPD6
  hgvsc: ENST00000433417.1:c.139-2712G>A
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390646
  ensembl transcript: ENST00000425813
  gene symbol: ENTPD6
  hgvsc: ENST00000425813.1:c.116G>A
  hgvsp: ENSP00000390646.1:p.Arg39Gln
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390511
  ensembl transcript: ENST00000418890
  gene symbol: ENTPD6
  hgvsc: ENST00000418890.1:c.65G>A
  hgvsp: ENSP00000390511.1:p.Arg22Gln
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000365840
  ensembl transcript: ENST00000376652
  gene symbol: ENTPD6
  hgvsc: ENST00000376652.4:c.116G>A
  hgvsp: ENSP00000365840.4:p.Arg39Gln
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401573
  ensembl transcript: ENST00000427553
  gene symbol: ENTPD6
  hgvsc: ENST00000427553.1:c.94-2712G>A
  variant of: http://identifiers.org/hgnc/3368
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1880
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17322
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9953
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4237
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15488
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg39Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: African
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ

20-25187773-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25187773
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 25187773
    reference: chr 20
allele count: 1
allele frequency: 8.308822307526131e-6
allele num: 120354
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000365840
  ensembl transcript: ENST00000376652
  gene symbol: ENTPD6
  hgvsc: ENST00000376652.4:c.116G>T
  hgvsp: ENSP00000365840.4:p.Arg39Leu
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390095
  ensembl transcript: ENST00000433417
  gene symbol: ENTPD6
  hgvsc: ENST00000433417.1:c.139-2712G>T
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000408098
  ensembl transcript: ENST00000439162
  gene symbol: ENTPD6
  hgvsc: ENST00000439162.1:c.62G>T
  hgvsp: ENSP00000408098.1:p.Arg21Leu
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401895
  ensembl transcript: ENST00000433259
  gene symbol: ENTPD6
  hgvsc: ENST00000433259.2:c.116G>T
  hgvsp: ENSP00000401895.2:p.Arg39Leu
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390646
  ensembl transcript: ENST00000425813
  gene symbol: ENTPD6
  hgvsc: ENST00000425813.1:c.116G>T
  hgvsp: ENSP00000390646.1:p.Arg39Leu
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000347084
  ensembl transcript: ENST00000354989
  gene symbol: ENTPD6
  hgvsc: ENST00000354989.5:c.65G>T
  hgvsp: ENSP00000347084.5:p.Arg22Leu
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401573
  ensembl transcript: ENST00000427553
  gene symbol: ENTPD6
  hgvsc: ENST00000427553.1:c.94-2712G>T
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000398844
  ensembl transcript: ENST00000435520
  gene symbol: ENTPD6
  hgvsc: ENST00000435520.1:c.113G>T
  hgvsp: ENSP00000398844.1:p.Arg38Leu
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000353131
  ensembl transcript: ENST00000360031
  gene symbol: ENTPD6
  hgvsc: ENST00000360031.2:c.113G>T
  hgvsp: ENSP00000353131.2:p.Arg38Leu
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000395064
  ensembl transcript: ENST00000417467
  gene symbol: ENTPD6
  hgvsc: ENST00000417467.1:c.62G>T
  hgvsp: ENSP00000395064.1:p.Arg21Leu
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390511
  ensembl transcript: ENST00000418890
  gene symbol: ENTPD6
  hgvsc: ENST00000418890.1:c.65G>T
  hgvsp: ENSP00000390511.1:p.Arg22Leu
  variant of: http://identifiers.org/hgnc/3368
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1880
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4237
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9039
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9953
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17322
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15488
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg39Leu
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ

20-25187779-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25187779
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 25187779
    reference: chr 20
allele count: 1
allele frequency: 8.301786544464368e-6
allele num: 120456
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000395064
  ensembl transcript: ENST00000417467
  gene symbol: ENTPD6
  hgvsc: ENST00000417467.1:c.68C>T
  hgvsp: ENSP00000395064.1:p.Ala23Val
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000408098
  ensembl transcript: ENST00000439162
  gene symbol: ENTPD6
  hgvsc: ENST00000439162.1:c.68C>T
  hgvsp: ENSP00000408098.1:p.Ala23Val
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390646
  ensembl transcript: ENST00000425813
  gene symbol: ENTPD6
  hgvsc: ENST00000425813.1:c.122C>T
  hgvsp: ENSP00000390646.1:p.Ala41Val
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000353131
  ensembl transcript: ENST00000360031
  gene symbol: ENTPD6
  hgvsc: ENST00000360031.2:c.119C>T
  hgvsp: ENSP00000353131.2:p.Ala40Val
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401895
  ensembl transcript: ENST00000433259
  gene symbol: ENTPD6
  hgvsc: ENST00000433259.2:c.122C>T
  hgvsp: ENSP00000401895.2:p.Ala41Val
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390511
  ensembl transcript: ENST00000418890
  gene symbol: ENTPD6
  hgvsc: ENST00000418890.1:c.71C>T
  hgvsp: ENSP00000390511.1:p.Ala24Val
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000347084
  ensembl transcript: ENST00000354989
  gene symbol: ENTPD6
  hgvsc: ENST00000354989.5:c.71C>T
  hgvsp: ENSP00000347084.5:p.Ala24Val
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000365840
  ensembl transcript: ENST00000376652
  gene symbol: ENTPD6
  hgvsc: ENST00000376652.4:c.122C>T
  hgvsp: ENSP00000365840.4:p.Ala41Val
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000398844
  ensembl transcript: ENST00000435520
  gene symbol: ENTPD6
  hgvsc: ENST00000435520.1:c.119C>T
  hgvsp: ENSP00000398844.1:p.Ala40Val
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401573
  ensembl transcript: ENST00000427553
  gene symbol: ENTPD6
  hgvsc: ENST00000427553.1:c.94-2706C>T
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390095
  ensembl transcript: ENST00000433417
  gene symbol: ENTPD6
  hgvsc: ENST00000433417.1:c.139-2706C>T
  variant of: http://identifiers.org/hgnc/3368
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15482
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9996
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17360
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9041
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4236
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1881
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala41Val
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum

20-25187780-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25187780
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 25187780
    reference: chr 20
allele count: 7
allele frequency: 5.809225049378413e-5
allele num: 120498
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000408098
  ensembl transcript: ENST00000439162
  gene symbol: ENTPD6
  hgvsc: ENST00000439162.1:c.69G>A
  hgvsp: ENST00000439162.1:c.69G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000347084
  ensembl transcript: ENST00000354989
  gene symbol: ENTPD6
  hgvsc: ENST00000354989.5:c.72G>A
  hgvsp: ENST00000354989.5:c.72G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000365840
  ensembl transcript: ENST00000376652
  gene symbol: ENTPD6
  hgvsc: ENST00000376652.4:c.123G>A
  hgvsp: ENST00000376652.4:c.123G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390095
  ensembl transcript: ENST00000433417
  gene symbol: ENTPD6
  hgvsc: ENST00000433417.1:c.139-2705G>A
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000353131
  ensembl transcript: ENST00000360031
  gene symbol: ENTPD6
  hgvsc: ENST00000360031.2:c.120G>A
  hgvsp: ENST00000360031.2:c.120G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000395064
  ensembl transcript: ENST00000417467
  gene symbol: ENTPD6
  hgvsc: ENST00000417467.1:c.69G>A
  hgvsp: ENST00000417467.1:c.69G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390511
  ensembl transcript: ENST00000418890
  gene symbol: ENTPD6
  hgvsc: ENST00000418890.1:c.72G>A
  hgvsp: ENST00000418890.1:c.72G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401573
  ensembl transcript: ENST00000427553
  gene symbol: ENTPD6
  hgvsc: ENST00000427553.1:c.94-2705G>A
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401895
  ensembl transcript: ENST00000433259
  gene symbol: ENTPD6
  hgvsc: ENST00000433259.2:c.123G>A
  hgvsp: ENST00000433259.2:c.123G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000398844
  ensembl transcript: ENST00000435520
  gene symbol: ENTPD6
  hgvsc: ENST00000435520.1:c.120G>A
  hgvsp: ENST00000435520.1:c.120G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390646
  ensembl transcript: ENST00000425813
  gene symbol: ENTPD6
  hgvsc: ENST00000425813.1:c.123G>A
  hgvsp: ENST00000425813.1:c.123G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4234
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10028
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17374
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9041
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1879
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15485
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ala41Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

20-25187804-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25187804
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 25187804
    reference: chr 20
allele count: 1
allele frequency: 8.279790686891435e-6
allele num: 120776
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000365840
  ensembl transcript: ENST00000376652
  gene symbol: ENTPD6
  hgvsc: ENST00000376652.4:c.147G>A
  hgvsp: ENST00000376652.4:c.147G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390646
  ensembl transcript: ENST00000425813
  gene symbol: ENTPD6
  hgvsc: ENST00000425813.1:c.147G>A
  hgvsp: ENST00000425813.1:c.147G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000398844
  ensembl transcript: ENST00000435520
  gene symbol: ENTPD6
  hgvsc: ENST00000435520.1:c.144G>A
  hgvsp: ENST00000435520.1:c.144G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401573
  ensembl transcript: ENST00000427553
  gene symbol: ENTPD6
  hgvsc: ENST00000427553.1:c.94-2681G>A
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401895
  ensembl transcript: ENST00000433259
  gene symbol: ENTPD6
  hgvsc: ENST00000433259.2:c.147G>A
  hgvsp: ENST00000433259.2:c.147G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000347084
  ensembl transcript: ENST00000354989
  gene symbol: ENTPD6
  hgvsc: ENST00000354989.5:c.96G>A
  hgvsp: ENST00000354989.5:c.96G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000408098
  ensembl transcript: ENST00000439162
  gene symbol: ENTPD6
  hgvsc: ENST00000439162.1:c.93G>A
  hgvsp: ENST00000439162.1:c.93G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000353131
  ensembl transcript: ENST00000360031
  gene symbol: ENTPD6
  hgvsc: ENST00000360031.2:c.144G>A
  hgvsp: ENST00000360031.2:c.144G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390095
  ensembl transcript: ENST00000433417
  gene symbol: ENTPD6
  hgvsc: ENST00000433417.1:c.139-2681G>A
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390511
  ensembl transcript: ENST00000418890
  gene symbol: ENTPD6
  hgvsc: ENST00000418890.1:c.96G>A
  hgvsp: ENST00000418890.1:c.96G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000395064
  ensembl transcript: ENST00000417467
  gene symbol: ENTPD6
  hgvsc: ENST00000417467.1:c.93G>A
  hgvsp: ENST00000417467.1:c.93G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17542
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9042
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10068
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1876
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15499
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4229
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu49Leu
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: Other
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

20-25187806-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25187806
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 25187806
    reference: chr 20
allele count: 1
allele frequency: 8.277460475126231e-6
allele num: 120810
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000398844
  ensembl transcript: ENST00000435520
  gene symbol: ENTPD6
  hgvsc: ENST00000435520.1:c.146G>A
  hgvsp: ENSP00000398844.1:p.Cys49Tyr
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000395064
  ensembl transcript: ENST00000417467
  gene symbol: ENTPD6
  hgvsc: ENST00000417467.1:c.95G>A
  hgvsp: ENSP00000395064.1:p.Cys32Tyr
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401573
  ensembl transcript: ENST00000427553
  gene symbol: ENTPD6
  hgvsc: ENST00000427553.1:c.94-2679G>A
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000347084
  ensembl transcript: ENST00000354989
  gene symbol: ENTPD6
  hgvsc: ENST00000354989.5:c.98G>A
  hgvsp: ENSP00000347084.5:p.Cys33Tyr
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390511
  ensembl transcript: ENST00000418890
  gene symbol: ENTPD6
  hgvsc: ENST00000418890.1:c.98G>A
  hgvsp: ENSP00000390511.1:p.Cys33Tyr
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390646
  ensembl transcript: ENST00000425813
  gene symbol: ENTPD6
  hgvsc: ENST00000425813.1:c.149G>A
  hgvsp: ENSP00000390646.1:p.Cys50Tyr
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000408098
  ensembl transcript: ENST00000439162
  gene symbol: ENTPD6
  hgvsc: ENST00000439162.1:c.95G>A
  hgvsp: ENSP00000408098.1:p.Cys32Tyr
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401895
  ensembl transcript: ENST00000433259
  gene symbol: ENTPD6
  hgvsc: ENST00000433259.2:c.149G>A
  hgvsp: ENSP00000401895.2:p.Cys50Tyr
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000365840
  ensembl transcript: ENST00000376652
  gene symbol: ENTPD6
  hgvsc: ENST00000376652.4:c.149G>A
  hgvsp: ENSP00000365840.4:p.Cys50Tyr
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000353131
  ensembl transcript: ENST00000360031
  gene symbol: ENTPD6
  hgvsc: ENST00000360031.2:c.146G>A
  hgvsp: ENSP00000353131.2:p.Cys49Tyr
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390095
  ensembl transcript: ENST00000433417
  gene symbol: ENTPD6
  hgvsc: ENST00000433417.1:c.139-2679G>A
  variant of: http://identifiers.org/hgnc/3368
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17573
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10065
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9040
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4228
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15497
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1874
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys50Tyr
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ

20-25187808-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25187808
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 25187808
    reference: chr 20
allele count: 1
allele frequency: 8.276501357346223e-6
allele num: 120824
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000347084
  ensembl transcript: ENST00000354989
  gene symbol: ENTPD6
  hgvsc: ENST00000354989.5:c.100G>A
  hgvsp: ENSP00000347084.5:p.Val34Met
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390511
  ensembl transcript: ENST00000418890
  gene symbol: ENTPD6
  hgvsc: ENST00000418890.1:c.100G>A
  hgvsp: ENSP00000390511.1:p.Val34Met
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401573
  ensembl transcript: ENST00000427553
  gene symbol: ENTPD6
  hgvsc: ENST00000427553.1:c.94-2677G>A
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000395064
  ensembl transcript: ENST00000417467
  gene symbol: ENTPD6
  hgvsc: ENST00000417467.1:c.97G>A
  hgvsp: ENSP00000395064.1:p.Val33Met
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000408098
  ensembl transcript: ENST00000439162
  gene symbol: ENTPD6
  hgvsc: ENST00000439162.1:c.97G>A
  hgvsp: ENSP00000408098.1:p.Val33Met
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390095
  ensembl transcript: ENST00000433417
  gene symbol: ENTPD6
  hgvsc: ENST00000433417.1:c.139-2677G>A
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000398844
  ensembl transcript: ENST00000435520
  gene symbol: ENTPD6
  hgvsc: ENST00000435520.1:c.148G>A
  hgvsp: ENSP00000398844.1:p.Val50Met
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390646
  ensembl transcript: ENST00000425813
  gene symbol: ENTPD6
  hgvsc: ENST00000425813.1:c.151G>A
  hgvsp: ENSP00000390646.1:p.Val51Met
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000365840
  ensembl transcript: ENST00000376652
  gene symbol: ENTPD6
  hgvsc: ENST00000376652.4:c.151G>A
  hgvsp: ENSP00000365840.4:p.Val51Met
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401895
  ensembl transcript: ENST00000433259
  gene symbol: ENTPD6
  hgvsc: ENST00000433259.2:c.151G>A
  hgvsp: ENSP00000401895.2:p.Val51Met
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000353131
  ensembl transcript: ENST00000360031
  gene symbol: ENTPD6
  hgvsc: ENST00000360031.2:c.148G>A
  hgvsp: ENSP00000353131.2:p.Val50Met
  variant of: http://identifiers.org/hgnc/3368
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15490
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10078
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17588
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9042
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4229
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1874
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val51Met
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

20-25187813-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25187813
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 25187813
    reference: chr 20
allele count: 4
allele frequency: 3.310052629836815e-5
allele num: 120844
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401895
  ensembl transcript: ENST00000433259
  gene symbol: ENTPD6
  hgvsc: ENST00000433259.2:c.156C>T
  hgvsp: ENST00000433259.2:c.156C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390646
  ensembl transcript: ENST00000425813
  gene symbol: ENTPD6
  hgvsc: ENST00000425813.1:c.156C>T
  hgvsp: ENST00000425813.1:c.156C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000395064
  ensembl transcript: ENST00000417467
  gene symbol: ENTPD6
  hgvsc: ENST00000417467.1:c.102C>T
  hgvsp: ENST00000417467.1:c.102C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000398844
  ensembl transcript: ENST00000435520
  gene symbol: ENTPD6
  hgvsc: ENST00000435520.1:c.153C>T
  hgvsp: ENST00000435520.1:c.153C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000365840
  ensembl transcript: ENST00000376652
  gene symbol: ENTPD6
  hgvsc: ENST00000376652.4:c.156C>T
  hgvsp: ENST00000376652.4:c.156C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390095
  ensembl transcript: ENST00000433417
  gene symbol: ENTPD6
  hgvsc: ENST00000433417.1:c.139-2672C>T
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000353131
  ensembl transcript: ENST00000360031
  gene symbol: ENTPD6
  hgvsc: ENST00000360031.2:c.153C>T
  hgvsp: ENST00000360031.2:c.153C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000347084
  ensembl transcript: ENST00000354989
  gene symbol: ENTPD6
  hgvsc: ENST00000354989.5:c.105C>T
  hgvsp: ENST00000354989.5:c.105C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401573
  ensembl transcript: ENST00000427553
  gene symbol: ENTPD6
  hgvsc: ENST00000427553.1:c.94-2672C>T
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000408098
  ensembl transcript: ENST00000439162
  gene symbol: ENTPD6
  hgvsc: ENST00000439162.1:c.102C>T
  hgvsp: ENST00000439162.1:c.102C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390511
  ensembl transcript: ENST00000418890
  gene symbol: ENTPD6
  hgvsc: ENST00000418890.1:c.105C>T
  hgvsp: ENST00000418890.1:c.105C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4227
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10089
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1871
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9038
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17576
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Gly52Gly
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

20-25187814-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25187814
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 25187814
    reference: chr 20
allele count: 1
allele frequency: 8.275131574592036e-6
allele num: 120844
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401573
  ensembl transcript: ENST00000427553
  gene symbol: ENTPD6
  hgvsc: ENST00000427553.1:c.94-2671G>A
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000347084
  ensembl transcript: ENST00000354989
  gene symbol: ENTPD6
  hgvsc: ENST00000354989.5:c.106G>A
  hgvsp: ENSP00000347084.5:p.Val36Met
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000395064
  ensembl transcript: ENST00000417467
  gene symbol: ENTPD6
  hgvsc: ENST00000417467.1:c.103G>A
  hgvsp: ENSP00000395064.1:p.Val35Met
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390095
  ensembl transcript: ENST00000433417
  gene symbol: ENTPD6
  hgvsc: ENST00000433417.1:c.139-2671G>A
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390511
  ensembl transcript: ENST00000418890
  gene symbol: ENTPD6
  hgvsc: ENST00000418890.1:c.106G>A
  hgvsp: ENSP00000390511.1:p.Val36Met
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000365840
  ensembl transcript: ENST00000376652
  gene symbol: ENTPD6
  hgvsc: ENST00000376652.4:c.157G>A
  hgvsp: ENSP00000365840.4:p.Val53Met
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000353131
  ensembl transcript: ENST00000360031
  gene symbol: ENTPD6
  hgvsc: ENST00000360031.2:c.154G>A
  hgvsp: ENSP00000353131.2:p.Val52Met
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401895
  ensembl transcript: ENST00000433259
  gene symbol: ENTPD6
  hgvsc: ENST00000433259.2:c.157G>A
  hgvsp: ENSP00000401895.2:p.Val53Met
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000408098
  ensembl transcript: ENST00000439162
  gene symbol: ENTPD6
  hgvsc: ENST00000439162.1:c.103G>A
  hgvsp: ENSP00000408098.1:p.Val35Met
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000398844
  ensembl transcript: ENST00000435520
  gene symbol: ENTPD6
  hgvsc: ENST00000435520.1:c.154G>A
  hgvsp: ENSP00000398844.1:p.Val52Met
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390646
  ensembl transcript: ENST00000425813
  gene symbol: ENTPD6
  hgvsc: ENST00000425813.1:c.157G>A
  hgvsp: ENSP00000390646.1:p.Val53Met
  variant of: http://identifiers.org/hgnc/3368
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1870
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17582
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4223
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9039
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15491
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10063
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val53Met
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
population: African
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: MQ

20-25187815-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25187815
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 25187815
    reference: chr 20
allele count: 7
allele frequency: 5.792496234877447e-5
allele num: 120846
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000353131
  ensembl transcript: ENST00000360031
  gene symbol: ENTPD6
  hgvsc: ENST00000360031.2:c.155T>C
  hgvsp: ENSP00000353131.2:p.Val52Ala
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000365840
  ensembl transcript: ENST00000376652
  gene symbol: ENTPD6
  hgvsc: ENST00000376652.4:c.158T>C
  hgvsp: ENSP00000365840.4:p.Val53Ala
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401573
  ensembl transcript: ENST00000427553
  gene symbol: ENTPD6
  hgvsc: ENST00000427553.1:c.94-2670T>C
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000347084
  ensembl transcript: ENST00000354989
  gene symbol: ENTPD6
  hgvsc: ENST00000354989.5:c.107T>C
  hgvsp: ENSP00000347084.5:p.Val36Ala
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390095
  ensembl transcript: ENST00000433417
  gene symbol: ENTPD6
  hgvsc: ENST00000433417.1:c.139-2670T>C
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390646
  ensembl transcript: ENST00000425813
  gene symbol: ENTPD6
  hgvsc: ENST00000425813.1:c.158T>C
  hgvsp: ENSP00000390646.1:p.Val53Ala
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000395064
  ensembl transcript: ENST00000417467
  gene symbol: ENTPD6
  hgvsc: ENST00000417467.1:c.104T>C
  hgvsp: ENSP00000395064.1:p.Val35Ala
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390511
  ensembl transcript: ENST00000418890
  gene symbol: ENTPD6
  hgvsc: ENST00000418890.1:c.107T>C
  hgvsp: ENSP00000390511.1:p.Val36Ala
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000408098
  ensembl transcript: ENST00000439162
  gene symbol: ENTPD6
  hgvsc: ENST00000439162.1:c.104T>C
  hgvsp: ENSP00000408098.1:p.Val35Ala
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000398844
  ensembl transcript: ENST00000435520
  gene symbol: ENTPD6
  hgvsc: ENST00000435520.1:c.155T>C
  hgvsp: ENSP00000398844.1:p.Val52Ala
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401895
  ensembl transcript: ENST00000433259
  gene symbol: ENTPD6
  hgvsc: ENST00000433259.2:c.158T>C
  hgvsp: ENSP00000401895.2:p.Val53Ala
  variant of: http://identifiers.org/hgnc/3368
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1869
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10017
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4222
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15482
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17581
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9038
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val53Ala
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: East Asian
population: Latino
reference allele: T
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff

20-25187829-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25187829
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 25187829
    reference: chr 20
allele count: 3
allele frequency: 2.482580559739164e-5
allele num: 120842
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401895
  ensembl transcript: ENST00000433259
  gene symbol: ENTPD6
  hgvsc: ENST00000433259.2:c.172G>A
  hgvsp: ENSP00000401895.2:p.Ala58Thr
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000395064
  ensembl transcript: ENST00000417467
  gene symbol: ENTPD6
  hgvsc: ENST00000417467.1:c.118G>A
  hgvsp: ENSP00000395064.1:p.Ala40Thr
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401573
  ensembl transcript: ENST00000427553
  gene symbol: ENTPD6
  hgvsc: ENST00000427553.1:c.94-2656G>A
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390095
  ensembl transcript: ENST00000433417
  gene symbol: ENTPD6
  hgvsc: ENST00000433417.1:c.139-2656G>A
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000408098
  ensembl transcript: ENST00000439162
  gene symbol: ENTPD6
  hgvsc: ENST00000439162.1:c.118G>A
  hgvsp: ENSP00000408098.1:p.Ala40Thr
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000347084
  ensembl transcript: ENST00000354989
  gene symbol: ENTPD6
  hgvsc: ENST00000354989.5:c.121G>A
  hgvsp: ENSP00000347084.5:p.Ala41Thr
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000398844
  ensembl transcript: ENST00000435520
  gene symbol: ENTPD6
  hgvsc: ENST00000435520.1:c.169G>A
  hgvsp: ENSP00000398844.1:p.Ala57Thr
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390511
  ensembl transcript: ENST00000418890
  gene symbol: ENTPD6
  hgvsc: ENST00000418890.1:c.121G>A
  hgvsp: ENSP00000390511.1:p.Ala41Thr
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000365840
  ensembl transcript: ENST00000376652
  gene symbol: ENTPD6
  hgvsc: ENST00000376652.4:c.172G>A
  hgvsp: ENSP00000365840.4:p.Ala58Thr
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000353131
  ensembl transcript: ENST00000360031
  gene symbol: ENTPD6
  hgvsc: ENST00000360031.2:c.169G>A
  hgvsp: ENSP00000353131.2:p.Ala57Thr
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390646
  ensembl transcript: ENST00000425813
  gene symbol: ENTPD6
  hgvsc: ENST00000425813.1:c.172G>A
  hgvsp: ENSP00000390646.1:p.Ala58Thr
  variant of: http://identifiers.org/hgnc/3368
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9899
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1867
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15482
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4224
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17574
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9031
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala58Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD

20-25187831-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25187831
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 25187831
    reference: chr 20
allele count: 1
allele frequency: 8.275542461808372e-6
allele num: 120838
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000353131
  ensembl transcript: ENST00000360031
  gene symbol: ENTPD6
  hgvsc: ENST00000360031.2:c.171C>G
  hgvsp: ENST00000360031.2:c.171C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401573
  ensembl transcript: ENST00000427553
  gene symbol: ENTPD6
  hgvsc: ENST00000427553.1:c.94-2654C>G
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390646
  ensembl transcript: ENST00000425813
  gene symbol: ENTPD6
  hgvsc: ENST00000425813.1:c.174C>G
  hgvsp: ENST00000425813.1:c.174C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000347084
  ensembl transcript: ENST00000354989
  gene symbol: ENTPD6
  hgvsc: ENST00000354989.5:c.123C>G
  hgvsp: ENST00000354989.5:c.123C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000395064
  ensembl transcript: ENST00000417467
  gene symbol: ENTPD6
  hgvsc: ENST00000417467.1:c.120C>G
  hgvsp: ENST00000417467.1:c.120C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401895
  ensembl transcript: ENST00000433259
  gene symbol: ENTPD6
  hgvsc: ENST00000433259.2:c.174C>G
  hgvsp: ENST00000433259.2:c.174C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000365840
  ensembl transcript: ENST00000376652
  gene symbol: ENTPD6
  hgvsc: ENST00000376652.4:c.174C>G
  hgvsp: ENST00000376652.4:c.174C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000398844
  ensembl transcript: ENST00000435520
  gene symbol: ENTPD6
  hgvsc: ENST00000435520.1:c.171C>G
  hgvsp: ENST00000435520.1:c.171C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390095
  ensembl transcript: ENST00000433417
  gene symbol: ENTPD6
  hgvsc: ENST00000433417.1:c.139-2654C>G
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390511
  ensembl transcript: ENST00000418890
  gene symbol: ENTPD6
  hgvsc: ENST00000418890.1:c.123C>G
  hgvsp: ENST00000418890.1:c.123C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000408098
  ensembl transcript: ENST00000439162
  gene symbol: ENTPD6
  hgvsc: ENST00000439162.1:c.120C>G
  hgvsp: ENST00000439162.1:c.120C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1868
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4223
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9880
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9030
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15477
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17565
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala58Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: African
population: European (Finnish)
population: South Asian
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum

20-25187831-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25187831
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 25187831
    reference: chr 20
allele count: 1
allele frequency: 8.275542461808372e-6
allele num: 120838
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401573
  ensembl transcript: ENST00000427553
  gene symbol: ENTPD6
  hgvsc: ENST00000427553.1:c.94-2654C>T
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000398844
  ensembl transcript: ENST00000435520
  gene symbol: ENTPD6
  hgvsc: ENST00000435520.1:c.171C>T
  hgvsp: ENST00000435520.1:c.171C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000395064
  ensembl transcript: ENST00000417467
  gene symbol: ENTPD6
  hgvsc: ENST00000417467.1:c.120C>T
  hgvsp: ENST00000417467.1:c.120C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390511
  ensembl transcript: ENST00000418890
  gene symbol: ENTPD6
  hgvsc: ENST00000418890.1:c.123C>T
  hgvsp: ENST00000418890.1:c.123C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000365840
  ensembl transcript: ENST00000376652
  gene symbol: ENTPD6
  hgvsc: ENST00000376652.4:c.174C>T
  hgvsp: ENST00000376652.4:c.174C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401895
  ensembl transcript: ENST00000433259
  gene symbol: ENTPD6
  hgvsc: ENST00000433259.2:c.174C>T
  hgvsp: ENST00000433259.2:c.174C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000347084
  ensembl transcript: ENST00000354989
  gene symbol: ENTPD6
  hgvsc: ENST00000354989.5:c.123C>T
  hgvsp: ENST00000354989.5:c.123C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390646
  ensembl transcript: ENST00000425813
  gene symbol: ENTPD6
  hgvsc: ENST00000425813.1:c.174C>T
  hgvsp: ENST00000425813.1:c.174C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000408098
  ensembl transcript: ENST00000439162
  gene symbol: ENTPD6
  hgvsc: ENST00000439162.1:c.120C>T
  hgvsp: ENST00000439162.1:c.120C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000353131
  ensembl transcript: ENST00000360031
  gene symbol: ENTPD6
  hgvsc: ENST00000360031.2:c.171C>T
  hgvsp: ENST00000360031.2:c.171C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390095
  ensembl transcript: ENST00000433417
  gene symbol: ENTPD6
  hgvsc: ENST00000433417.1:c.139-2654C>T
  variant of: http://identifiers.org/hgnc/3368
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4223
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1868
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9880
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9030
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17565
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15477
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala58Ala
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: C
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP

20-25187835-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25187835
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 25187835
    reference: chr 20
allele count: 1
allele frequency: 8.277049397430804e-6
allele num: 120816
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401573
  ensembl transcript: ENST00000427553
  gene symbol: ENTPD6
  hgvsc: ENST00000427553.1:c.94-2650A>G
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000347084
  ensembl transcript: ENST00000354989
  gene symbol: ENTPD6
  hgvsc: ENST00000354989.5:c.127A>G
  hgvsp: ENSP00000347084.5:p.Ile43Val
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000365840
  ensembl transcript: ENST00000376652
  gene symbol: ENTPD6
  hgvsc: ENST00000376652.4:c.178A>G
  hgvsp: ENSP00000365840.4:p.Ile60Val
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000353131
  ensembl transcript: ENST00000360031
  gene symbol: ENTPD6
  hgvsc: ENST00000360031.2:c.175A>G
  hgvsp: ENSP00000353131.2:p.Ile59Val
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000395064
  ensembl transcript: ENST00000417467
  gene symbol: ENTPD6
  hgvsc: ENST00000417467.1:c.124A>G
  hgvsp: ENSP00000395064.1:p.Ile42Val
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401895
  ensembl transcript: ENST00000433259
  gene symbol: ENTPD6
  hgvsc: ENST00000433259.2:c.178A>G
  hgvsp: ENSP00000401895.2:p.Ile60Val
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390511
  ensembl transcript: ENST00000418890
  gene symbol: ENTPD6
  hgvsc: ENST00000418890.1:c.127A>G
  hgvsp: ENSP00000390511.1:p.Ile43Val
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000398844
  ensembl transcript: ENST00000435520
  gene symbol: ENTPD6
  hgvsc: ENST00000435520.1:c.175A>G
  hgvsp: ENSP00000398844.1:p.Ile59Val
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390095
  ensembl transcript: ENST00000433417
  gene symbol: ENTPD6
  hgvsc: ENST00000433417.1:c.139-2650A>G
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390646
  ensembl transcript: ENST00000425813
  gene symbol: ENTPD6
  hgvsc: ENST00000425813.1:c.178A>G
  hgvsp: ENSP00000390646.1:p.Ile60Val
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000408098
  ensembl transcript: ENST00000439162
  gene symbol: ENTPD6
  hgvsc: ENST00000439162.1:c.124A>G
  hgvsp: ENSP00000408098.1:p.Ile42Val
  variant of: http://identifiers.org/hgnc/3368
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1868
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9029
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15471
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9801
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4219
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17522
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile60Val
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: DP

20-25187836-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25187836
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 25187836
    reference: chr 20
allele count: 1
allele frequency: 8.277049397430804e-6
allele num: 120816
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000408098
  ensembl transcript: ENST00000439162
  gene symbol: ENTPD6
  hgvsc: ENST00000439162.1:c.125T>A
  hgvsp: ENSP00000408098.1:p.Ile42Asn
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000353131
  ensembl transcript: ENST00000360031
  gene symbol: ENTPD6
  hgvsc: ENST00000360031.2:c.176T>A
  hgvsp: ENSP00000353131.2:p.Ile59Asn
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401573
  ensembl transcript: ENST00000427553
  gene symbol: ENTPD6
  hgvsc: ENST00000427553.1:c.94-2649T>A
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000398844
  ensembl transcript: ENST00000435520
  gene symbol: ENTPD6
  hgvsc: ENST00000435520.1:c.176T>A
  hgvsp: ENSP00000398844.1:p.Ile59Asn
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000347084
  ensembl transcript: ENST00000354989
  gene symbol: ENTPD6
  hgvsc: ENST00000354989.5:c.128T>A
  hgvsp: ENSP00000347084.5:p.Ile43Asn
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401895
  ensembl transcript: ENST00000433259
  gene symbol: ENTPD6
  hgvsc: ENST00000433259.2:c.179T>A
  hgvsp: ENSP00000401895.2:p.Ile60Asn
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390095
  ensembl transcript: ENST00000433417
  gene symbol: ENTPD6
  hgvsc: ENST00000433417.1:c.139-2649T>A
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000365840
  ensembl transcript: ENST00000376652
  gene symbol: ENTPD6
  hgvsc: ENST00000376652.4:c.179T>A
  hgvsp: ENSP00000365840.4:p.Ile60Asn
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390511
  ensembl transcript: ENST00000418890
  gene symbol: ENTPD6
  hgvsc: ENST00000418890.1:c.128T>A
  hgvsp: ENSP00000390511.1:p.Ile43Asn
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390646
  ensembl transcript: ENST00000425813
  gene symbol: ENTPD6
  hgvsc: ENST00000425813.1:c.179T>A
  hgvsp: ENSP00000390646.1:p.Ile60Asn
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000395064
  ensembl transcript: ENST00000417467
  gene symbol: ENTPD6
  hgvsc: ENST00000417467.1:c.125T>A
  hgvsp: ENSP00000395064.1:p.Ile42Asn
  variant of: http://identifiers.org/hgnc/3368
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1868
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17527
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15471
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9801
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9027
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4218
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile60Asn
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: QD

20-25187839-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25187839
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 25187839
    reference: chr 20
allele count: 1
allele frequency: 8.278008642241022e-6
allele num: 120802
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000353131
  ensembl transcript: ENST00000360031
  gene symbol: ENTPD6
  hgvsc: ENST00000360031.2:c.179A>G
  hgvsp: ENSP00000353131.2:p.Lys60Arg
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000395064
  ensembl transcript: ENST00000417467
  gene symbol: ENTPD6
  hgvsc: ENST00000417467.1:c.128A>G
  hgvsp: ENSP00000395064.1:p.Lys43Arg
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390511
  ensembl transcript: ENST00000418890
  gene symbol: ENTPD6
  hgvsc: ENST00000418890.1:c.131A>G
  hgvsp: ENSP00000390511.1:p.Lys44Arg
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000365840
  ensembl transcript: ENST00000376652
  gene symbol: ENTPD6
  hgvsc: ENST00000376652.4:c.182A>G
  hgvsp: ENSP00000365840.4:p.Lys61Arg
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000347084
  ensembl transcript: ENST00000354989
  gene symbol: ENTPD6
  hgvsc: ENST00000354989.5:c.131A>G
  hgvsp: ENSP00000347084.5:p.Lys44Arg
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000408098
  ensembl transcript: ENST00000439162
  gene symbol: ENTPD6
  hgvsc: ENST00000439162.1:c.128A>G
  hgvsp: ENSP00000408098.1:p.Lys43Arg
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401573
  ensembl transcript: ENST00000427553
  gene symbol: ENTPD6
  hgvsc: ENST00000427553.1:c.94-2646A>G
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401895
  ensembl transcript: ENST00000433259
  gene symbol: ENTPD6
  hgvsc: ENST00000433259.2:c.182A>G
  hgvsp: ENSP00000401895.2:p.Lys61Arg
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000398844
  ensembl transcript: ENST00000435520
  gene symbol: ENTPD6
  hgvsc: ENST00000435520.1:c.179A>G
  hgvsp: ENSP00000398844.1:p.Lys60Arg
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390095
  ensembl transcript: ENST00000433417
  gene symbol: ENTPD6
  hgvsc: ENST00000433417.1:c.139-2646A>G
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390646
  ensembl transcript: ENST00000425813
  gene symbol: ENTPD6
  hgvsc: ENST00000425813.1:c.182A>G
  hgvsp: ENSP00000390646.1:p.Lys61Arg
  variant of: http://identifiers.org/hgnc/3368
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15473
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9740
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17492
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4219
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9025
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1868
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Lys61Arg
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
reference allele: A
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: DP

20-25187847-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25187847
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 25187847
    reference: chr 20
allele count: 4
allele frequency: 3.312629399585921e-5
allele num: 120750
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401895
  ensembl transcript: ENST00000433259
  gene symbol: ENTPD6
  hgvsc: ENST00000433259.2:c.190C>T
  hgvsp: ENSP00000401895.2:p.Arg64Trp
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000365840
  ensembl transcript: ENST00000376652
  gene symbol: ENTPD6
  hgvsc: ENST00000376652.4:c.190C>T
  hgvsp: ENSP00000365840.4:p.Arg64Trp
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000347084
  ensembl transcript: ENST00000354989
  gene symbol: ENTPD6
  hgvsc: ENST00000354989.5:c.139C>T
  hgvsp: ENSP00000347084.5:p.Arg47Trp
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000395064
  ensembl transcript: ENST00000417467
  gene symbol: ENTPD6
  hgvsc: ENST00000417467.1:c.136C>T
  hgvsp: ENSP00000395064.1:p.Arg46Trp
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000353131
  ensembl transcript: ENST00000360031
  gene symbol: ENTPD6
  hgvsc: ENST00000360031.2:c.187C>T
  hgvsp: ENSP00000353131.2:p.Arg63Trp
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390646
  ensembl transcript: ENST00000425813
  gene symbol: ENTPD6
  hgvsc: ENST00000425813.1:c.190C>T
  hgvsp: ENSP00000390646.1:p.Arg64Trp
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000398844
  ensembl transcript: ENST00000435520
  gene symbol: ENTPD6
  hgvsc: ENST00000435520.1:c.187C>T
  hgvsp: ENSP00000398844.1:p.Arg63Trp
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390511
  ensembl transcript: ENST00000418890
  gene symbol: ENTPD6
  hgvsc: ENST00000418890.1:c.139C>T
  hgvsp: ENSP00000390511.1:p.Arg47Trp
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390095
  ensembl transcript: ENST00000433417
  gene symbol: ENTPD6
  hgvsc: ENST00000433417.1:c.139-2638C>T
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401573
  ensembl transcript: ENST00000427553
  gene symbol: ENTPD6
  hgvsc: ENST00000427553.1:c.94-2638C>T
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000408098
  ensembl transcript: ENST00000439162
  gene symbol: ENTPD6
  hgvsc: ENST00000439162.1:c.136C>T
  hgvsp: ENSP00000408098.1:p.Arg46Trp
  variant of: http://identifiers.org/hgnc/3368
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15475
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4220
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9623
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9019
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1868
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17420
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg64Trp
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: African
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum

20-25187848-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25187848
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 25187848
    reference: chr 20
allele count: 56
allele frequency: 4.637757975287375e-4
allele num: 120748
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000398844
  ensembl transcript: ENST00000435520
  gene symbol: ENTPD6
  hgvsc: ENST00000435520.1:c.188G>A
  hgvsp: ENSP00000398844.1:p.Arg63Gln
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401895
  ensembl transcript: ENST00000433259
  gene symbol: ENTPD6
  hgvsc: ENST00000433259.2:c.191G>A
  hgvsp: ENSP00000401895.2:p.Arg64Gln
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390511
  ensembl transcript: ENST00000418890
  gene symbol: ENTPD6
  hgvsc: ENST00000418890.1:c.140G>A
  hgvsp: ENSP00000390511.1:p.Arg47Gln
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000395064
  ensembl transcript: ENST00000417467
  gene symbol: ENTPD6
  hgvsc: ENST00000417467.1:c.137G>A
  hgvsp: ENSP00000395064.1:p.Arg46Gln
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401573
  ensembl transcript: ENST00000427553
  gene symbol: ENTPD6
  hgvsc: ENST00000427553.1:c.94-2637G>A
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390095
  ensembl transcript: ENST00000433417
  gene symbol: ENTPD6
  hgvsc: ENST00000433417.1:c.139-2637G>A
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000347084
  ensembl transcript: ENST00000354989
  gene symbol: ENTPD6
  hgvsc: ENST00000354989.5:c.140G>A
  hgvsp: ENSP00000347084.5:p.Arg47Gln
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000365840
  ensembl transcript: ENST00000376652
  gene symbol: ENTPD6
  hgvsc: ENST00000376652.4:c.191G>A
  hgvsp: ENSP00000365840.4:p.Arg64Gln
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390646
  ensembl transcript: ENST00000425813
  gene symbol: ENTPD6
  hgvsc: ENST00000425813.1:c.191G>A
  hgvsp: ENSP00000390646.1:p.Arg64Gln
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000408098
  ensembl transcript: ENST00000439162
  gene symbol: ENTPD6
  hgvsc: ENST00000439162.1:c.137G>A
  hgvsp: ENSP00000408098.1:p.Arg46Gln
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000353131
  ensembl transcript: ENST00000360031
  gene symbol: ENTPD6
  hgvsc: ENST00000360031.2:c.188G>A
  hgvsp: ENSP00000353131.2:p.Arg63Gln
  variant of: http://identifiers.org/hgnc/3368
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17463
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1863
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 15467
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 9608
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4217
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9015
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
hgvs: p.Arg64Gln
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum

20-25187855-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25187855
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 25187855
    reference: chr 20
allele count: 9
allele frequency: 7.455762475975876e-5
allele num: 120712
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000398844
  ensembl transcript: ENST00000435520
  gene symbol: ENTPD6
  hgvsc: ENST00000435520.1:c.195C>T
  hgvsp: ENST00000435520.1:c.195C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000395064
  ensembl transcript: ENST00000417467
  gene symbol: ENTPD6
  hgvsc: ENST00000417467.1:c.144C>T
  hgvsp: ENST00000417467.1:c.144C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390646
  ensembl transcript: ENST00000425813
  gene symbol: ENTPD6
  hgvsc: ENST00000425813.1:c.198C>T
  hgvsp: ENST00000425813.1:c.198C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000365840
  ensembl transcript: ENST00000376652
  gene symbol: ENTPD6
  hgvsc: ENST00000376652.4:c.198C>T
  hgvsp: ENST00000376652.4:c.198C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401573
  ensembl transcript: ENST00000427553
  gene symbol: ENTPD6
  hgvsc: ENST00000427553.1:c.94-2630C>T
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390095
  ensembl transcript: ENST00000433417
  gene symbol: ENTPD6
  hgvsc: ENST00000433417.1:c.139-2630C>T
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401895
  ensembl transcript: ENST00000433259
  gene symbol: ENTPD6
  hgvsc: ENST00000433259.2:c.198C>T
  hgvsp: ENST00000433259.2:c.198C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000353131
  ensembl transcript: ENST00000360031
  gene symbol: ENTPD6
  hgvsc: ENST00000360031.2:c.195C>T
  hgvsp: ENST00000360031.2:c.195C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000347084
  ensembl transcript: ENST00000354989
  gene symbol: ENTPD6
  hgvsc: ENST00000354989.5:c.147C>T
  hgvsp: ENST00000354989.5:c.147C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000408098
  ensembl transcript: ENST00000439162
  gene symbol: ENTPD6
  hgvsc: ENST00000439162.1:c.144C>T
  hgvsp: ENST00000439162.1:c.144C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390511
  ensembl transcript: ENST00000418890
  gene symbol: ENTPD6
  hgvsc: ENST00000418890.1:c.147C>T
  hgvsp: ENST00000418890.1:c.147C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9587
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17439
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1863
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9004
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15468
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4219
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Thr66Thr
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD

20-25187856-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25187856
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 25187856
    reference: chr 20
allele count: 40
allele frequency: 3.314550878355983e-4
allele num: 120680
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000365840
  ensembl transcript: ENST00000376652
  gene symbol: ENTPD6
  hgvsc: ENST00000376652.4:c.199G>A
  hgvsp: ENSP00000365840.4:p.Ala67Thr
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390646
  ensembl transcript: ENST00000425813
  gene symbol: ENTPD6
  hgvsc: ENST00000425813.1:c.199G>A
  hgvsp: ENSP00000390646.1:p.Ala67Thr
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000347084
  ensembl transcript: ENST00000354989
  gene symbol: ENTPD6
  hgvsc: ENST00000354989.5:c.148G>A
  hgvsp: ENSP00000347084.5:p.Ala50Thr
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390511
  ensembl transcript: ENST00000418890
  gene symbol: ENTPD6
  hgvsc: ENST00000418890.1:c.148G>A
  hgvsp: ENSP00000390511.1:p.Ala50Thr
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401573
  ensembl transcript: ENST00000427553
  gene symbol: ENTPD6
  hgvsc: ENST00000427553.1:c.94-2629G>A
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000395064
  ensembl transcript: ENST00000417467
  gene symbol: ENTPD6
  hgvsc: ENST00000417467.1:c.145G>A
  hgvsp: ENSP00000395064.1:p.Ala49Thr
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390095
  ensembl transcript: ENST00000433417
  gene symbol: ENTPD6
  hgvsc: ENST00000433417.1:c.139-2629G>A
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000353131
  ensembl transcript: ENST00000360031
  gene symbol: ENTPD6
  hgvsc: ENST00000360031.2:c.196G>A
  hgvsp: ENSP00000353131.2:p.Ala66Thr
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401895
  ensembl transcript: ENST00000433259
  gene symbol: ENTPD6
  hgvsc: ENST00000433259.2:c.199G>A
  hgvsp: ENSP00000401895.2:p.Ala67Thr
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000408098
  ensembl transcript: ENST00000439162
  gene symbol: ENTPD6
  hgvsc: ENST00000439162.1:c.145G>A
  hgvsp: ENSP00000408098.1:p.Ala49Thr
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000398844
  ensembl transcript: ENST00000435520
  gene symbol: ENTPD6
  hgvsc: ENST00000435520.1:c.196G>A
  hgvsp: ENSP00000398844.1:p.Ala66Thr
  variant of: http://identifiers.org/hgnc/3368
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9003
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1861
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 4216
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15464
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 17413
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9597
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Ala67Thr
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP

20-25187865-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25187865
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 25187865
    reference: chr 20
allele count: 1
allele frequency: 8.287613333112331e-6
allele num: 120662
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000365840
  ensembl transcript: ENST00000376652
  gene symbol: ENTPD6
  hgvsc: ENST00000376652.4:c.208G>A
  hgvsp: ENSP00000365840.4:p.Ala70Thr
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401573
  ensembl transcript: ENST00000427553
  gene symbol: ENTPD6
  hgvsc: ENST00000427553.1:c.94-2620G>A
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390095
  ensembl transcript: ENST00000433417
  gene symbol: ENTPD6
  hgvsc: ENST00000433417.1:c.139-2620G>A
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390646
  ensembl transcript: ENST00000425813
  gene symbol: ENTPD6
  hgvsc: ENST00000425813.1:c.208G>A
  hgvsp: ENSP00000390646.1:p.Ala70Thr
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000395064
  ensembl transcript: ENST00000417467
  gene symbol: ENTPD6
  hgvsc: ENST00000417467.1:c.154G>A
  hgvsp: ENSP00000395064.1:p.Ala52Thr
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000408098
  ensembl transcript: ENST00000439162
  gene symbol: ENTPD6
  hgvsc: ENST00000439162.1:c.154G>A
  hgvsp: ENSP00000408098.1:p.Ala52Thr
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000347084
  ensembl transcript: ENST00000354989
  gene symbol: ENTPD6
  hgvsc: ENST00000354989.5:c.157G>A
  hgvsp: ENSP00000347084.5:p.Ala53Thr
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000398844
  ensembl transcript: ENST00000435520
  gene symbol: ENTPD6
  hgvsc: ENST00000435520.1:c.205G>A
  hgvsp: ENSP00000398844.1:p.Ala69Thr
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401895
  ensembl transcript: ENST00000433259
  gene symbol: ENTPD6
  hgvsc: ENST00000433259.2:c.208G>A
  hgvsp: ENSP00000401895.2:p.Ala70Thr
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390511
  ensembl transcript: ENST00000418890
  gene symbol: ENTPD6
  hgvsc: ENST00000418890.1:c.157G>A
  hgvsp: ENSP00000390511.1:p.Ala53Thr
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000353131
  ensembl transcript: ENST00000360031
  gene symbol: ENTPD6
  hgvsc: ENST00000360031.2:c.205G>A
  hgvsp: ENSP00000353131.2:p.Ala69Thr
  variant of: http://identifiers.org/hgnc/3368
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17392
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 872
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1862
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9591
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15462
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4211
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9007
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala70Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: African
reference allele: G
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/20-25187867-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25187867
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 25187867
    reference: chr 20
allele count: 1
allele frequency: 8.285827919925758e-6
allele num: 120688
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000347084
  ensembl transcript: ENST00000354989
  gene symbol: ENTPD6
  hgvsc: ENST00000354989.5:c.159C>A
  hgvsp: ENST00000354989.5:c.159C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390646
  ensembl transcript: ENST00000425813
  gene symbol: ENTPD6
  hgvsc: ENST00000425813.1:c.210C>A
  hgvsp: ENST00000425813.1:c.210C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000398844
  ensembl transcript: ENST00000435520
  gene symbol: ENTPD6
  hgvsc: ENST00000435520.1:c.207C>A
  hgvsp: ENST00000435520.1:c.207C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401895
  ensembl transcript: ENST00000433259
  gene symbol: ENTPD6
  hgvsc: ENST00000433259.2:c.210C>A
  hgvsp: ENST00000433259.2:c.210C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000353131
  ensembl transcript: ENST00000360031
  gene symbol: ENTPD6
  hgvsc: ENST00000360031.2:c.207C>A
  hgvsp: ENST00000360031.2:c.207C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000365840
  ensembl transcript: ENST00000376652
  gene symbol: ENTPD6
  hgvsc: ENST00000376652.4:c.210C>A
  hgvsp: ENST00000376652.4:c.210C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390511
  ensembl transcript: ENST00000418890
  gene symbol: ENTPD6
  hgvsc: ENST00000418890.1:c.159C>A
  hgvsp: ENST00000418890.1:c.159C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000408098
  ensembl transcript: ENST00000439162
  gene symbol: ENTPD6
  hgvsc: ENST00000439162.1:c.156C>A
  hgvsp: ENST00000439162.1:c.156C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000395064
  ensembl transcript: ENST00000417467
  gene symbol: ENTPD6
  hgvsc: ENST00000417467.1:c.156C>A
  hgvsp: ENST00000417467.1:c.156C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401573
  ensembl transcript: ENST00000427553
  gene symbol: ENTPD6
  hgvsc: ENST00000427553.1:c.94-2618C>A
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390095
  ensembl transcript: ENST00000433417
  gene symbol: ENTPD6
  hgvsc: ENST00000433417.1:c.139-2618C>A
  variant of: http://identifiers.org/hgnc/3368
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 872
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17400
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4212
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9010
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9609
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15464
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala70Ala
num of homozygotes: 0
population: Latino
population: Other
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

20-25187875-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25187875
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 25187875
    reference: chr 20
allele count: 2
allele frequency: 1.658484808279156e-5
allele num: 120592
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000398844
  ensembl transcript: ENST00000435520
  gene symbol: ENTPD6
  hgvsc: ENST00000435520.1:c.215G>A
  hgvsp: ENSP00000398844.1:p.Ser72Asn
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000395064
  ensembl transcript: ENST00000417467
  gene symbol: ENTPD6
  hgvsc: ENST00000417467.1:c.164G>A
  hgvsp: ENSP00000395064.1:p.Ser55Asn
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401895
  ensembl transcript: ENST00000433259
  gene symbol: ENTPD6
  hgvsc: ENST00000433259.2:c.218G>A
  hgvsp: ENSP00000401895.2:p.Ser73Asn
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000347084
  ensembl transcript: ENST00000354989
  gene symbol: ENTPD6
  hgvsc: ENST00000354989.5:c.167G>A
  hgvsp: ENSP00000347084.5:p.Ser56Asn
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000365840
  ensembl transcript: ENST00000376652
  gene symbol: ENTPD6
  hgvsc: ENST00000376652.4:c.218G>A
  hgvsp: ENSP00000365840.4:p.Ser73Asn
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390095
  ensembl transcript: ENST00000433417
  gene symbol: ENTPD6
  hgvsc: ENST00000433417.1:c.139-2610G>A
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000408098
  ensembl transcript: ENST00000439162
  gene symbol: ENTPD6
  hgvsc: ENST00000439162.1:c.164G>A
  hgvsp: ENSP00000408098.1:p.Ser55Asn
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000353131
  ensembl transcript: ENST00000360031
  gene symbol: ENTPD6
  hgvsc: ENST00000360031.2:c.215G>A
  hgvsp: ENSP00000353131.2:p.Ser72Asn
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390646
  ensembl transcript: ENST00000425813
  gene symbol: ENTPD6
  hgvsc: ENST00000425813.1:c.218G>A
  hgvsp: ENSP00000390646.1:p.Ser73Asn
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401573
  ensembl transcript: ENST00000427553
  gene symbol: ENTPD6
  hgvsc: ENST00000427553.1:c.94-2610G>A
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390511
  ensembl transcript: ENST00000418890
  gene symbol: ENTPD6
  hgvsc: ENST00000418890.1:c.167G>A
  hgvsp: ENSP00000390511.1:p.Ser56Asn
  variant of: http://identifiers.org/hgnc/3368
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17334
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9419
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15466
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9007
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4212
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1859
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser73Asn
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

20-25187880-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25187880
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 25187880
    reference: chr 20
allele count: 5
allele frequency: 4.148620168931814e-5
allele num: 120522
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000365840
  ensembl transcript: ENST00000376652
  gene symbol: ENTPD6
  hgvsc: ENST00000376652.4:c.223A>G
  hgvsp: ENSP00000365840.4:p.Thr75Ala
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000347084
  ensembl transcript: ENST00000354989
  gene symbol: ENTPD6
  hgvsc: ENST00000354989.5:c.172A>G
  hgvsp: ENSP00000347084.5:p.Thr58Ala
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000408098
  ensembl transcript: ENST00000439162
  gene symbol: ENTPD6
  hgvsc: ENST00000439162.1:c.169A>G
  hgvsp: ENSP00000408098.1:p.Thr57Ala
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401895
  ensembl transcript: ENST00000433259
  gene symbol: ENTPD6
  hgvsc: ENST00000433259.2:c.223A>G
  hgvsp: ENSP00000401895.2:p.Thr75Ala
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000395064
  ensembl transcript: ENST00000417467
  gene symbol: ENTPD6
  hgvsc: ENST00000417467.1:c.169A>G
  hgvsp: ENSP00000395064.1:p.Thr57Ala
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401573
  ensembl transcript: ENST00000427553
  gene symbol: ENTPD6
  hgvsc: ENST00000427553.1:c.94-2605A>G
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390095
  ensembl transcript: ENST00000433417
  gene symbol: ENTPD6
  hgvsc: ENST00000433417.1:c.139-2605A>G
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000353131
  ensembl transcript: ENST00000360031
  gene symbol: ENTPD6
  hgvsc: ENST00000360031.2:c.220A>G
  hgvsp: ENSP00000353131.2:p.Thr74Ala
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000398844
  ensembl transcript: ENST00000435520
  gene symbol: ENTPD6
  hgvsc: ENST00000435520.1:c.220A>G
  hgvsp: ENSP00000398844.1:p.Thr74Ala
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390511
  ensembl transcript: ENST00000418890
  gene symbol: ENTPD6
  hgvsc: ENST00000418890.1:c.172A>G
  hgvsp: ENSP00000390511.1:p.Thr58Ala
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390646
  ensembl transcript: ENST00000425813
  gene symbol: ENTPD6
  hgvsc: ENST00000425813.1:c.223A>G
  hgvsp: ENSP00000390646.1:p.Thr75Ala
  variant of: http://identifiers.org/hgnc/3368
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9340
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17257
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1858
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9007
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4212
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Thr75Ala
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: A
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQ

http://identifiers.org/exac.variant/20-25187881-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25187881
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 25187881
    reference: chr 20
allele count: 1
allele frequency: 8.302337938363443e-6
allele num: 120448
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401573
  ensembl transcript: ENST00000427553
  gene symbol: ENTPD6
  hgvsc: ENST00000427553.1:c.94-2604C>A
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000347084
  ensembl transcript: ENST00000354989
  gene symbol: ENTPD6
  hgvsc: ENST00000354989.5:c.173C>A
  hgvsp: ENSP00000347084.5:p.Thr58Asn
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390511
  ensembl transcript: ENST00000418890
  gene symbol: ENTPD6
  hgvsc: ENST00000418890.1:c.173C>A
  hgvsp: ENSP00000390511.1:p.Thr58Asn
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000408098
  ensembl transcript: ENST00000439162
  gene symbol: ENTPD6
  hgvsc: ENST00000439162.1:c.170C>A
  hgvsp: ENSP00000408098.1:p.Thr57Asn
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401895
  ensembl transcript: ENST00000433259
  gene symbol: ENTPD6
  hgvsc: ENST00000433259.2:c.224C>A
  hgvsp: ENSP00000401895.2:p.Thr75Asn
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000395064
  ensembl transcript: ENST00000417467
  gene symbol: ENTPD6
  hgvsc: ENST00000417467.1:c.170C>A
  hgvsp: ENSP00000395064.1:p.Thr57Asn
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000365840
  ensembl transcript: ENST00000376652
  gene symbol: ENTPD6
  hgvsc: ENST00000376652.4:c.224C>A
  hgvsp: ENSP00000365840.4:p.Thr75Asn
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390646
  ensembl transcript: ENST00000425813
  gene symbol: ENTPD6
  hgvsc: ENST00000425813.1:c.224C>A
  hgvsp: ENSP00000390646.1:p.Thr75Asn
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000353131
  ensembl transcript: ENST00000360031
  gene symbol: ENTPD6
  hgvsc: ENST00000360031.2:c.221C>A
  hgvsp: ENSP00000353131.2:p.Thr74Asn
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390095
  ensembl transcript: ENST00000433417
  gene symbol: ENTPD6
  hgvsc: ENST00000433417.1:c.139-2604C>A
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000398844
  ensembl transcript: ENST00000435520
  gene symbol: ENTPD6
  hgvsc: ENST00000435520.1:c.221C>A
  hgvsp: ENSP00000398844.1:p.Thr74Asn
  variant of: http://identifiers.org/hgnc/3368
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9261
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9002
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4210
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17208
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15454
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1859
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr75Asn
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum

20-25187886-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25187886
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 25187886
    reference: chr 20
allele count: 1
allele frequency: 8.315593400745077e-6
allele num: 120256
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000347084
  ensembl transcript: ENST00000354989
  gene symbol: ENTPD6
  hgvsc: ENST00000354989.5:c.178G>A
  hgvsp: ENSP00000347084.5:p.Ala60Thr
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000353131
  ensembl transcript: ENST00000360031
  gene symbol: ENTPD6
  hgvsc: ENST00000360031.2:c.226G>A
  hgvsp: ENSP00000353131.2:p.Ala76Thr
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000398844
  ensembl transcript: ENST00000435520
  gene symbol: ENTPD6
  hgvsc: ENST00000435520.1:c.226G>A
  hgvsp: ENSP00000398844.1:p.Ala76Thr
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000395064
  ensembl transcript: ENST00000417467
  gene symbol: ENTPD6
  hgvsc: ENST00000417467.1:c.175G>A
  hgvsp: ENSP00000395064.1:p.Ala59Thr
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401573
  ensembl transcript: ENST00000427553
  gene symbol: ENTPD6
  hgvsc: ENST00000427553.1:c.94-2599G>A
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000365840
  ensembl transcript: ENST00000376652
  gene symbol: ENTPD6
  hgvsc: ENST00000376652.4:c.229G>A
  hgvsp: ENSP00000365840.4:p.Ala77Thr
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390511
  ensembl transcript: ENST00000418890
  gene symbol: ENTPD6
  hgvsc: ENST00000418890.1:c.178G>A
  hgvsp: ENSP00000390511.1:p.Ala60Thr
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401895
  ensembl transcript: ENST00000433259
  gene symbol: ENTPD6
  hgvsc: ENST00000433259.2:c.229G>A
  hgvsp: ENSP00000401895.2:p.Ala77Thr
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390646
  ensembl transcript: ENST00000425813
  gene symbol: ENTPD6
  hgvsc: ENST00000425813.1:c.229G>A
  hgvsp: ENSP00000390646.1:p.Ala77Thr
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390095
  ensembl transcript: ENST00000433417
  gene symbol: ENTPD6
  hgvsc: ENST00000433417.1:c.139-2599G>A
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000408098
  ensembl transcript: ENST00000439162
  gene symbol: ENTPD6
  hgvsc: ENST00000439162.1:c.175G>A
  hgvsp: ENSP00000408098.1:p.Ala59Thr
  variant of: http://identifiers.org/hgnc/3368
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1858
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15417
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8985
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17140
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9261
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4204
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala77Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: South Asian
population: East Asian
population: Latino
reference allele: G
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum

20-25187893-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25187893
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 25187893
    reference: chr 20
allele count: 1
allele frequency: 8.337641114575865e-6
allele num: 119938
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000353131
  ensembl transcript: ENST00000360031
  gene symbol: ENTPD6
  hgvsc: ENST00000360031.2:c.233C>T
  hgvsp: ENSP00000353131.2:p.Pro78Leu
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000347084
  ensembl transcript: ENST00000354989
  gene symbol: ENTPD6
  hgvsc: ENST00000354989.5:c.185C>T
  hgvsp: ENSP00000347084.5:p.Pro62Leu
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390095
  ensembl transcript: ENST00000433417
  gene symbol: ENTPD6
  hgvsc: ENST00000433417.1:c.139-2592C>T
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390511
  ensembl transcript: ENST00000418890
  gene symbol: ENTPD6
  hgvsc: ENST00000418890.1:c.185C>T
  hgvsp: ENSP00000390511.1:p.Pro62Leu
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401573
  ensembl transcript: ENST00000427553
  gene symbol: ENTPD6
  hgvsc: ENST00000427553.1:c.94-2592C>T
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000398844
  ensembl transcript: ENST00000435520
  gene symbol: ENTPD6
  hgvsc: ENST00000435520.1:c.233C>T
  hgvsp: ENSP00000398844.1:p.Pro78Leu
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000365840
  ensembl transcript: ENST00000376652
  gene symbol: ENTPD6
  hgvsc: ENST00000376652.4:c.236C>T
  hgvsp: ENSP00000365840.4:p.Pro79Leu
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000395064
  ensembl transcript: ENST00000417467
  gene symbol: ENTPD6
  hgvsc: ENST00000417467.1:c.182C>T
  hgvsp: ENSP00000395064.1:p.Pro61Leu
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390646
  ensembl transcript: ENST00000425813
  gene symbol: ENTPD6
  hgvsc: ENST00000425813.1:c.236C>T
  hgvsp: ENSP00000390646.1:p.Pro79Leu
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401895
  ensembl transcript: ENST00000433259
  gene symbol: ENTPD6
  hgvsc: ENST00000433259.2:c.236C>T
  hgvsp: ENSP00000401895.2:p.Pro79Leu
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000408098
  ensembl transcript: ENST00000439162
  gene symbol: ENTPD6
  hgvsc: ENST00000439162.1:c.182C>T
  hgvsp: ENSP00000408098.1:p.Pro61Leu
  variant of: http://identifiers.org/hgnc/3368
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1860
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4209
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9194
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15368
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8975
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17120
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro79Leu
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: European (Finnish)
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: DP

20-25187894-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25187894
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 25187894
    reference: chr 20
allele count: 5
allele frequency: 4.166527782407253e-5
allele num: 120004
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401895
  ensembl transcript: ENST00000433259
  gene symbol: ENTPD6
  hgvsc: ENST00000433259.2:c.237G>A
  hgvsp: ENST00000433259.2:c.237G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401573
  ensembl transcript: ENST00000427553
  gene symbol: ENTPD6
  hgvsc: ENST00000427553.1:c.94-2591G>A
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000408098
  ensembl transcript: ENST00000439162
  gene symbol: ENTPD6
  hgvsc: ENST00000439162.1:c.183G>A
  hgvsp: ENST00000439162.1:c.183G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000395064
  ensembl transcript: ENST00000417467
  gene symbol: ENTPD6
  hgvsc: ENST00000417467.1:c.183G>A
  hgvsp: ENST00000417467.1:c.183G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390646
  ensembl transcript: ENST00000425813
  gene symbol: ENTPD6
  hgvsc: ENST00000425813.1:c.237G>A
  hgvsp: ENST00000425813.1:c.237G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000398844
  ensembl transcript: ENST00000435520
  gene symbol: ENTPD6
  hgvsc: ENST00000435520.1:c.234G>A
  hgvsp: ENST00000435520.1:c.234G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000365840
  ensembl transcript: ENST00000376652
  gene symbol: ENTPD6
  hgvsc: ENST00000376652.4:c.237G>A
  hgvsp: ENST00000376652.4:c.237G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390095
  ensembl transcript: ENST00000433417
  gene symbol: ENTPD6
  hgvsc: ENST00000433417.1:c.139-2591G>A
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390511
  ensembl transcript: ENST00000418890
  gene symbol: ENTPD6
  hgvsc: ENST00000418890.1:c.186G>A
  hgvsp: ENST00000418890.1:c.186G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000347084
  ensembl transcript: ENST00000354989
  gene symbol: ENTPD6
  hgvsc: ENST00000354989.5:c.186G>A
  hgvsp: ENST00000354989.5:c.186G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000353131
  ensembl transcript: ENST00000360031
  gene symbol: ENTPD6
  hgvsc: ENST00000360031.2:c.234G>A
  hgvsp: ENST00000360031.2:c.234G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9166
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8982
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 893
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15369
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1862
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17160
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Pro79Pro
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD

20-25187898-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25187898
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 25187898
    reference: chr 20
allele count: 1
allele frequency: 8.334166750008334e-6
allele num: 119988
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000395064
  ensembl transcript: ENST00000417467
  gene symbol: ENTPD6
  hgvsc: ENST00000417467.1:c.187G>A
  hgvsp: ENSP00000395064.1:p.Ala63Thr
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390511
  ensembl transcript: ENST00000418890
  gene symbol: ENTPD6
  hgvsc: ENST00000418890.1:c.190G>A
  hgvsp: ENSP00000390511.1:p.Ala64Thr
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390646
  ensembl transcript: ENST00000425813
  gene symbol: ENTPD6
  hgvsc: ENST00000425813.1:c.241G>A
  hgvsp: ENSP00000390646.1:p.Ala81Thr
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000347084
  ensembl transcript: ENST00000354989
  gene symbol: ENTPD6
  hgvsc: ENST00000354989.5:c.190G>A
  hgvsp: ENSP00000347084.5:p.Ala64Thr
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000353131
  ensembl transcript: ENST00000360031
  gene symbol: ENTPD6
  hgvsc: ENST00000360031.2:c.238G>A
  hgvsp: ENSP00000353131.2:p.Ala80Thr
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000398844
  ensembl transcript: ENST00000435520
  gene symbol: ENTPD6
  hgvsc: ENST00000435520.1:c.238G>A
  hgvsp: ENSP00000398844.1:p.Ala80Thr
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390095
  ensembl transcript: ENST00000433417
  gene symbol: ENTPD6
  hgvsc: ENST00000433417.1:c.139-2587G>A
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401895
  ensembl transcript: ENST00000433259
  gene symbol: ENTPD6
  hgvsc: ENST00000433259.2:c.241G>A
  hgvsp: ENSP00000401895.2:p.Ala81Thr
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000365840
  ensembl transcript: ENST00000376652
  gene symbol: ENTPD6
  hgvsc: ENST00000376652.4:c.241G>A
  hgvsp: ENSP00000365840.4:p.Ala81Thr
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401573
  ensembl transcript: ENST00000427553
  gene symbol: ENTPD6
  hgvsc: ENST00000427553.1:c.94-2587G>A
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000408098
  ensembl transcript: ENST00000439162
  gene symbol: ENTPD6
  hgvsc: ENST00000439162.1:c.187G>A
  hgvsp: ENSP00000408098.1:p.Ala63Thr
  variant of: http://identifiers.org/hgnc/3368
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4194
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8964
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15317
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9141
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17231
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1853
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala81Thr
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

20-25187898-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25187898
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 25187898
    reference: chr 20
allele count: 1
allele frequency: 8.334166750008334e-6
allele num: 119988
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000395064
  ensembl transcript: ENST00000417467
  gene symbol: ENTPD6
  hgvsc: ENST00000417467.1:c.187G>T
  hgvsp: ENSP00000395064.1:p.Ala63Ser
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000408098
  ensembl transcript: ENST00000439162
  gene symbol: ENTPD6
  hgvsc: ENST00000439162.1:c.187G>T
  hgvsp: ENSP00000408098.1:p.Ala63Ser
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401895
  ensembl transcript: ENST00000433259
  gene symbol: ENTPD6
  hgvsc: ENST00000433259.2:c.241G>T
  hgvsp: ENSP00000401895.2:p.Ala81Ser
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000353131
  ensembl transcript: ENST00000360031
  gene symbol: ENTPD6
  hgvsc: ENST00000360031.2:c.238G>T
  hgvsp: ENSP00000353131.2:p.Ala80Ser
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000398844
  ensembl transcript: ENST00000435520
  gene symbol: ENTPD6
  hgvsc: ENST00000435520.1:c.238G>T
  hgvsp: ENSP00000398844.1:p.Ala80Ser
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390646
  ensembl transcript: ENST00000425813
  gene symbol: ENTPD6
  hgvsc: ENST00000425813.1:c.241G>T
  hgvsp: ENSP00000390646.1:p.Ala81Ser
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390511
  ensembl transcript: ENST00000418890
  gene symbol: ENTPD6
  hgvsc: ENST00000418890.1:c.190G>T
  hgvsp: ENSP00000390511.1:p.Ala64Ser
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401573
  ensembl transcript: ENST00000427553
  gene symbol: ENTPD6
  hgvsc: ENST00000427553.1:c.94-2587G>T
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000365840
  ensembl transcript: ENST00000376652
  gene symbol: ENTPD6
  hgvsc: ENST00000376652.4:c.241G>T
  hgvsp: ENSP00000365840.4:p.Ala81Ser
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000347084
  ensembl transcript: ENST00000354989
  gene symbol: ENTPD6
  hgvsc: ENST00000354989.5:c.190G>T
  hgvsp: ENSP00000347084.5:p.Ala64Ser
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390095
  ensembl transcript: ENST00000433417
  gene symbol: ENTPD6
  hgvsc: ENST00000433417.1:c.139-2587G>T
  variant of: http://identifiers.org/hgnc/3368
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8964
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17231
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4194
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15317
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1853
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9141
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala81Ser
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: Latino
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum

20-25187901-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25187901
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 25187901
    reference: chr 20
allele count: 9
allele frequency: 7.504502701620973e-5
allele num: 119928
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390095
  ensembl transcript: ENST00000433417
  gene symbol: ENTPD6
  hgvsc: ENST00000433417.1:c.139-2584C>T
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390511
  ensembl transcript: ENST00000418890
  gene symbol: ENTPD6
  hgvsc: ENST00000418890.1:c.193C>T
  hgvsp: ENSP00000390511.1:p.Arg65Trp
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000398844
  ensembl transcript: ENST00000435520
  gene symbol: ENTPD6
  hgvsc: ENST00000435520.1:c.241C>T
  hgvsp: ENSP00000398844.1:p.Arg81Trp
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401573
  ensembl transcript: ENST00000427553
  gene symbol: ENTPD6
  hgvsc: ENST00000427553.1:c.94-2584C>T
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000395064
  ensembl transcript: ENST00000417467
  gene symbol: ENTPD6
  hgvsc: ENST00000417467.1:c.190C>T
  hgvsp: ENSP00000395064.1:p.Arg64Trp
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000353131
  ensembl transcript: ENST00000360031
  gene symbol: ENTPD6
  hgvsc: ENST00000360031.2:c.241C>T
  hgvsp: ENSP00000353131.2:p.Arg81Trp
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000347084
  ensembl transcript: ENST00000354989
  gene symbol: ENTPD6
  hgvsc: ENST00000354989.5:c.193C>T
  hgvsp: ENSP00000347084.5:p.Arg65Trp
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401895
  ensembl transcript: ENST00000433259
  gene symbol: ENTPD6
  hgvsc: ENST00000433259.2:c.244C>T
  hgvsp: ENSP00000401895.2:p.Arg82Trp
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390646
  ensembl transcript: ENST00000425813
  gene symbol: ENTPD6
  hgvsc: ENST00000425813.1:c.244C>T
  hgvsp: ENSP00000390646.1:p.Arg82Trp
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000408098
  ensembl transcript: ENST00000439162
  gene symbol: ENTPD6
  hgvsc: ENST00000439162.1:c.190C>T
  hgvsp: ENSP00000408098.1:p.Arg64Trp
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000365840
  ensembl transcript: ENST00000376652
  gene symbol: ENTPD6
  hgvsc: ENST00000376652.4:c.244C>T
  hgvsp: ENSP00000365840.4:p.Arg82Trp
  variant of: http://identifiers.org/hgnc/3368
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4197
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17233
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 906
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8965
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15305
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9141
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1854
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Arg82Trp
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum

20-25187902-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25187902
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 25187902
    reference: chr 20
allele count: 77
allele frequency: 6.422661150407047e-4
allele num: 119888
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401895
  ensembl transcript: ENST00000433259
  gene symbol: ENTPD6
  hgvsc: ENST00000433259.2:c.245G>A
  hgvsp: ENSP00000401895.2:p.Arg82Gln
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000395064
  ensembl transcript: ENST00000417467
  gene symbol: ENTPD6
  hgvsc: ENST00000417467.1:c.191G>A
  hgvsp: ENSP00000395064.1:p.Arg64Gln
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000353131
  ensembl transcript: ENST00000360031
  gene symbol: ENTPD6
  hgvsc: ENST00000360031.2:c.242G>A
  hgvsp: ENSP00000353131.2:p.Arg81Gln
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401573
  ensembl transcript: ENST00000427553
  gene symbol: ENTPD6
  hgvsc: ENST00000427553.1:c.94-2583G>A
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390511
  ensembl transcript: ENST00000418890
  gene symbol: ENTPD6
  hgvsc: ENST00000418890.1:c.194G>A
  hgvsp: ENSP00000390511.1:p.Arg65Gln
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000347084
  ensembl transcript: ENST00000354989
  gene symbol: ENTPD6
  hgvsc: ENST00000354989.5:c.194G>A
  hgvsp: ENSP00000347084.5:p.Arg65Gln
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390646
  ensembl transcript: ENST00000425813
  gene symbol: ENTPD6
  hgvsc: ENST00000425813.1:c.245G>A
  hgvsp: ENSP00000390646.1:p.Arg82Gln
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000408098
  ensembl transcript: ENST00000439162
  gene symbol: ENTPD6
  hgvsc: ENST00000439162.1:c.191G>A
  hgvsp: ENSP00000408098.1:p.Arg64Gln
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000398844
  ensembl transcript: ENST00000435520
  gene symbol: ENTPD6
  hgvsc: ENST00000435520.1:c.242G>A
  hgvsp: ENSP00000398844.1:p.Arg81Gln
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390095
  ensembl transcript: ENST00000433417
  gene symbol: ENTPD6
  hgvsc: ENST00000433417.1:c.139-2583G>A
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000365840
  ensembl transcript: ENST00000376652
  gene symbol: ENTPD6
  hgvsc: ENST00000376652.4:c.245G>A
  hgvsp: ENSP00000365840.4:p.Arg82Gln
  variant of: http://identifiers.org/hgnc/3368
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 6.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 9119
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 8962
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4190
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 6.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15314
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1851
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 17292
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 868
  bin: 5.25e1
  variant carriers: 6
genotype quality: GenotypeQuality
hgvs: p.Arg82Gln
num of homozygotes: 1
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum

20-25187918-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25187918
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 25187918
    reference: chr 20
allele count: 1
allele frequency: 8.356592515835743e-6
allele num: 119666
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000353131
  ensembl transcript: ENST00000360031
  gene symbol: ENTPD6
  hgvsc: ENST00000360031.2:c.258C>T
  hgvsp: ENST00000360031.2:c.258C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401895
  ensembl transcript: ENST00000433259
  gene symbol: ENTPD6
  hgvsc: ENST00000433259.2:c.261C>T
  hgvsp: ENST00000433259.2:c.261C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390511
  ensembl transcript: ENST00000418890
  gene symbol: ENTPD6
  hgvsc: ENST00000418890.1:c.210C>T
  hgvsp: ENST00000418890.1:c.210C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401573
  ensembl transcript: ENST00000427553
  gene symbol: ENTPD6
  hgvsc: ENST00000427553.1:c.94-2567C>T
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000347084
  ensembl transcript: ENST00000354989
  gene symbol: ENTPD6
  hgvsc: ENST00000354989.5:c.210C>T
  hgvsp: ENST00000354989.5:c.210C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000395064
  ensembl transcript: ENST00000417467
  gene symbol: ENTPD6
  hgvsc: ENST00000417467.1:c.207C>T
  hgvsp: ENST00000417467.1:c.207C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000365840
  ensembl transcript: ENST00000376652
  gene symbol: ENTPD6
  hgvsc: ENST00000376652.4:c.261C>T
  hgvsp: ENST00000376652.4:c.261C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000408098
  ensembl transcript: ENST00000439162
  gene symbol: ENTPD6
  hgvsc: ENST00000439162.1:c.207C>T
  hgvsp: ENST00000439162.1:c.207C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000398844
  ensembl transcript: ENST00000435520
  gene symbol: ENTPD6
  hgvsc: ENST00000435520.1:c.258C>T
  hgvsp: ENST00000435520.1:c.258C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390646
  ensembl transcript: ENST00000425813
  gene symbol: ENTPD6
  hgvsc: ENST00000425813.1:c.261C>T
  hgvsp: ENST00000425813.1:c.261C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390095
  ensembl transcript: ENST00000433417
  gene symbol: ENTPD6
  hgvsc: ENST00000433417.1:c.139-2567C>T
  variant of: http://identifiers.org/hgnc/3368
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17454
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9196
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4193
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 867
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1847
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15354
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8948
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala87Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

20-25187922-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25187922
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 25187922
    reference: chr 20
allele count: 1
allele frequency: 8.365680631776201e-6
allele num: 119536
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401895
  ensembl transcript: ENST00000433259
  gene symbol: ENTPD6
  hgvsc: ENST00000433259.2:c.265A>G
  hgvsp: ENSP00000401895.2:p.Ser89Gly
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000347084
  ensembl transcript: ENST00000354989
  gene symbol: ENTPD6
  hgvsc: ENST00000354989.5:c.214A>G
  hgvsp: ENSP00000347084.5:p.Ser72Gly
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401573
  ensembl transcript: ENST00000427553
  gene symbol: ENTPD6
  hgvsc: ENST00000427553.1:c.94-2563A>G
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000395064
  ensembl transcript: ENST00000417467
  gene symbol: ENTPD6
  hgvsc: ENST00000417467.1:c.211A>G
  hgvsp: ENSP00000395064.1:p.Ser71Gly
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390646
  ensembl transcript: ENST00000425813
  gene symbol: ENTPD6
  hgvsc: ENST00000425813.1:c.265A>G
  hgvsp: ENSP00000390646.1:p.Ser89Gly
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000353131
  ensembl transcript: ENST00000360031
  gene symbol: ENTPD6
  hgvsc: ENST00000360031.2:c.262A>G
  hgvsp: ENSP00000353131.2:p.Ser88Gly
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000365840
  ensembl transcript: ENST00000376652
  gene symbol: ENTPD6
  hgvsc: ENST00000376652.4:c.265A>G
  hgvsp: ENSP00000365840.4:p.Ser89Gly
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390095
  ensembl transcript: ENST00000433417
  gene symbol: ENTPD6
  hgvsc: ENST00000433417.1:c.139-2563A>G
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390511
  ensembl transcript: ENST00000418890
  gene symbol: ENTPD6
  hgvsc: ENST00000418890.1:c.214A>G
  hgvsp: ENSP00000390511.1:p.Ser72Gly
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000408098
  ensembl transcript: ENST00000439162
  gene symbol: ENTPD6
  hgvsc: ENST00000439162.1:c.211A>G
  hgvsp: ENSP00000408098.1:p.Ser71Gly
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000398844
  ensembl transcript: ENST00000435520
  gene symbol: ENTPD6
  hgvsc: ENST00000435520.1:c.262A>G
  hgvsp: ENSP00000398844.1:p.Ser88Gly
  variant of: http://identifiers.org/hgnc/3368
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1845
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4187
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9141
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 867
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17472
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15345
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser89Gly
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP

20-25187924-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25187924
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 25187924
    reference: chr 20
allele count: 3
allele frequency: 2.51226824325456e-5
allele num: 119414
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000347084
  ensembl transcript: ENST00000354989
  gene symbol: ENTPD6
  hgvsc: ENST00000354989.5:c.216C>T
  hgvsp: ENST00000354989.5:c.216C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390095
  ensembl transcript: ENST00000433417
  gene symbol: ENTPD6
  hgvsc: ENST00000433417.1:c.139-2561C>T
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390646
  ensembl transcript: ENST00000425813
  gene symbol: ENTPD6
  hgvsc: ENST00000425813.1:c.267C>T
  hgvsp: ENST00000425813.1:c.267C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000398844
  ensembl transcript: ENST00000435520
  gene symbol: ENTPD6
  hgvsc: ENST00000435520.1:c.264C>T
  hgvsp: ENST00000435520.1:c.264C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401573
  ensembl transcript: ENST00000427553
  gene symbol: ENTPD6
  hgvsc: ENST00000427553.1:c.94-2561C>T
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000365840
  ensembl transcript: ENST00000376652
  gene symbol: ENTPD6
  hgvsc: ENST00000376652.4:c.267C>T
  hgvsp: ENST00000376652.4:c.267C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401895
  ensembl transcript: ENST00000433259
  gene symbol: ENTPD6
  hgvsc: ENST00000433259.2:c.267C>T
  hgvsp: ENST00000433259.2:c.267C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000395064
  ensembl transcript: ENST00000417467
  gene symbol: ENTPD6
  hgvsc: ENST00000417467.1:c.213C>T
  hgvsp: ENST00000417467.1:c.213C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000353131
  ensembl transcript: ENST00000360031
  gene symbol: ENTPD6
  hgvsc: ENST00000360031.2:c.264C>T
  hgvsp: ENST00000360031.2:c.264C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390511
  ensembl transcript: ENST00000418890
  gene symbol: ENTPD6
  hgvsc: ENST00000418890.1:c.216C>T
  hgvsp: ENST00000418890.1:c.216C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000408098
  ensembl transcript: ENST00000439162
  gene symbol: ENTPD6
  hgvsc: ENST00000439162.1:c.213C>T
  hgvsp: ENST00000439162.1:c.213C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 865
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8961
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1844
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17503
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8994
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15367
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser89Ser
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: QD

20-25187928-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25187928
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 25187928
    reference: chr 20
allele count: 1
allele frequency: 8.397574780403419e-6
allele num: 119082
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401895
  ensembl transcript: ENST00000433259
  gene symbol: ENTPD6
  hgvsc: ENST00000433259.2:c.271C>G
  hgvsp: ENSP00000401895.2:p.Leu91Val
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000353131
  ensembl transcript: ENST00000360031
  gene symbol: ENTPD6
  hgvsc: ENST00000360031.2:c.268C>G
  hgvsp: ENSP00000353131.2:p.Leu90Val
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000365840
  ensembl transcript: ENST00000376652
  gene symbol: ENTPD6
  hgvsc: ENST00000376652.4:c.271C>G
  hgvsp: ENSP00000365840.4:p.Leu91Val
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390095
  ensembl transcript: ENST00000433417
  gene symbol: ENTPD6
  hgvsc: ENST00000433417.1:c.139-2557C>G
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000395064
  ensembl transcript: ENST00000417467
  gene symbol: ENTPD6
  hgvsc: ENST00000417467.1:c.217C>G
  hgvsp: ENSP00000395064.1:p.Leu73Val
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000408098
  ensembl transcript: ENST00000439162
  gene symbol: ENTPD6
  hgvsc: ENST00000439162.1:c.217C>G
  hgvsp: ENSP00000408098.1:p.Leu73Val
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000398844
  ensembl transcript: ENST00000435520
  gene symbol: ENTPD6
  hgvsc: ENST00000435520.1:c.268C>G
  hgvsp: ENSP00000398844.1:p.Leu90Val
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000347084
  ensembl transcript: ENST00000354989
  gene symbol: ENTPD6
  hgvsc: ENST00000354989.5:c.220C>G
  hgvsp: ENSP00000347084.5:p.Leu74Val
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401573
  ensembl transcript: ENST00000427553
  gene symbol: ENTPD6
  hgvsc: ENST00000427553.1:c.94-2557C>G
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390646
  ensembl transcript: ENST00000425813
  gene symbol: ENTPD6
  hgvsc: ENST00000425813.1:c.271C>G
  hgvsp: ENSP00000390646.1:p.Leu91Val
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390511
  ensembl transcript: ENST00000418890
  gene symbol: ENTPD6
  hgvsc: ENST00000418890.1:c.220C>G
  hgvsp: ENSP00000390511.1:p.Leu74Val
  variant of: http://identifiers.org/hgnc/3368
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8739
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17494
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8955
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1844
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15349
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4188
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 865
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu91Val
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum

20-25187932-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25187932
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 25187932
    reference: chr 20
allele count: 5
allele frequency: 4.200198249357369e-5
allele num: 119042
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390095
  ensembl transcript: ENST00000433417
  gene symbol: ENTPD6
  hgvsc: ENST00000433417.1:c.139-2553G>A
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000365840
  ensembl transcript: ENST00000376652
  gene symbol: ENTPD6
  hgvsc: ENST00000376652.4:c.275G>A
  hgvsp: ENSP00000365840.4:p.Gly92Glu
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000408098
  ensembl transcript: ENST00000439162
  gene symbol: ENTPD6
  hgvsc: ENST00000439162.1:c.221G>A
  hgvsp: ENSP00000408098.1:p.Gly74Glu
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000395064
  ensembl transcript: ENST00000417467
  gene symbol: ENTPD6
  hgvsc: ENST00000417467.1:c.221G>A
  hgvsp: ENSP00000395064.1:p.Gly74Glu
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401573
  ensembl transcript: ENST00000427553
  gene symbol: ENTPD6
  hgvsc: ENST00000427553.1:c.94-2553G>A
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401895
  ensembl transcript: ENST00000433259
  gene symbol: ENTPD6
  hgvsc: ENST00000433259.2:c.275G>A
  hgvsp: ENSP00000401895.2:p.Gly92Glu
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000347084
  ensembl transcript: ENST00000354989
  gene symbol: ENTPD6
  hgvsc: ENST00000354989.5:c.224G>A
  hgvsp: ENSP00000347084.5:p.Gly75Glu
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390511
  ensembl transcript: ENST00000418890
  gene symbol: ENTPD6
  hgvsc: ENST00000418890.1:c.224G>A
  hgvsp: ENSP00000390511.1:p.Gly75Glu
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390646
  ensembl transcript: ENST00000425813
  gene symbol: ENTPD6
  hgvsc: ENST00000425813.1:c.275G>A
  hgvsp: ENSP00000390646.1:p.Gly92Glu
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000353131
  ensembl transcript: ENST00000360031
  gene symbol: ENTPD6
  hgvsc: ENST00000360031.2:c.272G>A
  hgvsp: ENSP00000353131.2:p.Gly91Glu
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000398844
  ensembl transcript: ENST00000435520
  gene symbol: ENTPD6
  hgvsc: ENST00000435520.1:c.272G>A
  hgvsp: ENSP00000398844.1:p.Gly91Glu
  variant of: http://identifiers.org/hgnc/3368
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1844
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15366
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8957
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1068
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4185
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8729
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 865
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17526
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly92Glu
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Finnish)
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

20-25187940-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25187940
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 25187940
    reference: chr 20
allele count: 1
allele frequency: 8.468260957929679e-6
allele num: 118088
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390095
  ensembl transcript: ENST00000433417
  gene symbol: ENTPD6
  hgvsc: ENST00000433417.1:c.139-2545G>A
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401573
  ensembl transcript: ENST00000427553
  gene symbol: ENTPD6
  hgvsc: ENST00000427553.1:c.94-2545G>A
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000353131
  ensembl transcript: ENST00000360031
  gene symbol: ENTPD6
  hgvsc: ENST00000360031.2:c.280G>A
  hgvsp: ENSP00000353131.2:p.Ala94Thr
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000395064
  ensembl transcript: ENST00000417467
  gene symbol: ENTPD6
  hgvsc: ENST00000417467.1:c.229G>A
  hgvsp: ENSP00000395064.1:p.Ala77Thr
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390511
  ensembl transcript: ENST00000418890
  gene symbol: ENTPD6
  hgvsc: ENST00000418890.1:c.232G>A
  hgvsp: ENSP00000390511.1:p.Ala78Thr
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000347084
  ensembl transcript: ENST00000354989
  gene symbol: ENTPD6
  hgvsc: ENST00000354989.5:c.232G>A
  hgvsp: ENSP00000347084.5:p.Ala78Thr
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000398844
  ensembl transcript: ENST00000435520
  gene symbol: ENTPD6
  hgvsc: ENST00000435520.1:c.280G>A
  hgvsp: ENSP00000398844.1:p.Ala94Thr
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401895
  ensembl transcript: ENST00000433259
  gene symbol: ENTPD6
  hgvsc: ENST00000433259.2:c.283G>A
  hgvsp: ENSP00000401895.2:p.Ala95Thr
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390646
  ensembl transcript: ENST00000425813
  gene symbol: ENTPD6
  hgvsc: ENST00000425813.1:c.283G>A
  hgvsp: ENSP00000390646.1:p.Ala95Thr
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000365840
  ensembl transcript: ENST00000376652
  gene symbol: ENTPD6
  hgvsc: ENST00000376652.4:c.283G>A
  hgvsp: ENSP00000365840.4:p.Ala95Thr
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000408098
  ensembl transcript: ENST00000439162
  gene symbol: ENTPD6
  hgvsc: ENST00000439162.1:c.229G>A
  hgvsp: ENSP00000408098.1:p.Ala77Thr
  variant of: http://identifiers.org/hgnc/3368
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4186
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1414
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7990
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8953
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1517
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1845
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15344
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala95Thr
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum

20-25187943-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25187943
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 25187943
    reference: chr 20
allele count: 1
allele frequency: 8.495743632440147e-6
allele num: 117706
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390095
  ensembl transcript: ENST00000433417
  gene symbol: ENTPD6
  hgvsc: ENST00000433417.1:c.139-2542G>C
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390646
  ensembl transcript: ENST00000425813
  gene symbol: ENTPD6
  hgvsc: ENST00000425813.1:c.286G>C
  hgvsp: ENSP00000390646.1:p.Asp96His
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401573
  ensembl transcript: ENST00000427553
  gene symbol: ENTPD6
  hgvsc: ENST00000427553.1:c.94-2542G>C
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000395064
  ensembl transcript: ENST00000417467
  gene symbol: ENTPD6
  hgvsc: ENST00000417467.1:c.232G>C
  hgvsp: ENSP00000395064.1:p.Asp78His
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000353131
  ensembl transcript: ENST00000360031
  gene symbol: ENTPD6
  hgvsc: ENST00000360031.2:c.283G>C
  hgvsp: ENSP00000353131.2:p.Asp95His
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000347084
  ensembl transcript: ENST00000354989
  gene symbol: ENTPD6
  hgvsc: ENST00000354989.5:c.235G>C
  hgvsp: ENSP00000347084.5:p.Asp79His
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000398844
  ensembl transcript: ENST00000435520
  gene symbol: ENTPD6
  hgvsc: ENST00000435520.1:c.283G>C
  hgvsp: ENSP00000398844.1:p.Asp95His
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000365840
  ensembl transcript: ENST00000376652
  gene symbol: ENTPD6
  hgvsc: ENST00000376652.4:c.286G>C
  hgvsp: ENSP00000365840.4:p.Asp96His
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390511
  ensembl transcript: ENST00000418890
  gene symbol: ENTPD6
  hgvsc: ENST00000418890.1:c.235G>C
  hgvsp: ENSP00000390511.1:p.Asp79His
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401895
  ensembl transcript: ENST00000433259
  gene symbol: ENTPD6
  hgvsc: ENST00000433259.2:c.286G>C
  hgvsp: ENSP00000401895.2:p.Asp96His
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000408098
  ensembl transcript: ENST00000439162
  gene symbol: ENTPD6
  hgvsc: ENST00000439162.1:c.232G>C
  hgvsp: ENSP00000408098.1:p.Asp78His
  variant of: http://identifiers.org/hgnc/3368
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15338
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1845
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7722
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8957
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4184
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17207
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1590
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp96His
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

20-25187945-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25187945
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 25187945
    reference: chr 20
allele count: 1
allele frequency: 8.50933474021001e-6
allele num: 117518
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000408098
  ensembl transcript: ENST00000439162
  gene symbol: ENTPD6
  hgvsc: ENST00000439162.1:c.234C>T
  hgvsp: ENST00000439162.1:c.234C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000353131
  ensembl transcript: ENST00000360031
  gene symbol: ENTPD6
  hgvsc: ENST00000360031.2:c.285C>T
  hgvsp: ENST00000360031.2:c.285C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000395064
  ensembl transcript: ENST00000417467
  gene symbol: ENTPD6
  hgvsc: ENST00000417467.1:c.234C>T
  hgvsp: ENST00000417467.1:c.234C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401895
  ensembl transcript: ENST00000433259
  gene symbol: ENTPD6
  hgvsc: ENST00000433259.2:c.288C>T
  hgvsp: ENST00000433259.2:c.288C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390511
  ensembl transcript: ENST00000418890
  gene symbol: ENTPD6
  hgvsc: ENST00000418890.1:c.237C>T
  hgvsp: ENST00000418890.1:c.237C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390095
  ensembl transcript: ENST00000433417
  gene symbol: ENTPD6
  hgvsc: ENST00000433417.1:c.139-2540C>T
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000347084
  ensembl transcript: ENST00000354989
  gene symbol: ENTPD6
  hgvsc: ENST00000354989.5:c.237C>T
  hgvsp: ENST00000354989.5:c.237C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000365840
  ensembl transcript: ENST00000376652
  gene symbol: ENTPD6
  hgvsc: ENST00000376652.4:c.288C>T
  hgvsp: ENST00000376652.4:c.288C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401573
  ensembl transcript: ENST00000427553
  gene symbol: ENTPD6
  hgvsc: ENST00000427553.1:c.94-2540C>T
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000398844
  ensembl transcript: ENST00000435520
  gene symbol: ENTPD6
  hgvsc: ENST00000435520.1:c.285C>T
  hgvsp: ENST00000435520.1:c.285C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390646
  ensembl transcript: ENST00000425813
  gene symbol: ENTPD6
  hgvsc: ENST00000425813.1:c.288C>T
  hgvsp: ENST00000425813.1:c.288C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15367
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1845
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17187
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8955
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1632
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1738
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4184
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp96Asp
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum

20-25187952-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25187952
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 25187952
    reference: chr 20
allele count: 9
allele frequency: 7.70152319014205e-5
allele num: 116860
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000353131
  ensembl transcript: ENST00000360031
  gene symbol: ENTPD6
  hgvsc: ENST00000360031.2:c.292G>A
  hgvsp: ENSP00000353131.2:p.Glu98Lys
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401895
  ensembl transcript: ENST00000433259
  gene symbol: ENTPD6
  hgvsc: ENST00000433259.2:c.295G>A
  hgvsp: ENSP00000401895.2:p.Glu99Lys
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401573
  ensembl transcript: ENST00000427553
  gene symbol: ENTPD6
  hgvsc: ENST00000427553.1:c.94-2533G>A
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000398844
  ensembl transcript: ENST00000435520
  gene symbol: ENTPD6
  hgvsc: ENST00000435520.1:c.292G>A
  hgvsp: ENSP00000398844.1:p.Glu98Lys
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000347084
  ensembl transcript: ENST00000354989
  gene symbol: ENTPD6
  hgvsc: ENST00000354989.5:c.244G>A
  hgvsp: ENSP00000347084.5:p.Glu82Lys
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000408098
  ensembl transcript: ENST00000439162
  gene symbol: ENTPD6
  hgvsc: ENST00000439162.1:c.241G>A
  hgvsp: ENSP00000408098.1:p.Glu81Lys
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000395064
  ensembl transcript: ENST00000417467
  gene symbol: ENTPD6
  hgvsc: ENST00000417467.1:c.241G>A
  hgvsp: ENSP00000395064.1:p.Glu81Lys
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390511
  ensembl transcript: ENST00000418890
  gene symbol: ENTPD6
  hgvsc: ENST00000418890.1:c.244G>A
  hgvsp: ENSP00000390511.1:p.Glu82Lys
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000365840
  ensembl transcript: ENST00000376652
  gene symbol: ENTPD6
  hgvsc: ENST00000376652.4:c.295G>A
  hgvsp: ENSP00000365840.4:p.Glu99Lys
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390646
  ensembl transcript: ENST00000425813
  gene symbol: ENTPD6
  hgvsc: ENST00000425813.1:c.295G>A
  hgvsp: ENSP00000390646.1:p.Glu99Lys
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390095
  ensembl transcript: ENST00000433417
  gene symbol: ENTPD6
  hgvsc: ENST00000433417.1:c.139-2533G>A
  variant of: http://identifiers.org/hgnc/3368
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1844
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8952
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4180
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2054
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17017
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7195
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1972
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15309
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu99Lys
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff

20-25187956-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25187956
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 25187956
    reference: chr 20
allele count: 1
allele frequency: 8.5966782435267e-6
allele num: 116324
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390095
  ensembl transcript: ENST00000433417
  gene symbol: ENTPD6
  hgvsc: ENST00000433417.1:c.139-2529T>A
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000347084
  ensembl transcript: ENST00000354989
  gene symbol: ENTPD6
  hgvsc: ENST00000354989.5:c.248T>A
  hgvsp: ENSP00000347084.5:p.Val83Asp
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000365840
  ensembl transcript: ENST00000376652
  gene symbol: ENTPD6
  hgvsc: ENST00000376652.4:c.299T>A
  hgvsp: ENSP00000365840.4:p.Val100Asp
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000398844
  ensembl transcript: ENST00000435520
  gene symbol: ENTPD6
  hgvsc: ENST00000435520.1:c.296T>A
  hgvsp: ENSP00000398844.1:p.Val99Asp
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390511
  ensembl transcript: ENST00000418890
  gene symbol: ENTPD6
  hgvsc: ENST00000418890.1:c.248T>A
  hgvsp: ENSP00000390511.1:p.Val83Asp
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000353131
  ensembl transcript: ENST00000360031
  gene symbol: ENTPD6
  hgvsc: ENST00000360031.2:c.296T>A
  hgvsp: ENSP00000353131.2:p.Val99Asp
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401895
  ensembl transcript: ENST00000433259
  gene symbol: ENTPD6
  hgvsc: ENST00000433259.2:c.299T>A
  hgvsp: ENSP00000401895.2:p.Val100Asp
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000395064
  ensembl transcript: ENST00000417467
  gene symbol: ENTPD6
  hgvsc: ENST00000417467.1:c.245T>A
  hgvsp: ENSP00000395064.1:p.Val82Asp
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390646
  ensembl transcript: ENST00000425813
  gene symbol: ENTPD6
  hgvsc: ENST00000425813.1:c.299T>A
  hgvsp: ENSP00000390646.1:p.Val100Asp
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000408098
  ensembl transcript: ENST00000439162
  gene symbol: ENTPD6
  hgvsc: ENST00000439162.1:c.245T>A
  hgvsp: ENSP00000408098.1:p.Val82Asp
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401573
  ensembl transcript: ENST00000427553
  gene symbol: ENTPD6
  hgvsc: ENST00000427553.1:c.94-2529T>A
  variant of: http://identifiers.org/hgnc/3368
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16841
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8951
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2226
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2248
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1844
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15309
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6835
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4181
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val100Asp
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
reference allele: T
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: QD

20-25187959-T-TC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25187959
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 25187960
    reference: chr 20
allele count: 1
allele frequency: 8.622324923692425e-6
allele num: 115978
alternate allele: TC
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390646
  ensembl transcript: ENST00000425813
  gene symbol: ENTPD6
  hgvsc: ENST00000425813.1:c.303dupC
  hgvsp: ENSP00000390646.1:p.Tyr102LeufsTer6
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000353131
  ensembl transcript: ENST00000360031
  gene symbol: ENTPD6
  hgvsc: ENST00000360031.2:c.300dupC
  hgvsp: ENSP00000353131.2:p.Tyr101LeufsTer6
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401895
  ensembl transcript: ENST00000433259
  gene symbol: ENTPD6
  hgvsc: ENST00000433259.2:c.303dupC
  hgvsp: ENSP00000401895.2:p.Tyr102LeufsTer6
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390095
  ensembl transcript: ENST00000433417
  gene symbol: ENTPD6
  hgvsc: ENST00000433417.1:c.139-2525dupC
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000398844
  ensembl transcript: ENST00000435520
  gene symbol: ENTPD6
  hgvsc: ENST00000435520.1:c.300dupC
  hgvsp: ENSP00000398844.1:p.Tyr101LeufsTer6
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000395064
  ensembl transcript: ENST00000417467
  gene symbol: ENTPD6
  hgvsc: ENST00000417467.1:c.249dupC
  hgvsp: ENSP00000395064.1:p.Tyr84LeufsTer6
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401573
  ensembl transcript: ENST00000427553
  gene symbol: ENTPD6
  hgvsc: ENST00000427553.1:c.94-2525dupC
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000365840
  ensembl transcript: ENST00000376652
  gene symbol: ENTPD6
  hgvsc: ENST00000376652.4:c.303dupC
  hgvsp: ENSP00000365840.4:p.Tyr102LeufsTer6
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000347084
  ensembl transcript: ENST00000354989
  gene symbol: ENTPD6
  hgvsc: ENST00000354989.5:c.252dupC
  hgvsp: ENSP00000347084.5:p.Tyr85LeufsTer6
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000408098
  ensembl transcript: ENST00000439162
  gene symbol: ENTPD6
  hgvsc: ENST00000439162.1:c.249dupC
  hgvsp: ENSP00000408098.1:p.Tyr84LeufsTer6
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390511
  ensembl transcript: ENST00000418890
  gene symbol: ENTPD6
  hgvsc: ENST00000418890.1:c.252dupC
  hgvsp: ENSP00000390511.1:p.Tyr85LeufsTer6
  variant of: http://identifiers.org/hgnc/3368
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2328
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16759
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1843
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2347
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4181
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15309
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6697
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Tyr102LeufsTer6
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS

20-25187962-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25187962
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 25187962
    reference: chr 20
allele count: 1
allele frequency: 8.637965586345104e-6
allele num: 115768
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390511
  ensembl transcript: ENST00000418890
  gene symbol: ENTPD6
  hgvsc: ENST00000418890.1:c.254A>G
  hgvsp: ENSP00000390511.1:p.Tyr85Cys
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000398844
  ensembl transcript: ENST00000435520
  gene symbol: ENTPD6
  hgvsc: ENST00000435520.1:c.302A>G
  hgvsp: ENSP00000398844.1:p.Tyr101Cys
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000408098
  ensembl transcript: ENST00000439162
  gene symbol: ENTPD6
  hgvsc: ENST00000439162.1:c.251A>G
  hgvsp: ENSP00000408098.1:p.Tyr84Cys
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000365840
  ensembl transcript: ENST00000376652
  gene symbol: ENTPD6
  hgvsc: ENST00000376652.4:c.305A>G
  hgvsp: ENSP00000365840.4:p.Tyr102Cys
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390646
  ensembl transcript: ENST00000425813
  gene symbol: ENTPD6
  hgvsc: ENST00000425813.1:c.305A>G
  hgvsp: ENSP00000390646.1:p.Tyr102Cys
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000353131
  ensembl transcript: ENST00000360031
  gene symbol: ENTPD6
  hgvsc: ENST00000360031.2:c.302A>G
  hgvsp: ENSP00000353131.2:p.Tyr101Cys
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000347084
  ensembl transcript: ENST00000354989
  gene symbol: ENTPD6
  hgvsc: ENST00000354989.5:c.254A>G
  hgvsp: ENSP00000347084.5:p.Tyr85Cys
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401895
  ensembl transcript: ENST00000433259
  gene symbol: ENTPD6
  hgvsc: ENST00000433259.2:c.305A>G
  hgvsp: ENSP00000401895.2:p.Tyr102Cys
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401573
  ensembl transcript: ENST00000427553
  gene symbol: ENTPD6
  hgvsc: ENST00000427553.1:c.94-2523A>G
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000395064
  ensembl transcript: ENST00000417467
  gene symbol: ENTPD6
  hgvsc: ENST00000417467.1:c.251A>G
  hgvsp: ENSP00000395064.1:p.Tyr84Cys
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390095
  ensembl transcript: ENST00000433417
  gene symbol: ENTPD6
  hgvsc: ENST00000433417.1:c.139-2523A>G
  variant of: http://identifiers.org/hgnc/3368
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4181
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2351
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15309
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8954
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2391
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1843
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6659
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16738
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr102Cys
num of homozygotes: 0
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: A
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ReadPosRankSum

20-25187963-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25187963
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 25187963
    reference: chr 20
allele count: 3
allele frequency: 2.5966382190524e-5
allele num: 115534
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000365840
  ensembl transcript: ENST00000376652
  gene symbol: ENTPD6
  hgvsc: ENST00000376652.4:c.306C>T
  hgvsp: ENST00000376652.4:c.306C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401573
  ensembl transcript: ENST00000427553
  gene symbol: ENTPD6
  hgvsc: ENST00000427553.1:c.94-2522C>T
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390511
  ensembl transcript: ENST00000418890
  gene symbol: ENTPD6
  hgvsc: ENST00000418890.1:c.255C>T
  hgvsp: ENST00000418890.1:c.255C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000398844
  ensembl transcript: ENST00000435520
  gene symbol: ENTPD6
  hgvsc: ENST00000435520.1:c.303C>T
  hgvsp: ENST00000435520.1:c.303C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000408098
  ensembl transcript: ENST00000439162
  gene symbol: ENTPD6
  hgvsc: ENST00000439162.1:c.252C>T
  hgvsp: ENST00000439162.1:c.252C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000353131
  ensembl transcript: ENST00000360031
  gene symbol: ENTPD6
  hgvsc: ENST00000360031.2:c.303C>T
  hgvsp: ENST00000360031.2:c.303C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000395064
  ensembl transcript: ENST00000417467
  gene symbol: ENTPD6
  hgvsc: ENST00000417467.1:c.252C>T
  hgvsp: ENST00000417467.1:c.252C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390646
  ensembl transcript: ENST00000425813
  gene symbol: ENTPD6
  hgvsc: ENST00000425813.1:c.306C>T
  hgvsp: ENST00000425813.1:c.306C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000347084
  ensembl transcript: ENST00000354989
  gene symbol: ENTPD6
  hgvsc: ENST00000354989.5:c.255C>T
  hgvsp: ENST00000354989.5:c.255C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390095
  ensembl transcript: ENST00000433417
  gene symbol: ENTPD6
  hgvsc: ENST00000433417.1:c.139-2522C>T
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401895
  ensembl transcript: ENST00000433259
  gene symbol: ENTPD6
  hgvsc: ENST00000433259.2:c.306C>T
  hgvsp: ENST00000433259.2:c.306C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3368
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16719
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4179
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2412
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1843
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2356
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15309
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6637
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8955
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Tyr102Tyr
num of homozygotes: 0
population: Other
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

20-25187964-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25187964
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 25187964
    reference: chr 20
allele count: 6
allele frequency: 5.1932764381048e-5
allele num: 115534
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000398844
  ensembl transcript: ENST00000435520
  gene symbol: ENTPD6
  hgvsc: ENST00000435520.1:c.304G>A
  hgvsp: ENSP00000398844.1:p.Gly102Arg
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000353131
  ensembl transcript: ENST00000360031
  gene symbol: ENTPD6
  hgvsc: ENST00000360031.2:c.304G>A
  hgvsp: ENSP00000353131.2:p.Gly102Arg
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000347084
  ensembl transcript: ENST00000354989
  gene symbol: ENTPD6
  hgvsc: ENST00000354989.5:c.256G>A
  hgvsp: ENSP00000347084.5:p.Gly86Arg
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000365840
  ensembl transcript: ENST00000376652
  gene symbol: ENTPD6
  hgvsc: ENST00000376652.4:c.307G>A
  hgvsp: ENSP00000365840.4:p.Gly103Arg
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000395064
  ensembl transcript: ENST00000417467
  gene symbol: ENTPD6
  hgvsc: ENST00000417467.1:c.253G>A
  hgvsp: ENSP00000395064.1:p.Gly85Arg
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000408098
  ensembl transcript: ENST00000439162
  gene symbol: ENTPD6
  hgvsc: ENST00000439162.1:c.253G>A
  hgvsp: ENSP00000408098.1:p.Gly85Arg
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401895
  ensembl transcript: ENST00000433259
  gene symbol: ENTPD6
  hgvsc: ENST00000433259.2:c.307G>A
  hgvsp: ENSP00000401895.2:p.Gly103Arg
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390646
  ensembl transcript: ENST00000425813
  gene symbol: ENTPD6
  hgvsc: ENST00000425813.1:c.307G>A
  hgvsp: ENSP00000390646.1:p.Gly103Arg
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390095
  ensembl transcript: ENST00000433417
  gene symbol: ENTPD6
  hgvsc: ENST00000433417.1:c.139-2521G>A
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000390511
  ensembl transcript: ENST00000418890
  gene symbol: ENTPD6
  hgvsc: ENST00000418890.1:c.256G>A
  hgvsp: ENSP00000390511.1:p.Gly86Arg
  variant of: http://identifiers.org/hgnc/3368
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197586
  ensembl protein: ENSP00000401573
  ensembl transcript: ENST00000427553
  gene symbol: ENTPD6
  hgvsc: ENST00000427553.1:c.94-2521G>A
  variant of: http://identifiers.org/hgnc/3368
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4188
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16699
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2455
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2368
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15298
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6636
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1842
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly103Arg
num of homozygotes: 0
reference allele: G

GenotypeQuality
all individuals: 8867
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2470
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 759
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4837
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 705
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 255
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3115
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1304
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3481
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 205
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 380
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 26340
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5227
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1603
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 5.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9228
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62512
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.752541184717841e-4
allele num: 11412
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 790
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8472
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11024
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.541e0

MQRankSum
type: SiteQuality
SIO_000300: 1.31e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.65e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.95e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

DP
type: SiteQuality
SIO_000300: 1.805147e6

FS
type: SiteQuality
SIO_000300: 4.046e0

QD
type: SiteQuality
SIO_000300: 1.177e1

VQSLOD
type: SiteQuality
SIO_000300: 1.01e-1

GenotypeQuality
all individuals: 68
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 208
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4840
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 598
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 746
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2470
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 178
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 700
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 371
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1305
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5228
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 3485
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26503
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3117
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8877
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1602
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.796622349982034e-4
allele num: 11132
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 794
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8482
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11418
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62564
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.096e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.217e0

DP
type: SiteQuality
SIO_000300: 1.806766e6

VQSLOD
type: SiteQuality
SIO_000300: -2.877e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 1.9659e1

MQ
type: SiteQuality
SIO_000300: 5.939e1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.58e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.12e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.14e0

GenotypeQuality
all individuals: 156
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4739
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3488
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8898
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 398
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 236
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1603
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 717
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 535
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3119
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5228
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1308
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2471
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26557
bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11424
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8496
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 790
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11370
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9252
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.59454029403323e-5
allele num: 62714
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.287e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.80923e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.57e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.362e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.91e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

MQ
type: SiteQuality
SIO_000300: 5.623e1

QD
type: SiteQuality
SIO_000300: 1.239e1

MQRankSum
type: SiteQuality
SIO_000300: 2.15e0

GenotypeQuality
all individuals: 4714
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26633
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 206
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 715
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8898
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5335
bin: 9.75e1
variant carriers: 13

GenotypeQuality
all individuals: 69
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 491
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1591
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 747
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 398
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3112
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3491
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1295
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 9
allele frequency: 1.433714595214579e-4
allele num: 62774
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9274
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11426
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8502
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 3.484320557491289e-4
allele num: 11480
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.46e-1

DP
type: SiteQuality
SIO_000300: 1.81988e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.12e-1

QD
type: SiteQuality
SIO_000300: 1.365e1

MQ
type: SiteQuality
SIO_000300: 5.973e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.98e-1

FS
type: SiteQuality
SIO_000300: 4.637e0

VQSLOD
type: SiteQuality
SIO_000300: 1.92e0

MQRankSum
type: SiteQuality
SIO_000300: 3.04e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.22e-2

GenotypeQuality
all individuals: 4714
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 715
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 491
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 398
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8898
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1591
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2456
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 747
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 206
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3491
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26633
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1295
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5335
bin: 9.75e1
variant carriers: 12

GenotypeQuality
all individuals: 157
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3112
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.352387673488591e-4
allele num: 8502
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11426
num of homozygotes: 0

African
type: Population
allele count: 8
allele frequency: 8.626266982963123e-4
allele num: 9274
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11480
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.186032433810176e-5
allele num: 62774
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.46e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.04e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.12e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.98e-1

DP
type: SiteQuality
SIO_000300: 1.81988e6

FS
type: SiteQuality
SIO_000300: 4.637e0

QD
type: SiteQuality
SIO_000300: 1.365e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.22e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.92e0

MQ
type: SiteQuality
SIO_000300: 5.973e1

GenotypeQuality
all individuals: 157
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 715
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 398
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 5.25e1
variant carriers: 2

GenotypeQuality
all individuals: 747
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3491
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8898
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5335
bin: 9.75e1
variant carriers: 271

GenotypeQuality
all individuals: 2456
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4714
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 491
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1591
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1295
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26633
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 206
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 4.25e1
variant carriers: 0

Other
type: Population
allele count: 2
allele frequency: 2.5e-3
allele num: 800
num of homozygotes: 0

African
type: Population
allele count: 11
allele frequency: 1.186111710157429e-3
allele num: 9274
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 3
allele frequency: 4.544077552256892e-4
allele num: 6602
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 193
allele frequency: 3.07452129862682e-3
allele num: 62774
num of homozygotes: 0

East Asian
type: Population
allele count: 28
allele frequency: 3.293342742884027e-3
allele num: 8502
num of homozygotes: 0

Latino
type: Population
allele count: 15
allele frequency: 1.312795378960266e-3
allele num: 11426
num of homozygotes: 0

South Asian
type: Population
allele count: 18
allele frequency: 1.56794425087108e-3
allele num: 11480
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.46e-1

MQ
type: SiteQuality
SIO_000300: 5.973e1

DP
type: SiteQuality
SIO_000300: 1.81988e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.12e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.22e-2

QD
type: SiteQuality
SIO_000300: 1.365e1

VQSLOD
type: SiteQuality
SIO_000300: 1.92e0

FS
type: SiteQuality
SIO_000300: 4.637e0

MQRankSum
type: SiteQuality
SIO_000300: 3.04e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.98e-1

GenotypeQuality
all individuals: 731
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2472
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8948
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1305
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 389
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 730
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1599
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3509
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3120
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4669
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 472
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5072
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 91
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26833
bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 802
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.183800821420612e-5
allele num: 62818
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11604
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11428
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.45e-1

DP
type: SiteQuality
SIO_000300: 1.809095e6

VQSLOD
type: SiteQuality
SIO_000300: 8.39e-1

FS
type: SiteQuality
SIO_000300: 9.238e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.21e1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.26e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.3e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 3.69e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.3e-2

GenotypeQuality
all individuals: 1305
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 472
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4669
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5072
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 55
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3509
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1599
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 210
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 731
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26833
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3120
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 730
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2472
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8948
bin: 6.75e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11428
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62818
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 802
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.617718028266115e-5
allele num: 11604
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 8.39e-1

QD
type: SiteQuality
SIO_000300: 1.21e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -1.45e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.3e-2

FS
type: SiteQuality
SIO_000300: 9.238e0

DP
type: SiteQuality
SIO_000300: 1.809095e6

ClippingRankSum
type: SiteQuality
SIO_000300: 3.69e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.26e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.3e-3

GenotypeQuality
all individuals: 193
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1304
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 731
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3511
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 448
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3124
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 725
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8953
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2472
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26909
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 393
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5075
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 1599
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11750
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11432
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9286
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8506
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.113479464257309e-4
allele num: 62866
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.37e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.32e-1

QD
type: SiteQuality
SIO_000300: 1.369e1

MQ
type: SiteQuality
SIO_000300: 5.951e1

FS
type: SiteQuality
SIO_000300: 1.268e0

VQSLOD
type: SiteQuality
SIO_000300: 3.9e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.21e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

DP
type: SiteQuality
SIO_000300: 1.810271e6

MQRankSum
type: SiteQuality
SIO_000300: 2.54e-1

GenotypeQuality
all individuals: 163
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 725
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5075
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 42
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26909
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8953
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 448
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 193
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 731
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3124
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 393
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2472
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4655
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1304
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3511
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1599
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11432
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8506
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11750
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9286
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.590684948939013e-5
allele num: 62866
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.32e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.54e-1

QD
type: SiteQuality
SIO_000300: 1.369e1

DP
type: SiteQuality
SIO_000300: 1.810271e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

VQSLOD
type: SiteQuality
SIO_000300: 3.9e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.37e0

FS
type: SiteQuality
SIO_000300: 1.268e0

MQ
type: SiteQuality
SIO_000300: 5.951e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.21e-1

GenotypeQuality
all individuals: 152
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8963
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 233
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5063
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3124
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3514
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4458
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 385
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 197
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 408
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 698
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2471
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1595
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26951
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 715
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1302
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9308
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11444
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8514
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.588915723910004e-5
allele num: 62936
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11988
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 804
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.12e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.83e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.2e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.13e0

DP
type: SiteQuality
SIO_000300: 1.814351e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -1.17e0

VQSLOD
type: SiteQuality
SIO_000300: -3.174e-1

QD
type: SiteQuality
SIO_000300: 1.356e1

GenotypeDepth
all individuals: 27
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 15464
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 585
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 207
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 371
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1594
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9052
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1303
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 571
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3735
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3530
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2478
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5066
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 3145
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28289
bin: 6.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11482
num of homozygotes: 0

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

African
type: Population
allele count: 2
allele frequency: 2.109259649862898e-4
allele num: 9482
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 3.012048192771085e-4
allele num: 13280
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63672
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 1.35e0

DP
type: SiteQuality
SIO_000300: 1.836001e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.9e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.66e-1

FS
type: SiteQuality
SIO_000300: 8.96e-1

QD
type: SiteQuality
SIO_000300: 1.144e1

VQSLOD
type: SiteQuality
SIO_000300: 8.67e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.44e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 29
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 467
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28555
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 353
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 554
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3535
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3624
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 534
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1593
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3148
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9072
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1302
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2485
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 193
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5065
bin: 9.75e1
variant carriers: 6

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11482
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8560
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.513317191283293e-4
allele num: 6608
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9518
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.410701052319549e-5
allele num: 13494
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.273722513253239e-5
allele num: 63758
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 832
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.768e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.38e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.3e-1

MQ
type: SiteQuality
SIO_000300: 5.917e1

DP
type: SiteQuality
SIO_000300: 1.839683e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 4.1e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.49e0

MQRankSum
type: SiteQuality
SIO_000300: 3.97e-1

QD
type: SiteQuality
SIO_000300: 1.072e1

GenotypeDepth
all individuals: 276
bin: 6.25e1
variant carriers: 2

GenotypeQuality
all individuals: 145
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2902
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3155
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1592
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1302
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 29487
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2494
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 420
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 304
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 430
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5085
bin: 9.75e1
variant carriers: 51

GenotypeQuality
all individuals: 3542
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9158
bin: 6.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.513317191283293e-4
allele num: 6608
num of homozygotes: 0

Latino
type: Population
allele count: 8
allele frequency: 6.957731779439903e-4
allele num: 11498
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 24
allele frequency: 3.734478573429185e-4
allele num: 64266
num of homozygotes: 0

South Asian
type: Population
allele count: 12
allele frequency: 8.339124391938846e-4
allele num: 14390
num of homozygotes: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 852
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.16767865483419e-4
allele num: 8564
num of homozygotes: 0

African
type: Population
allele count: 5
allele frequency: 5.170630816959669e-4
allele num: 9670
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.08e-1

MQ
type: SiteQuality
SIO_000300: 5.963e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.91e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.377e0

FS
type: SiteQuality
SIO_000300: 1.117e0

VQSLOD
type: SiteQuality
SIO_000300: 4.13e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.7e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-2

QD
type: SiteQuality
SIO_000300: 1.175e1

DP
type: SiteQuality
SIO_000300: 1.857906e6

GenotypeDepth
all individuals: 116
bin: 9.25e1
variant carriers: 112

GenotypeQuality
all individuals: 54
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3510
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3137
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 22
bin: 2.5e0
variant carriers: 1

GenotypeQuality
all individuals: 5529
bin: 9.75e1
variant carriers: 1529

GenotypeQuality
all individuals: 59
bin: 5.75e1
variant carriers: 2

GenotypeQuality
all individuals: 100
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 117
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2693
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 35
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1533
bin: 9.25e1
variant carriers: 3

GenotypeQuality
all individuals: 381
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 153
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2431
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 375
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 29806
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1251
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 9161
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 20
allele frequency: 2.058884084826024e-3
allele num: 9714
num of homozygotes: 0

South Asian
type: Population
allele count: 58
allele frequency: 3.969883641341547e-3
allele num: 14610
num of homozygotes: 0

Latino
type: Population
allele count: 81
allele frequency: 7.041029207232267e-3
allele num: 11504
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 142
allele frequency: 2.148910411622276e-2
allele num: 6608
num of homozygotes: 1

Other
type: Population
allele count: 17
allele frequency: 1.976744186046512e-2
allele num: 860
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1234
allele frequency: 1.914900220353186e-2
allele num: 64442
num of homozygotes: 15

East Asian
type: Population
allele count: 1
allele frequency: 1.167133520074697e-4
allele num: 8568
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.55e-1

DP
type: SiteQuality
SIO_000300: 1.929092e6

QD
type: SiteQuality
SIO_000300: 1.265e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.9e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.35e0

VQSLOD
type: SiteQuality
SIO_000300: 6.15e0

MQ
type: SiteQuality
SIO_000300: 5.955e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.09e-1

GenotypeDepth
all individuals: 124
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 375
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29806
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 269
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 59
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 381
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9161
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3510
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2693
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3137
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2431
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5529
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1251
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1533
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 1.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8568
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14610
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.551782998665467e-5
allele num: 64442
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 860
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11504
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9714
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 6.15e0

MQ
type: SiteQuality
SIO_000300: 5.955e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.09e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.55e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.35e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.5e-3

QD
type: SiteQuality
SIO_000300: 1.265e1

MQRankSum
type: SiteQuality
SIO_000300: 1.9e-1

DP
type: SiteQuality
SIO_000300: 1.929092e6

GenotypeDepth
all individuals: 22
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2507
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30888
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9459
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1567
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1273
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 339
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3638
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2478
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 338
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 250
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4104
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 43
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3228
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 4.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64608
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 862
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11516
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.047502047502048e-4
allele num: 9768
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14874
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.675e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

MQRankSum
type: SiteQuality
SIO_000300: -1.5e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.97e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.85e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.61e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.57e0

DP
type: SiteQuality
SIO_000300: 1.845673e6

QD
type: SiteQuality
SIO_000300: 1.403e1

GenotypeDepth
all individuals: 16226
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3228
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 339
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1273
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4104
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 115
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 338
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9459
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 250
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2507
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 43
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1567
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3638
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2478
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30888
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.166588894073728e-4
allele num: 8572
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9768
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64608
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 862
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11516
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14874
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.675e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.85e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.61e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.57e0

DP
type: SiteQuality
SIO_000300: 1.845673e6

MQRankSum
type: SiteQuality
SIO_000300: -1.5e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -4.97e-1

QD
type: SiteQuality
SIO_000300: 1.403e1

GenotypeDepth
all individuals: 13
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 796
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1276
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3674
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9714
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32710
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3273
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2506
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 36
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1567
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4104
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 133
bin: 3.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8606
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.080690766471071e-5
allele num: 65782
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16450
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 2.65e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.81e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -1.71e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.8e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 2.045e0

DP
type: SiteQuality
SIO_000300: 1.883383e6

QD
type: SiteQuality
SIO_000300: 9.220000000000001e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.721e0

GenotypeDepth
all individuals: 1878
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 58
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2508
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33054
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4099
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 9765
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3276
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 731
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1279
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3686
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1567
bin: 9.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10118
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.64902266043937e-5
allele num: 11562
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65960
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8612
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16496
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.74e-1

MQ
type: SiteQuality
SIO_000300: 5.894e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.38e0

QD
type: SiteQuality
SIO_000300: 1.364e1

MQRankSum
type: SiteQuality
SIO_000300: 3.47e-1

FS
type: SiteQuality
SIO_000300: 1.944e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.6e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.500000000000001e-2

DP
type: SiteQuality
SIO_000300: 1.885444e6

GenotypeDepth
all individuals: 888
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 716
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1278
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1569
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9773
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 1.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 36
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3680
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3280
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4099
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 69
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2508
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33143
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.212121212121212e-4
allele num: 16500
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8612
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.64902266043937e-5
allele num: 11562
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65986
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10126
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -6.51e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

QD
type: SiteQuality
SIO_000300: 1.437e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.133e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.3e-2

DP
type: SiteQuality
SIO_000300: 1.885948e6

VQSLOD
type: SiteQuality
SIO_000300: 6.17e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 5.42e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.77e-1

GenotypeDepth
all individuals: 13
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3275
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 700
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9769
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3678
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1278
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4094
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 33139
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2509
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1567
bin: 9.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10124
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.515243348081702e-5
allele num: 65996
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8612
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 5.600000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.013e1

MQRankSum
type: SiteQuality
SIO_000300: 1.08e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 2.73e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.23e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.46e0

DP
type: SiteQuality
SIO_000300: 1.886588e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.91e0

GenotypeDepth
all individuals: 9039
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 698
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9779
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33149
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1280
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3278
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4097
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 137
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1567
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2509
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3682
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.029201502483945e-5
allele num: 66024
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8614
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.865824782951855e-5
allele num: 10136
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.21e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.516e-1

QD
type: SiteQuality
SIO_000300: 1.188e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.07e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.94e-1

FS
type: SiteQuality
SIO_000300: 1.2451e1

MQRankSum
type: SiteQuality
SIO_000300: 1.46e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

DP
type: SiteQuality
SIO_000300: 1.886515e6

MQ
type: SiteQuality
SIO_000300: 5.965e1

GenotypeDepth
all individuals: 4
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9779
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 698
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1280
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2509
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 11
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3278
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3682
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4097
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1567
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33149
bin: 6.25e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8614
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10136
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.514600751241973e-5
allele num: 66024
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -4.94e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.46e-1

QD
type: SiteQuality
SIO_000300: 1.188e1

DP
type: SiteQuality
SIO_000300: 1.886515e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.07e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.21e-1

FS
type: SiteQuality
SIO_000300: 1.2451e1

VQSLOD
type: SiteQuality
SIO_000300: -6.516e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

MQ
type: SiteQuality
SIO_000300: 5.965e1

GenotypeDepth
all individuals: 3
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 647
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1568
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3687
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33279
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9788
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3283
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1278
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4094
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2510
bin: 8.25e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8614
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10160
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66100
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.05913717886573e-5
allele num: 16504
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.8e-1

VQSLOD
type: SiteQuality
SIO_000300: -7.131999999999999e-1

QD
type: SiteQuality
SIO_000300: 9.43e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

FS
type: SiteQuality
SIO_000300: 8.78e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.84e0

MQ
type: SiteQuality
SIO_000300: 5.927e1

DP
type: SiteQuality
SIO_000300: 1.887512e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.535e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.61e0

GenotypeDepth
all individuals: 186
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 106
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3280
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3688
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1278
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4095
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 23
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 623
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 33341
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1567
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2510
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9796
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.072214830047176e-5
allele num: 66136
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8614
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -7.21e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

DP
type: SiteQuality
SIO_000300: 1.888118e6

FS
type: SiteQuality
SIO_000300: 1.1e0

VQSLOD
type: SiteQuality
SIO_000300: 1.73e0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.24e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.6e-1

MQ
type: SiteQuality
SIO_000300: 5.964e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.25e-1

QD
type: SiteQuality
SIO_000300: 1.211e1

GenotypeDepth
all individuals: 12
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3689
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4082
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2498
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 446
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9820
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1565
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33358
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1274
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3276
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 5.75e1
variant carriers: 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: 1.508113651444773e-5
allele num: 66308
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10266
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.891267e6

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 9.389999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.79e-1

FS
type: SiteQuality
SIO_000300: 4.722e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.679e0

QD
type: SiteQuality
SIO_000300: 1.32e1

GenotypeDepth
all individuals: 4
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 18
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 444
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2498
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9824
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 79
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1565
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3279
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1274
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33535
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3692
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4081
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 62
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66328
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10278
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.05913717886573e-5
allele num: 16504
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.385e1

VQSLOD
type: SiteQuality
SIO_000300: 2.06e0

FS
type: SiteQuality
SIO_000300: 2.875e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.12e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 3.92e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.011e0

DP
type: SiteQuality
SIO_000300: 1.891579e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.14e-1

MQ
type: SiteQuality
SIO_000300: 5.979e1

GenotypeDepth
all individuals: 3
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 90
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 438
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2498
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9829
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33604
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3279
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3691
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1274
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1565
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4080
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5
bin: 1.75e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66336
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.05913717886573e-5
allele num: 16504
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.8e0

QD
type: SiteQuality
SIO_000300: 1.783e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.666e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.63e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.909e1

VQSLOD
type: SiteQuality
SIO_000300: -1.359e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.03e-1

DP
type: SiteQuality
SIO_000300: 1.891811e6

GenotypeDepth
all individuals: 15488
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 446
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2497
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9821
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4079
bin: 9.75e1
variant carriers: 4

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

GenotypeQuality
all individuals: 17
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3271
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1272
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1565
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3687
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33574
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10294
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.160092807424594e-4
allele num: 8620
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.64902266043937e-5
allele num: 11562
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.014408874419726e-5
allele num: 66348
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.24e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 1.891733e6

MQ
type: SiteQuality
SIO_000300: 5.921e1

VQSLOD
type: SiteQuality
SIO_000300: 3.18e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.65e-1

QD
type: SiteQuality
SIO_000300: 1.136e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.93e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.56e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.28e-1

GenotypeDepth
all individuals: 3
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 69
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9823
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 453
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1273
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33555
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4075
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2496
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3689
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3274
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1566
bin: 9.25e1
variant carriers: 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: 66348
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.059871530723549e-5
allele num: 16502
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10296
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -4.71e-1

DP
type: SiteQuality
SIO_000300: 1.891316e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.819e0

FS
type: SiteQuality
SIO_000300: 1.4101e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.37e0

VQSLOD
type: SiteQuality
SIO_000300: -2.26e0

QD
type: SiteQuality
SIO_000300: 9.23e0

MQRankSum
type: SiteQuality
SIO_000300: -6.39e-1

MQ
type: SiteQuality
SIO_000300: 5.911e1

GenotypeDepth
all individuals: 5
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 112
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33391
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9809
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1566
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2496
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 465
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3688
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3278
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4076
bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 37
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1272
bin: 8.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.043226623259179e-5
allele num: 66348
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10294
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -2.89e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.59e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.5e-2

QD
type: SiteQuality
SIO_000300: 1.227e1

DP
type: SiteQuality
SIO_000300: 1.890993e6

VQSLOD
type: SiteQuality
SIO_000300: 2.97e0

MQ
type: SiteQuality
SIO_000300: 5.983e1

FS
type: SiteQuality
SIO_000300: 1.115e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.71e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

GenotypeDepth
all individuals: 187
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 3272
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 18
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2494
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1272
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1563
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4070
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 522
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9811
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33327
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3677
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.521613311629589e-5
allele num: 66348
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10294
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.825e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.1e-1

FS
type: SiteQuality
SIO_000300: 5.91e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 5.964e1

QD
type: SiteQuality
SIO_000300: 1.284e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.6e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.25e-1

DP
type: SiteQuality
SIO_000300: 1.889437e6

VQSLOD
type: SiteQuality
SIO_000300: 1.66e0

GenotypeDepth
all individuals: 362
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3675
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9814
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3270
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1563
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33350
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4067
bin: 9.75e1
variant carriers: 1

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

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

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

GenotypeQuality
all individuals: 534
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2494
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1272
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 2.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66346
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8614
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.650519031141868e-5
allele num: 11560
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10296
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.255e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.77e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.88e-1

FS
type: SiteQuality
SIO_000300: 9.389999999999999e-1

MQ
type: SiteQuality
SIO_000300: 5.944e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 8.71e-1

DP
type: SiteQuality
SIO_000300: 1.889087e6

MQRankSum
type: SiteQuality
SIO_000300: -5.600000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.899e0

GenotypeDepth
all individuals: 40
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3675
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 4.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 534
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33350
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9814
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3270
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1563
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4067
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2494
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1272
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.507249871883761e-5
allele num: 66346
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10296
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8614
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: 6612
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.77e-1

MQ
type: SiteQuality
SIO_000300: 5.944e1

QD
type: SiteQuality
SIO_000300: 1.255e1

VQSLOD
type: SiteQuality
SIO_000300: 8.71e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.899e0

FS
type: SiteQuality
SIO_000300: 9.389999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.88e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.600000000000001e-1

DP
type: SiteQuality
SIO_000300: 1.889087e6

GenotypeDepth
all individuals: 5
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 3674
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 25
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 577
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3266
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9794
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1271
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 33169
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 187
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2492
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1565
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4064
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10286
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8614
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
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: 6612
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.507522537461935e-5
allele num: 66334
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.9e-1

MQ
type: SiteQuality
SIO_000300: 5.904e1

FS
type: SiteQuality
SIO_000300: 3.915e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.127e0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.78e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -4.576e-1

QD
type: SiteQuality
SIO_000300: 1.08e1

MQRankSum
type: SiteQuality
SIO_000300: 6.0e-2

DP
type: SiteQuality
SIO_000300: 1.887569e6

GenotypeDepth
all individuals: 112
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1565
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3675
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4065
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 187
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 31
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33209
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 576
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 165
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9790
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1269
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2492
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3265
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10286
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66334
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8614
num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -9.388e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.91e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

FS
type: SiteQuality
SIO_000300: 4.1576e1

MQRankSum
type: SiteQuality
SIO_000300: 4.24e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.474e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.34e0

DP
type: SiteQuality
SIO_000300: 1.887562e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.298e1

GenotypeDepth
all individuals: 112
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9777
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33074
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 608
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 161
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1268
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2492
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 39
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 201
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4062
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1564
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3269
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3672
bin: 7.75e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8610
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66330
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11558
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.72762645914397e-5
allele num: 10280
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

QD
type: SiteQuality
SIO_000300: 7.2e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.672e0

MQ
type: SiteQuality
SIO_000300: 5.94e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.07e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.49e0

FS
type: SiteQuality
SIO_000300: 1.865e0

VQSLOD
type: SiteQuality
SIO_000300: -5.499000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.39e-1

DP
type: SiteQuality
SIO_000300: 1.886582e6

GenotypeDepth
all individuals: 40
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 245
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32709
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 204
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 220
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3665
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2489
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4062
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 3253
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9697
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1266
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1560
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 675
bin: 2.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.05766900896535e-5
allele num: 16508
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.508295625942685e-5
allele num: 66300
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.162790697674419e-4
allele num: 8600
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.72951936174353e-5
allele num: 10278
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 6.3e-2

QD
type: SiteQuality
SIO_000300: 1.162e1

DP
type: SiteQuality
SIO_000300: 1.884903e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 9.69e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.51e0

FS
type: SiteQuality
SIO_000300: 4.645e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.18e-1

GenotypeDepth
all individuals: 362
bin: 5.75e1
variant carriers: 5

GenotypeQuality
all individuals: 238
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3662
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32943
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9702
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3255
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 184
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4069
bin: 9.75e1
variant carriers: 56

GenotypeQuality
all individuals: 20
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 215
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 678
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1261
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2486
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1559
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8600
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10276
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 56
allele frequency: 8.447729672650475e-4
allele num: 66290
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11558
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

QD
type: SiteQuality
SIO_000300: 1.393e1

MQ
type: SiteQuality
SIO_000300: 5.961e1

DP
type: SiteQuality
SIO_000300: 1.886473e6

VQSLOD
type: SiteQuality
SIO_000300: 3.43e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.6e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.27e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.78e-1

FS
type: SiteQuality
SIO_000300: 1.733e0

MQRankSum
type: SiteQuality
SIO_000300: 2.97e-1

GenotypeDepth
all individuals: 12
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 182
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 222
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3654
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2486
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4026
bin: 9.75e1
variant carriers: 9

GenotypeQuality
all individuals: 721
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 252
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32862
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9706
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 167
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1261
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1557
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3258
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.733307377846993e-5
allele num: 10274
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.658008658008658e-5
allele num: 11550
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.508932882665379e-5
allele num: 66272
num of homozygotes: 0

South Asian
type: Population
allele count: 5
allele frequency: 3.028834504482675e-4
allele num: 16508
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8598
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.513775355737209e-4
allele num: 6606
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.768e0

QD
type: SiteQuality
SIO_000300: 1.18e1

MQRankSum
type: SiteQuality
SIO_000300: 2.58e-1

MQ
type: SiteQuality
SIO_000300: 5.96e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.33e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.84e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.7e0

DP
type: SiteQuality
SIO_000300: 1.883117e6

VQSLOD
type: SiteQuality
SIO_000300: 2.59e0

GenotypeDepth
all individuals: 356
bin: 5.75e1
variant carriers: 4

GenotypeQuality
all individuals: 1259
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 164
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4027
bin: 9.75e1
variant carriers: 40

GenotypeQuality
all individuals: 8
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1557
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3255
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 739
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2481
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 219
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3649
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 258
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32765
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9709
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 4.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

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

African
type: Population
allele count: 3
allele frequency: 2.923406743324888e-4
allele num: 10262
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 37
allele frequency: 5.584231338102569e-4
allele num: 66258
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8594
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.43e0

MQ
type: SiteQuality
SIO_000300: 5.95e1

QD
type: SiteQuality
SIO_000300: 1.271e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -5.06e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.29e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.3e-2

FS
type: SiteQuality
SIO_000300: 5.2e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.36e-1

DP
type: SiteQuality
SIO_000300: 1.88322e6

GenotypeDepth
all individuals: 352
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1558
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1258
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 789
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 260
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3654
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2483
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 237
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9710
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3256
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3985
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 32918
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66254
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11550
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.737098344693281e-5
allele num: 10270
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.880247e6

FS
type: SiteQuality
SIO_000300: 1.564e1

MQRankSum
type: SiteQuality
SIO_000300: 2.14e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.0e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.34e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

QD
type: SiteQuality
SIO_000300: 1.464e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.47e0

VQSLOD
type: SiteQuality
SIO_000300: -2.023e0

GenotypeDepth
all individuals: 1861
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33055
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1558
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2485
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3247
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 234
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 3984
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3649
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9709
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 792
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1259
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 251
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 4.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11550
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.733307377846993e-5
allele num: 10274
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8584
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66272
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.51e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.67e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 5.907e1

QD
type: SiteQuality
SIO_000300: 1.047e1

DP
type: SiteQuality
SIO_000300: 1.880495e6

FS
type: SiteQuality
SIO_000300: 1.0735e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.875e0

VQSLOD
type: SiteQuality
SIO_000300: -1.687e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.22e-1

GenotypeDepth
all individuals: 2
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 870
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1557
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 32678
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3650
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3984
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1258
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2482
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 200
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 303
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3240
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 296
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9681
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11542
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16484
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10272
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.332633543270352e-4
allele num: 8574
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66220
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.407e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 6.860000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.193e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.45e-1

QD
type: SiteQuality
SIO_000300: 1.011e1

MQRankSum
type: SiteQuality
SIO_000300: -3.3e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 2.54e0

DP
type: SiteQuality
SIO_000300: 1.877883e6

GenotypeDepth
all individuals: 15447
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9666
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 247
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1556
bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 24
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3235
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 902
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3983
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 2480
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32515
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3645
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1259
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 354
bin: 3.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10260
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66198
num of homozygotes: 0

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

East Asian
type: Population
allele count: 5
allele frequency: 5.842486562280906e-4
allele num: 8558
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16476
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.522e0

DP
type: SiteQuality
SIO_000300: 1.876091e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.3e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.3e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.16e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.28e0

VQSLOD
type: SiteQuality
SIO_000300: 4.2e-1

QD
type: SiteQuality
SIO_000300: 1.211e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.45e-1

MQ
type: SiteQuality
SIO_000300: 5.956e1

GenotypeDepth
all individuals: 4
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3981
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 10
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3642
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 165
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9612
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 347
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1259
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 194
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2479
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 301
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3230
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1556
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 413
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 919
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32139
bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16460
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8558
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11532
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10250
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.511715797430083e-5
allele num: 66150
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.657e0

DP
type: SiteQuality
SIO_000300: 1.874587e6

QD
type: SiteQuality
SIO_000300: 5.54e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.065e0

MQ
type: SiteQuality
SIO_000300: 5.899e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.259e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.45e0

FS
type: SiteQuality
SIO_000300: 1.76e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.1e-3

MQRankSum
type: SiteQuality
SIO_000300: 6.78e-1

GenotypeDepth
all individuals: 12
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3979
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 247
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 951
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9533
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 360
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2475
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1552
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 356
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3628
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3210
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 443
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1257
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32027
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66044
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6594
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.786651008025054e-5
allele num: 10218
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16426
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: 11522
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.247e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.43e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.872348e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.89e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.95e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -1.89e-1

FS
type: SiteQuality
SIO_000300: 1.121e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.12e-1

GenotypeDepth
all individuals: 4
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 207
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 410
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 284
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1550
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 355
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9437
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3978
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 962
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3619
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31736
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1251
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 370
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3187
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 443
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2472
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8542
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65900
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.858044164037855e-5
allele num: 10144
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16344
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.283e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.02e0

VQSLOD
type: SiteQuality
SIO_000300: 1.94e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.38e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.35e-1

MQ
type: SiteQuality
SIO_000300: 5.972e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 3.08e-1

QD
type: SiteQuality
SIO_000300: 1.022e1

DP
type: SiteQuality
SIO_000300: 1.869945e6

GenotypeDepth
all individuals: 4208
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2467
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1025
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1246
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3185
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9492
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 394
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 266
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1549
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 374
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 178
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32033
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3608
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 430
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3975
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 136
bin: 5.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8544
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.677542519958348e-5
allele num: 11524
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.034072635698898e-5
allele num: 65918
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.116207951070337e-5
allele num: 16350
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.825112988799372e-5
allele num: 10178
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.9e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 5.968e1

DP
type: SiteQuality
SIO_000300: 1.870647e6

VQSLOD
type: SiteQuality
SIO_000300: 1.81e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.54e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.89e-1

FS
type: SiteQuality
SIO_000300: 2.174e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.47e0

QD
type: SiteQuality
SIO_000300: 1.346e1

GenotypeDepth
all individuals: 178
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 80
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 226
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1248
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2466
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 367
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 425
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 358
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9476
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32087
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1070
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 182
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3193
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3608
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1548
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3970
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 63
bin: 1.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8542
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.680555555555556e-5
allele num: 11520
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16294
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10186
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65956
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

MQRankSum
type: SiteQuality
SIO_000300: 6.02e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.64e-1

FS
type: SiteQuality
SIO_000300: 1.351e0

DP
type: SiteQuality
SIO_000300: 1.868434e6

VQSLOD
type: SiteQuality
SIO_000300: 1.09e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.577e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.6e-2

MQ
type: SiteQuality
SIO_000300: 5.964e1

QD
type: SiteQuality
SIO_000300: 1.225e1

GenotypeDepth
all individuals: 178
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 425
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 182
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1070
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1248
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 358
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3608
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9476
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1548
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 226
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3970
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 367
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3193
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32087
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2466
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8542
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.516162290011523e-5
allele num: 65956
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16294
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10186
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11520
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.6e-2

QD
type: SiteQuality
SIO_000300: 1.225e1

FS
type: SiteQuality
SIO_000300: 1.351e0

MQRankSum
type: SiteQuality
SIO_000300: 6.02e-1

MQ
type: SiteQuality
SIO_000300: 5.964e1

DP
type: SiteQuality
SIO_000300: 1.868434e6

ClippingRankSum
type: SiteQuality
SIO_000300: 4.64e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.09e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.577e0

GenotypeDepth
all individuals: 38
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 3597
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32149
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1122
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3968
bin: 9.75e1
variant carriers: 9

GenotypeQuality
all individuals: 3191
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2470
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 417
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1247
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 348
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 207
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9469
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1546
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 342
bin: 3.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8540
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.55000455000455e-5
allele num: 65934
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6584
num of homozygotes: 0

South Asian
type: Population
allele count: 5
allele frequency: 3.076923076923077e-4
allele num: 16250
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10196
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.679048776254123e-5
allele num: 11522
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.0e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

DP
type: SiteQuality
SIO_000300: 1.868369e6

QD
type: SiteQuality
SIO_000300: 1.526e1

MQRankSum
type: SiteQuality
SIO_000300: 2.95e-1

MQ
type: SiteQuality
SIO_000300: 5.973e1

FS
type: SiteQuality
SIO_000300: 1.0593e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.8e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.16e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.56e0

GenotypeDepth
all individuals: 5
bin: 8.75e1
variant carriers: 3

GenotypeQuality
all individuals: 9493
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1247
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32230
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3194
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1112
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3590
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 389
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 308
bin: 3.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 2468
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1544
bin: 9.25e1
variant carriers: 1

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

GenotypeQuality
all individuals: 3991
bin: 9.75e1
variant carriers: 74

GenotypeQuality
all individuals: 111
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 329
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 5.25e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.51666818333485e-5
allele num: 65934
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16220
num of homozygotes: 0

African
type: Population
allele count: 68
allele frequency: 6.669282071400549e-3
allele num: 10196
num of homozygotes: 1

Latino
type: Population
allele count: 7
allele frequency: 6.079555323953448e-4
allele num: 11514
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: 1
allele frequency: 1.108647450110865e-3
allele num: 902
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6584
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.04e0

DP
type: SiteQuality
SIO_000300: 1.870091e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.27e0

MQ
type: SiteQuality
SIO_000300: 5.968e1

MQRankSum
type: SiteQuality
SIO_000300: 2.89e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -3.07e-1

FS
type: SiteQuality
SIO_000300: 2.454e0

QD
type: SiteQuality
SIO_000300: 1.55e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.01e-1

GenotypeDepth
all individuals: 100
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3924
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 253
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1544
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 180
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1245
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32561
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3206
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9548
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3610
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1253
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2481
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 75
bin: 4.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65938
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.17096018735363e-4
allele num: 8540
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11520
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10214
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15978
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.1e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.88e-1

MQ
type: SiteQuality
SIO_000300: 5.841e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.701e0

DP
type: SiteQuality
SIO_000300: 1.868928e6

FS
type: SiteQuality
SIO_000300: 1.752e0

QD
type: SiteQuality
SIO_000300: 1.243e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.96e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.826e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

GenotypeDepth
all individuals: 8956
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9541
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1337
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 234
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3607
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 167
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 249
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3200
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3924
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 32634
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1544
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1253
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2476
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10224
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8534
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.294058408862034e-5
allele num: 15888
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11516
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65898
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -5.512e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.02e0

QD
type: SiteQuality
SIO_000300: 1.444e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.095e0

MQ
type: SiteQuality
SIO_000300: 5.953e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.19e-1

FS
type: SiteQuality
SIO_000300: 8.52e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.53e-1

DP
type: SiteQuality
SIO_000300: 1.868096e6

GenotypeDepth
all individuals: 4195
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2472
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 187
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9502
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32437
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1251
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1426
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 191
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 243
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3593
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1542
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3180
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 258
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3924
bin: 9.75e1
variant carriers: 3

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11516
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65892
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10218
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.900899759219364e-4
allele num: 15782
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8534
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 886
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.24e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 9.379999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.169e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.631e0

VQSLOD
type: SiteQuality
SIO_000300: 8.2e-1

FS
type: SiteQuality
SIO_000300: 2.11e0

DP
type: SiteQuality
SIO_000300: 1.867736e6

QD
type: SiteQuality
SIO_000300: 1.356e1

GenotypeDepth
all individuals: 2
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 231
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3922
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 12
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 214
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 165
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32153
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 175
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 263
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9510
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2470
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3180
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1542
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3584
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1253
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1699
bin: 2.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8534
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65798
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10222
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.433350488934638e-5
allele num: 15544
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 882
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.707e0

FS
type: SiteQuality
SIO_000300: 9.743e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.115e0

QD
type: SiteQuality
SIO_000300: 1.456e1

MQRankSum
type: SiteQuality
SIO_000300: -4.21e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.949e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.86343e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 1.42e0

GenotypeDepth
all individuals: 13
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2468
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 228
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 238
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9519
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1253
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 73
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3180
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32469
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1723
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3591
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3923
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 155
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1540
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 1.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65808
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 882
num of homozygotes: 0

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

African
type: Population
allele count: 5
allele frequency: 4.883766360617308e-4
allele num: 10238
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11510
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15478
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.98e-1

DP
type: SiteQuality
SIO_000300: 1.8639e6

MQ
type: SiteQuality
SIO_000300: 5.948e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.17e-1

QD
type: SiteQuality
SIO_000300: 1.255e1

MQRankSum
type: SiteQuality
SIO_000300: -8.159999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.3e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.4e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.55e0

GenotypeDepth
all individuals: 17304
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1255
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 286
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31509
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2464
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 273
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2555
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3579
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1540
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9406
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3920
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3178
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10240
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.524715640533041e-5
allele num: 65586
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14760
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11504
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8536
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.665e0

QD
type: SiteQuality
SIO_000300: 1.266e1

DP
type: SiteQuality
SIO_000300: 1.850895e6

MQRankSum
type: SiteQuality
SIO_000300: -1.093e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

MQ
type: SiteQuality
SIO_000300: 5.951e1

FS
type: SiteQuality
SIO_000300: 1.675e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.05e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.44e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.76e-1

GenotypeDepth
all individuals: 10
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3173
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3918
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 302
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 283
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31070
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 37
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1539
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1257
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3577
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2463
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2863
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9379
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 4.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.172058134083451e-4
allele num: 8532
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10238
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65468
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14514
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -8.2e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.34e-2

MQ
type: SiteQuality
SIO_000300: 5.956e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.871e0

QD
type: SiteQuality
SIO_000300: 1.592e1

FS
type: SiteQuality
SIO_000300: 6.795e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

DP
type: SiteQuality
SIO_000300: 1.845765e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.61e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.97e-1

GenotypeDepth
all individuals: 7621
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 189
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9360
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 280
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1539
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1256
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30939
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 301
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2957
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3918
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2464
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3575
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3172
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 4.25e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10230
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65424
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11500
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8532
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.955070246209486e-5
allele num: 14378
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.274e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.87e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.569e0

MQRankSum
type: SiteQuality
SIO_000300: -4.19e-1

VQSLOD
type: SiteQuality
SIO_000300: -8.840000000000001e-2

QD
type: SiteQuality
SIO_000300: 1.247e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.844733e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.54e0

GenotypeDepth
all individuals: 176
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 3571
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9356
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1535
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1255
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 291
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3919
bin: 9.75e1
variant carriers: 9

GenotypeQuality
all individuals: 64
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3168
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3567
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 296
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 30618
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2464
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10216
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.172058134083451e-4
allele num: 8532
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.225602843398597e-4
allele num: 65274
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13882
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: 1.35e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.06e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.41e-1

QD
type: SiteQuality
SIO_000300: 1.113e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.57e-1

FS
type: SiteQuality
SIO_000300: 1.098e0

VQSLOD
type: SiteQuality
SIO_000300: 4.6e-1

DP
type: SiteQuality
SIO_000300: 1.834916e6

MQ
type: SiteQuality
SIO_000300: 5.893e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

GenotypeDepth
all individuals: 338
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 257
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1534
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 310
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3569
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9315
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3924
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2465
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 324
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3151
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3910
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 30087
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1257
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10190
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65170
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 862
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8522
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13496
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.70170553428472e-5
allele num: 11492
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -5.538999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.36e-1

FS
type: SiteQuality
SIO_000300: 5.848e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.94e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -2.058e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -5.93e-1

DP
type: SiteQuality
SIO_000300: 1.826757e6

QD
type: SiteQuality
SIO_000300: 1.657e1

GenotypeDepth
all individuals: 8951
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3155
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3910
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3570
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 156
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1535
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9316
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29885
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 306
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4070
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 320
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2466
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 332
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1256
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11492
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10190
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65096
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 850
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.17343346632246e-4
allele num: 8522
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13236
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.23e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.21e-1

MQ
type: SiteQuality
SIO_000300: 5.983e1

QD
type: SiteQuality
SIO_000300: 1.478e1

MQRankSum
type: SiteQuality
SIO_000300: 9.79e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.169e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.454e0

DP
type: SiteQuality
SIO_000300: 1.822683e6

FS
type: SiteQuality
SIO_000300: 1.304e0

GenotypeDepth
all individuals: 173
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29880
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1535
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 332
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 357
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 283
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2467
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1256
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4121
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3571
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3908
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 142
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9303
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3153
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10184
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 848
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11494
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.537468097536976e-5
allele num: 65042
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13092
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8516
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.821173e6

VQSLOD
type: SiteQuality
SIO_000300: -8.890000000000001e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -9.16e-1

MQ
type: SiteQuality
SIO_000300: 5.908e1

MQRankSum
type: SiteQuality
SIO_000300: 1.02e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.83e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

FS
type: SiteQuality
SIO_000300: 9.429999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.016e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.48e0

GenotypeDepth
all individuals: 2
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 264
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 395
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3571
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 316
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3153
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3908
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 40
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29843
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4115
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1534
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2467
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9302
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1256
bin: 8.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11494
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10186
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.078343851008158e-5
allele num: 64970
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 7.733952049497293e-5
allele num: 12930
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.820487e6

MQRankSum
type: SiteQuality
SIO_000300: -8.0e-3

FS
type: SiteQuality
SIO_000300: 2.422e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.35e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.31e-1

MQ
type: SiteQuality
SIO_000300: 5.934e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.086e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.62e0

QD
type: SiteQuality
SIO_000300: 9.300000000000001e0

GenotypeDepth
all individuals: 8959
bin: 3.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 267
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9300
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 5.25e1
variant carriers: 0