19-1506801-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1506801
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1506801
    reference: chr 19
allele count: 2
allele frequency: 1.149029070435482e-4
allele num: 17406
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590562
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590562.1:n.1158G>C
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000585700
  gene symbol: ADAMTSL5
  hgvsc: ENST00000585700.1:n.1057G>C
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000399364
  ensembl transcript: ENST00000413997
  gene symbol: ADAMTSL5
  hgvsc: ENST00000413997.2:c.1009G>C
  hgvsp: ENSP00000399364.2:p.Val337Leu
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000466231
  ensembl transcript: ENST00000590090
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590090.1:c.343G>C
  hgvsp: ENSP00000466231.1:p.Val115Leu
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590682
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590682.1:n.308G>C
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000378850
  ensembl transcript: ENST00000395467
  gene symbol: ADAMTSL5
  hgvsc: ENST00000395467.2:c.286G>C
  hgvsp: ENSP00000378850.2:p.Val96Leu
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000327608
  ensembl transcript: ENST00000330475
  gene symbol: ADAMTSL5
  hgvsc: ENST00000330475.4:c.979G>C
  hgvsp: ENSP00000327608.3:p.Val327Leu
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590440
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590440.1:n.1017G>C
  variant of: http://identifiers.org/hgnc/27912
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1771
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1514
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32990
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3512
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7030
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1156
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4771
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30738
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 937
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Val327Leu
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

19-1506801-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1506801
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1506801
    reference: chr 19
allele count: 0
allele frequency: 0.0e0
allele num: 17406
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000466231
  ensembl transcript: ENST00000590090
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590090.1:c.343G>A
  hgvsp: ENSP00000466231.1:p.Val115Met
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590562
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590562.1:n.1158G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000327608
  ensembl transcript: ENST00000330475
  gene symbol: ADAMTSL5
  hgvsc: ENST00000330475.4:c.979G>A
  hgvsp: ENSP00000327608.3:p.Val327Met
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000399364
  ensembl transcript: ENST00000413997
  gene symbol: ADAMTSL5
  hgvsc: ENST00000413997.2:c.1009G>A
  hgvsp: ENSP00000399364.2:p.Val337Met
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000585700
  gene symbol: ADAMTSL5
  hgvsc: ENST00000585700.1:n.1057G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000378850
  ensembl transcript: ENST00000395467
  gene symbol: ADAMTSL5
  hgvsc: ENST00000395467.2:c.286G>A
  hgvsp: ENSP00000378850.2:p.Val96Met
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590440
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590440.1:n.1017G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590682
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590682.1:n.308G>A
  variant of: http://identifiers.org/hgnc/27912
canonical: true
consequence: missense
filter: AC_Adj0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32990
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1771
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1514
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7030
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3512
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 386
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 242
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 379
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3832
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3450
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Val327Met
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: QD

19-1506802-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1506802
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1506802
    reference: chr 19
allele count: 0
allele frequency: 0.0e0
allele num: 17448
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000378850
  ensembl transcript: ENST00000395467
  gene symbol: ADAMTSL5
  hgvsc: ENST00000395467.2:c.285G>A
  hgvsp: ENST00000395467.2:c.285G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000466231
  ensembl transcript: ENST00000590090
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590090.1:c.342G>A
  hgvsp: ENST00000590090.1:c.342G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000327608
  ensembl transcript: ENST00000330475
  gene symbol: ADAMTSL5
  hgvsc: ENST00000330475.4:c.978G>A
  hgvsp: ENST00000330475.4:c.978G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000399364
  ensembl transcript: ENST00000413997
  gene symbol: ADAMTSL5
  hgvsc: ENST00000413997.2:c.1008G>A
  hgvsp: ENST00000413997.2:c.1008G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590562
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590562.1:n.1157G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590682
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590682.1:n.307G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000585700
  gene symbol: ADAMTSL5
  hgvsc: ENST00000585700.1:n.1056G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590440
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590440.1:n.1016G>A
  variant of: http://identifiers.org/hgnc/27912
canonical: true
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 3499
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1501
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33113
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1797
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6999
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1001
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3087
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4982
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31182
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 247
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 923
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Gly326Gly
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD

19-1506804-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1506804
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1506804
    reference: chr 19
allele count: 1
allele frequency: 5.730659025787966e-5
allele num: 17450
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000378850
  ensembl transcript: ENST00000395467
  gene symbol: ADAMTSL5
  hgvsc: ENST00000395467.2:c.283G>C
  hgvsp: ENSP00000378850.2:p.Gly95Arg
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000585700
  gene symbol: ADAMTSL5
  hgvsc: ENST00000585700.1:n.1054G>C
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590682
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590682.1:n.305G>C
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000399364
  ensembl transcript: ENST00000413997
  gene symbol: ADAMTSL5
  hgvsc: ENST00000413997.2:c.1006G>C
  hgvsp: ENSP00000399364.2:p.Gly336Arg
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590562
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590562.1:n.1155G>C
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000466231
  ensembl transcript: ENST00000590090
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590090.1:c.340G>C
  hgvsp: ENSP00000466231.1:p.Gly114Arg
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000327608
  ensembl transcript: ENST00000330475
  gene symbol: ADAMTSL5
  hgvsc: ENST00000330475.4:c.976G>C
  hgvsp: ENSP00000327608.3:p.Gly326Arg
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590440
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590440.1:n.1014G>C
  variant of: http://identifiers.org/hgnc/27912
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1829
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3521
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33121
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1415
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6558
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 261
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 870
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 982
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 404
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 924
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Gly326Arg
num of homozygotes: 0
population: African
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

http://identifiers.org/exac.variant/19-1506806-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1506806
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1506806
    reference: chr 19
allele count: 2
allele frequency: 1.155001155001155e-4
allele num: 17316
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000399364
  ensembl transcript: ENST00000413997
  gene symbol: ADAMTSL5
  hgvsc: ENST00000413997.2:c.1004G>T
  hgvsp: ENSP00000399364.2:p.Arg335Leu
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590562
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590562.1:n.1153G>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000585700
  gene symbol: ADAMTSL5
  hgvsc: ENST00000585700.1:n.1052G>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590440
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590440.1:n.1012G>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000378850
  ensembl transcript: ENST00000395467
  gene symbol: ADAMTSL5
  hgvsc: ENST00000395467.2:c.281G>T
  hgvsp: ENSP00000378850.2:p.Arg94Leu
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000466231
  ensembl transcript: ENST00000590090
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590090.1:c.338G>T
  hgvsp: ENSP00000466231.1:p.Arg113Leu
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000327608
  ensembl transcript: ENST00000330475
  gene symbol: ADAMTSL5
  hgvsc: ENST00000330475.4:c.974G>T
  hgvsp: ENSP00000327608.3:p.Arg325Leu
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590682
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590682.1:n.303G>T
  variant of: http://identifiers.org/hgnc/27912
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6208
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3541
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32984
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1856
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1349
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 411
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4461
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30793
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 370
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 802
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Arg325Leu
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ

19-1506807-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1506807
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1506807
    reference: chr 19
allele count: 0
allele frequency: 0.0e0
allele num: 17452
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590440
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590440.1:n.1011C>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000466231
  ensembl transcript: ENST00000590090
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590090.1:c.337C>T
  hgvsp: ENSP00000466231.1:p.Arg113Trp
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000378850
  ensembl transcript: ENST00000395467
  gene symbol: ADAMTSL5
  hgvsc: ENST00000395467.2:c.280C>T
  hgvsp: ENSP00000378850.2:p.Arg94Trp
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590682
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590682.1:n.302C>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590562
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590562.1:n.1152C>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000399364
  ensembl transcript: ENST00000413997
  gene symbol: ADAMTSL5
  hgvsc: ENST00000413997.2:c.1003C>T
  hgvsp: ENSP00000399364.2:p.Arg335Trp
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000327608
  ensembl transcript: ENST00000330475
  gene symbol: ADAMTSL5
  hgvsc: ENST00000330475.4:c.973C>T
  hgvsp: ENSP00000327608.3:p.Arg325Trp
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000585700
  gene symbol: ADAMTSL5
  hgvsc: ENST00000585700.1:n.1051C>T
  variant of: http://identifiers.org/hgnc/27912
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3587
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5999
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1312
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33087
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1875
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4553
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 382
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 349
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2768
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 413
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 655
  bin: 1.75e1
  variant carriers: 1
hgvs: p.Arg325Trp
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff

19-1506809-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1506809
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1506809
    reference: chr 19
allele count: 0
allele frequency: 0.0e0
allele num: 17456
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000399364
  ensembl transcript: ENST00000413997
  gene symbol: ADAMTSL5
  hgvsc: ENST00000413997.2:c.1001C>T
  hgvsp: ENSP00000399364.2:p.Pro334Leu
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000585700
  gene symbol: ADAMTSL5
  hgvsc: ENST00000585700.1:n.1049C>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590682
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590682.1:n.300C>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000327608
  ensembl transcript: ENST00000330475
  gene symbol: ADAMTSL5
  hgvsc: ENST00000330475.4:c.971C>T
  hgvsp: ENSP00000327608.3:p.Pro324Leu
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590562
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590562.1:n.1150C>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000378850
  ensembl transcript: ENST00000395467
  gene symbol: ADAMTSL5
  hgvsc: ENST00000395467.2:c.278C>T
  hgvsp: ENSP00000378850.2:p.Pro93Leu
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000466231
  ensembl transcript: ENST00000590090
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590090.1:c.335C>T
  hgvsp: ENSP00000466231.1:p.Pro112Leu
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590440
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590440.1:n.1009C>T
  variant of: http://identifiers.org/hgnc/27912
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32959
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1242
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3637
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1908
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5396
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 738
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 346
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 684
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 271
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 382
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Pro324Leu
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum

http://identifiers.org/exac.variant/19-1506821-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1506821
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1506821
    reference: chr 19
allele count: 8
allele frequency: 4.548555833522856e-4
allele num: 17588
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000585700
  gene symbol: ADAMTSL5
  hgvsc: ENST00000585700.1:n.1037G>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000399364
  ensembl transcript: ENST00000413997
  gene symbol: ADAMTSL5
  hgvsc: ENST00000413997.2:c.989G>T
  hgvsp: ENSP00000399364.2:p.Arg330Met
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000466231
  ensembl transcript: ENST00000590090
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590090.1:c.323G>T
  hgvsp: ENSP00000466231.1:p.Arg108Met
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000378850
  ensembl transcript: ENST00000395467
  gene symbol: ADAMTSL5
  hgvsc: ENST00000395467.2:c.266G>T
  hgvsp: ENSP00000378850.2:p.Arg89Met
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000327608
  ensembl transcript: ENST00000330475
  gene symbol: ADAMTSL5
  hgvsc: ENST00000330475.4:c.959G>T
  hgvsp: ENSP00000327608.3:p.Arg320Met
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590562
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590562.1:n.1138G>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590440
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590440.1:n.997G>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590682
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590682.1:n.288G>T
  variant of: http://identifiers.org/hgnc/27912
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1999
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3764
  bin: 7.5e0
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 930
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3953
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31996
  bin: 2.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2822
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2959
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 289
  bin: 2.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 263
  bin: 3.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.75e1
  variant carriers: 1
hgvs: p.Arg320Met
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: Other
population: South Asian
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

19-1506824-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1506824
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1506824
    reference: chr 19
allele count: 58
allele frequency: 3.292835244691723e-3
allele num: 17614
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000466231
  ensembl transcript: ENST00000590090
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590090.1:c.320T>A
  hgvsp: ENSP00000466231.1:p.Leu107Gln
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590682
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590682.1:n.285T>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590440
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590440.1:n.994T>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000585700
  gene symbol: ADAMTSL5
  hgvsc: ENST00000585700.1:n.1034T>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000327608
  ensembl transcript: ENST00000330475
  gene symbol: ADAMTSL5
  hgvsc: ENST00000330475.4:c.956T>A
  hgvsp: ENSP00000327608.3:p.Leu319Gln
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000378850
  ensembl transcript: ENST00000395467
  gene symbol: ADAMTSL5
  hgvsc: ENST00000395467.2:c.263T>A
  hgvsp: ENSP00000378850.2:p.Leu88Gln
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000399364
  ensembl transcript: ENST00000413997
  gene symbol: ADAMTSL5
  hgvsc: ENST00000413997.2:c.986T>A
  hgvsp: ENSP00000399364.2:p.Leu329Gln
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590562
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590562.1:n.1135T>A
  variant of: http://identifiers.org/hgnc/27912
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 865
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31467
  bin: 2.5e0
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 2021
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 1.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 4014
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3469
  bin: 7.5e0
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 4.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 1.75e1
  variant carriers: 15
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 442
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2558
  bin: 2.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 492
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3080
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 418
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Leu319Gln
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum

19-1506828-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1506828
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1506828
    reference: chr 19
allele count: 1
allele frequency: 5.657388549445576e-5
allele num: 17676
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000466231
  ensembl transcript: ENST00000590090
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590090.1:c.316C>T
  hgvsp: ENSP00000466231.1:p.Pro106Ser
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000399364
  ensembl transcript: ENST00000413997
  gene symbol: ADAMTSL5
  hgvsc: ENST00000413997.2:c.982C>T
  hgvsp: ENSP00000399364.2:p.Pro328Ser
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000327608
  ensembl transcript: ENST00000330475
  gene symbol: ADAMTSL5
  hgvsc: ENST00000330475.4:c.952C>T
  hgvsp: ENSP00000327608.3:p.Pro318Ser
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000585700
  gene symbol: ADAMTSL5
  hgvsc: ENST00000585700.1:n.1030C>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590440
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590440.1:n.990C>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590562
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590562.1:n.1131C>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000378850
  ensembl transcript: ENST00000395467
  gene symbol: ADAMTSL5
  hgvsc: ENST00000395467.2:c.259C>T
  hgvsp: ENSP00000378850.2:p.Pro87Ser
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590682
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590682.1:n.281C>T
  variant of: http://identifiers.org/hgnc/27912
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4098
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2055
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30748
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3013
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27697
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 286
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 444
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 418
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3379
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 241
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Pro318Ser
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD

19-1506842-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1506842
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1506842
    reference: chr 19
allele count: 0
allele frequency: 0.0e0
allele num: 18052
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000378850
  ensembl transcript: ENST00000395467
  gene symbol: ADAMTSL5
  hgvsc: ENST00000395467.2:c.245A>C
  hgvsp: ENSP00000378850.2:p.Gln82Pro
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590562
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590562.1:n.1117A>C
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000466231
  ensembl transcript: ENST00000590090
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590090.1:c.302A>C
  hgvsp: ENSP00000466231.1:p.Gln101Pro
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590682
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590682.1:n.267A>C
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000399364
  ensembl transcript: ENST00000413997
  gene symbol: ADAMTSL5
  hgvsc: ENST00000413997.2:c.968A>C
  hgvsp: ENSP00000399364.2:p.Gln323Pro
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590440
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590440.1:n.976A>C
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000327608
  ensembl transcript: ENST00000330475
  gene symbol: ADAMTSL5
  hgvsc: ENST00000330475.4:c.938A>C
  hgvsp: ENSP00000327608.3:p.Gln313Pro
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000585700
  gene symbol: ADAMTSL5
  hgvsc: ENST00000585700.1:n.1016A>C
  variant of: http://identifiers.org/hgnc/27912
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28644
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4430
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2096
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2163
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 425
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 295
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 433
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1640
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Gln313Pro
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum

19-1506869-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1506869
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1506869
    reference: chr 19
allele count: 1
allele frequency: 5.416531253385332e-5
allele num: 18462
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000378850
  ensembl transcript: ENST00000395467
  gene symbol: ADAMTSL5
  hgvsc: ENST00000395467.2:c.218G>A
  hgvsp: ENSP00000378850.2:p.Arg73His
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000585700
  gene symbol: ADAMTSL5
  hgvsc: ENST00000585700.1:n.989G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000399364
  ensembl transcript: ENST00000413997
  gene symbol: ADAMTSL5
  hgvsc: ENST00000413997.2:c.941G>A
  hgvsp: ENSP00000399364.2:p.Arg314His
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590440
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590440.1:n.949G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590562
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590562.1:n.1090G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590682
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590682.1:n.240G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000466231
  ensembl transcript: ENST00000590090
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590090.1:c.275G>A
  hgvsp: ENSP00000466231.1:p.Arg92His
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000327608
  ensembl transcript: ENST00000330475
  gene symbol: ADAMTSL5
  hgvsc: ENST00000330475.4:c.911G>A
  hgvsp: ENSP00000327608.3:p.Arg304His
  variant of: http://identifiers.org/hgnc/27912
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4651
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 935
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23565
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2409
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5616
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20082
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Arg304His
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: African
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: FS

19-1506870-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1506870
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1506870
    reference: chr 19
allele count: 0
allele frequency: 0.0e0
allele num: 18474
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000378850
  ensembl transcript: ENST00000395467
  gene symbol: ADAMTSL5
  hgvsc: ENST00000395467.2:c.217C>T
  hgvsp: ENSP00000378850.2:p.Arg73Cys
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590682
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590682.1:n.239C>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000466231
  ensembl transcript: ENST00000590090
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590090.1:c.274C>T
  hgvsp: ENSP00000466231.1:p.Arg92Cys
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000399364
  ensembl transcript: ENST00000413997
  gene symbol: ADAMTSL5
  hgvsc: ENST00000413997.2:c.940C>T
  hgvsp: ENSP00000399364.2:p.Arg314Cys
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000585700
  gene symbol: ADAMTSL5
  hgvsc: ENST00000585700.1:n.988C>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000327608
  ensembl transcript: ENST00000330475
  gene symbol: ADAMTSL5
  hgvsc: ENST00000330475.4:c.910C>T
  hgvsp: ENSP00000327608.3:p.Arg304Cys
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590440
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590440.1:n.948C>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590562
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590562.1:n.1089C>T
  variant of: http://identifiers.org/hgnc/27912
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4647
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1173
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2427
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23149
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 940
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 471
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3691
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 299
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 980
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Arg304Cys
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: DP

19-1506876-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1506876
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1506876
    reference: chr 19
allele count: 2
allele frequency: 1.080497028633171e-4
allele num: 18510
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000466231
  ensembl transcript: ENST00000590090
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590090.1:c.268C>T
  hgvsp: ENSP00000466231.1:p.Arg90Trp
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000327608
  ensembl transcript: ENST00000330475
  gene symbol: ADAMTSL5
  hgvsc: ENST00000330475.4:c.904C>T
  hgvsp: ENSP00000327608.3:p.Arg302Trp
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000399364
  ensembl transcript: ENST00000413997
  gene symbol: ADAMTSL5
  hgvsc: ENST00000413997.2:c.934C>T
  hgvsp: ENSP00000399364.2:p.Arg312Trp
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590562
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590562.1:n.1083C>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000378850
  ensembl transcript: ENST00000395467
  gene symbol: ADAMTSL5
  hgvsc: ENST00000395467.2:c.211C>T
  hgvsp: ENSP00000378850.2:p.Arg71Trp
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590440
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590440.1:n.942C>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590682
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590682.1:n.233C>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000585700
  gene symbol: ADAMTSL5
  hgvsc: ENST00000585700.1:n.982C>T
  variant of: http://identifiers.org/hgnc/27912
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4675
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22272
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2448
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5666
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3677
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Arg302Trp
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: BaseQRankSum

19-1506912-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1506912
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1506912
    reference: chr 19
allele count: 1
allele frequency: 5.441288497116117e-5
allele num: 18378
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000378850
  ensembl transcript: ENST00000395467
  gene symbol: ADAMTSL5
  hgvsc: ENST00000395467.2:c.175C>T
  hgvsp: ENSP00000378850.2:p.Pro59Ser
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590562
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590562.1:n.1047C>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000327608
  ensembl transcript: ENST00000330475
  gene symbol: ADAMTSL5
  hgvsc: ENST00000330475.4:c.868C>T
  hgvsp: ENSP00000327608.3:p.Pro290Ser
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000399364
  ensembl transcript: ENST00000413997
  gene symbol: ADAMTSL5
  hgvsc: ENST00000413997.2:c.898C>T
  hgvsp: ENSP00000399364.2:p.Pro300Ser
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000466231
  ensembl transcript: ENST00000590090
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590090.1:c.232C>T
  hgvsp: ENSP00000466231.1:p.Pro78Ser
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590682
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590682.1:n.197C>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000585700
  gene symbol: ADAMTSL5
  hgvsc: ENST00000585700.1:n.946C>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590440
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590440.1:n.906C>T
  variant of: http://identifiers.org/hgnc/27912
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2451
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4479
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 949
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20233
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 467
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Pro290Ser
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: South Asian
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

19-1506912-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1506912
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1506912
    reference: chr 19
allele count: 1
allele frequency: 5.441288497116117e-5
allele num: 18378
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590682
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590682.1:n.197C>G
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000327608
  ensembl transcript: ENST00000330475
  gene symbol: ADAMTSL5
  hgvsc: ENST00000330475.4:c.868C>G
  hgvsp: ENSP00000327608.3:p.Pro290Ala
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000466231
  ensembl transcript: ENST00000590090
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590090.1:c.232C>G
  hgvsp: ENSP00000466231.1:p.Pro78Ala
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000378850
  ensembl transcript: ENST00000395467
  gene symbol: ADAMTSL5
  hgvsc: ENST00000395467.2:c.175C>G
  hgvsp: ENSP00000378850.2:p.Pro59Ala
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000399364
  ensembl transcript: ENST00000413997
  gene symbol: ADAMTSL5
  hgvsc: ENST00000413997.2:c.898C>G
  hgvsp: ENSP00000399364.2:p.Pro300Ala
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590440
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590440.1:n.906C>G
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590562
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590562.1:n.1047C>G
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000585700
  gene symbol: ADAMTSL5
  hgvsc: ENST00000585700.1:n.946C>G
  variant of: http://identifiers.org/hgnc/27912
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 949
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4479
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20233
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2451
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 302
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1157
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 467
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Pro290Ala
num of homozygotes: 0
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD

19-1506942-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1506942
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1506942
    reference: chr 19
allele count: 1
allele frequency: 5.544466622310933e-5
allele num: 18036
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590682
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590682.1:n.182-15C>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000399364
  ensembl transcript: ENST00000413997
  gene symbol: ADAMTSL5
  hgvsc: ENST00000413997.2:c.883-15C>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000466231
  ensembl transcript: ENST00000590090
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590090.1:c.217-15C>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000585700
  gene symbol: ADAMTSL5
  hgvsc: ENST00000585700.1:n.931-15C>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000378850
  ensembl transcript: ENST00000395467
  gene symbol: ADAMTSL5
  hgvsc: ENST00000395467.2:c.160-15C>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000327608
  ensembl transcript: ENST00000330475
  gene symbol: ADAMTSL5
  hgvsc: ENST00000330475.4:c.853-15C>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590440
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590440.1:n.891-15C>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590562
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590562.1:n.1032-15C>T
  variant of: http://identifiers.org/hgnc/27912
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1210
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2278
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19737
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4165
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 182
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 464
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3333
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 213
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 422
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQ

19-1506966-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1506966
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1506966
    reference: chr 19
allele count: 1
allele frequency: 5.631899076368552e-5
allele num: 17756
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000327608
  ensembl transcript: ENST00000330475
  gene symbol: ADAMTSL5
  hgvsc: ENST00000330475.4:c.853-39C>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590562
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590562.1:n.1032-39C>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000585700
  gene symbol: ADAMTSL5
  hgvsc: ENST00000585700.1:n.931-39C>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000378850
  ensembl transcript: ENST00000395467
  gene symbol: ADAMTSL5
  hgvsc: ENST00000395467.2:c.160-39C>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000466231
  ensembl transcript: ENST00000590090
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590090.1:c.217-39C>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590682
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590682.1:n.182-39C>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000399364
  ensembl transcript: ENST00000413997
  gene symbol: ADAMTSL5
  hgvsc: ENST00000413997.2:c.883-39C>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590440
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590440.1:n.891-39C>T
  variant of: http://identifiers.org/hgnc/27912
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1272
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20578
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3840
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2065
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1106
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 459
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 290
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15265
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 287
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 348
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4478
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 210
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: African
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: DP

19-1506978-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1506978
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1506978
    reference: chr 19
allele count: 6
allele frequency: 3.503445054303398e-4
allele num: 17126
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000378850
  ensembl transcript: ENST00000395467
  gene symbol: ADAMTSL5
  hgvsc: ENST00000395467.2:c.160-51A>G
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000466231
  ensembl transcript: ENST00000590090
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590090.1:c.217-51A>G
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000327608
  ensembl transcript: ENST00000330475
  gene symbol: ADAMTSL5
  hgvsc: ENST00000330475.4:c.853-51A>G
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000585700
  gene symbol: ADAMTSL5
  hgvsc: ENST00000585700.1:n.931-51A>G
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590682
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590682.1:n.182-51A>G
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000399364
  ensembl transcript: ENST00000413997
  gene symbol: ADAMTSL5
  hgvsc: ENST00000413997.2:c.883-51A>G
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590562
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590562.1:n.1032-51A>G
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590440
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590440.1:n.891-51A>G
  variant of: http://identifiers.org/hgnc/27912
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1469
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22838
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 940
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2039
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3808
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 462
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 420
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 460
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 274
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 848
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 253
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 199
  bin: 5.25e1
  variant carriers: 1
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD

http://identifiers.org/exac.variant/19-1507192-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1507192
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1507192
    reference: chr 19
allele count: 1
allele frequency: 9.240777703851557e-6
allele num: 108216
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000585700
  gene symbol: ADAMTSL5
  hgvsc: ENST00000585700.1:n.930+49G>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000378850
  ensembl transcript: ENST00000395467
  gene symbol: ADAMTSL5
  hgvsc: ENST00000395467.2:c.159+49G>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000399364
  ensembl transcript: ENST00000413997
  gene symbol: ADAMTSL5
  hgvsc: ENST00000413997.2:c.882+49G>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590682
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590682.1:n.181+49G>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590440
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590440.1:n.890+49G>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000327608
  ensembl transcript: ENST00000330475
  gene symbol: ADAMTSL5
  hgvsc: ENST00000330475.4:c.852+49G>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000466231
  ensembl transcript: ENST00000590090
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590090.1:c.216+49G>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590562
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590562.1:n.1031+49G>T
  variant of: http://identifiers.org/hgnc/27912
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4854
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1596
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4950
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12464
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2862
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1340
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1640
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4189
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14861
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1563
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7714
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 561
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15457
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1032
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 607
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3390
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3215
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2013
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10522
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: FS

19-1507193-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1507193
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1507193
    reference: chr 19
allele count: 3
allele frequency: 2.771874711263051e-5
allele num: 108230
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000399364
  ensembl transcript: ENST00000413997
  gene symbol: ADAMTSL5
  hgvsc: ENST00000413997.2:c.882+48A>G
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000327608
  ensembl transcript: ENST00000330475
  gene symbol: ADAMTSL5
  hgvsc: ENST00000330475.4:c.852+48A>G
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000585700
  gene symbol: ADAMTSL5
  hgvsc: ENST00000585700.1:n.930+48A>G
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590440
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590440.1:n.890+48A>G
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000466231
  ensembl transcript: ENST00000590090
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590090.1:c.216+48A>G
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590682
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590682.1:n.181+48A>G
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000378850
  ensembl transcript: ENST00000395467
  gene symbol: ADAMTSL5
  hgvsc: ENST00000395467.2:c.159+48A>G
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590562
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590562.1:n.1031+48A>G
  variant of: http://identifiers.org/hgnc/27912
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14870
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4928
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12454
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4181
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1505
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1593
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4941
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1639
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7709
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2864
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3913
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 617
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15643
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 779
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3226
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 319
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 434
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4842
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: T
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum

19-1507202-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1507202
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1507202
    reference: chr 19
allele count: 1
allele frequency: 9.233269315999409e-6
allele num: 108304
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590440
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590440.1:n.890+39T>C
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000466231
  ensembl transcript: ENST00000590090
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590090.1:c.216+39T>C
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590682
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590682.1:n.181+39T>C
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000327608
  ensembl transcript: ENST00000330475
  gene symbol: ADAMTSL5
  hgvsc: ENST00000330475.4:c.852+39T>C
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000585700
  gene symbol: ADAMTSL5
  hgvsc: ENST00000585700.1:n.930+39T>C
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590562
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590562.1:n.1031+39T>C
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000378850
  ensembl transcript: ENST00000395467
  gene symbol: ADAMTSL5
  hgvsc: ENST00000395467.2:c.159+39T>C
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000399364
  ensembl transcript: ENST00000413997
  gene symbol: ADAMTSL5
  hgvsc: ENST00000413997.2:c.882+39T>C
  variant of: http://identifiers.org/hgnc/27912
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7706
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1637
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15264
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4155
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1633
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4932
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1193
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5420
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12544
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2862
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10511
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17056
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 216
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1276
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2902
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3387
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 526
  bin: 1.25e1
  variant carriers: 1
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: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum

19-1507203-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1507203
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1507203
    reference: chr 19
allele count: 16
allele frequency: 1.477841612325199e-4
allele num: 108266
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000466231
  ensembl transcript: ENST00000590090
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590090.1:c.216+38C>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590682
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590682.1:n.181+38C>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000585700
  gene symbol: ADAMTSL5
  hgvsc: ENST00000585700.1:n.930+38C>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000378850
  ensembl transcript: ENST00000395467
  gene symbol: ADAMTSL5
  hgvsc: ENST00000395467.2:c.159+38C>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590440
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590440.1:n.890+38C>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000399364
  ensembl transcript: ENST00000413997
  gene symbol: ADAMTSL5
  hgvsc: ENST00000413997.2:c.882+38C>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590562
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590562.1:n.1031+38C>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000327608
  ensembl transcript: ENST00000330475
  gene symbol: ADAMTSL5
  hgvsc: ENST00000330475.4:c.852+38C>T
  variant of: http://identifiers.org/hgnc/27912
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12556
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7704
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1173
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4936
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2864
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15287
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1639
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5441
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1641
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4146
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 566
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3439
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3898
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2903
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4789
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: DP

19-1507206-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1507206
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1507206
    reference: chr 19
allele count: 1
allele frequency: 9.228838273838089e-6
allele num: 108356
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590562
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590562.1:n.1031+35C>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590682
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590682.1:n.181+35C>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000327608
  ensembl transcript: ENST00000330475
  gene symbol: ADAMTSL5
  hgvsc: ENST00000330475.4:c.852+35C>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000399364
  ensembl transcript: ENST00000413997
  gene symbol: ADAMTSL5
  hgvsc: ENST00000413997.2:c.882+35C>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000585700
  gene symbol: ADAMTSL5
  hgvsc: ENST00000585700.1:n.930+35C>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000378850
  ensembl transcript: ENST00000395467
  gene symbol: ADAMTSL5
  hgvsc: ENST00000395467.2:c.159+35C>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590440
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590440.1:n.890+35C>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000466231
  ensembl transcript: ENST00000590090
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590090.1:c.216+35C>A
  variant of: http://identifiers.org/hgnc/27912
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2862
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4934
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15498
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4117
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5492
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12594
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1071
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7704
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1671
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1638
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3392
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3460
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1242
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 351
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 550
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4786
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/19-1507207-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1507207
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1507207
    reference: chr 19
allele count: 1
allele frequency: 9.222710001106724e-6
allele num: 108428
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590682
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590682.1:n.181+34T>G
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000327608
  ensembl transcript: ENST00000330475
  gene symbol: ADAMTSL5
  hgvsc: ENST00000330475.4:c.852+34T>G
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590562
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590562.1:n.1031+34T>G
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000585700
  gene symbol: ADAMTSL5
  hgvsc: ENST00000585700.1:n.930+34T>G
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000466231
  ensembl transcript: ENST00000590090
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590090.1:c.216+34T>G
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000399364
  ensembl transcript: ENST00000413997
  gene symbol: ADAMTSL5
  hgvsc: ENST00000413997.2:c.882+34T>G
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000378850
  ensembl transcript: ENST00000395467
  gene symbol: ADAMTSL5
  hgvsc: ENST00000395467.2:c.159+34T>G
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590440
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590440.1:n.890+34T>G
  variant of: http://identifiers.org/hgnc/27912
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4928
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15565
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4111
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1680
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12599
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1637
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5541
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7708
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2863
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 505
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 318
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 332
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 447
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7576
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1286
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: African
reference allele: A
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: DP

http://identifiers.org/exac.variant/19-1507208-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1507208
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1507208
    reference: chr 19
allele count: 3
allele frequency: 2.765792676180994e-5
allele num: 108468
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000327608
  ensembl transcript: ENST00000330475
  gene symbol: ADAMTSL5
  hgvsc: ENST00000330475.4:c.852+33G>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000399364
  ensembl transcript: ENST00000413997
  gene symbol: ADAMTSL5
  hgvsc: ENST00000413997.2:c.882+33G>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590562
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590562.1:n.1031+33G>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000585700
  gene symbol: ADAMTSL5
  hgvsc: ENST00000585700.1:n.930+33G>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000378850
  ensembl transcript: ENST00000395467
  gene symbol: ADAMTSL5
  hgvsc: ENST00000395467.2:c.159+33G>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590682
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590682.1:n.181+33G>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000466231
  ensembl transcript: ENST00000590090
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590090.1:c.216+33G>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590440
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590440.1:n.890+33G>T
  variant of: http://identifiers.org/hgnc/27912
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4929
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15609
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1636
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4111
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7708
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2860
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5583
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12604
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10507
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4797
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3893
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1345
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 470
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 282
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: FS
site quality: ClippingRankSum

19-1507208-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1507208
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1507208
    reference: chr 19
allele count: 3
allele frequency: 2.765792676180994e-5
allele num: 108468
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000327608
  ensembl transcript: ENST00000330475
  gene symbol: ADAMTSL5
  hgvsc: ENST00000330475.4:c.852+33G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590562
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590562.1:n.1031+33G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000585700
  gene symbol: ADAMTSL5
  hgvsc: ENST00000585700.1:n.930+33G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000399364
  ensembl transcript: ENST00000413997
  gene symbol: ADAMTSL5
  hgvsc: ENST00000413997.2:c.882+33G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000466231
  ensembl transcript: ENST00000590090
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590090.1:c.216+33G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590682
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590682.1:n.181+33G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590440
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590440.1:n.890+33G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000378850
  ensembl transcript: ENST00000395467
  gene symbol: ADAMTSL5
  hgvsc: ENST00000395467.2:c.159+33G>A
  variant of: http://identifiers.org/hgnc/27912
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2860
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15609
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4111
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7708
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5583
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4929
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1636
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12604
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3534
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 429
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1996
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3399
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 324
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 470
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17587
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: VQSLOD

19-1507211-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1507211
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1507211
    reference: chr 19
allele count: 2
allele frequency: 1.842367073215667e-5
allele num: 108556
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590440
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590440.1:n.890+30G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000585700
  gene symbol: ADAMTSL5
  hgvsc: ENST00000585700.1:n.930+30G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000466231
  ensembl transcript: ENST00000590090
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590090.1:c.216+30G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000327608
  ensembl transcript: ENST00000330475
  gene symbol: ADAMTSL5
  hgvsc: ENST00000330475.4:c.852+30G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000378850
  ensembl transcript: ENST00000395467
  gene symbol: ADAMTSL5
  hgvsc: ENST00000395467.2:c.159+30G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590682
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590682.1:n.181+30G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000399364
  ensembl transcript: ENST00000413997
  gene symbol: ADAMTSL5
  hgvsc: ENST00000413997.2:c.882+30G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590562
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590562.1:n.1031+30G>A
  variant of: http://identifiers.org/hgnc/27912
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5756
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4057
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1743
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15679
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12621
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1636
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4930
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2860
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7711
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1482
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 363
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 282
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7592
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum

19-1507214-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1507214
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1507214
    reference: chr 19
allele count: 2
allele frequency: 1.841078135356064e-5
allele num: 108632
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000585700
  gene symbol: ADAMTSL5
  hgvsc: ENST00000585700.1:n.930+27G>C
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000399364
  ensembl transcript: ENST00000413997
  gene symbol: ADAMTSL5
  hgvsc: ENST00000413997.2:c.882+27G>C
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590440
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590440.1:n.890+27G>C
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000466231
  ensembl transcript: ENST00000590090
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590090.1:c.216+27G>C
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000378850
  ensembl transcript: ENST00000395467
  gene symbol: ADAMTSL5
  hgvsc: ENST00000395467.2:c.159+27G>C
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590682
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590682.1:n.181+27G>C
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000327608
  ensembl transcript: ENST00000330475
  gene symbol: ADAMTSL5
  hgvsc: ENST00000330475.4:c.852+27G>C
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590562
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590562.1:n.1031+27G>C
  variant of: http://identifiers.org/hgnc/27912
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1776
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12625
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4015
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7711
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2859
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5893
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1636
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4930
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15710
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18044
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 348
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2902
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

19-1507218-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1507218
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1507218
    reference: chr 19
allele count: 2
allele frequency: 1.838708491155812e-5
allele num: 108772
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000327608
  ensembl transcript: ENST00000330475
  gene symbol: ADAMTSL5
  hgvsc: ENST00000330475.4:c.852+23G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590440
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590440.1:n.890+23G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000585700
  gene symbol: ADAMTSL5
  hgvsc: ENST00000585700.1:n.930+23G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000378850
  ensembl transcript: ENST00000395467
  gene symbol: ADAMTSL5
  hgvsc: ENST00000395467.2:c.159+23G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000466231
  ensembl transcript: ENST00000590090
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590090.1:c.216+23G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000399364
  ensembl transcript: ENST00000413997
  gene symbol: ADAMTSL5
  hgvsc: ENST00000413997.2:c.882+23G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590682
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590682.1:n.181+23G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590562
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590562.1:n.1031+23G>A
  variant of: http://identifiers.org/hgnc/27912
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1636
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12639
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4930
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7708
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3925
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15806
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6033
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1848
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2860
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3532
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 323
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1597
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 315
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7643
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4819
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2903
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ

19-1507220-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1507220
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1507220
    reference: chr 19
allele count: 5
allele frequency: 4.594659168182904e-5
allele num: 108822
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590440
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590440.1:n.890+21G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000466231
  ensembl transcript: ENST00000590090
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590090.1:c.216+21G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590682
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590682.1:n.181+21G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000327608
  ensembl transcript: ENST00000330475
  gene symbol: ADAMTSL5
  hgvsc: ENST00000330475.4:c.852+21G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000585700
  gene symbol: ADAMTSL5
  hgvsc: ENST00000585700.1:n.930+21G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000399364
  ensembl transcript: ENST00000413997
  gene symbol: ADAMTSL5
  hgvsc: ENST00000413997.2:c.882+21G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000378850
  ensembl transcript: ENST00000395467
  gene symbol: ADAMTSL5
  hgvsc: ENST00000395467.2:c.159+21G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590562
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590562.1:n.1031+21G>A
  variant of: http://identifiers.org/hgnc/27912
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2859
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7709
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3894
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6107
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1636
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1875
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4930
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15817
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12643
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 280
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18323
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1995
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4820
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 234
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3542
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: Other
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum

19-1507231-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1507231
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1507231
    reference: chr 19
allele count: 2
allele frequency: 1.832307241278218e-5
allele num: 109152
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000378850
  ensembl transcript: ENST00000395467
  gene symbol: ADAMTSL5
  hgvsc: ENST00000395467.2:c.159+10G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000466231
  ensembl transcript: ENST00000590090
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590090.1:c.216+10G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590562
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590562.1:n.1031+10G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000399364
  ensembl transcript: ENST00000413997
  gene symbol: ADAMTSL5
  hgvsc: ENST00000413997.2:c.882+10G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000585700
  gene symbol: ADAMTSL5
  hgvsc: ENST00000585700.1:n.930+10G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000327608
  ensembl transcript: ENST00000330475
  gene symbol: ADAMTSL5
  hgvsc: ENST00000330475.4:c.852+10G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590440
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590440.1:n.890+10G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590682
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590682.1:n.181+10G>A
  variant of: http://identifiers.org/hgnc/27912
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4927
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2859
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6348
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15960
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3627
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7710
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1636
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2096
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12671
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3332
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3431
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 287
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 285
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3906
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: DP

19-1507235-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1507235
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1507235
    reference: chr 19
allele count: 1
allele frequency: 9.150302875025163e-6
allele num: 109286
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000585700
  gene symbol: ADAMTSL5
  hgvsc: ENST00000585700.1:n.930+6A>C
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000378850
  ensembl transcript: ENST00000395467
  gene symbol: ADAMTSL5
  hgvsc: ENST00000395467.2:c.159+6A>C
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000399364
  ensembl transcript: ENST00000413997
  gene symbol: ADAMTSL5
  hgvsc: ENST00000413997.2:c.882+6A>C
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000327608
  ensembl transcript: ENST00000330475
  gene symbol: ADAMTSL5
  hgvsc: ENST00000330475.4:c.852+6A>C
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590682
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590682.1:n.181+6A>C
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000466231
  ensembl transcript: ENST00000590090
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590090.1:c.216+6A>C
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590562
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590562.1:n.1031+6A>C
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590440
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590440.1:n.890+6A>C
  variant of: http://identifiers.org/hgnc/27912
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2859
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6444
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3512
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7712
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1636
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2177
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4928
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12677
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16003
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7713
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3260
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 222
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3434
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 276
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 4.75e1
  variant carriers: 0
hgvs: c.852+6A>C
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
population: African
reference allele: T
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum

19-1507240-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1507240
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1507240
    reference: chr 19
allele count: 2
allele frequency: 1.827318410232983e-5
allele num: 109450
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590562
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590562.1:n.1031+1G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000399364
  ensembl transcript: ENST00000413997
  gene symbol: ADAMTSL5
  hgvsc: ENST00000413997.2:c.882+1G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000378850
  ensembl transcript: ENST00000395467
  gene symbol: ADAMTSL5
  hgvsc: ENST00000395467.2:c.159+1G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590440
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590440.1:n.890+1G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000466231
  ensembl transcript: ENST00000590090
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590090.1:c.216+1G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000585700
  gene symbol: ADAMTSL5
  hgvsc: ENST00000585700.1:n.930+1G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000327608
  ensembl transcript: ENST00000330475
  gene symbol: ADAMTSL5
  hgvsc: ENST00000330475.4:c.852+1G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590682
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590682.1:n.181+1G>A
  variant of: http://identifiers.org/hgnc/27912
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2268
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7714
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3377
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1636
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2860
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12673
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6497
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4926
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16049
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 18892
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 335
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3146
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3435
  bin: 7.25e1
  variant carriers: 0
hgvs: c.852+1G>A
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: African
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

19-1507241-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1507241
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1507241
    reference: chr 19
allele count: 1
allele frequency: 9.134255284166682e-6
allele num: 109478
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000466231
  ensembl transcript: ENST00000590090
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590090.1:c.216G>A
  hgvsp: ENST00000590090.1:c.216G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000399364
  ensembl transcript: ENST00000413997
  gene symbol: ADAMTSL5
  hgvsc: ENST00000413997.2:c.882G>A
  hgvsp: ENST00000413997.2:c.882G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590682
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590682.1:n.181G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590562
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590562.1:n.1031G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000327608
  ensembl transcript: ENST00000330475
  gene symbol: ADAMTSL5
  hgvsc: ENST00000330475.4:c.852G>A
  hgvsp: ENST00000330475.4:c.852G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000585700
  gene symbol: ADAMTSL5
  hgvsc: ENST00000585700.1:n.930G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000378850
  ensembl transcript: ENST00000395467
  gene symbol: ADAMTSL5
  hgvsc: ENST00000395467.2:c.159G>A
  hgvsp: ENST00000395467.2:c.159G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590440
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590440.1:n.890G>A
  variant of: http://identifiers.org/hgnc/27912
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16051
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2860
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2292
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4926
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12673
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3352
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7715
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1636
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6518
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2906
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4830
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10497
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3143
  bin: 7.5e0
  variant carriers: 0
hgvs: c.852G>A
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

http://identifiers.org/exac.variant/19-1507245-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1507245
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1507245
    reference: chr 19
allele count: 1
allele frequency: 9.125253225777015e-6
allele num: 109586
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590440
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590440.1:n.886T>G
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000378850
  ensembl transcript: ENST00000395467
  gene symbol: ADAMTSL5
  hgvsc: ENST00000395467.2:c.155T>G
  hgvsp: ENSP00000378850.2:p.Leu52Arg
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000399364
  ensembl transcript: ENST00000413997
  gene symbol: ADAMTSL5
  hgvsc: ENST00000413997.2:c.878T>G
  hgvsp: ENSP00000399364.2:p.Leu293Arg
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590562
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590562.1:n.1027T>G
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000585700
  gene symbol: ADAMTSL5
  hgvsc: ENST00000585700.1:n.926T>G
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590682
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590682.1:n.177T>G
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000466231
  ensembl transcript: ENST00000590090
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590090.1:c.212T>G
  hgvsp: ENSP00000466231.1:p.Leu71Arg
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000327608
  ensembl transcript: ENST00000330475
  gene symbol: ADAMTSL5
  hgvsc: ENST00000330475.4:c.848T>G
  hgvsp: ENSP00000327608.3:p.Leu283Arg
  variant of: http://identifiers.org/hgnc/27912
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 16085
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12680
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3209
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6543
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2860
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4925
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7717
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2407
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1636
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3040
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 286
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10496
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 308
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1936
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Leu283Arg
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

19-1507246-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1507246
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1507246
    reference: chr 19
allele count: 2
allele frequency: 1.824284880326912e-5
allele num: 109632
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590562
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590562.1:n.1026C>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000399364
  ensembl transcript: ENST00000413997
  gene symbol: ADAMTSL5
  hgvsc: ENST00000413997.2:c.877C>T
  hgvsp: ENST00000413997.2:c.877C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000466231
  ensembl transcript: ENST00000590090
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590090.1:c.211C>T
  hgvsp: ENST00000590090.1:c.211C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590682
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590682.1:n.176C>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000378850
  ensembl transcript: ENST00000395467
  gene symbol: ADAMTSL5
  hgvsc: ENST00000395467.2:c.154C>T
  hgvsp: ENST00000395467.2:c.154C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000585700
  gene symbol: ADAMTSL5
  hgvsc: ENST00000585700.1:n.925C>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590440
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590440.1:n.885C>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000327608
  ensembl transcript: ENST00000330475
  gene symbol: ADAMTSL5
  hgvsc: ENST00000330475.4:c.847C>T
  hgvsp: ENST00000330475.4:c.847C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27912
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12678
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16089
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6570
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1636
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3173
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2431
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2860
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7715
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4926
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2906
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 307
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3006
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7748
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Leu283Leu
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: African
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum

19-1507250-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1507250
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1507250
    reference: chr 19
allele count: 1
allele frequency: 9.115770282588878e-6
allele num: 109700
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000399364
  ensembl transcript: ENST00000413997
  gene symbol: ADAMTSL5
  hgvsc: ENST00000413997.2:c.873G>A
  hgvsp: ENST00000413997.2:c.873G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000327608
  ensembl transcript: ENST00000330475
  gene symbol: ADAMTSL5
  hgvsc: ENST00000330475.4:c.843G>A
  hgvsp: ENST00000330475.4:c.843G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590682
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590682.1:n.172G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000466231
  ensembl transcript: ENST00000590090
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590090.1:c.207G>A
  hgvsp: ENST00000590090.1:c.207G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000378850
  ensembl transcript: ENST00000395467
  gene symbol: ADAMTSL5
  hgvsc: ENST00000395467.2:c.150G>A
  hgvsp: ENST00000395467.2:c.150G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590562
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590562.1:n.1022G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590440
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590440.1:n.881G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000585700
  gene symbol: ADAMTSL5
  hgvsc: ENST00000585700.1:n.921G>A
  variant of: http://identifiers.org/hgnc/27912
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16119
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12687
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1636
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7715
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2580
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4926
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6598
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2998
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2860
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7755
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19054
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 314
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Leu281Leu
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: MQRankSum

19-1507259-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1507259
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1507259
    reference: chr 19
allele count: 1
allele frequency: 9.09487776484284e-6
allele num: 109952
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000466231
  ensembl transcript: ENST00000590090
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590090.1:c.198C>G
  hgvsp: ENST00000590090.1:c.198C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000585700
  gene symbol: ADAMTSL5
  hgvsc: ENST00000585700.1:n.912C>G
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590440
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590440.1:n.872C>G
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000327608
  ensembl transcript: ENST00000330475
  gene symbol: ADAMTSL5
  hgvsc: ENST00000330475.4:c.834C>G
  hgvsp: ENST00000330475.4:c.834C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590562
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590562.1:n.1013C>G
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000378850
  ensembl transcript: ENST00000395467
  gene symbol: ADAMTSL5
  hgvsc: ENST00000395467.2:c.141C>G
  hgvsp: ENST00000395467.2:c.141C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590682
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590682.1:n.163C>G
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000399364
  ensembl transcript: ENST00000413997
  gene symbol: ADAMTSL5
  hgvsc: ENST00000413997.2:c.864C>G
  hgvsp: ENST00000413997.2:c.864C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/27912
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2986
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7717
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6642
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2550
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12687
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16176
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4927
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1636
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2860
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3908
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19161
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2449
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4836
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Ser278Ser
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ

19-1507262-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1507262
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1507262
    reference: chr 19
allele count: 1
allele frequency: 9.088760838347299e-6
allele num: 110026
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000399364
  ensembl transcript: ENST00000413997
  gene symbol: ADAMTSL5
  hgvsc: ENST00000413997.2:c.861C>T
  hgvsp: ENST00000413997.2:c.861C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000327608
  ensembl transcript: ENST00000330475
  gene symbol: ADAMTSL5
  hgvsc: ENST00000330475.4:c.831C>T
  hgvsp: ENST00000330475.4:c.831C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000585700
  gene symbol: ADAMTSL5
  hgvsc: ENST00000585700.1:n.909C>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000378850
  ensembl transcript: ENST00000395467
  gene symbol: ADAMTSL5
  hgvsc: ENST00000395467.2:c.138C>T
  hgvsp: ENST00000395467.2:c.138C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590562
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590562.1:n.1010C>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590682
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590682.1:n.160C>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000466231
  ensembl transcript: ENST00000590090
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590090.1:c.195C>T
  hgvsp: ENST00000590090.1:c.195C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590440
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590440.1:n.869C>T
  variant of: http://identifiers.org/hgnc/27912
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7718
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16174
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3114
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6650
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2860
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2398
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4926
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12686
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1636
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2301
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 222
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19136
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2638
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4835
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Thr277Thr
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum

19-1507267-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1507267
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1507267
    reference: chr 19
allele count: 1
allele frequency: 9.07424547648863e-6
allele num: 110202
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000327608
  ensembl transcript: ENST00000330475
  gene symbol: ADAMTSL5
  hgvsc: ENST00000330475.4:c.826C>T
  hgvsp: ENSP00000327608.3:p.Pro276Ser
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590682
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590682.1:n.155C>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000466231
  ensembl transcript: ENST00000590090
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590090.1:c.190C>T
  hgvsp: ENSP00000466231.1:p.Pro64Ser
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000585700
  gene symbol: ADAMTSL5
  hgvsc: ENST00000585700.1:n.904C>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000399364
  ensembl transcript: ENST00000413997
  gene symbol: ADAMTSL5
  hgvsc: ENST00000413997.2:c.856C>T
  hgvsp: ENSP00000399364.2:p.Pro286Ser
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590440
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590440.1:n.864C>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000378850
  ensembl transcript: ENST00000395467
  gene symbol: ADAMTSL5
  hgvsc: ENST00000395467.2:c.133C>T
  hgvsp: ENSP00000378850.2:p.Pro45Ser
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590562
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590562.1:n.1005C>T
  variant of: http://identifiers.org/hgnc/27912
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2140
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16218
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4928
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2861
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7721
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1636
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6630
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12681
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3305
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3449
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7774
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19145
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Pro276Ser
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: QD

19-1507269-CCG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1507269
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1507267
    reference: chr 19
allele count: 1
allele frequency: 9.062567969259769e-6
allele num: 110344
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000466231
  ensembl transcript: ENST00000590090
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590090.1:c.186_187delCG
  hgvsp: ENSP00000466231.1:p.Gly63AlafsTer5
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590682
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590682.1:n.151_152delCG
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000327608
  ensembl transcript: ENST00000330475
  gene symbol: ADAMTSL5
  hgvsc: ENST00000330475.4:c.822_823delCG
  hgvsp: ENSP00000327608.3:p.Gly275AlafsTer5
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000585700
  gene symbol: ADAMTSL5
  hgvsc: ENST00000585700.1:n.900_901delCG
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000399364
  ensembl transcript: ENST00000413997
  gene symbol: ADAMTSL5
  hgvsc: ENST00000413997.2:c.852_853delCG
  hgvsp: ENSP00000399364.2:p.Gly285AlafsTer5
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590562
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590562.1:n.1001_1002delCG
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590440
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590440.1:n.860_861delCG
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000378850
  ensembl transcript: ENST00000395467
  gene symbol: ADAMTSL5
  hgvsc: ENST00000395467.2:c.129_130delCG
  hgvsp: ENSP00000378850.2:p.Gly44AlafsTer5
  variant of: http://identifiers.org/hgnc/27912
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1997
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12684
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6647
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7718
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16231
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3400
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2860
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1636
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4928
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19190
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2002
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7775
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3450
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Gly275AlafsTer5
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: Other
reference allele: CCG
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum

19-1507270-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1507270
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1507270
    reference: chr 19
allele count: 232
allele frequency: 2.101144761628749e-3
allele num: 110416
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590682
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590682.1:n.152G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000378850
  ensembl transcript: ENST00000395467
  gene symbol: ADAMTSL5
  hgvsc: ENST00000395467.2:c.130G>A
  hgvsp: ENSP00000378850.2:p.Gly44Arg
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000399364
  ensembl transcript: ENST00000413997
  gene symbol: ADAMTSL5
  hgvsc: ENST00000413997.2:c.853G>A
  hgvsp: ENSP00000399364.2:p.Gly285Arg
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590562
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590562.1:n.1002G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000466231
  ensembl transcript: ENST00000590090
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590090.1:c.187G>A
  hgvsp: ENSP00000466231.1:p.Gly63Arg
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000327608
  ensembl transcript: ENST00000330475
  gene symbol: ADAMTSL5
  hgvsc: ENST00000330475.4:c.823G>A
  hgvsp: ENSP00000327608.3:p.Gly275Arg
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590440
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590440.1:n.861G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000585700
  gene symbol: ADAMTSL5
  hgvsc: ENST00000585700.1:n.901G>A
  variant of: http://identifiers.org/hgnc/27912
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16211
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7682
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3413
  bin: 7.5e0
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 1.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 1.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4904
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 6619
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1929
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 9.75e1
  variant carriers: 163
genotype depth: GenotypeDepth
  all individuals: 1621
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12664
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2846
  bin: 4.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2894
  bin: 9.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Gly275Arg
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD

19-1507271-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1507271
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1507271
    reference: chr 19
allele count: 1
allele frequency: 9.050428990334141e-6
allele num: 110492
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000585700
  gene symbol: ADAMTSL5
  hgvsc: ENST00000585700.1:n.900C>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000466231
  ensembl transcript: ENST00000590090
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590090.1:c.186C>T
  hgvsp: ENST00000590090.1:c.186C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000327608
  ensembl transcript: ENST00000330475
  gene symbol: ADAMTSL5
  hgvsc: ENST00000330475.4:c.822C>T
  hgvsp: ENST00000330475.4:c.822C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590682
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590682.1:n.151C>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000399364
  ensembl transcript: ENST00000413997
  gene symbol: ADAMTSL5
  hgvsc: ENST00000413997.2:c.852C>T
  hgvsp: ENST00000413997.2:c.852C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590440
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590440.1:n.860C>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000378850
  ensembl transcript: ENST00000395467
  gene symbol: ADAMTSL5
  hgvsc: ENST00000395467.2:c.129C>T
  hgvsp: ENST00000395467.2:c.129C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590562
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590562.1:n.1001C>T
  variant of: http://identifiers.org/hgnc/27912
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1630
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3524
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1811
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16276
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6645
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7706
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4917
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12717
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2858
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1992
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3248
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19257
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7802
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1757
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ala274Ala
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: QD

19-1507272-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1507272
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1507272
    reference: chr 19
allele count: 0
allele frequency: 0.0e0
allele num: 110530
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000399364
  ensembl transcript: ENST00000413997
  gene symbol: ADAMTSL5
  hgvsc: ENST00000413997.2:c.851C>A
  hgvsp: ENSP00000399364.2:p.Ala284Asp
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000327608
  ensembl transcript: ENST00000330475
  gene symbol: ADAMTSL5
  hgvsc: ENST00000330475.4:c.821C>A
  hgvsp: ENSP00000327608.3:p.Ala274Asp
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000585700
  gene symbol: ADAMTSL5
  hgvsc: ENST00000585700.1:n.899C>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000378850
  ensembl transcript: ENST00000395467
  gene symbol: ADAMTSL5
  hgvsc: ENST00000395467.2:c.128C>A
  hgvsp: ENSP00000378850.2:p.Ala43Asp
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590562
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590562.1:n.1000C>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000466231
  ensembl transcript: ENST00000590090
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590090.1:c.185C>A
  hgvsp: ENSP00000466231.1:p.Ala62Asp
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590440
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590440.1:n.859C>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590682
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590682.1:n.150C>A
  variant of: http://identifiers.org/hgnc/27912
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3602
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1717
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12719
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6644
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1631
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16288
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2858
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7706
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4917
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 315
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19267
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1670
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ala274Asp
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum

19-1507275-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1507275
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1507275
    reference: chr 19
allele count: 1
allele frequency: 9.030650026188885e-6
allele num: 110734
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000466231
  ensembl transcript: ENST00000590090
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590090.1:c.182C>T
  hgvsp: ENSP00000466231.1:p.Ala61Val
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590440
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590440.1:n.856C>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000399364
  ensembl transcript: ENST00000413997
  gene symbol: ADAMTSL5
  hgvsc: ENST00000413997.2:c.848C>T
  hgvsp: ENSP00000399364.2:p.Ala283Val
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590682
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590682.1:n.147C>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000585700
  gene symbol: ADAMTSL5
  hgvsc: ENST00000585700.1:n.896C>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000327608
  ensembl transcript: ENST00000330475
  gene symbol: ADAMTSL5
  hgvsc: ENST00000330475.4:c.818C>T
  hgvsp: ENSP00000327608.3:p.Ala273Val
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000378850
  ensembl transcript: ENST00000395467
  gene symbol: ADAMTSL5
  hgvsc: ENST00000395467.2:c.125C>T
  hgvsp: ENSP00000378850.2:p.Ala42Val
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590562
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590562.1:n.997C>T
  variant of: http://identifiers.org/hgnc/27912
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4917
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3771
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2858
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7704
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16303
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1466
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12725
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1631
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6677
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1992
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2905
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3593
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ala273Val
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ

http://identifiers.org/exac.variant/19-1507280-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1507280
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1507280
    reference: chr 19
allele count: 1
allele frequency: 9.008846687447073e-6
allele num: 111002
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000585700
  gene symbol: ADAMTSL5
  hgvsc: ENST00000585700.1:n.891G>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000399364
  ensembl transcript: ENST00000413997
  gene symbol: ADAMTSL5
  hgvsc: ENST00000413997.2:c.843G>T
  hgvsp: ENSP00000399364.2:p.Leu281Phe
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000378850
  ensembl transcript: ENST00000395467
  gene symbol: ADAMTSL5
  hgvsc: ENST00000395467.2:c.120G>T
  hgvsp: ENSP00000378850.2:p.Leu40Phe
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000327608
  ensembl transcript: ENST00000330475
  gene symbol: ADAMTSL5
  hgvsc: ENST00000330475.4:c.813G>T
  hgvsp: ENSP00000327608.3:p.Leu271Phe
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590682
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590682.1:n.142G>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000466231
  ensembl transcript: ENST00000590090
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590090.1:c.177G>T
  hgvsp: ENSP00000466231.1:p.Leu59Phe
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590440
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590440.1:n.851G>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590562
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590562.1:n.992G>T
  variant of: http://identifiers.org/hgnc/27912
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7702
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12722
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4917
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3918
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1179
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16318
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1631
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2858
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6772
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 185
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3910
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4846
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3825
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Leu271Phe
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: DP

19-1507283-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1507283
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1507283
    reference: chr 19
allele count: 1
allele frequency: 8.992158837493705e-6
allele num: 111208
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000399364
  ensembl transcript: ENST00000413997
  gene symbol: ADAMTSL5
  hgvsc: ENST00000413997.2:c.840A>G
  hgvsp: ENST00000413997.2:c.840A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000378850
  ensembl transcript: ENST00000395467
  gene symbol: ADAMTSL5
  hgvsc: ENST00000395467.2:c.117A>G
  hgvsp: ENST00000395467.2:c.117A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000327608
  ensembl transcript: ENST00000330475
  gene symbol: ADAMTSL5
  hgvsc: ENST00000330475.4:c.810A>G
  hgvsp: ENST00000330475.4:c.810A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000466231
  ensembl transcript: ENST00000590090
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590090.1:c.174A>G
  hgvsp: ENST00000590090.1:c.174A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590440
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590440.1:n.848A>G
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590682
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590682.1:n.139A>G
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000585700
  gene symbol: ADAMTSL5
  hgvsc: ENST00000585700.1:n.888A>G
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590562
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590562.1:n.989A>G
  variant of: http://identifiers.org/hgnc/27912
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1631
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4918
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16318
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6813
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4002
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12721
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2857
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7701
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 190
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3909
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10416
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Thr270Thr
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: T
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD

19-1507293-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1507293
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1507293
    reference: chr 19
allele count: 1
allele frequency: 8.953032392071195e-6
allele num: 111694
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000399364
  ensembl transcript: ENST00000413997
  gene symbol: ADAMTSL5
  hgvsc: ENST00000413997.2:c.830C>T
  hgvsp: ENSP00000399364.2:p.Pro277Leu
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000465064
  ensembl transcript: ENST00000587828
  gene symbol: ADAMTSL5
  hgvsc: ENST00000587828.1:c.*725C>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590682
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590682.1:n.129C>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000378850
  ensembl transcript: ENST00000395467
  gene symbol: ADAMTSL5
  hgvsc: ENST00000395467.2:c.107C>T
  hgvsp: ENSP00000378850.2:p.Pro36Leu
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590440
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590440.1:n.838C>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000327608
  ensembl transcript: ENST00000330475
  gene symbol: ADAMTSL5
  hgvsc: ENST00000330475.4:c.800C>T
  hgvsp: ENSP00000327608.3:p.Pro267Leu
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000585700
  gene symbol: ADAMTSL5
  hgvsc: ENST00000585700.1:n.878C>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590562
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590562.1:n.979C>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000466231
  ensembl transcript: ENST00000590090
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590090.1:c.164C>T
  hgvsp: ENSP00000466231.1:p.Pro55Leu
  variant of: http://identifiers.org/hgnc/27912
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4068
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1631
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4918
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7701
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16334
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6946
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12723
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2857
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4125
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2903
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 722
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Pro267Leu
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

19-1507297-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1507297
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1507297
    reference: chr 19
allele count: 1
allele frequency: 8.9394264463992e-6
allele num: 111864
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000399364
  ensembl transcript: ENST00000413997
  gene symbol: ADAMTSL5
  hgvsc: ENST00000413997.2:c.826G>C
  hgvsp: ENSP00000399364.2:p.Gly276Arg
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000327608
  ensembl transcript: ENST00000330475
  gene symbol: ADAMTSL5
  hgvsc: ENST00000330475.4:c.796G>C
  hgvsp: ENSP00000327608.3:p.Gly266Arg
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000466231
  ensembl transcript: ENST00000590090
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590090.1:c.160G>C
  hgvsp: ENSP00000466231.1:p.Gly54Arg
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000585700
  gene symbol: ADAMTSL5
  hgvsc: ENST00000585700.1:n.874G>C
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000378850
  ensembl transcript: ENST00000395467
  gene symbol: ADAMTSL5
  hgvsc: ENST00000395467.2:c.103G>C
  hgvsp: ENSP00000378850.2:p.Gly35Arg
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000465064
  ensembl transcript: ENST00000587828
  gene symbol: ADAMTSL5
  hgvsc: ENST00000587828.1:c.*721G>C
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590682
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590682.1:n.125G>C
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590562
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590562.1:n.975G>C
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590440
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590440.1:n.834G>C
  variant of: http://identifiers.org/hgnc/27912
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12721
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4918
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16341
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6998
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4044
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2855
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1631
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7702
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1991
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4119
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 661
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4843
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Gly266Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: Other
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: QD

19-1507303-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1507303
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1507303
    reference: chr 19
allele count: 28
allele frequency: 2.49946440048561e-4
allele num: 112024
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000378850
  ensembl transcript: ENST00000395467
  gene symbol: ADAMTSL5
  hgvsc: ENST00000395467.2:c.97G>A
  hgvsp: ENSP00000378850.2:p.Asp33Asn
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590682
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590682.1:n.119G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590440
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590440.1:n.828G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000327608
  ensembl transcript: ENST00000330475
  gene symbol: ADAMTSL5
  hgvsc: ENST00000330475.4:c.790G>A
  hgvsp: ENSP00000327608.3:p.Asp264Asn
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590562
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590562.1:n.969G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000585700
  gene symbol: ADAMTSL5
  hgvsc: ENST00000585700.1:n.868G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000465064
  ensembl transcript: ENST00000587828
  gene symbol: ADAMTSL5
  hgvsc: ENST00000587828.1:c.*715G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000399364
  ensembl transcript: ENST00000413997
  gene symbol: ADAMTSL5
  hgvsc: ENST00000413997.2:c.820G>A
  hgvsp: ENSP00000399364.2:p.Asp274Asn
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000466231
  ensembl transcript: ENST00000590090
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590090.1:c.154G>A
  hgvsp: ENSP00000466231.1:p.Asp52Asn
  variant of: http://identifiers.org/hgnc/27912
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7700
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16332
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4914
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2851
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4038
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1628
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7064
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12719
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 9.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3452
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7821
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4139
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Asp264Asn
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD

19-1507304-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1507304
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1507304
    reference: chr 19
allele count: 5
allele frequency: 4.46149727848666e-5
allele num: 112070
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000466231
  ensembl transcript: ENST00000590090
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590090.1:c.153A>C
  hgvsp: ENST00000590090.1:c.153A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000399364
  ensembl transcript: ENST00000413997
  gene symbol: ADAMTSL5
  hgvsc: ENST00000413997.2:c.819A>C
  hgvsp: ENST00000413997.2:c.819A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590440
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590440.1:n.827A>C
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000327608
  ensembl transcript: ENST00000330475
  gene symbol: ADAMTSL5
  hgvsc: ENST00000330475.4:c.789A>C
  hgvsp: ENST00000330475.4:c.789A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000378850
  ensembl transcript: ENST00000395467
  gene symbol: ADAMTSL5
  hgvsc: ENST00000395467.2:c.96A>C
  hgvsp: ENST00000395467.2:c.96A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590682
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590682.1:n.118A>C
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000585700
  gene symbol: ADAMTSL5
  hgvsc: ENST00000585700.1:n.867A>C
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000465064
  ensembl transcript: ENST00000587828
  gene symbol: ADAMTSL5
  hgvsc: ENST00000587828.1:c.*714A>C
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590562
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590562.1:n.968A>C
  variant of: http://identifiers.org/hgnc/27912
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12718
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1628
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16336
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7080
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4918
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4036
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2851
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7713
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4846
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Arg263Arg
num of homozygotes: 0
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: FS
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

19-1507305-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1507305
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1507305
    reference: chr 19
allele count: 6
allele frequency: 5.353128011134506e-5
allele num: 112084
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000399364
  ensembl transcript: ENST00000413997
  gene symbol: ADAMTSL5
  hgvsc: ENST00000413997.2:c.818G>A
  hgvsp: ENSP00000399364.2:p.Arg273Gln
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590562
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590562.1:n.967G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000327608
  ensembl transcript: ENST00000330475
  gene symbol: ADAMTSL5
  hgvsc: ENST00000330475.4:c.788G>A
  hgvsp: ENSP00000327608.3:p.Arg263Gln
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000465064
  ensembl transcript: ENST00000587828
  gene symbol: ADAMTSL5
  hgvsc: ENST00000587828.1:c.*713G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590682
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590682.1:n.117G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000585700
  gene symbol: ADAMTSL5
  hgvsc: ENST00000585700.1:n.866G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000466231
  ensembl transcript: ENST00000590090
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590090.1:c.152G>A
  hgvsp: ENSP00000466231.1:p.Arg51Gln
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000378850
  ensembl transcript: ENST00000395467
  gene symbol: ADAMTSL5
  hgvsc: ENST00000395467.2:c.95G>A
  hgvsp: ENSP00000378850.2:p.Arg32Gln
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590440
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590440.1:n.826G>A
  variant of: http://identifiers.org/hgnc/27912
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16336
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4914
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1628
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7711
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2851
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12723
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4016
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7096
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 204
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4114
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Arg263Gln
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Latino
reference allele: C
site quality: MQ
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum

19-1507306-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1507306
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1507306
    reference: chr 19
allele count: 1
allele frequency: 8.914244963451595e-6
allele num: 112180
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000378850
  ensembl transcript: ENST00000395467
  gene symbol: ADAMTSL5
  hgvsc: ENST00000395467.2:c.94C>T
  hgvsp: ENSP00000378850.2:p.Arg32Ter
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000585700
  gene symbol: ADAMTSL5
  hgvsc: ENST00000585700.1:n.865C>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590440
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590440.1:n.825C>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000465064
  ensembl transcript: ENST00000587828
  gene symbol: ADAMTSL5
  hgvsc: ENST00000587828.1:c.*712C>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000399364
  ensembl transcript: ENST00000413997
  gene symbol: ADAMTSL5
  hgvsc: ENST00000413997.2:c.817C>T
  hgvsp: ENSP00000399364.2:p.Arg273Ter
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000466231
  ensembl transcript: ENST00000590090
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590090.1:c.151C>T
  hgvsp: ENSP00000466231.1:p.Arg51Ter
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590562
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590562.1:n.966C>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590682
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590682.1:n.116C>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000327608
  ensembl transcript: ENST00000330475
  gene symbol: ADAMTSL5
  hgvsc: ENST00000330475.4:c.787C>T
  hgvsp: ENSP00000327608.3:p.Arg263Ter
  variant of: http://identifiers.org/hgnc/27912
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3995
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4915
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7144
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12723
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2852
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16343
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1628
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7714
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1989
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg263Ter
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ClippingRankSum

http://identifiers.org/exac.variant/19-1507315-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1507315
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1507315
    reference: chr 19
allele count: 1
allele frequency: 8.887782853689319e-6
allele num: 112514
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000465064
  ensembl transcript: ENST00000587828
  gene symbol: ADAMTSL5
  hgvsc: ENST00000587828.1:c.*703G>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590562
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590562.1:n.957G>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590682
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590682.1:n.107G>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000585700
  gene symbol: ADAMTSL5
  hgvsc: ENST00000585700.1:n.856G>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590440
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590440.1:n.816G>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000399364
  ensembl transcript: ENST00000413997
  gene symbol: ADAMTSL5
  hgvsc: ENST00000413997.2:c.808G>T
  hgvsp: ENSP00000399364.2:p.Val270Phe
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000466231
  ensembl transcript: ENST00000590090
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590090.1:c.142G>T
  hgvsp: ENSP00000466231.1:p.Val48Phe
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000378850
  ensembl transcript: ENST00000395467
  gene symbol: ADAMTSL5
  hgvsc: ENST00000395467.2:c.85G>T
  hgvsp: ENSP00000378850.2:p.Val29Phe
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000327608
  ensembl transcript: ENST00000330475
  gene symbol: ADAMTSL5
  hgvsc: ENST00000330475.4:c.778G>T
  hgvsp: ENSP00000327608.3:p.Val260Phe
  variant of: http://identifiers.org/hgnc/27912
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4916
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7713
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3873
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16359
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1630
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12730
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7205
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2852
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3911
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4088
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 503
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Val260Phe
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum

19-1507315-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1507315
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1507315
    reference: chr 19
allele count: 1
allele frequency: 8.887782853689319e-6
allele num: 112514
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000585700
  gene symbol: ADAMTSL5
  hgvsc: ENST00000585700.1:n.856G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000378850
  ensembl transcript: ENST00000395467
  gene symbol: ADAMTSL5
  hgvsc: ENST00000395467.2:c.85G>A
  hgvsp: ENSP00000378850.2:p.Val29Ile
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000399364
  ensembl transcript: ENST00000413997
  gene symbol: ADAMTSL5
  hgvsc: ENST00000413997.2:c.808G>A
  hgvsp: ENSP00000399364.2:p.Val270Ile
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590682
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590682.1:n.107G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590440
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590440.1:n.816G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000327608
  ensembl transcript: ENST00000330475
  gene symbol: ADAMTSL5
  hgvsc: ENST00000330475.4:c.778G>A
  hgvsp: ENSP00000327608.3:p.Val260Ile
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000465064
  ensembl transcript: ENST00000587828
  gene symbol: ADAMTSL5
  hgvsc: ENST00000587828.1:c.*703G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000466231
  ensembl transcript: ENST00000590090
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590090.1:c.142G>A
  hgvsp: ENSP00000466231.1:p.Val48Ile
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590562
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590562.1:n.957G>A
  variant of: http://identifiers.org/hgnc/27912
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12730
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7713
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7205
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16359
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3873
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1630
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2852
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4916
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3911
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 176
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2904
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Val260Ile
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum

19-1507316-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1507316
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1507316
    reference: chr 19
allele count: 10
allele frequency: 8.885729518393461e-5
allele num: 112540
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000378850
  ensembl transcript: ENST00000395467
  gene symbol: ADAMTSL5
  hgvsc: ENST00000395467.2:c.84G>A
  hgvsp: ENST00000395467.2:c.84G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590562
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590562.1:n.956G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590682
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590682.1:n.106G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000327608
  ensembl transcript: ENST00000330475
  gene symbol: ADAMTSL5
  hgvsc: ENST00000330475.4:c.777G>A
  hgvsp: ENST00000330475.4:c.777G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590440
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590440.1:n.815G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000465064
  ensembl transcript: ENST00000587828
  gene symbol: ADAMTSL5
  hgvsc: ENST00000587828.1:c.*702G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000466231
  ensembl transcript: ENST00000590090
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590090.1:c.141G>A
  hgvsp: ENST00000590090.1:c.141G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000399364
  ensembl transcript: ENST00000413997
  gene symbol: ADAMTSL5
  hgvsc: ENST00000413997.2:c.807G>A
  hgvsp: ENST00000413997.2:c.807G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000585700
  gene symbol: ADAMTSL5
  hgvsc: ENST00000585700.1:n.855G>A
  variant of: http://identifiers.org/hgnc/27912
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7167
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16361
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2852
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3865
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4915
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7711
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12731
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1629
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 218
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3909
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 491
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4091
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Val259Val
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum

19-1507317-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1507317
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1507317
    reference: chr 19
allele count: 3
allele frequency: 2.665103139491498e-5
allele num: 112566
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000399364
  ensembl transcript: ENST00000413997
  gene symbol: ADAMTSL5
  hgvsc: ENST00000413997.2:c.806T>C
  hgvsp: ENSP00000399364.2:p.Val269Ala
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590440
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590440.1:n.814T>C
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000378850
  ensembl transcript: ENST00000395467
  gene symbol: ADAMTSL5
  hgvsc: ENST00000395467.2:c.83T>C
  hgvsp: ENSP00000378850.2:p.Val28Ala
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000466231
  ensembl transcript: ENST00000590090
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590090.1:c.140T>C
  hgvsp: ENSP00000466231.1:p.Val47Ala
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000465064
  ensembl transcript: ENST00000587828
  gene symbol: ADAMTSL5
  hgvsc: ENST00000587828.1:c.*701T>C
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000327608
  ensembl transcript: ENST00000330475
  gene symbol: ADAMTSL5
  hgvsc: ENST00000330475.4:c.776T>C
  hgvsp: ENSP00000327608.3:p.Val259Ala
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000585700
  gene symbol: ADAMTSL5
  hgvsc: ENST00000585700.1:n.854T>C
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590562
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590562.1:n.955T>C
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590682
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590682.1:n.105T>C
  variant of: http://identifiers.org/hgnc/27912
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4915
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7182
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16366
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12734
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1628
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2852
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7712
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3862
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4101
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3443
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Val259Ala
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Other
reference allele: A
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: QD

19-1507319-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1507319
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1507319
    reference: chr 19
allele count: 8
allele frequency: 7.102903311728669e-5
allele num: 112630
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000465064
  ensembl transcript: ENST00000587828
  gene symbol: ADAMTSL5
  hgvsc: ENST00000587828.1:c.*699T>C
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000585700
  gene symbol: ADAMTSL5
  hgvsc: ENST00000585700.1:n.852T>C
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000327608
  ensembl transcript: ENST00000330475
  gene symbol: ADAMTSL5
  hgvsc: ENST00000330475.4:c.774T>C
  hgvsp: ENST00000330475.4:c.774T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590682
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590682.1:n.103T>C
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000466231
  ensembl transcript: ENST00000590090
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590090.1:c.138T>C
  hgvsp: ENST00000590090.1:c.138T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000399364
  ensembl transcript: ENST00000413997
  gene symbol: ADAMTSL5
  hgvsc: ENST00000413997.2:c.804T>C
  hgvsp: ENST00000413997.2:c.804T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000378850
  ensembl transcript: ENST00000395467
  gene symbol: ADAMTSL5
  hgvsc: ENST00000395467.2:c.81T>C
  hgvsp: ENST00000395467.2:c.81T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590440
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590440.1:n.812T>C
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590562
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590562.1:n.953T>C
  variant of: http://identifiers.org/hgnc/27912
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 16365
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4914
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3832
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2852
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7710
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7180
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1628
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12733
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1989
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4089
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10405
  bin: 9.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 1.25e1
  variant carriers: 0
hgvs: p.His258His
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: Latino
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP

19-1507320-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1507320
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1507320
    reference: chr 19
allele count: 1
allele frequency: 8.878156184523599e-6
allele num: 112636
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590440
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590440.1:n.811A>G
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000585700
  gene symbol: ADAMTSL5
  hgvsc: ENST00000585700.1:n.851A>G
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590562
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590562.1:n.952A>G
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000465064
  ensembl transcript: ENST00000587828
  gene symbol: ADAMTSL5
  hgvsc: ENST00000587828.1:c.*698A>G
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000327608
  ensembl transcript: ENST00000330475
  gene symbol: ADAMTSL5
  hgvsc: ENST00000330475.4:c.773A>G
  hgvsp: ENSP00000327608.3:p.His258Arg
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000378850
  ensembl transcript: ENST00000395467
  gene symbol: ADAMTSL5
  hgvsc: ENST00000395467.2:c.80A>G
  hgvsp: ENSP00000378850.2:p.His27Arg
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000399364
  ensembl transcript: ENST00000413997
  gene symbol: ADAMTSL5
  hgvsc: ENST00000413997.2:c.803A>G
  hgvsp: ENSP00000399364.2:p.His268Arg
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000466231
  ensembl transcript: ENST00000590090
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590090.1:c.137A>G
  hgvsp: ENSP00000466231.1:p.His46Arg
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590682
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590682.1:n.102A>G
  variant of: http://identifiers.org/hgnc/27912
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7177
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2853
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12732
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7709
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3829
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1628
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16363
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4915
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 194
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4075
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 221
  bin: 2.75e1
  variant carriers: 0
hgvs: p.His258Arg
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: East Asian
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum

19-1507321-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1507321
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1507321
    reference: chr 19
allele count: 1
allele frequency: 8.877368037924116e-6
allele num: 112646
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000465064
  ensembl transcript: ENST00000587828
  gene symbol: ADAMTSL5
  hgvsc: ENST00000587828.1:c.*697C>G
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000466231
  ensembl transcript: ENST00000590090
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590090.1:c.136C>G
  hgvsp: ENSP00000466231.1:p.His46Asp
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590682
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590682.1:n.101C>G
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000378850
  ensembl transcript: ENST00000395467
  gene symbol: ADAMTSL5
  hgvsc: ENST00000395467.2:c.79C>G
  hgvsp: ENSP00000378850.2:p.His27Asp
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590440
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590440.1:n.810C>G
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000585700
  gene symbol: ADAMTSL5
  hgvsc: ENST00000585700.1:n.850C>G
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000399364
  ensembl transcript: ENST00000413997
  gene symbol: ADAMTSL5
  hgvsc: ENST00000413997.2:c.802C>G
  hgvsp: ENSP00000399364.2:p.His268Asp
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590562
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590562.1:n.951C>G
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000327608
  ensembl transcript: ENST00000330475
  gene symbol: ADAMTSL5
  hgvsc: ENST00000330475.4:c.772C>G
  hgvsp: ENSP00000327608.3:p.His258Asp
  variant of: http://identifiers.org/hgnc/27912
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2854
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4915
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7168
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1628
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7710
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12731
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16360
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3820
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 498
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3442
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 146
  bin: 1.75e1
  variant carriers: 0
hgvs: p.His258Asp
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff

19-1507322-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1507322
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1507322
    reference: chr 19
allele count: 217
allele frequency: 1.926594101248291e-3
allele num: 112634
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000399364
  ensembl transcript: ENST00000413997
  gene symbol: ADAMTSL5
  hgvsc: ENST00000413997.2:c.801G>A
  hgvsp: ENST00000413997.2:c.801G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000327608
  ensembl transcript: ENST00000330475
  gene symbol: ADAMTSL5
  hgvsc: ENST00000330475.4:c.771G>A
  hgvsp: ENST00000330475.4:c.771G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000466231
  ensembl transcript: ENST00000590090
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590090.1:c.135G>A
  hgvsp: ENST00000590090.1:c.135G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000465064
  ensembl transcript: ENST00000587828
  gene symbol: ADAMTSL5
  hgvsc: ENST00000587828.1:c.*696G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000585700
  gene symbol: ADAMTSL5
  hgvsc: ENST00000585700.1:n.849G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590562
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590562.1:n.950G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590440
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590440.1:n.809G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590682
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590682.1:n.100G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000378850
  ensembl transcript: ENST00000395467
  gene symbol: ADAMTSL5
  hgvsc: ENST00000395467.2:c.78G>A
  hgvsp: ENST00000395467.2:c.78G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27912
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4899
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 3780
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 16332
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 12710
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2835
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1618
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 7091
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 6.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 1.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 9.75e1
  variant carriers: 131
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 7679
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 5.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 209
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1979
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10524
  bin: 9.75e1
  variant carriers: 215
genotype quality: GenotypeQuality
  all individuals: 19673
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Thr257Thr
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff

19-1507323-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1507323
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1507323
    reference: chr 19
allele count: 3
allele frequency: 2.662312306982358e-5
allele num: 112684
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000327608
  ensembl transcript: ENST00000330475
  gene symbol: ADAMTSL5
  hgvsc: ENST00000330475.4:c.770C>T
  hgvsp: ENSP00000327608.3:p.Thr257Met
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000378850
  ensembl transcript: ENST00000395467
  gene symbol: ADAMTSL5
  hgvsc: ENST00000395467.2:c.77C>T
  hgvsp: ENSP00000378850.2:p.Thr26Met
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590682
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590682.1:n.99C>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590562
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590562.1:n.949C>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000466231
  ensembl transcript: ENST00000590090
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590090.1:c.134C>T
  hgvsp: ENSP00000466231.1:p.Thr45Met
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590440
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590440.1:n.808C>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000585700
  gene symbol: ADAMTSL5
  hgvsc: ENST00000585700.1:n.848C>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000399364
  ensembl transcript: ENST00000413997
  gene symbol: ADAMTSL5
  hgvsc: ENST00000413997.2:c.800C>T
  hgvsp: ENSP00000399364.2:p.Thr267Met
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000465064
  ensembl transcript: ENST00000587828
  gene symbol: ADAMTSL5
  hgvsc: ENST00000587828.1:c.*695C>T
  variant of: http://identifiers.org/hgnc/27912
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12752
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1619
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3776
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4918
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2838
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7700
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7112
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16415
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10342
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 7857
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 228
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4061
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Thr257Met
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: DP

19-1507323-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1507323
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1507323
    reference: chr 19
allele count: 1
allele frequency: 8.874374356607859e-6
allele num: 112684
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000327608
  ensembl transcript: ENST00000330475
  gene symbol: ADAMTSL5
  hgvsc: ENST00000330475.4:c.770C>G
  hgvsp: ENSP00000327608.3:p.Thr257Arg
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000466231
  ensembl transcript: ENST00000590090
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590090.1:c.134C>G
  hgvsp: ENSP00000466231.1:p.Thr45Arg
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000399364
  ensembl transcript: ENST00000413997
  gene symbol: ADAMTSL5
  hgvsc: ENST00000413997.2:c.800C>G
  hgvsp: ENSP00000399364.2:p.Thr267Arg
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590682
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590682.1:n.99C>G
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000378850
  ensembl transcript: ENST00000395467
  gene symbol: ADAMTSL5
  hgvsc: ENST00000395467.2:c.77C>G
  hgvsp: ENSP00000378850.2:p.Thr26Arg
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590440
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590440.1:n.808C>G
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590562
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590562.1:n.949C>G
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000465064
  ensembl transcript: ENST00000587828
  gene symbol: ADAMTSL5
  hgvsc: ENST00000587828.1:c.*695C>G
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000585700
  gene symbol: ADAMTSL5
  hgvsc: ENST00000585700.1:n.848C>G
  variant of: http://identifiers.org/hgnc/27912
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7112
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3776
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7700
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1619
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16415
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4918
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12752
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2838
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4061
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Thr257Arg
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD

19-1507327-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1507327
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1507327
    reference: chr 19
allele count: 6
allele frequency: 5.321979776476849e-5
allele num: 112740
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000399364
  ensembl transcript: ENST00000413997
  gene symbol: ADAMTSL5
  hgvsc: ENST00000413997.2:c.796G>A
  hgvsp: ENSP00000399364.2:p.Gly266Ser
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000378850
  ensembl transcript: ENST00000395467
  gene symbol: ADAMTSL5
  hgvsc: ENST00000395467.2:c.73G>A
  hgvsp: ENSP00000378850.2:p.Gly25Ser
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590440
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590440.1:n.804G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000585700
  gene symbol: ADAMTSL5
  hgvsc: ENST00000585700.1:n.844G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000465064
  ensembl transcript: ENST00000587828
  gene symbol: ADAMTSL5
  hgvsc: ENST00000587828.1:c.*691G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590682
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590682.1:n.95G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000327608
  ensembl transcript: ENST00000330475
  gene symbol: ADAMTSL5
  hgvsc: ENST00000330475.4:c.766G>A
  hgvsp: ENSP00000327608.3:p.Gly256Ser
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000466231
  ensembl transcript: ENST00000590090
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590090.1:c.130G>A
  hgvsp: ENSP00000466231.1:p.Gly44Ser
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590562
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590562.1:n.945G>A
  variant of: http://identifiers.org/hgnc/27912
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1620
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7700
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16434
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4918
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12749
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2837
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3690
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7017
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 220
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3445
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 568
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Gly256Ser
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: DP

19-1507328-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1507328
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1507328
    reference: chr 19
allele count: 1
allele frequency: 8.868235753179262e-6
allele num: 112762
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590562
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590562.1:n.944C>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000378850
  ensembl transcript: ENST00000395467
  gene symbol: ADAMTSL5
  hgvsc: ENST00000395467.2:c.72C>T
  hgvsp: ENST00000395467.2:c.72C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000466231
  ensembl transcript: ENST00000590090
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590090.1:c.129C>T
  hgvsp: ENST00000590090.1:c.129C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000399364
  ensembl transcript: ENST00000413997
  gene symbol: ADAMTSL5
  hgvsc: ENST00000413997.2:c.795C>T
  hgvsp: ENST00000413997.2:c.795C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590682
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590682.1:n.94C>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000465064
  ensembl transcript: ENST00000587828
  gene symbol: ADAMTSL5
  hgvsc: ENST00000587828.1:c.*690C>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000585700
  gene symbol: ADAMTSL5
  hgvsc: ENST00000585700.1:n.843C>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590440
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590440.1:n.803C>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000327608
  ensembl transcript: ENST00000330475
  gene symbol: ADAMTSL5
  hgvsc: ENST00000330475.4:c.765C>T
  hgvsp: ENST00000330475.4:c.765C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/27912
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7701
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7030
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3688
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4919
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1619
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16431
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2837
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12750
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19763
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 568
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ala255Ala
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

19-1507328-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1507328
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1507328
    reference: chr 19
allele count: 1
allele frequency: 8.868235753179262e-6
allele num: 112762
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590682
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590682.1:n.94C>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590562
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590562.1:n.944C>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000327608
  ensembl transcript: ENST00000330475
  gene symbol: ADAMTSL5
  hgvsc: ENST00000330475.4:c.765C>A
  hgvsp: ENST00000330475.4:c.765C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000378850
  ensembl transcript: ENST00000395467
  gene symbol: ADAMTSL5
  hgvsc: ENST00000395467.2:c.72C>A
  hgvsp: ENST00000395467.2:c.72C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000466231
  ensembl transcript: ENST00000590090
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590090.1:c.129C>A
  hgvsp: ENST00000590090.1:c.129C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590440
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590440.1:n.803C>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000399364
  ensembl transcript: ENST00000413997
  gene symbol: ADAMTSL5
  hgvsc: ENST00000413997.2:c.795C>A
  hgvsp: ENST00000413997.2:c.795C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000465064
  ensembl transcript: ENST00000587828
  gene symbol: ADAMTSL5
  hgvsc: ENST00000587828.1:c.*690C>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000585700
  gene symbol: ADAMTSL5
  hgvsc: ENST00000585700.1:n.843C>A
  variant of: http://identifiers.org/hgnc/27912
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12750
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1619
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16431
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3688
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4919
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7030
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2837
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7701
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 568
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3919
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ala255Ala
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP

19-1507331-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1507331
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1507331
    reference: chr 19
allele count: 11
allele frequency: 9.7531564760959e-5
allele num: 112784
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000399364
  ensembl transcript: ENST00000413997
  gene symbol: ADAMTSL5
  hgvsc: ENST00000413997.2:c.792G>A
  hgvsp: ENST00000413997.2:c.792G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000378850
  ensembl transcript: ENST00000395467
  gene symbol: ADAMTSL5
  hgvsc: ENST00000395467.2:c.69G>A
  hgvsp: ENST00000395467.2:c.69G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000465064
  ensembl transcript: ENST00000587828
  gene symbol: ADAMTSL5
  hgvsc: ENST00000587828.1:c.*687G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590682
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590682.1:n.91G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590440
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590440.1:n.800G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000466231
  ensembl transcript: ENST00000590090
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590090.1:c.126G>A
  hgvsp: ENST00000590090.1:c.126G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000585700
  gene symbol: ADAMTSL5
  hgvsc: ENST00000585700.1:n.840G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000327608
  ensembl transcript: ENST00000330475
  gene symbol: ADAMTSL5
  hgvsc: ENST00000330475.4:c.762G>A
  hgvsp: ENST00000330475.4:c.762G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590562
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590562.1:n.941G>A
  variant of: http://identifiers.org/hgnc/27912
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12744
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1067
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6953
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2836
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7704
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3661
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16441
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1619
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4918
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 19708
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2891
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7851
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4832
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 583
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ala254Ala
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: DP

19-1507332-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1507332
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1507332
    reference: chr 19
allele count: 3
allele frequency: 2.660376354574961e-5
allele num: 112766
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000465064
  ensembl transcript: ENST00000587828
  gene symbol: ADAMTSL5
  hgvsc: ENST00000587828.1:c.*686C>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000585700
  gene symbol: ADAMTSL5
  hgvsc: ENST00000585700.1:n.839C>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000378850
  ensembl transcript: ENST00000395467
  gene symbol: ADAMTSL5
  hgvsc: ENST00000395467.2:c.68C>T
  hgvsp: ENSP00000378850.2:p.Ala23Val
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000466231
  ensembl transcript: ENST00000590090
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590090.1:c.125C>T
  hgvsp: ENSP00000466231.1:p.Ala42Val
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000327608
  ensembl transcript: ENST00000330475
  gene symbol: ADAMTSL5
  hgvsc: ENST00000330475.4:c.761C>T
  hgvsp: ENSP00000327608.3:p.Ala254Val
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590440
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590440.1:n.799C>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590562
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590562.1:n.940C>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000399364
  ensembl transcript: ENST00000413997
  gene symbol: ADAMTSL5
  hgvsc: ENST00000413997.2:c.791C>T
  hgvsp: ENSP00000399364.2:p.Ala264Val
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590682
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590682.1:n.90C>T
  variant of: http://identifiers.org/hgnc/27912
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1619
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12749
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4917
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6930
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16447
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1095
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2836
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3647
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7703
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4832
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3918
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19686
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ala254Val
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD

19-1507336-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1507336
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1507336
    reference: chr 19
allele count: 6
allele frequency: 5.321507760532151e-5
allele num: 112750
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000465064
  ensembl transcript: ENST00000587828
  gene symbol: ADAMTSL5
  hgvsc: ENST00000587828.1:c.*682G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590562
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590562.1:n.936G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000378850
  ensembl transcript: ENST00000395467
  gene symbol: ADAMTSL5
  hgvsc: ENST00000395467.2:c.64G>A
  hgvsp: ENSP00000378850.2:p.Glu22Lys
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590440
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590440.1:n.795G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000327608
  ensembl transcript: ENST00000330475
  gene symbol: ADAMTSL5
  hgvsc: ENST00000330475.4:c.757G>A
  hgvsp: ENSP00000327608.3:p.Glu253Lys
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000466231
  ensembl transcript: ENST00000590090
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590090.1:c.121G>A
  hgvsp: ENSP00000466231.1:p.Glu41Lys
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000590682
  gene symbol: ADAMTSL5
  hgvsc: ENST00000590682.1:n.86G>A
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000399364
  ensembl transcript: ENST00000413997
  gene symbol: ADAMTSL5
  hgvsc: ENST00000413997.2:c.787G>A
  hgvsp: ENSP00000399364.2:p.Glu263Lys
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000185761
  ensembl transcript: ENST00000585700
  gene symbol: ADAMTSL5
  hgvsc: ENST00000585700.1:n.835G>A
  variant of: http://identifiers.org/hgnc/27912
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7703
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3616
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 16458
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1156
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6832
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1619
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4919
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2836
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12742
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 661
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4067
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 264
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19620
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Glu253Lys
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum

19-1507341-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1507341
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 1507341
    reference: chr 19
allele count: 2
allele frequency: 1.776609163750067e-5
allele num: 112574
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000465064
  ensembl transcript: ENST00000587828
  gene symbol: ADAMTSL5
  hgvsc: ENST00000587828.1:c.*677C>T
  variant of: http://identifiers.org/hgnc/27912
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000185761
  ensembl protein: ENSP00000378850
  ensembl transcript: ENST00000395467
  gene symbol: ADAMTSL5
  hgvsc: ENST00000395467.2:c.59C>T
  hgvsp: ENSP00000378850.2:p.Thr20Ile
  variant of: http://identifiers.org/hgnc/27912
canonical: true
consequence: missense
filter: PASS
hgvs: p.Thr251Ile
num of homozygotes: 0
reference allele: G

GenotypeQuality
all individuals: 350
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3450
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 242
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 388
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 365
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 379
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 969
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3832
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 386
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 237
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1636
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 328
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 582
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 164
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7652
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.85143997718848e-4
allele num: 7014
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.43e-1

VQSLOD
type: SiteQuality
SIO_000300: -8.702e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.63e-1

QD
type: SiteQuality
SIO_000300: 1.498e1

FS
type: SiteQuality
SIO_000300: 8.042e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.97e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.99e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.2e-1

DP
type: SiteQuality
SIO_000300: 3.38797e5

GenotypeQuality
all individuals: 1156
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 969
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30738
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 350
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 237
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4771
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 937
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 365
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 388
bin: 9.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 328
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7014
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1636
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 164
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 582
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7652
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.99e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.63e-1

DP
type: SiteQuality
SIO_000300: 3.38797e5

MQRankSum
type: SiteQuality
SIO_000300: 1.43e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.97e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -7.2e-1

VQSLOD
type: SiteQuality
SIO_000300: -8.702e-1

FS
type: SiteQuality
SIO_000300: 8.042e0

QD
type: SiteQuality
SIO_000300: 1.498e1

GenotypeQuality
all individuals: 102
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 371
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 355
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 348
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 392
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 383
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 135
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 947
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3919
bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 28
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 332
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 166
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7660
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7038
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1644
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.76e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.29e-1

DP
type: SiteQuality
SIO_000300: 3.3966e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.74e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.61e-1

FS
type: SiteQuality
SIO_000300: 2.105e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.28e0

QD
type: SiteQuality
SIO_000300: 2.62e0

VQSLOD
type: SiteQuality
SIO_000300: -1.992e0

GenotypeQuality
all individuals: 223
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3961
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2954
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 31113
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4750
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 371
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 371
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 333
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 409
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1628
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 318
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 168
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7698
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 26
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.420454545454545e-4
allele num: 7040
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.88e-2

DP
type: SiteQuality
SIO_000300: 3.3665e5

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.96e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.2e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.074e0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 7.43e0

GenotypeQuality
all individuals: 347
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 404
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 90
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 822
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3230
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 331
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 260
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3986
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 990
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 213
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 105
bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 168
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 322
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.295672454003628e-4
allele num: 7718
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1594
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 22
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6944
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.824817518248175e-3
allele num: 548
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.607e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.62e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.920000000000001e-2

DP
type: SiteQuality
SIO_000300: 3.34436e5

QD
type: SiteQuality
SIO_000300: 2.049e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.4e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.92e-1

FS
type: SiteQuality
SIO_000300: 1.6965e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.4e-1

MQ
type: SiteQuality
SIO_000300: 5.855e1

GenotypeQuality
all individuals: 1010
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 195
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 331
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31210
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 754
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 270
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4119
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 409
bin: 9.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 26
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1622
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 172
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7032
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 320
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7730
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -6.671e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.04e0

FS
type: SiteQuality
SIO_000300: 9.249000000000001e0

QD
type: SiteQuality
SIO_000300: 7.7e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.84e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.286e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.29e-1

DP
type: SiteQuality
SIO_000300: 3.34126e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.84e-2

GenotypeQuality
all individuals: 52
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1024
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4162
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 423
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 30881
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 190
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 410
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2777
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 84
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4041
bin: 2.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 320
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 26
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 536
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1622
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7742
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 174
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7036
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.23e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.58e-1

DP
type: SiteQuality
SIO_000300: 3.29769e5

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.23e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 6.91e0

VQSLOD
type: SiteQuality
SIO_000300: -2.064e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.84e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.231e0

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

GenotypeQuality
all individuals: 545
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1090
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4551
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 454
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 119
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29462
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 424
bin: 9.75e1
variant carriers: 11

GenotypeQuality
all individuals: 415
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 439
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 281
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 8.476970895733258e-4
allele num: 7078
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 18
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 328
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 180
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 2.56278831368529e-4
allele num: 7804
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 526
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.21e-1

FS
type: SiteQuality
SIO_000300: 1.909e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.98e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.31e0

QD
type: SiteQuality
SIO_000300: 1.512e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.06e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.067e0

DP
type: SiteQuality
SIO_000300: 3.19886e5

ClippingRankSum
type: SiteQuality
SIO_000300: 3.58e-1

GenotypeQuality
all individuals: 28809
bin: 7.5e0
variant carriers: 3

GenotypeQuality
all individuals: 4599
bin: 6.25e1
variant carriers: 2

GenotypeQuality
all individuals: 119
bin: 8.75e1
variant carriers: 2

GenotypeQuality
all individuals: 441
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 265
bin: 2.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1096
bin: 6.75e1
variant carriers: 4

GenotypeQuality
all individuals: 113
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 239
bin: 3.25e1
variant carriers: 2

GenotypeQuality
all individuals: 283
bin: 8.25e1
variant carriers: 2

GenotypeQuality
all individuals: 64
bin: 4.75e1
variant carriers: 2

GenotypeQuality
all individuals: 149
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 464
bin: 9.75e1
variant carriers: 58

GenotypeQuality
all individuals: 56
bin: 4.25e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16
num of homozygotes: 0

African
type: Population
allele count: 58
allele frequency: 3.460620525059666e-2
allele num: 1676
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7074
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7810
num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 178
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.34e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.969999999999999e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 4.67e0

QD
type: SiteQuality
SIO_000300: 1.391e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.04e-1

DP
type: SiteQuality
SIO_000300: 3.17857e5

MQRankSum
type: SiteQuality
SIO_000300: 2.22e-1

GenotypeQuality
all individuals: 132
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 424
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 225
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 459
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 436
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1105
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4707
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2197
bin: 2.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7816
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 5.88235294117647e-4
allele num: 1700
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 182
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7098
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 322
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 18
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -5.33e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.05e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.457e0

FS
type: SiteQuality
SIO_000300: 4.123e0

QD
type: SiteQuality
SIO_000300: 7.34e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.91e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.62e-1

DP
type: SiteQuality
SIO_000300: 3.13183e5

MQ
type: SiteQuality
SIO_000300: 5.911e1

VQSLOD
type: SiteQuality
SIO_000300: -1.704e0

GenotypeQuality
all individuals: 44
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 251
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 3265
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 25568
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 299
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 460
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 197
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5155
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1160
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 342
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 26
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 568
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7858
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1794
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 182
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7282
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.38e0

MQRankSum
type: SiteQuality
SIO_000300: -1.56e-1

DP
type: SiteQuality
SIO_000300: 3.08119e5

QD
type: SiteQuality
SIO_000300: 1.097e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.04e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.11e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.7e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.2e-1

GenotypeQuality
all individuals: 151
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 40
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1026
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1188
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 298
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3571
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 470
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 426
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 446
bin: 7.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 350
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7570
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 184
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.272912423625254e-4
allele num: 7856
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1898
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.48e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.729999999999999e-2

DP
type: SiteQuality
SIO_000300: 2.97674e5

BaseQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.122e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.14e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.14e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

FS
type: SiteQuality
SIO_000300: 7.091e0

GenotypeQuality
all individuals: 137
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 446
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19541
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1198
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 426
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5628
bin: 6.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7854
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1900
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 574
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7580
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 348
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 184
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.466e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.74e-2

MQRankSum
type: SiteQuality
SIO_000300: -5.5e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.5e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.754e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.5e-1

QD
type: SiteQuality
SIO_000300: 5.29e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.9661e5

GenotypeQuality
all individuals: 446
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18634
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 960
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 300
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 471
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 427
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 40
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1205
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 352
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 574
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.317523056653491e-4
allele num: 7590
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1922
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.273236567354214e-4
allele num: 7854
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 184
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.61e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 5.19e-1

QD
type: SiteQuality
SIO_000300: 1.181e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.05e0

MQRankSum
type: SiteQuality
SIO_000300: -5.19e-1

FS
type: SiteQuality
SIO_000300: 1.425e0

VQSLOD
type: SiteQuality
SIO_000300: -1.976e0

MQ
type: SiteQuality
SIO_000300: 5.935e1

DP
type: SiteQuality
SIO_000300: 2.94637e5

BaseQRankSum
type: SiteQuality
SIO_000300: 1.66e0

GenotypeQuality
all individuals: 17581
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1157
bin: 2.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 2675
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 441
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 424
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 29
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 302
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1193
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5504
bin: 6.25e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 1
allele frequency: 2.631578947368421e-2
allele num: 38
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7548
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1878
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 342
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 178
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7832
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.053e1

VQSLOD
type: SiteQuality
SIO_000300: -1.666e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.79e-2

FS
type: SiteQuality
SIO_000300: 2.511e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.82e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.76e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.31e-1

DP
type: SiteQuality
SIO_000300: 2.88052e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.31e-1

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

GenotypeQuality
all individuals: 44
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 29
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 441
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17581
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2675
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 145
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 424
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1193
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5504
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1878
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 5.617977528089887e-3
allele num: 178
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 342
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7548
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 38
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7832
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.88052e5

BaseQRankSum
type: SiteQuality
SIO_000300: -5.82e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.31e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.31e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.79e-2

FS
type: SiteQuality
SIO_000300: 2.511e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.76e-1

QD
type: SiteQuality
SIO_000300: 1.053e1

VQSLOD
type: SiteQuality
SIO_000300: -1.666e0

GenotypeQuality
all individuals: 296
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4977
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16450
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 434
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1142
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 184
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 53
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1178
bin: 2.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7326
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 172
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.279754287176862e-4
allele num: 7814
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 40
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1808
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 330
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 546
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -5.15e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.53e-1

QD
type: SiteQuality
SIO_000300: 1.208e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.51e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.315e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.59e-2

DP
type: SiteQuality
SIO_000300: 2.79373e5

BaseQRankSum
type: SiteQuality
SIO_000300: -1.259e0

FS
type: SiteQuality
SIO_000300: 9.1e-1

MQ
type: SiteQuality
SIO_000300: 5.946e1

GenotypeQuality
all individuals: 96
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 987
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 419
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 301
bin: 3.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.280409731113956e-4
allele num: 7810
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7110
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 538
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 168
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 312
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1774
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 2.28e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.82e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.48e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.96e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.638e0

QD
type: SiteQuality
SIO_000300: 1.41e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.5e-2

MQ
type: SiteQuality
SIO_000300: 5.903e1

DP
type: SiteQuality
SIO_000300: 2.73432e5

GenotypeQuality
all individuals: 478
bin: 1.25e1
variant carriers: 1

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 296
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7804
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 308
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 6.195786864931846e-4
allele num: 1614
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 168
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.505253677574302e-4
allele num: 6662
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.361e0

MQRankSum
type: SiteQuality
SIO_000300: -4.27e-1

DP
type: SiteQuality
SIO_000300: 2.82283e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.72e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.172e0

QD
type: SiteQuality
SIO_000300: 1.63e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.15e0

FS
type: SiteQuality
SIO_000300: 9.954000000000001e0

MQ
type: SiteQuality
SIO_000300: 5.739e1

VQSLOD
type: SiteQuality
SIO_000300: -6.506999999999999e-1

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 523
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 170
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variant carriers: 0

GenotypeQuality
all individuals: 327
bin: 4.25e1
variant carriers: 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: 6230
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.006846556584777e-4
allele num: 9932
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9004
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62368
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.483e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.365e0

DP
type: SiteQuality
SIO_000300: 1.809867e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.9e-3

MQRankSum
type: SiteQuality
SIO_000300: 2.61e0

QD
type: SiteQuality
SIO_000300: 1.433e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.93e-1

MQ
type: SiteQuality
SIO_000300: 5.866e1

FS
type: SiteQuality
SIO_000300: 3.68e0

GenotypeQuality
all individuals: 486
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2003
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 163
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 7400
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GenotypeQuality
all individuals: 10519
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1024
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variant carriers: 0

GenotypeQuality
all individuals: 2902
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3386
bin: 7.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9928
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62368
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.531904874028726e-4
allele num: 8494
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9012
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6246
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.332e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.22e0

MQ
type: SiteQuality
SIO_000300: 5.951e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.5e-3

VQSLOD
type: SiteQuality
SIO_000300: 8.59e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.13e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.19e-1

DP
type: SiteQuality
SIO_000300: 1.809944e6

FS
type: SiteQuality
SIO_000300: 1.82e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.47e-1

GenotypeQuality
all individuals: 440
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 563
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3429
bin: 7.5e0
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7500
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4796
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variant carriers: 0

GenotypeQuality
all individuals: 368
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variant carriers: 0

GenotypeQuality
all individuals: 537
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variant carriers: 0

GenotypeQuality
all individuals: 33
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variant carriers: 0

GenotypeQuality
all individuals: 3901
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variant carriers: 0

GenotypeQuality
all individuals: 164
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1995
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9934
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9012
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11430
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6262
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.602255976414792e-5
allele num: 62412
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.888e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.22e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.219e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.88e-1

QD
type: SiteQuality
SIO_000300: 7.82e0

MQRankSum
type: SiteQuality
SIO_000300: 7.86e-1

DP
type: SiteQuality
SIO_000300: 1.818467e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.444e0

GenotypeQuality
all individuals: 430
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 354
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variant carriers: 0

GenotypeQuality
all individuals: 10514
bin: 9.75e1
variant carriers: 16

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1993
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GenotypeQuality
all individuals: 16993
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variant carriers: 0

GenotypeQuality
all individuals: 530
bin: 3.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6260
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9014
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 16
allele frequency: 2.56492465533825e-4
allele num: 62380
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9926
num of homozygotes: 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: 8496
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.604e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.3e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.8e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.91e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.72e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.6e-3

QD
type: SiteQuality
SIO_000300: 1.441e1

MQ
type: SiteQuality
SIO_000300: 5.956e1

DP
type: SiteQuality
SIO_000300: 1.819568e6

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9936
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11438
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6290
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9014
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.601845325815339e-5
allele num: 62428
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.53e-1

QD
type: SiteQuality
SIO_000300: 2.287e1

DP
type: SiteQuality
SIO_000300: 1.823608e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.4e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.92e0

MQ
type: SiteQuality
SIO_000300: 5.273e1

MQRankSum
type: SiteQuality
SIO_000300: -2.8e0

VQSLOD
type: SiteQuality
SIO_000300: -8.202e-1

GenotypeQuality
all individuals: 307
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1996
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 4798
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.600717121270329e-5
allele num: 62472
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6300
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9018
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9948
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -9.929e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.8e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.855e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.64e0

MQ
type: SiteQuality
SIO_000300: 5.245e1

QD
type: SiteQuality
SIO_000300: 2.252e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.93e-1

DP
type: SiteQuality
SIO_000300: 1.824992e6

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

GenotypeQuality
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GenotypeQuality
all individuals: 114
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GenotypeQuality
all individuals: 7586
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GenotypeQuality
all individuals: 17587
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GenotypeQuality
all individuals: 1996
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variant carriers: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.741258741258741e-5
allele num: 11440
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8494
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.200204813108039e-5
allele num: 62496
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6304
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9956
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.800000000000001e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.7e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.83e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.48e0

QD
type: SiteQuality
SIO_000300: 1.505e1

VQSLOD
type: SiteQuality
SIO_000300: 3.56e0

DP
type: SiteQuality
SIO_000300: 1.826329e6

MQ
type: SiteQuality
SIO_000300: 5.942e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.7e-1

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 3

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2903
bin: 9.25e1
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GenotypeQuality
all individuals: 114
bin: 4.25e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6304
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.800307219662058e-5
allele num: 62496
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9956
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8494
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.48e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.800000000000001e-3

QD
type: SiteQuality
SIO_000300: 1.505e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.7e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.7e-1

MQ
type: SiteQuality
SIO_000300: 5.942e1

DP
type: SiteQuality
SIO_000300: 1.826329e6

MQRankSum
type: SiteQuality
SIO_000300: 2.83e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.56e0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.177301624676242e-4
allele num: 8494
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11442
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9024
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6336
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62540
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9962
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.319261213720317e-3
allele num: 758
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.99e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.2e-1

MQ
type: SiteQuality
SIO_000300: 5.979e1

DP
type: SiteQuality
SIO_000300: 1.829664e6

QD
type: SiteQuality
SIO_000300: 1.44e1

FS
type: SiteQuality
SIO_000300: 1.542e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

VQSLOD
type: SiteQuality
SIO_000300: 9.13e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.79e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.53e-1

GenotypeQuality
all individuals: 3900
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9028
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62576
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9966
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11448
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.355157795572303e-4
allele num: 8492
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6360
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -1.148e0

FS
type: SiteQuality
SIO_000300: 1.1387e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.82e-1

MQ
type: SiteQuality
SIO_000300: 5.959e1

QD
type: SiteQuality
SIO_000300: 1.484e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.32e0

DP
type: SiteQuality
SIO_000300: 1.831788e6

MQRankSum
type: SiteQuality
SIO_000300: -8.500000000000001e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.71e-1

GenotypeQuality
all individuals: 36
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 2

GenotypeQuality
all individuals: 137
bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.192949966474025e-5
allele num: 62638
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9984
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 766
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6398
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8494
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11450
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9042
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.4e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.01e-1

QD
type: SiteQuality
SIO_000300: 1.215e1

MQRankSum
type: SiteQuality
SIO_000300: 1.74e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.835527e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.56e0

VQSLOD
type: SiteQuality
SIO_000300: 5.81e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 7651
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10504
bin: 9.75e1
variant carriers: 5

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 44
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GenotypeQuality
all individuals: 226
bin: 2.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6404
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9992
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62664
num of homozygotes: 0

East Asian
type: Population
allele count: 4
allele frequency: 4.709206498704968e-4
allele num: 8494
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.104972375690608e-4
allele num: 9050
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11452
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 766
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.137e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.06e-1

QD
type: SiteQuality
SIO_000300: 1.395e1

MQ
type: SiteQuality
SIO_000300: 5.944e1

VQSLOD
type: SiteQuality
SIO_000300: 1.57e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.9e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -3.176e0

MQRankSum
type: SiteQuality
SIO_000300: -8.3e-2

DP
type: SiteQuality
SIO_000300: 1.837122e6

ClippingRankSum
type: SiteQuality
SIO_000300: -8.46e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10040
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 768
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11456
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.182888789865682e-5
allele num: 62836
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6482
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8496
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9074
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VQSLOD
type: SiteQuality
SIO_000300: -1.744e0

MQ
type: SiteQuality
SIO_000300: 5.751e1

QD
type: SiteQuality
SIO_000300: 1.064e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.5e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 1.9e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.31e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.68e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.772e0

FS
type: SiteQuality
SIO_000300: 1.188e0

DP
type: SiteQuality
SIO_000300: 1.844523e6

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.589370291490511e-5
allele num: 62918
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11462
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9090
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 770
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10056
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.09e0

DP
type: SiteQuality
SIO_000300: 1.847169e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.4e-3

VQSLOD
type: SiteQuality
SIO_000300: 9.340000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.475e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.48e0

FS
type: SiteQuality
SIO_000300: 1.181e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.39e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.39e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8500
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63004
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6514
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 772
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.722958827634333e-5
allele num: 11464
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.932459276916965e-5
allele num: 10068
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9128
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.43e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.096e0

MQ
type: SiteQuality
SIO_000300: 5.948e1

FS
type: SiteQuality
SIO_000300: 5.31e-1

QD
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 6.98e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.11e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.04e0

DP
type: SiteQuality
SIO_000300: 1.84956e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 57
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 32
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 3435
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10074
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6516
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11464
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 772
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.586797841954935e-5
allele num: 63020
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.0e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.26e0

FS
type: SiteQuality
SIO_000300: 1.3682e1

DP
type: SiteQuality
SIO_000300: 1.849948e6

VQSLOD
type: SiteQuality
SIO_000300: -2.087e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.8e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.692e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.99e-1

QD
type: SiteQuality
SIO_000300: 1.274e1

MQ
type: SiteQuality
SIO_000300: 5.875e1

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9150
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 776
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10082
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.585087496829825e-5
allele num: 63088
num of homozygotes: 0

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11466
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.62e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.1e-3

QD
type: SiteQuality
SIO_000300: 1.179e1

MQ
type: SiteQuality
SIO_000300: 5.933e1

FS
type: SiteQuality
SIO_000300: 2.5928e1

VQSLOD
type: SiteQuality
SIO_000300: -4.184e0

MQRankSum
type: SiteQuality
SIO_000300: -6.36e-1

DP
type: SiteQuality
SIO_000300: 1.852088e6

ClippingRankSum
type: SiteQuality
SIO_000300: 4.63e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.9e-2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 9158
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6526
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11466
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.584334104375931e-5
allele num: 63118
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 776
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.9147332936744e-5
allele num: 10086
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.86e0

QD
type: SiteQuality
SIO_000300: 1.139e1

DP
type: SiteQuality
SIO_000300: 1.852653e6

MQ
type: SiteQuality
SIO_000300: 5.976e1

FS
type: SiteQuality
SIO_000300: 6.45e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.9e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.283e0

MQRankSum
type: SiteQuality
SIO_000300: 9.69e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.88e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.137e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63162
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11466
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10096
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 1.091941471937104e-4
allele num: 9158
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 776
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.3e-3

VQSLOD
type: SiteQuality
SIO_000300: -8.881e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.36e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.54e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.899e0

DP
type: SiteQuality
SIO_000300: 1.854835e6

MQ
type: SiteQuality
SIO_000300: 5.833e1

QD
type: SiteQuality
SIO_000300: 1.568e1

MQRankSum
type: SiteQuality
SIO_000300: 7.099999999999999e-2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 25
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variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.175364362952515e-4
allele num: 8508
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11466
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9254
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63274
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 778
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10114
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6558
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.1066e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.06e0

VQSLOD
type: SiteQuality
SIO_000300: -1.281e0

QD
type: SiteQuality
SIO_000300: 1.081e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.26e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.3e-3

MQRankSum
type: SiteQuality
SIO_000300: 4.52e-1

DP
type: SiteQuality
SIO_000300: 1.859678e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.31e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 1.077121930202499e-4
allele num: 9284
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11466
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 778
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63304
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8508
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.36e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.13e0

MQ
type: SiteQuality
SIO_000300: 5.981e1

VQSLOD
type: SiteQuality
SIO_000300: 3.77e-1

MQRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.212e1

FS
type: SiteQuality
SIO_000300: 4.249e0

DP
type: SiteQuality
SIO_000300: 1.860915e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.2e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.897e0

GenotypeQuality
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variant carriers: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11470
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8520
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.578880889225717e-5
allele num: 63336
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9392
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10138
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6564
num of homozygotes: 0

Other
type: Population
allele count: 0
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num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.39e-1

VQSLOD
type: SiteQuality
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BaseQRankSum
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MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 2.612e0

MQ
type: SiteQuality
SIO_000300: 5.919e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-3

DP
type: SiteQuality
SIO_000300: 1.86362e6

QD
type: SiteQuality
SIO_000300: 1.402e1

GenotypeQuality
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variant carriers: 0

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

East Asian
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allele count: 1
allele frequency: 1.172332942555686e-4
allele num: 8530
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6564
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63382
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11472
num of homozygotes: 0

Other
type: Population
allele count: 0
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allele num: 782
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.86e-1

DP
type: SiteQuality
SIO_000300: 1.865092e6

MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.93e1

VQSLOD
type: SiteQuality
SIO_000300: 1.3e-1

FS
type: SiteQuality
SIO_000300: 2.095e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.34e-1

GenotypeQuality
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variant carriers: 2

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

African
type: Population
allele count: 5
allele frequency: 4.928050463236743e-4
allele num: 10146
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 4
allele frequency: 6.091989034419738e-4
allele num: 6566
num of homozygotes: 0

Latino
type: Population
allele count: 11
allele frequency: 9.590235396687009e-4
allele num: 11470
num of homozygotes: 0

East Asian
type: Population
allele count: 1
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allele num: 8534
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Other
type: Population
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allele frequency: 1.278772378516624e-3
allele num: 782
num of homozygotes: 0

South Asian
type: Population
allele count: 77
allele frequency: 8.091635140815468e-3
allele num: 9516
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European (Non-Finnish)
type: Population
allele count: 133
allele frequency: 2.097725623797357e-3
allele num: 63402
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.97e1

BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.885142e6

FS
type: SiteQuality
SIO_000300: 5.36e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -2.38e-1

ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 2.8e-1

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
type: Population
allele count: 0
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allele num: 9570
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10152
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11470
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.576839383140433e-5
allele num: 63418
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8532
num of homozygotes: 0

European (Finnish)
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allele count: 0
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Other
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ClippingRankSum
type: SiteQuality
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DP
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ReadPosRankSum
type: SiteQuality
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BaseQRankSum
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InbreedingCoeff
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SIO_000300: -1.6e-3

MQRankSum
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FS
type: SiteQuality
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MQ
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VQSLOD
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QD
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

Other
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allele frequency: 0.0e0
allele num: 786
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11470
num of homozygotes: 0

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

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 8536
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 63438
num of homozygotes: 0

FS
type: SiteQuality
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MQ
type: SiteQuality
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InbreedingCoeff
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SIO_000300: -2.3e-3

VQSLOD
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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DP
type: SiteQuality
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QD
type: SiteQuality
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ReadPosRankSum
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SIO_000300: 3.61e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10166
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.574803149606299e-5
allele num: 63500
num of homozygotes: 0

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

South Asian
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allele frequency: 0.0e0
allele num: 9862
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11472
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10186
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6564
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Other
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8556
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.573069057731634e-5
allele num: 63570
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.032e0

ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -4.438e-1

MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 3.294e0

MQ
type: SiteQuality
SIO_000300: 5.979e1

BaseQRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.139e1

DP
type: SiteQuality
SIO_000300: 1.872744e6

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

Latino
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allele count: 1
allele frequency: 8.712319219376198e-5
allele num: 11478
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6566
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10196
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 63634
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8562
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ReadPosRankSum
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InbreedingCoeff
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.981e1

MQRankSum
type: SiteQuality
SIO_000300: 9.429999999999999e-1

FS
type: SiteQuality
SIO_000300: 7.68e-1

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 9.790483649892304e-5
allele num: 10214
num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 800
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 10288
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 63768
num of homozygotes: 0

VQSLOD
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BaseQRankSum
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InbreedingCoeff
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QD
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MQRankSum
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FS
type: SiteQuality
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MQ
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ClippingRankSum
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DP
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

European (Non-Finnish)
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allele frequency: 1.56710336613803e-5
allele num: 63812
num of homozygotes: 0

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

Latino
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Other
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African
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European (Non-Finnish)
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allele frequency: 4.385964912280702e-4
allele num: 63840
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European (Finnish)
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East Asian
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FS
type: SiteQuality
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VQSLOD
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DP
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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ReadPosRankSum
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ClippingRankSum
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MQ
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele num: 10216
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Latino
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num of homozygotes: 0

European (Non-Finnish)
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European (Finnish)
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East Asian
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South Asian
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FS
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DP
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MQ
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VQSLOD
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MQRankSum
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InbreedingCoeff
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ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 6
allele frequency: 9.397024275646045e-5
allele num: 63850
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10218
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6572
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.978e1

DP
type: SiteQuality
SIO_000300: 1.882192e6

QD
type: SiteQuality
SIO_000300: 1.255e1

VQSLOD
type: SiteQuality
SIO_000300: 1.1e0

InbreedingCoeff
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SIO_000300: -8.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 1.47e0

MQRankSum
type: SiteQuality
SIO_000300: 6.17e-1

FS
type: SiteQuality
SIO_000300: 1.118e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.03e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.24e0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8580
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 63872
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6574
num of homozygotes: 0

African
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allele frequency: 0.0e0
allele num: 10218
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11488
num of homozygotes: 0

South Asian
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allele frequency: 9.391435011269723e-5
allele num: 10648
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.936e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.06e-1

MQRankSum
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BaseQRankSum
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SIO_000300: -1.289e0

InbreedingCoeff
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SIO_000300: -5.999999999999999e-4

QD
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VQSLOD
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SIO_000300: -2.519e0

FS
type: SiteQuality
SIO_000300: 2.216e0

DP
type: SiteQuality
SIO_000300: 1.882461e6

ClippingRankSum
type: SiteQuality
SIO_000300: 6.1e-2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 10222
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11488
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 10854
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
allele num: 810
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.562988433885589e-5
allele num: 63980
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.67e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

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

DP
type: SiteQuality
SIO_000300: 1.884386e6

VQSLOD
type: SiteQuality
SIO_000300: 6.66e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.49e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8586
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10222
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6574
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.213193292795283e-5
allele num: 10854
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63980
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11488
num of homozygotes: 0

Other
type: Population
allele count: 0
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allele num: 810
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -4.67e-1

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.295e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.49e-1

BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.884386e6

FS
type: SiteQuality
SIO_000300: 4.51e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.67e-1

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8586
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11490
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63984
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10224
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South Asian
type: Population
allele count: 10
allele frequency: 9.201324990798675e-4
allele num: 10868
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 810
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6578
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.0e0

VQSLOD
type: SiteQuality
SIO_000300: 9.88e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.11e-1

MQ
type: SiteQuality
SIO_000300: 5.975e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.77e-1

QD
type: SiteQuality
SIO_000300: 1.127e1

FS
type: SiteQuality
SIO_000300: 5.53e-1

DP
type: SiteQuality
SIO_000300: 1.884559e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.867e0

GenotypeQuality
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variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8586
num of homozygotes: 0

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

European (Non-Finnish)
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allele frequency: 4.688672168042011e-5
allele num: 63984
num of homozygotes: 0

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

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

Other
type: Population
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num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.426e0

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

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

European (Non-Finnish)
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African
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East Asian
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Other
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Latino
type: Population
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South Asian
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allele frequency: 7.313951362223441e-4
allele num: 10938
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
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ClippingRankSum
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MQ
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BaseQRankSum
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MQRankSum
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QD
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VQSLOD
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DP
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

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

African
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European (Non-Finnish)
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European (Finnish)
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East Asian
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Other
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South Asian
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allele num: 10948
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.9e-2

FS
type: SiteQuality
SIO_000300: 9.17e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.66e0

MQ
type: SiteQuality
SIO_000300: 5.971e1

MQRankSum
type: SiteQuality
SIO_000300: -1.299e0

QD
type: SiteQuality
SIO_000300: 1.914e1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.14e-1

DP
type: SiteQuality
SIO_000300: 1.884256e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.55e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

GenotypeQuality
all individuals: 520
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 230
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4018
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 184
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3432
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 5.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 7817
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 3.75e1
variant carriers: 2

GenotypeQuality
all individuals: 4829
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2885
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3901
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 31
allele frequency: 4.711246200607902e-3
allele num: 6580
num of homozygotes: 0

Latino
type: Population
allele count: 46
allele frequency: 4.002784545770972e-3
allele num: 11492
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 116
allele frequency: 1.812613288330521e-3
allele num: 63996
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10228
num of homozygotes: 0

South Asian
type: Population
allele count: 24
allele frequency: 2.193383293730579e-3
allele num: 10942
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8588
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 808
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.39e0

VQSLOD
type: SiteQuality
SIO_000300: 4.26e0

QD
type: SiteQuality
SIO_000300: 1.26e1

FS
type: SiteQuality
SIO_000300: 5.600000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.04e-1

DP
type: SiteQuality
SIO_000300: 1.899493e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.29e-1

MQ
type: SiteQuality
SIO_000300: 5.971e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.76e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.7e-3

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

GenotypeQuality
all individuals: 99
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19809
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 516
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3917
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4844
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3448
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1986
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2891
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 208
bin: 3.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10228
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.685742846432588e-5
allele num: 64024
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11492
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 810
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8592
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10960
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.92e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.13e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.2e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -3.61e-1

QD
type: SiteQuality
SIO_000300: 1.219e1

MQ
type: SiteQuality
SIO_000300: 5.995e1

FS
type: SiteQuality
SIO_000300: 3.478e0

VQSLOD
type: SiteQuality
SIO_000300: 9.64e-1

DP
type: SiteQuality
SIO_000300: 1.883658e6

GenotypeQuality
all individuals: 228
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19809
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 516
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1986
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7857
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2891
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3917
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4844
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10342
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3448
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11492
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 810
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10228
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.561914282144196e-5
allele num: 64024
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10960
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8592
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.61e-1

DP
type: SiteQuality
SIO_000300: 1.883658e6

FS
type: SiteQuality
SIO_000300: 3.478e0

QD
type: SiteQuality
SIO_000300: 1.219e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.92e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

MQRankSum
type: SiteQuality
SIO_000300: 9.13e-1

MQ
type: SiteQuality
SIO_000300: 5.995e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.2e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.64e-1

GenotypeQuality
all individuals: 7851
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 254
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1986
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 179
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4839
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4002
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 19695
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3919
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10340
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 84
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2893
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 2
allele frequency: 1.955416503715291e-4
allele num: 10228
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.094216078574027e-5
allele num: 10996
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.684572142410993e-5
allele num: 64040
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 814
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8594
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11490
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 2.671e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.02e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.11e0

VQSLOD
type: SiteQuality
SIO_000300: 1.65e0

MQ
type: SiteQuality
SIO_000300: 5.964e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -5.4e-2

MQRankSum
type: SiteQuality
SIO_000300: -8.44e-1

QD
type: SiteQuality
SIO_000300: 1.245e1

DP
type: SiteQuality
SIO_000300: 1.883067e6

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

GenotypeQuality
all individuals: 251
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 213
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1986
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7853
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3445
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4049
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4838
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2892
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10337
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3919
bin: 8.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 814
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8592
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11492
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10228
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11018
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.561524047470331e-5
allele num: 64040
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.984e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

FS
type: SiteQuality
SIO_000300: 2.057e0

VQSLOD
type: SiteQuality
SIO_000300: 6.1e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.99e0

DP
type: SiteQuality
SIO_000300: 1.882853e6

ClippingRankSum
type: SiteQuality
SIO_000300: 5.580000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.32e0

QD
type: SiteQuality
SIO_000300: 1.303e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.26e0

GenotypeQuality
all individuals: 147
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4838
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 213
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4049
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2892
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 251
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7853
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3445
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10337
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 19763
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1986
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8592
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10228
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11492
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.520218911523259e-4
allele num: 6578
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11018
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64040
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 814
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.32e0

FS
type: SiteQuality
SIO_000300: 2.057e0

MQ
type: SiteQuality
SIO_000300: 5.984e1

VQSLOD
type: SiteQuality
SIO_000300: 6.1e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.580000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.303e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.26e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.99e0

DP
type: SiteQuality
SIO_000300: 1.882853e6

GenotypeQuality
all individuals: 94
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4077
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 93
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3918
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 260
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 220
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3451
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 37
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10340
bin: 9.75e1
variant carriers: 10

GenotypeQuality
all individuals: 1985
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.775171065493646e-5
allele num: 10230
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 814
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 6
allele frequency: 9.121313469139556e-4
allele num: 6578
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.703220191470844e-5
allele num: 11490
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.561524047470331e-5
allele num: 64040
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.163602513381429e-4
allele num: 8594
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.05961224859576e-5
allele num: 11038
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.56e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.34e-1

FS
type: SiteQuality
SIO_000300: 1.2e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.79e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.87e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.15e-1

QD
type: SiteQuality
SIO_000300: 1.455e1

MQ
type: SiteQuality
SIO_000300: 5.939e1

DP
type: SiteQuality
SIO_000300: 1.882676e6

GenotypeQuality
all individuals: 92
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7852
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 597
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2892
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4071
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 10333
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 218
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1985
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3452
bin: 7.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 814
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11030
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10228
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8594
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.123535842573794e-5
allele num: 64030
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.70170553428472e-5
allele num: 11492
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.21e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -4.51e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.872e0

DP
type: SiteQuality
SIO_000300: 1.882132e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.75e-1

MQ
type: SiteQuality
SIO_000300: 5.92e1

VQSLOD
type: SiteQuality
SIO_000300: 4.13e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

QD
type: SiteQuality
SIO_000300: 1.168e1

GenotypeQuality
all individuals: 46
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1984
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 50
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 217
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4831
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3455
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10335
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 7857
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2892
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3918
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.704735376044568e-5
allele num: 11488
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10226
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 2.724795640326976e-4
allele num: 11010
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 810
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8594
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6580
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.122950563692576e-5
allele num: 64042
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.064e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.04e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.860000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.24e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

DP
type: SiteQuality
SIO_000300: 1.880917e6

MQRankSum
type: SiteQuality
SIO_000300: 1.62e0

QD
type: SiteQuality
SIO_000300: 1.214e1

MQ
type: SiteQuality
SIO_000300: 5.968e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.32e-1