17-58233889-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58233889
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 58233889
    reference: chr 17
allele count: 5
allele frequency: 4.126910759681733e-5
allele num: 121156
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167434
  ensembl protein: ENSP00000466964
  ensembl transcript: ENST00000591725
  gene symbol: CA4
  hgvsc: ENST00000591725.1:c.-158-32C>T
  variant of: http://identifiers.org/hgnc/1375
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167434
  ensembl transcript: ENST00000585705
  gene symbol: CA4
  hgvsc: ENST00000585705.1:n.206-32C>T
  variant of: http://identifiers.org/hgnc/1375
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167434
  ensembl protein: ENSP00000300900
  ensembl transcript: ENST00000300900
  gene symbol: CA4
  hgvsc: ENST00000300900.4:c.113-32C>T
  variant of: http://identifiers.org/hgnc/1375
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167434
  ensembl protein: ENSP00000467465
  ensembl transcript: ENST00000586876
  gene symbol: CA4
  hgvsc: ENST00000586876.1:c.113-32C>T
  variant of: http://identifiers.org/hgnc/1375
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13803
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1439
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13941
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 975
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2209
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3454
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2352
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5740
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8781
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3700
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18752
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7495
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2130
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15711
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3463
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3279
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: South Asian
reference allele: C
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum

15-58974405-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58974405
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 58974405
    reference: chr 15
allele count: 1
allele frequency: 8.251505899826718e-6
allele num: 121190
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000386056
  ensembl transcript: ENST00000402627
  gene symbol: ADAM10
  hgvsc: ENST00000402627.1:c.56-41376A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000391930
  ensembl transcript: ENST00000439637
  gene symbol: ADAM10
  hgvsc: ENST00000439637.1:c.315A>G
  hgvsp: ENST00000439637.1:c.315A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000453952
  ensembl transcript: ENST00000559053
  gene symbol: ADAM10
  hgvsc: ENST00000559053.1:c.56-41376A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000379444
  ensembl transcript: ENST00000396140
  gene symbol: ADAM10
  hgvsc: ENST00000396140.2:c.56-41376A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000558733
  gene symbol: ADAM10
  hgvsc: ENST00000558733.1:n.551A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000260408
  ensembl transcript: ENST00000260408
  gene symbol: ADAM10
  hgvsc: ENST00000260408.3:c.315A>G
  hgvsp: ENST00000260408.3:c.315A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000560608
  gene symbol: ADAM10
  hgvsc: ENST00000560608.1:n.464-2924A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000497846
  gene symbol: ADAM10
  hgvsc: ENST00000497846.1:n.432A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452639
  ensembl transcript: ENST00000561288
  gene symbol: ADAM10
  hgvsc: ENST00000561288.1:c.55+67274A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452704
  ensembl transcript: ENST00000558004
  gene symbol: ADAM10
  hgvsc: ENST00000558004.1:c.331+16074A>G
  variant of: http://identifiers.org/hgnc/188
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8015
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20164
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18324
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5335
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3516
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1617
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3832
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Gly105Gly
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum

15-58974423-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58974423
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 58974423
    reference: chr 15
allele count: 1
allele frequency: 8.251369727374745e-6
allele num: 121192
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000558733
  gene symbol: ADAM10
  hgvsc: ENST00000558733.1:n.533C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452704
  ensembl transcript: ENST00000558004
  gene symbol: ADAM10
  hgvsc: ENST00000558004.1:c.331+16056C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000379444
  ensembl transcript: ENST00000396140
  gene symbol: ADAM10
  hgvsc: ENST00000396140.2:c.56-41394C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452639
  ensembl transcript: ENST00000561288
  gene symbol: ADAM10
  hgvsc: ENST00000561288.1:c.55+67256C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000260408
  ensembl transcript: ENST00000260408
  gene symbol: ADAM10
  hgvsc: ENST00000260408.3:c.297C>T
  hgvsp: ENST00000260408.3:c.297C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000453952
  ensembl transcript: ENST00000559053
  gene symbol: ADAM10
  hgvsc: ENST00000559053.1:c.56-41394C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000386056
  ensembl transcript: ENST00000402627
  gene symbol: ADAM10
  hgvsc: ENST00000402627.1:c.56-41394C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000391930
  ensembl transcript: ENST00000439637
  gene symbol: ADAM10
  hgvsc: ENST00000439637.1:c.297C>T
  hgvsp: ENST00000439637.1:c.297C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000497846
  gene symbol: ADAM10
  hgvsc: ENST00000497846.1:n.414C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000560608
  gene symbol: ADAM10
  hgvsc: ENST00000560608.1:n.464-2942C>T
  variant of: http://identifiers.org/hgnc/188
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20205
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8014
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3516
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18326
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5285
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 858
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1616
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3355
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34279
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Thr99Thr
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD

15-58974430-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58974430
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 58974430
    reference: chr 15
allele count: 1
allele frequency: 8.250144377526608e-6
allele num: 121210
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452639
  ensembl transcript: ENST00000561288
  gene symbol: ADAM10
  hgvsc: ENST00000561288.1:c.55+67249A>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000260408
  ensembl transcript: ENST00000260408
  gene symbol: ADAM10
  hgvsc: ENST00000260408.3:c.290A>C
  hgvsp: ENSP00000260408.3:p.Tyr97Ser
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000497846
  gene symbol: ADAM10
  hgvsc: ENST00000497846.1:n.407A>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452704
  ensembl transcript: ENST00000558004
  gene symbol: ADAM10
  hgvsc: ENST00000558004.1:c.331+16049A>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000391930
  ensembl transcript: ENST00000439637
  gene symbol: ADAM10
  hgvsc: ENST00000439637.1:c.290A>C
  hgvsp: ENSP00000391930.1:p.Tyr97Ser
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000558733
  gene symbol: ADAM10
  hgvsc: ENST00000558733.1:n.526A>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000379444
  ensembl transcript: ENST00000396140
  gene symbol: ADAM10
  hgvsc: ENST00000396140.2:c.56-41401A>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000560608
  gene symbol: ADAM10
  hgvsc: ENST00000560608.1:n.464-2949A>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000386056
  ensembl transcript: ENST00000402627
  gene symbol: ADAM10
  hgvsc: ENST00000402627.1:c.56-41401A>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000453952
  ensembl transcript: ENST00000559053
  gene symbol: ADAM10
  hgvsc: ENST00000559053.1:c.56-41401A>C
  variant of: http://identifiers.org/hgnc/188
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 858
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18328
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5246
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20220
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1617
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8012
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3518
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3500
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11359
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Tyr97Ser
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: Other
population: South Asian
reference allele: T
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum

15-58974435-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58974435
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 58974435
    reference: chr 15
allele count: 1
allele frequency: 8.249736008447729e-6
allele num: 121216
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000391930
  ensembl transcript: ENST00000439637
  gene symbol: ADAM10
  hgvsc: ENST00000439637.1:c.285T>C
  hgvsp: ENST00000439637.1:c.285T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000558733
  gene symbol: ADAM10
  hgvsc: ENST00000558733.1:n.521T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000453952
  ensembl transcript: ENST00000559053
  gene symbol: ADAM10
  hgvsc: ENST00000559053.1:c.56-41406T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000379444
  ensembl transcript: ENST00000396140
  gene symbol: ADAM10
  hgvsc: ENST00000396140.2:c.56-41406T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000386056
  ensembl transcript: ENST00000402627
  gene symbol: ADAM10
  hgvsc: ENST00000402627.1:c.56-41406T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000260408
  ensembl transcript: ENST00000260408
  gene symbol: ADAM10
  hgvsc: ENST00000260408.3:c.285T>C
  hgvsp: ENST00000260408.3:c.285T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000497846
  gene symbol: ADAM10
  hgvsc: ENST00000497846.1:n.402T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452704
  ensembl transcript: ENST00000558004
  gene symbol: ADAM10
  hgvsc: ENST00000558004.1:c.331+16044T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452639
  ensembl transcript: ENST00000561288
  gene symbol: ADAM10
  hgvsc: ENST00000561288.1:c.55+67244T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000560608
  gene symbol: ADAM10
  hgvsc: ENST00000560608.1:n.464-2954T>C
  variant of: http://identifiers.org/hgnc/188
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18332
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3515
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1617
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20218
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8012
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5228
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Leu95Leu
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum

15-58974437-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58974437
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 58974437
    reference: chr 15
allele count: 1
allele frequency: 8.250144377526608e-6
allele num: 121210
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000391930
  ensembl transcript: ENST00000439637
  gene symbol: ADAM10
  hgvsc: ENST00000439637.1:c.283C>G
  hgvsp: ENSP00000391930.1:p.Leu95Val
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000379444
  ensembl transcript: ENST00000396140
  gene symbol: ADAM10
  hgvsc: ENST00000396140.2:c.56-41408C>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452639
  ensembl transcript: ENST00000561288
  gene symbol: ADAM10
  hgvsc: ENST00000561288.1:c.55+67242C>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000497846
  gene symbol: ADAM10
  hgvsc: ENST00000497846.1:n.400C>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000260408
  ensembl transcript: ENST00000260408
  gene symbol: ADAM10
  hgvsc: ENST00000260408.3:c.283C>G
  hgvsp: ENSP00000260408.3:p.Leu95Val
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000386056
  ensembl transcript: ENST00000402627
  gene symbol: ADAM10
  hgvsc: ENST00000402627.1:c.56-41408C>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000453952
  ensembl transcript: ENST00000559053
  gene symbol: ADAM10
  hgvsc: ENST00000559053.1:c.56-41408C>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000560608
  gene symbol: ADAM10
  hgvsc: ENST00000560608.1:n.464-2956C>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452704
  ensembl transcript: ENST00000558004
  gene symbol: ADAM10
  hgvsc: ENST00000558004.1:c.331+16042C>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000558733
  gene symbol: ADAM10
  hgvsc: ENST00000558733.1:n.519C>G
  variant of: http://identifiers.org/hgnc/188
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8008
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3516
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18331
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1616
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5220
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20222
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3820
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34229
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Leu95Val
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: Latino
population: European (Finnish)
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD

15-58974438-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58974438
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 58974438
    reference: chr 15
allele count: 7
allele frequency: 5.775196356676127e-5
allele num: 121208
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000260408
  ensembl transcript: ENST00000260408
  gene symbol: ADAM10
  hgvsc: ENST00000260408.3:c.282A>T
  hgvsp: ENST00000260408.3:c.282A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000453952
  ensembl transcript: ENST00000559053
  gene symbol: ADAM10
  hgvsc: ENST00000559053.1:c.56-41409A>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000560608
  gene symbol: ADAM10
  hgvsc: ENST00000560608.1:n.464-2957A>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000558733
  gene symbol: ADAM10
  hgvsc: ENST00000558733.1:n.518A>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000386056
  ensembl transcript: ENST00000402627
  gene symbol: ADAM10
  hgvsc: ENST00000402627.1:c.56-41409A>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000379444
  ensembl transcript: ENST00000396140
  gene symbol: ADAM10
  hgvsc: ENST00000396140.2:c.56-41409A>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000391930
  ensembl transcript: ENST00000439637
  gene symbol: ADAM10
  hgvsc: ENST00000439637.1:c.282A>T
  hgvsp: ENST00000439637.1:c.282A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000497846
  gene symbol: ADAM10
  hgvsc: ENST00000497846.1:n.399A>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452639
  ensembl transcript: ENST00000561288
  gene symbol: ADAM10
  hgvsc: ENST00000561288.1:c.55+67241A>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452704
  ensembl transcript: ENST00000558004
  gene symbol: ADAM10
  hgvsc: ENST00000558004.1:c.331+16041A>T
  variant of: http://identifiers.org/hgnc/188
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20218
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 18329
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5217
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1617
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8009
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3516
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11360
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Val94Val
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum

15-58974440-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58974440
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 58974440
    reference: chr 15
allele count: 1
allele frequency: 8.25082508250825e-6
allele num: 121200
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000497846
  gene symbol: ADAM10
  hgvsc: ENST00000497846.1:n.397G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000453952
  ensembl transcript: ENST00000559053
  gene symbol: ADAM10
  hgvsc: ENST00000559053.1:c.56-41411G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000379444
  ensembl transcript: ENST00000396140
  gene symbol: ADAM10
  hgvsc: ENST00000396140.2:c.56-41411G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000260408
  ensembl transcript: ENST00000260408
  gene symbol: ADAM10
  hgvsc: ENST00000260408.3:c.280G>A
  hgvsp: ENSP00000260408.3:p.Val94Ile
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000558733
  gene symbol: ADAM10
  hgvsc: ENST00000558733.1:n.516G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000560608
  gene symbol: ADAM10
  hgvsc: ENST00000560608.1:n.464-2959G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452639
  ensembl transcript: ENST00000561288
  gene symbol: ADAM10
  hgvsc: ENST00000561288.1:c.55+67239G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000391930
  ensembl transcript: ENST00000439637
  gene symbol: ADAM10
  hgvsc: ENST00000439637.1:c.280G>A
  hgvsp: ENSP00000391930.1:p.Val94Ile
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452704
  ensembl transcript: ENST00000558004
  gene symbol: ADAM10
  hgvsc: ENST00000558004.1:c.331+16039G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000386056
  ensembl transcript: ENST00000402627
  gene symbol: ADAM10
  hgvsc: ENST00000402627.1:c.56-41411G>A
  variant of: http://identifiers.org/hgnc/188
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5218
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20218
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1617
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8007
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18328
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3515
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3343
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Val94Ile
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQ

15-58974456-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58974456
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 58974456
    reference: chr 15
allele count: 2
allele frequency: 1.650355651642929e-5
allele num: 121186
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000453952
  ensembl transcript: ENST00000559053
  gene symbol: ADAM10
  hgvsc: ENST00000559053.1:c.56-41427A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000260408
  ensembl transcript: ENST00000260408
  gene symbol: ADAM10
  hgvsc: ENST00000260408.3:c.264A>G
  hgvsp: ENST00000260408.3:c.264A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000558733
  gene symbol: ADAM10
  hgvsc: ENST00000558733.1:n.500A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000560608
  gene symbol: ADAM10
  hgvsc: ENST00000560608.1:n.464-2975A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000561149
  gene symbol: ADAM10
  hgvsc: ENST00000561149.1:n.524A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000497846
  gene symbol: ADAM10
  hgvsc: ENST00000497846.1:n.381A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000391930
  ensembl transcript: ENST00000439637
  gene symbol: ADAM10
  hgvsc: ENST00000439637.1:c.264A>G
  hgvsp: ENST00000439637.1:c.264A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000379444
  ensembl transcript: ENST00000396140
  gene symbol: ADAM10
  hgvsc: ENST00000396140.2:c.56-41427A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452704
  ensembl transcript: ENST00000558004
  gene symbol: ADAM10
  hgvsc: ENST00000558004.1:c.331+16023A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452639
  ensembl transcript: ENST00000561288
  gene symbol: ADAM10
  hgvsc: ENST00000561288.1:c.55+67223A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000386056
  ensembl transcript: ENST00000402627
  gene symbol: ADAM10
  hgvsc: ENST00000402627.1:c.56-41427A>G
  variant of: http://identifiers.org/hgnc/188
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8002
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5262
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18300
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20157
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3511
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1613
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Val88Val
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: East Asian
reference allele: T
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: QD

15-58974464-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58974464
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 58974464
    reference: chr 15
allele count: 1
allele frequency: 8.25218682950982e-6
allele num: 121180
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452639
  ensembl transcript: ENST00000561288
  gene symbol: ADAM10
  hgvsc: ENST00000561288.1:c.55+67215T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000260408
  ensembl transcript: ENST00000260408
  gene symbol: ADAM10
  hgvsc: ENST00000260408.3:c.256T>C
  hgvsp: ENSP00000260408.3:p.Phe86Leu
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452704
  ensembl transcript: ENST00000558004
  gene symbol: ADAM10
  hgvsc: ENST00000558004.1:c.331+16015T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000497846
  gene symbol: ADAM10
  hgvsc: ENST00000497846.1:n.373T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000561149
  gene symbol: ADAM10
  hgvsc: ENST00000561149.1:n.516T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000386056
  ensembl transcript: ENST00000402627
  gene symbol: ADAM10
  hgvsc: ENST00000402627.1:c.56-41435T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000379444
  ensembl transcript: ENST00000396140
  gene symbol: ADAM10
  hgvsc: ENST00000396140.2:c.56-41435T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000391930
  ensembl transcript: ENST00000439637
  gene symbol: ADAM10
  hgvsc: ENST00000439637.1:c.256T>C
  hgvsp: ENSP00000391930.1:p.Phe86Leu
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000453952
  ensembl transcript: ENST00000559053
  gene symbol: ADAM10
  hgvsc: ENST00000559053.1:c.56-41435T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000558733
  gene symbol: ADAM10
  hgvsc: ENST00000558733.1:n.492T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000560608
  gene symbol: ADAM10
  hgvsc: ENST00000560608.1:n.464-2983T>C
  variant of: http://identifiers.org/hgnc/188
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1613
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5295
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18278
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20172
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7994
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3511
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3485
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Phe86Leu
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD

15-58974473-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58974473
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 58974473
    reference: chr 15
allele count: 1
allele frequency: 8.250688932525866e-6
allele num: 121202
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000558733
  gene symbol: ADAM10
  hgvsc: ENST00000558733.1:n.483A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000260408
  ensembl transcript: ENST00000260408
  gene symbol: ADAM10
  hgvsc: ENST00000260408.3:c.247A>G
  hgvsp: ENSP00000260408.3:p.Ser83Gly
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000386056
  ensembl transcript: ENST00000402627
  gene symbol: ADAM10
  hgvsc: ENST00000402627.1:c.56-41444A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452704
  ensembl transcript: ENST00000558004
  gene symbol: ADAM10
  hgvsc: ENST00000558004.1:c.331+16006A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000379444
  ensembl transcript: ENST00000396140
  gene symbol: ADAM10
  hgvsc: ENST00000396140.2:c.56-41444A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000560608
  gene symbol: ADAM10
  hgvsc: ENST00000560608.1:n.464-2992A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452639
  ensembl transcript: ENST00000561288
  gene symbol: ADAM10
  hgvsc: ENST00000561288.1:c.55+67206A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000497846
  gene symbol: ADAM10
  hgvsc: ENST00000497846.1:n.364A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000391930
  ensembl transcript: ENST00000439637
  gene symbol: ADAM10
  hgvsc: ENST00000439637.1:c.247A>G
  hgvsp: ENSP00000391930.1:p.Ser83Gly
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000561149
  gene symbol: ADAM10
  hgvsc: ENST00000561149.1:n.507A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000453952
  ensembl transcript: ENST00000559053
  gene symbol: ADAM10
  hgvsc: ENST00000559053.1:c.56-41444A>G
  variant of: http://identifiers.org/hgnc/188
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20214
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5308
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1612
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18264
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7983
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3511
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ser83Gly
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum

15-58974499-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58974499
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 58974499
    reference: chr 15
allele count: 1
allele frequency: 8.256274768824306e-6
allele num: 121120
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000260408
  ensembl transcript: ENST00000260408
  gene symbol: ADAM10
  hgvsc: ENST00000260408.3:c.221G>A
  hgvsp: ENSP00000260408.3:p.Arg74Gln
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000386056
  ensembl transcript: ENST00000402627
  gene symbol: ADAM10
  hgvsc: ENST00000402627.1:c.56-41470G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000561149
  gene symbol: ADAM10
  hgvsc: ENST00000561149.1:n.481G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452704
  ensembl transcript: ENST00000558004
  gene symbol: ADAM10
  hgvsc: ENST00000558004.1:c.331+15980G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000560608
  gene symbol: ADAM10
  hgvsc: ENST00000560608.1:n.464-3018G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000391930
  ensembl transcript: ENST00000439637
  gene symbol: ADAM10
  hgvsc: ENST00000439637.1:c.221G>A
  hgvsp: ENSP00000391930.1:p.Arg74Gln
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452639
  ensembl transcript: ENST00000561288
  gene symbol: ADAM10
  hgvsc: ENST00000561288.1:c.55+67180G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000379444
  ensembl transcript: ENST00000396140
  gene symbol: ADAM10
  hgvsc: ENST00000396140.2:c.56-41470G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000558733
  gene symbol: ADAM10
  hgvsc: ENST00000558733.1:n.457G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000497846
  gene symbol: ADAM10
  hgvsc: ENST00000497846.1:n.338G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000453952
  ensembl transcript: ENST00000559053
  gene symbol: ADAM10
  hgvsc: ENST00000559053.1:c.56-41470G>A
  variant of: http://identifiers.org/hgnc/188
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20206
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5299
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18228
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1614
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7978
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3510
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3297
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Arg74Gln
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff

15-58974501-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58974501
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 58974501
    reference: chr 15
allele count: 12
allele frequency: 9.90916597853014e-5
allele num: 121100
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000558733
  gene symbol: ADAM10
  hgvsc: ENST00000558733.1:n.455A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000260408
  ensembl transcript: ENST00000260408
  gene symbol: ADAM10
  hgvsc: ENST00000260408.3:c.219A>G
  hgvsp: ENST00000260408.3:c.219A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000391930
  ensembl transcript: ENST00000439637
  gene symbol: ADAM10
  hgvsc: ENST00000439637.1:c.219A>G
  hgvsp: ENST00000439637.1:c.219A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452639
  ensembl transcript: ENST00000561288
  gene symbol: ADAM10
  hgvsc: ENST00000561288.1:c.55+67178A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000386056
  ensembl transcript: ENST00000402627
  gene symbol: ADAM10
  hgvsc: ENST00000402627.1:c.56-41472A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000379444
  ensembl transcript: ENST00000396140
  gene symbol: ADAM10
  hgvsc: ENST00000396140.2:c.56-41472A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000561149
  gene symbol: ADAM10
  hgvsc: ENST00000561149.1:n.479A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452704
  ensembl transcript: ENST00000558004
  gene symbol: ADAM10
  hgvsc: ENST00000558004.1:c.331+15978A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000497846
  gene symbol: ADAM10
  hgvsc: ENST00000497846.1:n.336A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000560608
  gene symbol: ADAM10
  hgvsc: ENST00000560608.1:n.464-3020A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000453952
  ensembl transcript: ENST00000559053
  gene symbol: ADAM10
  hgvsc: ENST00000559053.1:c.56-41472A>G
  variant of: http://identifiers.org/hgnc/188
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18217
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1609
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 20201
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7970
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3505
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5290
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Leu73Leu
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

15-58974507-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58974507
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 58974507
    reference: chr 15
allele count: 1
allele frequency: 8.261049153242462e-6
allele num: 121050
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000386056
  ensembl transcript: ENST00000402627
  gene symbol: ADAM10
  hgvsc: ENST00000402627.1:c.56-41478C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000453952
  ensembl transcript: ENST00000559053
  gene symbol: ADAM10
  hgvsc: ENST00000559053.1:c.56-41478C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000497846
  gene symbol: ADAM10
  hgvsc: ENST00000497846.1:n.330C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000561149
  gene symbol: ADAM10
  hgvsc: ENST00000561149.1:n.473C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000379444
  ensembl transcript: ENST00000396140
  gene symbol: ADAM10
  hgvsc: ENST00000396140.2:c.56-41478C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000558733
  gene symbol: ADAM10
  hgvsc: ENST00000558733.1:n.449C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452639
  ensembl transcript: ENST00000561288
  gene symbol: ADAM10
  hgvsc: ENST00000561288.1:c.55+67172C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000391930
  ensembl transcript: ENST00000439637
  gene symbol: ADAM10
  hgvsc: ENST00000439637.1:c.213C>T
  hgvsp: ENST00000439637.1:c.213C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000560608
  gene symbol: ADAM10
  hgvsc: ENST00000560608.1:n.464-3026C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000260408
  ensembl transcript: ENST00000260408
  gene symbol: ADAM10
  hgvsc: ENST00000260408.3:c.213C>T
  hgvsp: ENST00000260408.3:c.213C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452704
  ensembl transcript: ENST00000558004
  gene symbol: ADAM10
  hgvsc: ENST00000558004.1:c.331+15972C>T
  variant of: http://identifiers.org/hgnc/188
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18208
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5248
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20176
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1610
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7970
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3502
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Phe71Phe
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
reference allele: G
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

15-58974512-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58974512
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 58974512
    reference: chr 15
allele count: 1
allele frequency: 8.26296045347127e-6
allele num: 121022
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000453952
  ensembl transcript: ENST00000559053
  gene symbol: ADAM10
  hgvsc: ENST00000559053.1:c.56-41483C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000386056
  ensembl transcript: ENST00000402627
  gene symbol: ADAM10
  hgvsc: ENST00000402627.1:c.56-41483C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000391930
  ensembl transcript: ENST00000439637
  gene symbol: ADAM10
  hgvsc: ENST00000439637.1:c.208C>T
  hgvsp: ENSP00000391930.1:p.His70Tyr
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452704
  ensembl transcript: ENST00000558004
  gene symbol: ADAM10
  hgvsc: ENST00000558004.1:c.331+15967C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452639
  ensembl transcript: ENST00000561288
  gene symbol: ADAM10
  hgvsc: ENST00000561288.1:c.55+67167C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000560608
  gene symbol: ADAM10
  hgvsc: ENST00000560608.1:n.464-3031C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000260408
  ensembl transcript: ENST00000260408
  gene symbol: ADAM10
  hgvsc: ENST00000260408.3:c.208C>T
  hgvsp: ENSP00000260408.3:p.His70Tyr
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000379444
  ensembl transcript: ENST00000396140
  gene symbol: ADAM10
  hgvsc: ENST00000396140.2:c.56-41483C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000558733
  gene symbol: ADAM10
  hgvsc: ENST00000558733.1:n.444C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000497846
  gene symbol: ADAM10
  hgvsc: ENST00000497846.1:n.325C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000561149
  gene symbol: ADAM10
  hgvsc: ENST00000561149.1:n.468C>T
  variant of: http://identifiers.org/hgnc/188
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20139
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5230
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3502
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7968
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18195
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1609
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His70Tyr
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: QD

15-58974537-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58974537
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 58974537
    reference: chr 15
allele count: 1
allele frequency: 8.3099270388406e-6
allele num: 120338
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000379444
  ensembl transcript: ENST00000396140
  gene symbol: ADAM10
  hgvsc: ENST00000396140.2:c.56-41508C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000453952
  ensembl transcript: ENST00000559053
  gene symbol: ADAM10
  hgvsc: ENST00000559053.1:c.56-41508C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000558733
  gene symbol: ADAM10
  hgvsc: ENST00000558733.1:n.443-24C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000497846
  gene symbol: ADAM10
  hgvsc: ENST00000497846.1:n.324-24C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000561149
  gene symbol: ADAM10
  hgvsc: ENST00000561149.1:n.467-24C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000386056
  ensembl transcript: ENST00000402627
  gene symbol: ADAM10
  hgvsc: ENST00000402627.1:c.56-41508C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000391930
  ensembl transcript: ENST00000439637
  gene symbol: ADAM10
  hgvsc: ENST00000439637.1:c.207-24C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452639
  ensembl transcript: ENST00000561288
  gene symbol: ADAM10
  hgvsc: ENST00000561288.1:c.55+67142C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452704
  ensembl transcript: ENST00000558004
  gene symbol: ADAM10
  hgvsc: ENST00000558004.1:c.331+15942C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000260408
  ensembl transcript: ENST00000260408
  gene symbol: ADAM10
  hgvsc: ENST00000260408.3:c.207-24C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000560608
  gene symbol: ADAM10
  hgvsc: ENST00000560608.1:n.464-3056C>T
  variant of: http://identifiers.org/hgnc/188
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17711
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1600
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7895
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2023
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4167
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19114
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3465
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: G
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum

15-58974540-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58974540
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 58974540
    reference: chr 15
allele count: 1
allele frequency: 8.319190709127816e-6
allele num: 120204
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000497846
  gene symbol: ADAM10
  hgvsc: ENST00000497846.1:n.324-27G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000391930
  ensembl transcript: ENST00000439637
  gene symbol: ADAM10
  hgvsc: ENST00000439637.1:c.207-27G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000260408
  ensembl transcript: ENST00000260408
  gene symbol: ADAM10
  hgvsc: ENST00000260408.3:c.207-27G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452704
  ensembl transcript: ENST00000558004
  gene symbol: ADAM10
  hgvsc: ENST00000558004.1:c.331+15939G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000558733
  gene symbol: ADAM10
  hgvsc: ENST00000558733.1:n.443-27G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000379444
  ensembl transcript: ENST00000396140
  gene symbol: ADAM10
  hgvsc: ENST00000396140.2:c.56-41511G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000561149
  gene symbol: ADAM10
  hgvsc: ENST00000561149.1:n.467-27G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000560608
  gene symbol: ADAM10
  hgvsc: ENST00000560608.1:n.464-3059G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000453952
  ensembl transcript: ENST00000559053
  gene symbol: ADAM10
  hgvsc: ENST00000559053.1:c.56-41511G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000386056
  ensembl transcript: ENST00000402627
  gene symbol: ADAM10
  hgvsc: ENST00000402627.1:c.56-41511G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452639
  ensembl transcript: ENST00000561288
  gene symbol: ADAM10
  hgvsc: ENST00000561288.1:c.55+67139G>A
  variant of: http://identifiers.org/hgnc/188
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 3455
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7848
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1598
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2450
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4004
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17521
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18704
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3087
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

15-58974543-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58974543
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 58974543
    reference: chr 15
allele count: 1
allele frequency: 8.328891257995735e-6
allele num: 120064
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000558733
  gene symbol: ADAM10
  hgvsc: ENST00000558733.1:n.443-30G>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452704
  ensembl transcript: ENST00000558004
  gene symbol: ADAM10
  hgvsc: ENST00000558004.1:c.331+15936G>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000497846
  gene symbol: ADAM10
  hgvsc: ENST00000497846.1:n.324-30G>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000453952
  ensembl transcript: ENST00000559053
  gene symbol: ADAM10
  hgvsc: ENST00000559053.1:c.56-41514G>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000386056
  ensembl transcript: ENST00000402627
  gene symbol: ADAM10
  hgvsc: ENST00000402627.1:c.56-41514G>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000560608
  gene symbol: ADAM10
  hgvsc: ENST00000560608.1:n.464-3062G>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000260408
  ensembl transcript: ENST00000260408
  gene symbol: ADAM10
  hgvsc: ENST00000260408.3:c.207-30G>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452639
  ensembl transcript: ENST00000561288
  gene symbol: ADAM10
  hgvsc: ENST00000561288.1:c.55+67136G>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000391930
  ensembl transcript: ENST00000439637
  gene symbol: ADAM10
  hgvsc: ENST00000439637.1:c.207-30G>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000379444
  ensembl transcript: ENST00000396140
  gene symbol: ADAM10
  hgvsc: ENST00000396140.2:c.56-41514G>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000561149
  gene symbol: ADAM10
  hgvsc: ENST00000561149.1:n.467-30G>C
  variant of: http://identifiers.org/hgnc/188
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 3447
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18005
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1803
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7789
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1596
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3801
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17103
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3043
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum

15-58974545-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58974545
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 58974545
    reference: chr 15
allele count: 1
allele frequency: 8.335556148306214e-6
allele num: 119968
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000560608
  gene symbol: ADAM10
  hgvsc: ENST00000560608.1:n.464-3064C>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000386056
  ensembl transcript: ENST00000402627
  gene symbol: ADAM10
  hgvsc: ENST00000402627.1:c.56-41516C>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000260408
  ensembl transcript: ENST00000260408
  gene symbol: ADAM10
  hgvsc: ENST00000260408.3:c.207-32C>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452639
  ensembl transcript: ENST00000561288
  gene symbol: ADAM10
  hgvsc: ENST00000561288.1:c.55+67134C>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000561149
  gene symbol: ADAM10
  hgvsc: ENST00000561149.1:n.467-32C>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000497846
  gene symbol: ADAM10
  hgvsc: ENST00000497846.1:n.324-32C>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000453952
  ensembl transcript: ENST00000559053
  gene symbol: ADAM10
  hgvsc: ENST00000559053.1:c.56-41516C>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000558733
  gene symbol: ADAM10
  hgvsc: ENST00000558733.1:n.443-32C>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452704
  ensembl transcript: ENST00000558004
  gene symbol: ADAM10
  hgvsc: ENST00000558004.1:c.331+15934C>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000391930
  ensembl transcript: ENST00000439637
  gene symbol: ADAM10
  hgvsc: ENST00000439637.1:c.207-32C>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000379444
  ensembl transcript: ENST00000396140
  gene symbol: ADAM10
  hgvsc: ENST00000396140.2:c.56-41516C>A
  variant of: http://identifiers.org/hgnc/188
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3657
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2551
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7753
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3372
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3435
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16797
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1593
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17394
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1000
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff

15-58974547-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58974547
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 58974547
    reference: chr 15
allele count: 1
allele frequency: 8.340840089413805e-6
allele num: 119892
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000497846
  gene symbol: ADAM10
  hgvsc: ENST00000497846.1:n.324-34T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000560608
  gene symbol: ADAM10
  hgvsc: ENST00000560608.1:n.464-3066T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000561149
  gene symbol: ADAM10
  hgvsc: ENST00000561149.1:n.467-34T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452639
  ensembl transcript: ENST00000561288
  gene symbol: ADAM10
  hgvsc: ENST00000561288.1:c.55+67132T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000386056
  ensembl transcript: ENST00000402627
  gene symbol: ADAM10
  hgvsc: ENST00000402627.1:c.56-41518T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000391930
  ensembl transcript: ENST00000439637
  gene symbol: ADAM10
  hgvsc: ENST00000439637.1:c.207-34T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000260408
  ensembl transcript: ENST00000260408
  gene symbol: ADAM10
  hgvsc: ENST00000260408.3:c.207-34T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452704
  ensembl transcript: ENST00000558004
  gene symbol: ADAM10
  hgvsc: ENST00000558004.1:c.331+15932T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000558733
  gene symbol: ADAM10
  hgvsc: ENST00000558733.1:n.443-34T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000379444
  ensembl transcript: ENST00000396140
  gene symbol: ADAM10
  hgvsc: ENST00000396140.2:c.56-41518T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000453952
  ensembl transcript: ENST00000559053
  gene symbol: ADAM10
  hgvsc: ENST00000559053.1:c.56-41518T>C
  variant of: http://identifiers.org/hgnc/188
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 7660
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16436
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3729
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1591
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16313
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3428
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3918
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3425
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27815
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

15-58974550-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58974550
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 58974550
    reference: chr 15
allele count: 1
allele frequency: 8.362882183715796e-6
allele num: 119576
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000558733
  gene symbol: ADAM10
  hgvsc: ENST00000558733.1:n.443-37A>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000560608
  gene symbol: ADAM10
  hgvsc: ENST00000560608.1:n.464-3069A>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000260408
  ensembl transcript: ENST00000260408
  gene symbol: ADAM10
  hgvsc: ENST00000260408.3:c.207-37A>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000379444
  ensembl transcript: ENST00000396140
  gene symbol: ADAM10
  hgvsc: ENST00000396140.2:c.56-41521A>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000561149
  gene symbol: ADAM10
  hgvsc: ENST00000561149.1:n.467-37A>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452639
  ensembl transcript: ENST00000561288
  gene symbol: ADAM10
  hgvsc: ENST00000561288.1:c.55+67129A>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452704
  ensembl transcript: ENST00000558004
  gene symbol: ADAM10
  hgvsc: ENST00000558004.1:c.331+15929A>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000386056
  ensembl transcript: ENST00000402627
  gene symbol: ADAM10
  hgvsc: ENST00000402627.1:c.56-41521A>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000497846
  gene symbol: ADAM10
  hgvsc: ENST00000497846.1:n.324-37A>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000391930
  ensembl transcript: ENST00000439637
  gene symbol: ADAM10
  hgvsc: ENST00000439637.1:c.207-37A>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000453952
  ensembl transcript: ENST00000559053
  gene symbol: ADAM10
  hgvsc: ENST00000559053.1:c.56-41521A>C
  variant of: http://identifiers.org/hgnc/188
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15557
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1585
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3406
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3896
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15750
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5279
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3404
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7567
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 375
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: QD
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum

15-58974559-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58974559
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 58974559
    reference: chr 15
allele count: 1
allele frequency: 8.473427331887202e-6
allele num: 118016
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000260408
  ensembl transcript: ENST00000260408
  gene symbol: ADAM10
  hgvsc: ENST00000260408.3:c.207-46G>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000379444
  ensembl transcript: ENST00000396140
  gene symbol: ADAM10
  hgvsc: ENST00000396140.2:c.56-41530G>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000497846
  gene symbol: ADAM10
  hgvsc: ENST00000497846.1:n.324-46G>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000561149
  gene symbol: ADAM10
  hgvsc: ENST00000561149.1:n.467-46G>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000558733
  gene symbol: ADAM10
  hgvsc: ENST00000558733.1:n.443-46G>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000386056
  ensembl transcript: ENST00000402627
  gene symbol: ADAM10
  hgvsc: ENST00000402627.1:c.56-41530G>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000391930
  ensembl transcript: ENST00000439637
  gene symbol: ADAM10
  hgvsc: ENST00000439637.1:c.207-46G>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000560608
  gene symbol: ADAM10
  hgvsc: ENST00000560608.1:n.464-3078G>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452639
  ensembl transcript: ENST00000561288
  gene symbol: ADAM10
  hgvsc: ENST00000561288.1:c.55+67120G>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452704
  ensembl transcript: ENST00000558004
  gene symbol: ADAM10
  hgvsc: ENST00000558004.1:c.331+15920G>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000453952
  ensembl transcript: ENST00000559053
  gene symbol: ADAM10
  hgvsc: ENST00000559053.1:c.56-41530G>C
  variant of: http://identifiers.org/hgnc/188
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3800
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11332
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3230
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 975
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1547
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9792
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9409
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10153
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6637
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 841
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2681
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: C
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

15-58974562-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58974562
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 58974562
    reference: chr 15
allele count: 6
allele frequency: 5.248150027115442e-5
allele num: 114326
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000497846
  gene symbol: ADAM10
  hgvsc: ENST00000497846.1:n.324-49T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000560608
  gene symbol: ADAM10
  hgvsc: ENST00000560608.1:n.464-3081T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000379444
  ensembl transcript: ENST00000396140
  gene symbol: ADAM10
  hgvsc: ENST00000396140.2:c.56-41533T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452639
  ensembl transcript: ENST00000561288
  gene symbol: ADAM10
  hgvsc: ENST00000561288.1:c.55+67117T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000386056
  ensembl transcript: ENST00000402627
  gene symbol: ADAM10
  hgvsc: ENST00000402627.1:c.56-41533T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000391930
  ensembl transcript: ENST00000439637
  gene symbol: ADAM10
  hgvsc: ENST00000439637.1:c.207-49T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000260408
  ensembl transcript: ENST00000260408
  gene symbol: ADAM10
  hgvsc: ENST00000260408.3:c.207-49T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000561149
  gene symbol: ADAM10
  hgvsc: ENST00000561149.1:n.467-49T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452704
  ensembl transcript: ENST00000558004
  gene symbol: ADAM10
  hgvsc: ENST00000558004.1:c.331+15917T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000558733
  gene symbol: ADAM10
  hgvsc: ENST00000558733.1:n.443-49T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000453952
  ensembl transcript: ENST00000559053
  gene symbol: ADAM10
  hgvsc: ENST00000559053.1:c.56-41533T>C
  variant of: http://identifiers.org/hgnc/188
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12427
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11880
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1398
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1211
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9051
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2777
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4164
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8688
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5265
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 968
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ

15-58983253-A-AACATCATAAGCAAATGAAGTAATAAGAGGCTGGCTTAACATTCTAAAATCATCAATGTAATTCACCGCATTCAAAGGG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58983253
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 58983331
    reference: chr 15
allele count: 1
allele frequency: 9.917486512218343e-6
allele num: 100832
alternate allele: AACATCATAAGCAAATGAAGTAATAAGAGGCTGGCTTAACATTCTAAAATCATCAATGTAATTCACCGCATTCAAAGGG
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452704
  ensembl transcript: ENST00000558004
  gene symbol: ADAM10
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000391930
  ensembl transcript: ENST00000439637
  gene symbol: ADAM10
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000379444
  ensembl transcript: ENST00000396140
  gene symbol: ADAM10
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000558733
  gene symbol: ADAM10
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000497846
  gene symbol: ADAM10
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000560608
  gene symbol: ADAM10
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000561149
  gene symbol: ADAM10
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452639
  ensembl transcript: ENST00000561288
  gene symbol: ADAM10
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000260408
  ensembl transcript: ENST00000260408
  gene symbol: ADAM10
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000386056
  ensembl transcript: ENST00000402627
  gene symbol: ADAM10
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000453952
  ensembl transcript: ENST00000559053
  gene symbol: ADAM10
  variant of: http://identifiers.org/hgnc/188
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.95to100.00
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13263
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11793
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7627
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8816
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11548
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2230
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2586
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1617
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3382
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 758
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3824
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: European (Finnish)
reference allele: A
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ

15-58983266-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58983266
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 58983266
    reference: chr 15
allele count: 1
allele frequency: 1.003029148027042e-5
allele num: 99698
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452639
  ensembl transcript: ENST00000561288
  gene symbol: ADAM10
  hgvsc: ENST00000561288.1:c.55+58413A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000560608
  gene symbol: ADAM10
  hgvsc: ENST00000560608.1:n.464-11785A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000453952
  ensembl transcript: ENST00000559053
  gene symbol: ADAM10
  hgvsc: ENST00000559053.1:c.56-50237A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000561149
  gene symbol: ADAM10
  hgvsc: ENST00000561149.1:n.467-8753A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000260408
  ensembl transcript: ENST00000260408
  gene symbol: ADAM10
  hgvsc: ENST00000260408.3:c.207-8753A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452704
  ensembl transcript: ENST00000558004
  gene symbol: ADAM10
  hgvsc: ENST00000558004.1:c.331+7213A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000558733
  gene symbol: ADAM10
  hgvsc: ENST00000558733.1:n.443-8753A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000379444
  ensembl transcript: ENST00000396140
  gene symbol: ADAM10
  hgvsc: ENST00000396140.2:c.56-50237A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000391930
  ensembl transcript: ENST00000439637
  gene symbol: ADAM10
  hgvsc: ENST00000439637.1:c.207-8753A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000497846
  gene symbol: ADAM10
  hgvsc: ENST00000497846.1:n.324-8753A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000386056
  ensembl transcript: ENST00000402627
  gene symbol: ADAM10
  hgvsc: ENST00000402627.1:c.56-50237A>G
  variant of: http://identifiers.org/hgnc/188
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9622
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9898
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8216
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12559
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2205
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2153
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13203
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16006
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum

15-58983270-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58983270
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 58983270
    reference: chr 15
allele count: 2
allele frequency: 2.015722636565209e-5
allele num: 99220
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000560608
  gene symbol: ADAM10
  hgvsc: ENST00000560608.1:n.464-11789A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452704
  ensembl transcript: ENST00000558004
  gene symbol: ADAM10
  hgvsc: ENST00000558004.1:c.331+7209A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000386056
  ensembl transcript: ENST00000402627
  gene symbol: ADAM10
  hgvsc: ENST00000402627.1:c.56-50241A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000391930
  ensembl transcript: ENST00000439637
  gene symbol: ADAM10
  hgvsc: ENST00000439637.1:c.207-8757A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000379444
  ensembl transcript: ENST00000396140
  gene symbol: ADAM10
  hgvsc: ENST00000396140.2:c.56-50241A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000497846
  gene symbol: ADAM10
  hgvsc: ENST00000497846.1:n.324-8757A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000453952
  ensembl transcript: ENST00000559053
  gene symbol: ADAM10
  hgvsc: ENST00000559053.1:c.56-50241A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000561149
  gene symbol: ADAM10
  hgvsc: ENST00000561149.1:n.467-8757A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000558733
  gene symbol: ADAM10
  hgvsc: ENST00000558733.1:n.443-8757A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452639
  ensembl transcript: ENST00000561288
  gene symbol: ADAM10
  hgvsc: ENST00000561288.1:c.55+58409A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000260408
  ensembl transcript: ENST00000260408
  gene symbol: ADAM10
  hgvsc: ENST00000260408.3:c.207-8757A>G
  variant of: http://identifiers.org/hgnc/188
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2064
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12652
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9016
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8386
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2137
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13671
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9927
  bin: 1.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1989
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

15-58983272-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58983272
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 58983272
    reference: chr 15
allele count: 1
allele frequency: 1.011879464918139e-5
allele num: 98826
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000561149
  gene symbol: ADAM10
  hgvsc: ENST00000561149.1:n.467-8759G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000391930
  ensembl transcript: ENST00000439637
  gene symbol: ADAM10
  hgvsc: ENST00000439637.1:c.207-8759G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000386056
  ensembl transcript: ENST00000402627
  gene symbol: ADAM10
  hgvsc: ENST00000402627.1:c.56-50243G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452639
  ensembl transcript: ENST00000561288
  gene symbol: ADAM10
  hgvsc: ENST00000561288.1:c.55+58407G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000560608
  gene symbol: ADAM10
  hgvsc: ENST00000560608.1:n.464-11791G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000558733
  gene symbol: ADAM10
  hgvsc: ENST00000558733.1:n.443-8759G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000260408
  ensembl transcript: ENST00000260408
  gene symbol: ADAM10
  hgvsc: ENST00000260408.3:c.207-8759G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000497846
  gene symbol: ADAM10
  hgvsc: ENST00000497846.1:n.324-8759G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000453952
  ensembl transcript: ENST00000559053
  gene symbol: ADAM10
  hgvsc: ENST00000559053.1:c.56-50243G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452704
  ensembl transcript: ENST00000558004
  gene symbol: ADAM10
  hgvsc: ENST00000558004.1:c.331+7207G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000379444
  ensembl transcript: ENST00000396140
  gene symbol: ADAM10
  hgvsc: ENST00000396140.2:c.56-50243G>A
  variant of: http://identifiers.org/hgnc/188
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14199
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2046
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9600
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8858
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8459
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2058
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12634
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 769
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum

15-58983273-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58983273
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 58983273
    reference: chr 15
allele count: 5
allele frequency: 5.043780010491062e-5
allele num: 99132
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000260408
  ensembl transcript: ENST00000260408
  gene symbol: ADAM10
  hgvsc: ENST00000260408.3:c.207-8760C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000379444
  ensembl transcript: ENST00000396140
  gene symbol: ADAM10
  hgvsc: ENST00000396140.2:c.56-50244C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000386056
  ensembl transcript: ENST00000402627
  gene symbol: ADAM10
  hgvsc: ENST00000402627.1:c.56-50244C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000497846
  gene symbol: ADAM10
  hgvsc: ENST00000497846.1:n.324-8760C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452704
  ensembl transcript: ENST00000558004
  gene symbol: ADAM10
  hgvsc: ENST00000558004.1:c.331+7206C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000560608
  gene symbol: ADAM10
  hgvsc: ENST00000560608.1:n.464-11792C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000453952
  ensembl transcript: ENST00000559053
  gene symbol: ADAM10
  hgvsc: ENST00000559053.1:c.56-50244C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000391930
  ensembl transcript: ENST00000439637
  gene symbol: ADAM10
  hgvsc: ENST00000439637.1:c.207-8760C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452639
  ensembl transcript: ENST00000561288
  gene symbol: ADAM10
  hgvsc: ENST00000561288.1:c.55+58406C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000561149
  gene symbol: ADAM10
  hgvsc: ENST00000561149.1:n.467-8760C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000558733
  gene symbol: ADAM10
  hgvsc: ENST00000558733.1:n.443-8760C>T
  variant of: http://identifiers.org/hgnc/188
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8536
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2001
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12622
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8783
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14636
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1981
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9307
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4205
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: African
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ

15-58983279-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58983279
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 58983279
    reference: chr 15
allele count: 2
allele frequency: 2.011141725157372e-5
allele num: 99446
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452704
  ensembl transcript: ENST00000558004
  gene symbol: ADAM10
  hgvsc: ENST00000558004.1:c.331+7200T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452639
  ensembl transcript: ENST00000561288
  gene symbol: ADAM10
  hgvsc: ENST00000561288.1:c.55+58400T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000386056
  ensembl transcript: ENST00000402627
  gene symbol: ADAM10
  hgvsc: ENST00000402627.1:c.56-50250T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000560608
  gene symbol: ADAM10
  hgvsc: ENST00000560608.1:n.464-11798T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000379444
  ensembl transcript: ENST00000396140
  gene symbol: ADAM10
  hgvsc: ENST00000396140.2:c.56-50250T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000561149
  gene symbol: ADAM10
  hgvsc: ENST00000561149.1:n.467-8766T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000391930
  ensembl transcript: ENST00000439637
  gene symbol: ADAM10
  hgvsc: ENST00000439637.1:c.207-8766T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000497846
  gene symbol: ADAM10
  hgvsc: ENST00000497846.1:n.324-8766T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000558733
  gene symbol: ADAM10
  hgvsc: ENST00000558733.1:n.443-8766T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000260408
  ensembl transcript: ENST00000260408
  gene symbol: ADAM10
  hgvsc: ENST00000260408.3:c.207-8766T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000453952
  ensembl transcript: ENST00000559053
  gene symbol: ADAM10
  hgvsc: ENST00000559053.1:c.56-50250T>C
  variant of: http://identifiers.org/hgnc/188
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8648
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1895
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8455
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15922
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1879
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12614
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8444
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12740
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: African
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: QD

15-58983280-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58983280
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 58983280
    reference: chr 15
allele count: 5
allele frequency: 5.026034860577793e-5
allele num: 99482
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000558733
  gene symbol: ADAM10
  hgvsc: ENST00000558733.1:n.443-8767A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000379444
  ensembl transcript: ENST00000396140
  gene symbol: ADAM10
  hgvsc: ENST00000396140.2:c.56-50251A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000391930
  ensembl transcript: ENST00000439637
  gene symbol: ADAM10
  hgvsc: ENST00000439637.1:c.207-8767A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452639
  ensembl transcript: ENST00000561288
  gene symbol: ADAM10
  hgvsc: ENST00000561288.1:c.55+58399A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000260408
  ensembl transcript: ENST00000260408
  gene symbol: ADAM10
  hgvsc: ENST00000260408.3:c.207-8767A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452704
  ensembl transcript: ENST00000558004
  gene symbol: ADAM10
  hgvsc: ENST00000558004.1:c.331+7199A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000386056
  ensembl transcript: ENST00000402627
  gene symbol: ADAM10
  hgvsc: ENST00000402627.1:c.56-50251A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000561149
  gene symbol: ADAM10
  hgvsc: ENST00000561149.1:n.467-8767A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000560608
  gene symbol: ADAM10
  hgvsc: ENST00000560608.1:n.464-11799A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000497846
  gene symbol: ADAM10
  hgvsc: ENST00000497846.1:n.324-8767A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000453952
  ensembl transcript: ENST00000559053
  gene symbol: ADAM10
  hgvsc: ENST00000559053.1:c.56-50251A>G
  variant of: http://identifiers.org/hgnc/188
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8357
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8422
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8679
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12623
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1850
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16048
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1877
  bin: 3.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 753
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
reference allele: T
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum

15-58983300-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58983300
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 58983300
    reference: chr 15
allele count: 2
allele frequency: 1.999000499750125e-5
allele num: 100050
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452704
  ensembl transcript: ENST00000558004
  gene symbol: ADAM10
  hgvsc: ENST00000558004.1:c.331+7179T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000260408
  ensembl transcript: ENST00000260408
  gene symbol: ADAM10
  hgvsc: ENST00000260408.3:c.207-8787T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000453952
  ensembl transcript: ENST00000559053
  gene symbol: ADAM10
  hgvsc: ENST00000559053.1:c.56-50271T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000558733
  gene symbol: ADAM10
  hgvsc: ENST00000558733.1:n.443-8787T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000391930
  ensembl transcript: ENST00000439637
  gene symbol: ADAM10
  hgvsc: ENST00000439637.1:c.207-8787T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452639
  ensembl transcript: ENST00000561288
  gene symbol: ADAM10
  hgvsc: ENST00000561288.1:c.55+58379T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000379444
  ensembl transcript: ENST00000396140
  gene symbol: ADAM10
  hgvsc: ENST00000396140.2:c.56-50271T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000561149
  gene symbol: ADAM10
  hgvsc: ENST00000561149.1:n.467-8787T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000560608
  gene symbol: ADAM10
  hgvsc: ENST00000560608.1:n.464-11819T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000497846
  gene symbol: ADAM10
  hgvsc: ENST00000497846.1:n.324-8787T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000386056
  ensembl transcript: ENST00000402627
  gene symbol: ADAM10
  hgvsc: ENST00000402627.1:c.56-50271T>C
  variant of: http://identifiers.org/hgnc/188
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7645
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1686
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8503
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18038
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12208
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7989
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1773
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2722
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ

15-58983308-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58983308
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 58983308
    reference: chr 15
allele count: 1
allele frequency: 9.945894334818586e-6
allele num: 100544
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000386056
  ensembl transcript: ENST00000402627
  gene symbol: ADAM10
  hgvsc: ENST00000402627.1:c.56-50279C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452639
  ensembl transcript: ENST00000561288
  gene symbol: ADAM10
  hgvsc: ENST00000561288.1:c.55+58371C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000561149
  gene symbol: ADAM10
  hgvsc: ENST00000561149.1:n.467-8795C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000560608
  gene symbol: ADAM10
  hgvsc: ENST00000560608.1:n.464-11827C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452704
  ensembl transcript: ENST00000558004
  gene symbol: ADAM10
  hgvsc: ENST00000558004.1:c.331+7171C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000497846
  gene symbol: ADAM10
  hgvsc: ENST00000497846.1:n.324-8795C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000379444
  ensembl transcript: ENST00000396140
  gene symbol: ADAM10
  hgvsc: ENST00000396140.2:c.56-50279C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000391930
  ensembl transcript: ENST00000439637
  gene symbol: ADAM10
  hgvsc: ENST00000439637.1:c.207-8795C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000558733
  gene symbol: ADAM10
  hgvsc: ENST00000558733.1:n.443-8795C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000260408
  ensembl transcript: ENST00000260408
  gene symbol: ADAM10
  hgvsc: ENST00000260408.3:c.207-8795C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000453952
  ensembl transcript: ENST00000559053
  gene symbol: ADAM10
  hgvsc: ENST00000559053.1:c.56-50279C>T
  variant of: http://identifiers.org/hgnc/188
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11917
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18933
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7396
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8275
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7894
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1619
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1805
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 784
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: FS

15-58983309-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58983309
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 58983309
    reference: chr 15
allele count: 0
allele frequency: 0.0e0
allele num: 100754
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000391930
  ensembl transcript: ENST00000439637
  gene symbol: ADAM10
  hgvsc: ENST00000439637.1:c.207-8796A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000453952
  ensembl transcript: ENST00000559053
  gene symbol: ADAM10
  hgvsc: ENST00000559053.1:c.56-50280A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452639
  ensembl transcript: ENST00000561288
  gene symbol: ADAM10
  hgvsc: ENST00000561288.1:c.55+58370A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000386056
  ensembl transcript: ENST00000402627
  gene symbol: ADAM10
  hgvsc: ENST00000402627.1:c.56-50280A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000497846
  gene symbol: ADAM10
  hgvsc: ENST00000497846.1:n.324-8796A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000379444
  ensembl transcript: ENST00000396140
  gene symbol: ADAM10
  hgvsc: ENST00000396140.2:c.56-50280A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452704
  ensembl transcript: ENST00000558004
  gene symbol: ADAM10
  hgvsc: ENST00000558004.1:c.331+7170A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000558733
  gene symbol: ADAM10
  hgvsc: ENST00000558733.1:n.443-8796A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000561149
  gene symbol: ADAM10
  hgvsc: ENST00000561149.1:n.467-8796A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000260408
  ensembl transcript: ENST00000260408
  gene symbol: ADAM10
  hgvsc: ENST00000260408.3:c.207-8796A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000560608
  gene symbol: ADAM10
  hgvsc: ENST00000560608.1:n.464-11828A>G
  variant of: http://identifiers.org/hgnc/188
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8243
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11839
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19199
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1611
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1797
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7253
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7897
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4658
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: DP

15-58983310-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58983310
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 58983310
    reference: chr 15
allele count: 1
allele frequency: 9.910999226942061e-6
allele num: 100898
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000497846
  gene symbol: ADAM10
  hgvsc: ENST00000497846.1:n.324-8797T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000560608
  gene symbol: ADAM10
  hgvsc: ENST00000560608.1:n.464-11829T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000453952
  ensembl transcript: ENST00000559053
  gene symbol: ADAM10
  hgvsc: ENST00000559053.1:c.56-50281T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000558733
  gene symbol: ADAM10
  hgvsc: ENST00000558733.1:n.443-8797T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000561149
  gene symbol: ADAM10
  hgvsc: ENST00000561149.1:n.467-8797T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000391930
  ensembl transcript: ENST00000439637
  gene symbol: ADAM10
  hgvsc: ENST00000439637.1:c.207-8797T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000379444
  ensembl transcript: ENST00000396140
  gene symbol: ADAM10
  hgvsc: ENST00000396140.2:c.56-50281T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000386056
  ensembl transcript: ENST00000402627
  gene symbol: ADAM10
  hgvsc: ENST00000402627.1:c.56-50281T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452704
  ensembl transcript: ENST00000558004
  gene symbol: ADAM10
  hgvsc: ENST00000558004.1:c.331+7169T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452639
  ensembl transcript: ENST00000561288
  gene symbol: ADAM10
  hgvsc: ENST00000561288.1:c.55+58369T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000260408
  ensembl transcript: ENST00000260408
  gene symbol: ADAM10
  hgvsc: ENST00000260408.3:c.207-8797T>C
  variant of: http://identifiers.org/hgnc/188
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7940
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8166
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11754
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1603
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19478
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7096
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1812
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1627
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

15-58983314-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58983314
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 58983314
    reference: chr 15
allele count: 19
allele frequency: 1.88070397719399e-4
allele num: 101026
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000560608
  gene symbol: ADAM10
  hgvsc: ENST00000560608.1:n.464-11833C>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452639
  ensembl transcript: ENST00000561288
  gene symbol: ADAM10
  hgvsc: ENST00000561288.1:c.55+58365C>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000379444
  ensembl transcript: ENST00000396140
  gene symbol: ADAM10
  hgvsc: ENST00000396140.2:c.56-50285C>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000260408
  ensembl transcript: ENST00000260408
  gene symbol: ADAM10
  hgvsc: ENST00000260408.3:c.207-8801C>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000386056
  ensembl transcript: ENST00000402627
  gene symbol: ADAM10
  hgvsc: ENST00000402627.1:c.56-50285C>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000558733
  gene symbol: ADAM10
  hgvsc: ENST00000558733.1:n.443-8801C>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000453952
  ensembl transcript: ENST00000559053
  gene symbol: ADAM10
  hgvsc: ENST00000559053.1:c.56-50285C>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000497846
  gene symbol: ADAM10
  hgvsc: ENST00000497846.1:n.324-8801C>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000561149
  gene symbol: ADAM10
  hgvsc: ENST00000561149.1:n.467-8801C>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452704
  ensembl transcript: ENST00000558004
  gene symbol: ADAM10
  hgvsc: ENST00000558004.1:c.331+7165C>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000391930
  ensembl transcript: ENST00000439637
  gene symbol: ADAM10
  hgvsc: ENST00000439637.1:c.207-8801C>A
  variant of: http://identifiers.org/hgnc/188
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11713
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8085
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7957
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19598
  bin: 2.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1585
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1840
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7078
  bin: 1.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 815
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum

15-58983318-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58983318
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 58983318
    reference: chr 15
allele count: 20358
allele frequency: 1.995060857294055e-1
allele num: 102042
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000497846
  gene symbol: ADAM10
  hgvsc: ENST00000497846.1:n.324-8805C>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000453952
  ensembl transcript: ENST00000559053
  gene symbol: ADAM10
  hgvsc: ENST00000559053.1:c.56-50289C>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000558733
  gene symbol: ADAM10
  hgvsc: ENST00000558733.1:n.443-8805C>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000391930
  ensembl transcript: ENST00000439637
  gene symbol: ADAM10
  hgvsc: ENST00000439637.1:c.207-8805C>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452639
  ensembl transcript: ENST00000561288
  gene symbol: ADAM10
  hgvsc: ENST00000561288.1:c.55+58361C>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000260408
  ensembl transcript: ENST00000260408
  gene symbol: ADAM10
  hgvsc: ENST00000260408.3:c.207-8805C>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000561149
  gene symbol: ADAM10
  hgvsc: ENST00000561149.1:n.467-8805C>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000379444
  ensembl transcript: ENST00000396140
  gene symbol: ADAM10
  hgvsc: ENST00000396140.2:c.56-50289C>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000560608
  gene symbol: ADAM10
  hgvsc: ENST00000560608.1:n.464-11837C>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000386056
  ensembl transcript: ENST00000402627
  gene symbol: ADAM10
  hgvsc: ENST00000402627.1:c.56-50289C>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452704
  ensembl transcript: ENST00000558004
  gene symbol: ADAM10
  hgvsc: ENST00000558004.1:c.331+7161C>G
  variant of: http://identifiers.org/hgnc/188
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10838
  bin: 1.25e1
  variant carriers: 3477
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 4.25e1
  variant carriers: 226
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 6.25e1
  variant carriers: 48
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 4.75e1
  variant carriers: 120
genotype depth: GenotypeDepth
  all individuals: 1281
  bin: 2.5e0
  variant carriers: 91
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.25e1
  variant carriers: 52
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 7.25e1
  variant carriers: 45
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.75e1
  variant carriers: 61
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.75e1
  variant carriers: 51
genotype depth: GenotypeDepth
  all individuals: 8723
  bin: 2.75e1
  variant carriers: 2568
genotype depth: GenotypeDepth
  all individuals: 17745
  bin: 2.25e1
  variant carriers: 4331
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.75e1
  variant carriers: 47
genotype depth: GenotypeDepth
  all individuals: 2421
  bin: 3.25e1
  variant carriers: 1153
genotype depth: GenotypeDepth
  all individuals: 6968
  bin: 7.5e0
  variant carriers: 1042
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 9.25e1
  variant carriers: 55
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 5.25e1
  variant carriers: 61
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 6.75e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 9.75e1
  variant carriers: 397
genotype depth: GenotypeDepth
  all individuals: 9199
  bin: 1.75e1
  variant carriers: 5363
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 3.75e1
  variant carriers: 443
genotype quality: GenotypeQuality
  all individuals: 1120
  bin: 2.5e0
  variant carriers: 72
num of homozygotes: 2033
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD

15-58983325-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58983325
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 58983325
    reference: chr 15
allele count: 1
allele frequency: 1.005854070691424e-5
allele num: 99418
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452704
  ensembl transcript: ENST00000558004
  gene symbol: ADAM10
  hgvsc: ENST00000558004.1:c.331+7154A>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000386056
  ensembl transcript: ENST00000402627
  gene symbol: ADAM10
  hgvsc: ENST00000402627.1:c.56-50296A>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000391930
  ensembl transcript: ENST00000439637
  gene symbol: ADAM10
  hgvsc: ENST00000439637.1:c.207-8812A>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000260408
  ensembl transcript: ENST00000260408
  gene symbol: ADAM10
  hgvsc: ENST00000260408.3:c.207-8812A>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000497846
  gene symbol: ADAM10
  hgvsc: ENST00000497846.1:n.324-8812A>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452639
  ensembl transcript: ENST00000561288
  gene symbol: ADAM10
  hgvsc: ENST00000561288.1:c.55+58354A>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000379444
  ensembl transcript: ENST00000396140
  gene symbol: ADAM10
  hgvsc: ENST00000396140.2:c.56-50296A>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000561149
  gene symbol: ADAM10
  hgvsc: ENST00000561149.1:n.467-8812A>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000560608
  gene symbol: ADAM10
  hgvsc: ENST00000560608.1:n.464-11844A>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000453952
  ensembl transcript: ENST00000559053
  gene symbol: ADAM10
  hgvsc: ENST00000559053.1:c.56-50296A>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000558733
  gene symbol: ADAM10
  hgvsc: ENST00000558733.1:n.443-8812A>C
  variant of: http://identifiers.org/hgnc/188
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1645
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16705
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8823
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1754
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7659
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8064
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13236
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3891
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
reference allele: T
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: DP

http://identifiers.org/exac.variant/15-58983327-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58983327
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 58983327
    reference: chr 15
allele count: 1
allele frequency: 1.010121416594275e-5
allele num: 98998
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000561149
  gene symbol: ADAM10
  hgvsc: ENST00000561149.1:n.467-8814G>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000453952
  ensembl transcript: ENST00000559053
  gene symbol: ADAM10
  hgvsc: ENST00000559053.1:c.56-50298G>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000386056
  ensembl transcript: ENST00000402627
  gene symbol: ADAM10
  hgvsc: ENST00000402627.1:c.56-50298G>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452704
  ensembl transcript: ENST00000558004
  gene symbol: ADAM10
  hgvsc: ENST00000558004.1:c.331+7152G>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452639
  ensembl transcript: ENST00000561288
  gene symbol: ADAM10
  hgvsc: ENST00000561288.1:c.55+58352G>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000560608
  gene symbol: ADAM10
  hgvsc: ENST00000560608.1:n.464-11846G>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000260408
  ensembl transcript: ENST00000260408
  gene symbol: ADAM10
  hgvsc: ENST00000260408.3:c.207-8814G>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000379444
  ensembl transcript: ENST00000396140
  gene symbol: ADAM10
  hgvsc: ENST00000396140.2:c.56-50298G>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000558733
  gene symbol: ADAM10
  hgvsc: ENST00000558733.1:n.443-8814G>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000391930
  ensembl transcript: ENST00000439637
  gene symbol: ADAM10
  hgvsc: ENST00000439637.1:c.207-8814G>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000497846
  gene symbol: ADAM10
  hgvsc: ENST00000497846.1:n.324-8814G>T
  variant of: http://identifiers.org/hgnc/188
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1810
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1648
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13148
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8820
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16835
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8089
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7545
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 755
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD

15-58983327-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58983327
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 58983327
    reference: chr 15
allele count: 1
allele frequency: 1.010121416594275e-5
allele num: 98998
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000560608
  gene symbol: ADAM10
  hgvsc: ENST00000560608.1:n.464-11846G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000391930
  ensembl transcript: ENST00000439637
  gene symbol: ADAM10
  hgvsc: ENST00000439637.1:c.207-8814G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000379444
  ensembl transcript: ENST00000396140
  gene symbol: ADAM10
  hgvsc: ENST00000396140.2:c.56-50298G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452704
  ensembl transcript: ENST00000558004
  gene symbol: ADAM10
  hgvsc: ENST00000558004.1:c.331+7152G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000260408
  ensembl transcript: ENST00000260408
  gene symbol: ADAM10
  hgvsc: ENST00000260408.3:c.207-8814G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452639
  ensembl transcript: ENST00000561288
  gene symbol: ADAM10
  hgvsc: ENST00000561288.1:c.55+58352G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000386056
  ensembl transcript: ENST00000402627
  gene symbol: ADAM10
  hgvsc: ENST00000402627.1:c.56-50298G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000561149
  gene symbol: ADAM10
  hgvsc: ENST00000561149.1:n.467-8814G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000497846
  gene symbol: ADAM10
  hgvsc: ENST00000497846.1:n.324-8814G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000453952
  ensembl transcript: ENST00000559053
  gene symbol: ADAM10
  hgvsc: ENST00000559053.1:c.56-50298G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000558733
  gene symbol: ADAM10
  hgvsc: ENST00000558733.1:n.443-8814G>A
  variant of: http://identifiers.org/hgnc/188
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13148
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1810
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16835
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8089
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7545
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1648
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8820
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 714
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: African
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQ

15-58983328-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58983328
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 58983328
    reference: chr 15
allele count: 20
allele frequency: 2.018326403746014e-4
allele num: 99092
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000391930
  ensembl transcript: ENST00000439637
  gene symbol: ADAM10
  hgvsc: ENST00000439637.1:c.207-8815C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000561149
  gene symbol: ADAM10
  hgvsc: ENST00000561149.1:n.467-8815C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000560608
  gene symbol: ADAM10
  hgvsc: ENST00000560608.1:n.464-11847C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000453952
  ensembl transcript: ENST00000559053
  gene symbol: ADAM10
  hgvsc: ENST00000559053.1:c.56-50299C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000497846
  gene symbol: ADAM10
  hgvsc: ENST00000497846.1:n.324-8815C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000260408
  ensembl transcript: ENST00000260408
  gene symbol: ADAM10
  hgvsc: ENST00000260408.3:c.207-8815C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000386056
  ensembl transcript: ENST00000402627
  gene symbol: ADAM10
  hgvsc: ENST00000402627.1:c.56-50299C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452639
  ensembl transcript: ENST00000561288
  gene symbol: ADAM10
  hgvsc: ENST00000561288.1:c.55+58351C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000379444
  ensembl transcript: ENST00000396140
  gene symbol: ADAM10
  hgvsc: ENST00000396140.2:c.56-50299C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452704
  ensembl transcript: ENST00000558004
  gene symbol: ADAM10
  hgvsc: ENST00000558004.1:c.331+7151C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000558733
  gene symbol: ADAM10
  hgvsc: ENST00000558733.1:n.443-8815C>T
  variant of: http://identifiers.org/hgnc/188
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1658
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8862
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8089
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 13188
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7412
  bin: 1.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1792
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16906
  bin: 2.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 19768
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

15-58983329-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58983329
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 58983329
    reference: chr 15
allele count: 0
allele frequency: 0.0e0
allele num: 98924
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000386056
  ensembl transcript: ENST00000402627
  gene symbol: ADAM10
  hgvsc: ENST00000402627.1:c.56-50300C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000391930
  ensembl transcript: ENST00000439637
  gene symbol: ADAM10
  hgvsc: ENST00000439637.1:c.207-8816C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452704
  ensembl transcript: ENST00000558004
  gene symbol: ADAM10
  hgvsc: ENST00000558004.1:c.331+7150C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000379444
  ensembl transcript: ENST00000396140
  gene symbol: ADAM10
  hgvsc: ENST00000396140.2:c.56-50300C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000560608
  gene symbol: ADAM10
  hgvsc: ENST00000560608.1:n.464-11848C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000561149
  gene symbol: ADAM10
  hgvsc: ENST00000561149.1:n.467-8816C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000497846
  gene symbol: ADAM10
  hgvsc: ENST00000497846.1:n.324-8816C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452639
  ensembl transcript: ENST00000561288
  gene symbol: ADAM10
  hgvsc: ENST00000561288.1:c.55+58350C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000453952
  ensembl transcript: ENST00000559053
  gene symbol: ADAM10
  hgvsc: ENST00000559053.1:c.56-50300C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000558733
  gene symbol: ADAM10
  hgvsc: ENST00000558733.1:n.443-8816C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000260408
  ensembl transcript: ENST00000260408
  gene symbol: ADAM10
  hgvsc: ENST00000260408.3:c.207-8816C>T
  variant of: http://identifiers.org/hgnc/188
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 7518
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13312
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16730
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1672
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7947
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8958
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1769
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4606
  bin: 3.25e1
  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: MQ
site quality: QD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD

15-58983335-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58983335
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 58983335
    reference: chr 15
allele count: 71
allele frequency: 7.410190577577389e-4
allele num: 95814
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000561149
  gene symbol: ADAM10
  hgvsc: ENST00000561149.1:n.467-8822A>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000260408
  ensembl transcript: ENST00000260408
  gene symbol: ADAM10
  hgvsc: ENST00000260408.3:c.207-8822A>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000386056
  ensembl transcript: ENST00000402627
  gene symbol: ADAM10
  hgvsc: ENST00000402627.1:c.56-50306A>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000453952
  ensembl transcript: ENST00000559053
  gene symbol: ADAM10
  hgvsc: ENST00000559053.1:c.56-50306A>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000558733
  gene symbol: ADAM10
  hgvsc: ENST00000558733.1:n.443-8822A>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452639
  ensembl transcript: ENST00000561288
  gene symbol: ADAM10
  hgvsc: ENST00000561288.1:c.55+58344A>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000379444
  ensembl transcript: ENST00000396140
  gene symbol: ADAM10
  hgvsc: ENST00000396140.2:c.56-50306A>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000497846
  gene symbol: ADAM10
  hgvsc: ENST00000497846.1:n.324-8822A>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000560608
  gene symbol: ADAM10
  hgvsc: ENST00000560608.1:n.464-11854A>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452704
  ensembl transcript: ENST00000558004
  gene symbol: ADAM10
  hgvsc: ENST00000558004.1:c.331+7144A>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000391930
  ensembl transcript: ENST00000439637
  gene symbol: ADAM10
  hgvsc: ENST00000439637.1:c.207-8822A>C
  variant of: http://identifiers.org/hgnc/188
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.95to100.00
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1627
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13829
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1608
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 9375
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7623
  bin: 2.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16427
  bin: 2.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 9.75e1
  variant carriers: 37
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7512
  bin: 1.75e1
  variant carriers: 14
genotype quality: GenotypeQuality
  all individuals: 1718
  bin: 7.5e0
  variant carriers: 5
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
reference allele: T
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum

15-58983336-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58983336
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 58983336
    reference: chr 15
allele count: 1
allele frequency: 1.021325271672522e-5
allele num: 97912
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000391930
  ensembl transcript: ENST00000439637
  gene symbol: ADAM10
  hgvsc: ENST00000439637.1:c.207-8823C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000379444
  ensembl transcript: ENST00000396140
  gene symbol: ADAM10
  hgvsc: ENST00000396140.2:c.56-50307C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452704
  ensembl transcript: ENST00000558004
  gene symbol: ADAM10
  hgvsc: ENST00000558004.1:c.331+7143C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000497846
  gene symbol: ADAM10
  hgvsc: ENST00000497846.1:n.324-8823C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000386056
  ensembl transcript: ENST00000402627
  gene symbol: ADAM10
  hgvsc: ENST00000402627.1:c.56-50307C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000453952
  ensembl transcript: ENST00000559053
  gene symbol: ADAM10
  hgvsc: ENST00000559053.1:c.56-50307C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000558733
  gene symbol: ADAM10
  hgvsc: ENST00000558733.1:n.443-8823C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000561149
  gene symbol: ADAM10
  hgvsc: ENST00000561149.1:n.467-8823C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000260408
  ensembl transcript: ENST00000260408
  gene symbol: ADAM10
  hgvsc: ENST00000260408.3:c.207-8823C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000560608
  gene symbol: ADAM10
  hgvsc: ENST00000560608.1:n.464-11855C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452639
  ensembl transcript: ENST00000561288
  gene symbol: ADAM10
  hgvsc: ENST00000561288.1:c.55+58343C>T
  variant of: http://identifiers.org/hgnc/188
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7442
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16246
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1580
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9575
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13898
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7634
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1657
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2450
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD

http://identifiers.org/exac.variant/15-58983338-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58983338
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 58983338
    reference: chr 15
allele count: 13
allele frequency: 1.32688264233368e-4
allele num: 97974
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000497846
  gene symbol: ADAM10
  hgvsc: ENST00000497846.1:n.324-8825T>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452639
  ensembl transcript: ENST00000561288
  gene symbol: ADAM10
  hgvsc: ENST00000561288.1:c.55+58341T>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000391930
  ensembl transcript: ENST00000439637
  gene symbol: ADAM10
  hgvsc: ENST00000439637.1:c.207-8825T>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000561149
  gene symbol: ADAM10
  hgvsc: ENST00000561149.1:n.467-8825T>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000560608
  gene symbol: ADAM10
  hgvsc: ENST00000560608.1:n.464-11857T>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000379444
  ensembl transcript: ENST00000396140
  gene symbol: ADAM10
  hgvsc: ENST00000396140.2:c.56-50309T>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452704
  ensembl transcript: ENST00000558004
  gene symbol: ADAM10
  hgvsc: ENST00000558004.1:c.331+7141T>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000453952
  ensembl transcript: ENST00000559053
  gene symbol: ADAM10
  hgvsc: ENST00000559053.1:c.56-50309T>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000386056
  ensembl transcript: ENST00000402627
  gene symbol: ADAM10
  hgvsc: ENST00000402627.1:c.56-50309T>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000558733
  gene symbol: ADAM10
  hgvsc: ENST00000558733.1:n.443-8825T>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000260408
  ensembl transcript: ENST00000260408
  gene symbol: ADAM10
  hgvsc: ENST00000260408.3:c.207-8825T>G
  variant of: http://identifiers.org/hgnc/188
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1648
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16299
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 9687
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1574
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7242
  bin: 1.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7617
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13976
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4026
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: East Asian
population: Latino
reference allele: A
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ

15-58983345-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58983345
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 58983345
    reference: chr 15
allele count: 2
allele frequency: 2.068894176062894e-5
allele num: 96670
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000561149
  gene symbol: ADAM10
  hgvsc: ENST00000561149.1:n.467-8832T>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452704
  ensembl transcript: ENST00000558004
  gene symbol: ADAM10
  hgvsc: ENST00000558004.1:c.331+7134T>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000497846
  gene symbol: ADAM10
  hgvsc: ENST00000497846.1:n.324-8832T>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000391930
  ensembl transcript: ENST00000439637
  gene symbol: ADAM10
  hgvsc: ENST00000439637.1:c.207-8832T>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000386056
  ensembl transcript: ENST00000402627
  gene symbol: ADAM10
  hgvsc: ENST00000402627.1:c.56-50316T>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452639
  ensembl transcript: ENST00000561288
  gene symbol: ADAM10
  hgvsc: ENST00000561288.1:c.55+58334T>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000560608
  gene symbol: ADAM10
  hgvsc: ENST00000560608.1:n.464-11864T>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000453952
  ensembl transcript: ENST00000559053
  gene symbol: ADAM10
  hgvsc: ENST00000559053.1:c.56-50316T>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000558733
  gene symbol: ADAM10
  hgvsc: ENST00000558733.1:n.443-8832T>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000260408
  ensembl transcript: ENST00000260408
  gene symbol: ADAM10
  hgvsc: ENST00000260408.3:c.207-8832T>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000379444
  ensembl transcript: ENST00000396140
  gene symbol: ADAM10
  hgvsc: ENST00000396140.2:c.56-50316T>A
  variant of: http://identifiers.org/hgnc/188
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14513
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1683
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7531
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15259
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1615
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10218
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7231
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15959
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
reference allele: A
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ

15-58983357-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58983357
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 58983357
    reference: chr 15
allele count: 1
allele frequency: 1.046287770988533e-5
allele num: 95576
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452704
  ensembl transcript: ENST00000558004
  gene symbol: ADAM10
  hgvsc: ENST00000558004.1:c.331+7122T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000379444
  ensembl transcript: ENST00000396140
  gene symbol: ADAM10
  hgvsc: ENST00000396140.2:c.56-50328T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000260408
  ensembl transcript: ENST00000260408
  gene symbol: ADAM10
  hgvsc: ENST00000260408.3:c.207-8844T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000386056
  ensembl transcript: ENST00000402627
  gene symbol: ADAM10
  hgvsc: ENST00000402627.1:c.56-50328T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000453952
  ensembl transcript: ENST00000559053
  gene symbol: ADAM10
  hgvsc: ENST00000559053.1:c.56-50328T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000560608
  gene symbol: ADAM10
  hgvsc: ENST00000560608.1:n.464-11876T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000558733
  gene symbol: ADAM10
  hgvsc: ENST00000558733.1:n.443-8844T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000561149
  gene symbol: ADAM10
  hgvsc: ENST00000561149.1:n.467-8844T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452639
  ensembl transcript: ENST00000561288
  gene symbol: ADAM10
  hgvsc: ENST00000561288.1:c.55+58322T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000497846
  gene symbol: ADAM10
  hgvsc: ENST00000497846.1:n.324-8844T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000391930
  ensembl transcript: ENST00000439637
  gene symbol: ADAM10
  hgvsc: ENST00000439637.1:c.207-8844T>C
  variant of: http://identifiers.org/hgnc/188
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 11001
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6439
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1628
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14807
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1603
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6807
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15773
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 716
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: Other
population: East Asian
population: European (Finnish)
reference allele: A
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff

15-58983358-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58983358
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 58983358
    reference: chr 15
allele count: 209
allele frequency: 2.189077654649433e-3
allele num: 95474
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000453952
  ensembl transcript: ENST00000559053
  gene symbol: ADAM10
  hgvsc: ENST00000559053.1:c.56-50329A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000560608
  gene symbol: ADAM10
  hgvsc: ENST00000560608.1:n.464-11877A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000379444
  ensembl transcript: ENST00000396140
  gene symbol: ADAM10
  hgvsc: ENST00000396140.2:c.56-50329A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000558733
  gene symbol: ADAM10
  hgvsc: ENST00000558733.1:n.443-8845A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000386056
  ensembl transcript: ENST00000402627
  gene symbol: ADAM10
  hgvsc: ENST00000402627.1:c.56-50329A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452704
  ensembl transcript: ENST00000558004
  gene symbol: ADAM10
  hgvsc: ENST00000558004.1:c.331+7121A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000497846
  gene symbol: ADAM10
  hgvsc: ENST00000497846.1:n.324-8845A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000260408
  ensembl transcript: ENST00000260408
  gene symbol: ADAM10
  hgvsc: ENST00000260408.3:c.207-8845A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000561149
  gene symbol: ADAM10
  hgvsc: ENST00000561149.1:n.467-8845A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000391930
  ensembl transcript: ENST00000439637
  gene symbol: ADAM10
  hgvsc: ENST00000439637.1:c.207-8845A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452639
  ensembl transcript: ENST00000561288
  gene symbol: ADAM10
  hgvsc: ENST00000561288.1:c.55+58321A>G
  variant of: http://identifiers.org/hgnc/188
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1630
  bin: 3.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11033
  bin: 7.5e0
  variant carriers: 37
genotype depth: GenotypeDepth
  all individuals: 15635
  bin: 2.25e1
  variant carriers: 48
genotype depth: GenotypeDepth
  all individuals: 1594
  bin: 2.5e0
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 14898
  bin: 1.25e1
  variant carriers: 58
genotype depth: GenotypeDepth
  all individuals: 6788
  bin: 2.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6468
  bin: 1.75e1
  variant carriers: 51
genotype quality: GenotypeQuality
  all individuals: 17458
  bin: 6.25e1
  variant carriers: 5
num of homozygotes: 3
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: South Asian
reference allele: T
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/15-58983365-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58983365
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 58983365
    reference: chr 15
allele count: 1
allele frequency: 1.060130608090917e-5
allele num: 94328
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000560608
  gene symbol: ADAM10
  hgvsc: ENST00000560608.1:n.464-11884G>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000260408
  ensembl transcript: ENST00000260408
  gene symbol: ADAM10
  hgvsc: ENST00000260408.3:c.207-8852G>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000558733
  gene symbol: ADAM10
  hgvsc: ENST00000558733.1:n.443-8852G>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452639
  ensembl transcript: ENST00000561288
  gene symbol: ADAM10
  hgvsc: ENST00000561288.1:c.55+58314G>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000561149
  gene symbol: ADAM10
  hgvsc: ENST00000561149.1:n.467-8852G>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000379444
  ensembl transcript: ENST00000396140
  gene symbol: ADAM10
  hgvsc: ENST00000396140.2:c.56-50336G>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000386056
  ensembl transcript: ENST00000402627
  gene symbol: ADAM10
  hgvsc: ENST00000402627.1:c.56-50336G>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000391930
  ensembl transcript: ENST00000439637
  gene symbol: ADAM10
  hgvsc: ENST00000439637.1:c.207-8852G>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000497846
  gene symbol: ADAM10
  hgvsc: ENST00000497846.1:n.324-8852G>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452704
  ensembl transcript: ENST00000558004
  gene symbol: ADAM10
  hgvsc: ENST00000558004.1:c.331+7114G>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000453952
  ensembl transcript: ENST00000559053
  gene symbol: ADAM10
  hgvsc: ENST00000559053.1:c.56-50336G>T
  variant of: http://identifiers.org/hgnc/188
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11496
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15027
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1680
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15341
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6186
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6721
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1598
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2140
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD

15-58983366-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58983366
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 58983366
    reference: chr 15
allele count: 1
allele frequency: 1.065802655980219e-5
allele num: 93826
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000560608
  gene symbol: ADAM10
  hgvsc: ENST00000560608.1:n.464-11885G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000561149
  gene symbol: ADAM10
  hgvsc: ENST00000561149.1:n.467-8853G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000497846
  gene symbol: ADAM10
  hgvsc: ENST00000497846.1:n.324-8853G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000453952
  ensembl transcript: ENST00000559053
  gene symbol: ADAM10
  hgvsc: ENST00000559053.1:c.56-50337G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000260408
  ensembl transcript: ENST00000260408
  gene symbol: ADAM10
  hgvsc: ENST00000260408.3:c.207-8853G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000391930
  ensembl transcript: ENST00000439637
  gene symbol: ADAM10
  hgvsc: ENST00000439637.1:c.207-8853G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000379444
  ensembl transcript: ENST00000396140
  gene symbol: ADAM10
  hgvsc: ENST00000396140.2:c.56-50337G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452639
  ensembl transcript: ENST00000561288
  gene symbol: ADAM10
  hgvsc: ENST00000561288.1:c.55+58313G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452704
  ensembl transcript: ENST00000558004
  gene symbol: ADAM10
  hgvsc: ENST00000558004.1:c.331+7113G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000558733
  gene symbol: ADAM10
  hgvsc: ENST00000558733.1:n.443-8853G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000386056
  ensembl transcript: ENST00000402627
  gene symbol: ADAM10
  hgvsc: ENST00000402627.1:c.56-50337G>A
  variant of: http://identifiers.org/hgnc/188
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15340
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1697
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11554
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6686
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6165
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1599
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15001
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4188
  bin: 2.75e1
  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: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ

15-58983367-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58983367
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 58983367
    reference: chr 15
allele count: 1
allele frequency: 1.071007818357074e-5
allele num: 93370
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452639
  ensembl transcript: ENST00000561288
  gene symbol: ADAM10
  hgvsc: ENST00000561288.1:c.55+58312C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000391930
  ensembl transcript: ENST00000439637
  gene symbol: ADAM10
  hgvsc: ENST00000439637.1:c.207-8854C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000497846
  gene symbol: ADAM10
  hgvsc: ENST00000497846.1:n.324-8854C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000560608
  gene symbol: ADAM10
  hgvsc: ENST00000560608.1:n.464-11886C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000379444
  ensembl transcript: ENST00000396140
  gene symbol: ADAM10
  hgvsc: ENST00000396140.2:c.56-50338C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000558733
  gene symbol: ADAM10
  hgvsc: ENST00000558733.1:n.443-8854C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000386056
  ensembl transcript: ENST00000402627
  gene symbol: ADAM10
  hgvsc: ENST00000402627.1:c.56-50338C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000561149
  gene symbol: ADAM10
  hgvsc: ENST00000561149.1:n.467-8854C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452704
  ensembl transcript: ENST00000558004
  gene symbol: ADAM10
  hgvsc: ENST00000558004.1:c.331+7112C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000260408
  ensembl transcript: ENST00000260408
  gene symbol: ADAM10
  hgvsc: ENST00000260408.3:c.207-8854C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000453952
  ensembl transcript: ENST00000559053
  gene symbol: ADAM10
  hgvsc: ENST00000559053.1:c.56-50338C>T
  variant of: http://identifiers.org/hgnc/188
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1575
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15004
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11700
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6649
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1691
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15357
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6071
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 309
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: African
population: European (Finnish)
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum

15-58983373-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58983373
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 58983373
    reference: chr 15
allele count: 1
allele frequency: 1.071972214480201e-5
allele num: 93286
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452639
  ensembl transcript: ENST00000561288
  gene symbol: ADAM10
  hgvsc: ENST00000561288.1:c.55+58306G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000558733
  gene symbol: ADAM10
  hgvsc: ENST00000558733.1:n.443-8860G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000561149
  gene symbol: ADAM10
  hgvsc: ENST00000561149.1:n.467-8860G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000386056
  ensembl transcript: ENST00000402627
  gene symbol: ADAM10
  hgvsc: ENST00000402627.1:c.56-50344G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000391930
  ensembl transcript: ENST00000439637
  gene symbol: ADAM10
  hgvsc: ENST00000439637.1:c.207-8860G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000260408
  ensembl transcript: ENST00000260408
  gene symbol: ADAM10
  hgvsc: ENST00000260408.3:c.207-8860G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000453952
  ensembl transcript: ENST00000559053
  gene symbol: ADAM10
  hgvsc: ENST00000559053.1:c.56-50344G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452704
  ensembl transcript: ENST00000558004
  gene symbol: ADAM10
  hgvsc: ENST00000558004.1:c.331+7106G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000379444
  ensembl transcript: ENST00000396140
  gene symbol: ADAM10
  hgvsc: ENST00000396140.2:c.56-50344G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000560608
  gene symbol: ADAM10
  hgvsc: ENST00000560608.1:n.464-11892G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000497846
  gene symbol: ADAM10
  hgvsc: ENST00000497846.1:n.324-8860G>A
  variant of: http://identifiers.org/hgnc/188
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 12173
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1587
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1646
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6289
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15632
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15055
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5673
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2144
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

15-58983380-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58983380
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 58983380
    reference: chr 15
allele count: 1
allele frequency: 1.08084738434933e-5
allele num: 92520
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000260408
  ensembl transcript: ENST00000260408
  gene symbol: ADAM10
  hgvsc: ENST00000260408.3:c.207-8867T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000386056
  ensembl transcript: ENST00000402627
  gene symbol: ADAM10
  hgvsc: ENST00000402627.1:c.56-50351T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000561149
  gene symbol: ADAM10
  hgvsc: ENST00000561149.1:n.467-8867T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000391930
  ensembl transcript: ENST00000439637
  gene symbol: ADAM10
  hgvsc: ENST00000439637.1:c.207-8867T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452704
  ensembl transcript: ENST00000558004
  gene symbol: ADAM10
  hgvsc: ENST00000558004.1:c.331+7099T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000560608
  gene symbol: ADAM10
  hgvsc: ENST00000560608.1:n.464-11899T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000497846
  gene symbol: ADAM10
  hgvsc: ENST00000497846.1:n.324-8867T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000379444
  ensembl transcript: ENST00000396140
  gene symbol: ADAM10
  hgvsc: ENST00000396140.2:c.56-50351T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000453952
  ensembl transcript: ENST00000559053
  gene symbol: ADAM10
  hgvsc: ENST00000559053.1:c.56-50351T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000558733
  gene symbol: ADAM10
  hgvsc: ENST00000558733.1:n.443-8867T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452639
  ensembl transcript: ENST00000561288
  gene symbol: ADAM10
  hgvsc: ENST00000561288.1:c.55+58299T>C
  variant of: http://identifiers.org/hgnc/188
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5469
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1614
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15724
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12586
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1593
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15107
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5963
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 474
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD

15-58983383-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58983383
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 58983383
    reference: chr 15
allele count: 7
allele frequency: 7.599279154091669e-5
allele num: 92114
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000379444
  ensembl transcript: ENST00000396140
  gene symbol: ADAM10
  hgvsc: ENST00000396140.2:c.56-50354A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452704
  ensembl transcript: ENST00000558004
  gene symbol: ADAM10
  hgvsc: ENST00000558004.1:c.331+7096A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000260408
  ensembl transcript: ENST00000260408
  gene symbol: ADAM10
  hgvsc: ENST00000260408.3:c.207-8870A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000391930
  ensembl transcript: ENST00000439637
  gene symbol: ADAM10
  hgvsc: ENST00000439637.1:c.207-8870A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000560608
  gene symbol: ADAM10
  hgvsc: ENST00000560608.1:n.464-11902A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000497846
  gene symbol: ADAM10
  hgvsc: ENST00000497846.1:n.324-8870A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000558733
  gene symbol: ADAM10
  hgvsc: ENST00000558733.1:n.443-8870A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000386056
  ensembl transcript: ENST00000402627
  gene symbol: ADAM10
  hgvsc: ENST00000402627.1:c.56-50354A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000453952
  ensembl transcript: ENST00000559053
  gene symbol: ADAM10
  hgvsc: ENST00000559053.1:c.56-50354A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452639
  ensembl transcript: ENST00000561288
  gene symbol: ADAM10
  hgvsc: ENST00000561288.1:c.55+58296A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000561149
  gene symbol: ADAM10
  hgvsc: ENST00000561149.1:n.467-8870A>G
  variant of: http://identifiers.org/hgnc/188
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1613
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15528
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5823
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12714
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15196
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1625
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5558
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 952
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: QD

15-58983391-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58983391
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 58983391
    reference: chr 15
allele count: 1
allele frequency: 1.094379268079146e-5
allele num: 91376
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000391930
  ensembl transcript: ENST00000439637
  gene symbol: ADAM10
  hgvsc: ENST00000439637.1:c.207-8878G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000558733
  gene symbol: ADAM10
  hgvsc: ENST00000558733.1:n.443-8878G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452639
  ensembl transcript: ENST00000561288
  gene symbol: ADAM10
  hgvsc: ENST00000561288.1:c.55+58288G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452704
  ensembl transcript: ENST00000558004
  gene symbol: ADAM10
  hgvsc: ENST00000558004.1:c.331+7088G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000379444
  ensembl transcript: ENST00000396140
  gene symbol: ADAM10
  hgvsc: ENST00000396140.2:c.56-50362G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000386056
  ensembl transcript: ENST00000402627
  gene symbol: ADAM10
  hgvsc: ENST00000402627.1:c.56-50362G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000560608
  gene symbol: ADAM10
  hgvsc: ENST00000560608.1:n.464-11910G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000497846
  gene symbol: ADAM10
  hgvsc: ENST00000497846.1:n.324-8878G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000260408
  ensembl transcript: ENST00000260408
  gene symbol: ADAM10
  hgvsc: ENST00000260408.3:c.207-8878G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000561149
  gene symbol: ADAM10
  hgvsc: ENST00000561149.1:n.467-8878G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000453952
  ensembl transcript: ENST00000559053
  gene symbol: ADAM10
  hgvsc: ENST00000559053.1:c.56-50362G>A
  variant of: http://identifiers.org/hgnc/188
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5824
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13065
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1596
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5657
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15398
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14904
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1619
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 667
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

15-58983409-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58983409
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 58983409
    reference: chr 15
allele count: 1
allele frequency: 1.110222932764899e-5
allele num: 90072
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000561149
  gene symbol: ADAM10
  hgvsc: ENST00000561149.1:n.467-8896C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000497846
  gene symbol: ADAM10
  hgvsc: ENST00000497846.1:n.324-8896C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000560608
  gene symbol: ADAM10
  hgvsc: ENST00000560608.1:n.464-11928C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000391930
  ensembl transcript: ENST00000439637
  gene symbol: ADAM10
  hgvsc: ENST00000439637.1:c.207-8896C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000386056
  ensembl transcript: ENST00000402627
  gene symbol: ADAM10
  hgvsc: ENST00000402627.1:c.56-50380C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000379444
  ensembl transcript: ENST00000396140
  gene symbol: ADAM10
  hgvsc: ENST00000396140.2:c.56-50380C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000453952
  ensembl transcript: ENST00000559053
  gene symbol: ADAM10
  hgvsc: ENST00000559053.1:c.56-50380C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000260408
  ensembl transcript: ENST00000260408
  gene symbol: ADAM10
  hgvsc: ENST00000260408.3:c.207-8896C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452704
  ensembl transcript: ENST00000558004
  gene symbol: ADAM10
  hgvsc: ENST00000558004.1:c.331+7070C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000558733
  gene symbol: ADAM10
  hgvsc: ENST00000558733.1:n.443-8896C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452639
  ensembl transcript: ENST00000561288
  gene symbol: ADAM10
  hgvsc: ENST00000561288.1:c.55+58270C>T
  variant of: http://identifiers.org/hgnc/188
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5261
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7410
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13825
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1479
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12737
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15734
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1632
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4258
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD

15-58983410-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58983410
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 58983410
    reference: chr 15
allele count: 1
allele frequency: 1.110469506507351e-5
allele num: 90052
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452704
  ensembl transcript: ENST00000558004
  gene symbol: ADAM10
  hgvsc: ENST00000558004.1:c.331+7069C>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452639
  ensembl transcript: ENST00000561288
  gene symbol: ADAM10
  hgvsc: ENST00000561288.1:c.55+58269C>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000391930
  ensembl transcript: ENST00000439637
  gene symbol: ADAM10
  hgvsc: ENST00000439637.1:c.207-8897C>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000560608
  gene symbol: ADAM10
  hgvsc: ENST00000560608.1:n.464-11929C>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000558733
  gene symbol: ADAM10
  hgvsc: ENST00000558733.1:n.443-8897C>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000386056
  ensembl transcript: ENST00000402627
  gene symbol: ADAM10
  hgvsc: ENST00000402627.1:c.56-50381C>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000497846
  gene symbol: ADAM10
  hgvsc: ENST00000497846.1:n.324-8897C>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000561149
  gene symbol: ADAM10
  hgvsc: ENST00000561149.1:n.467-8897C>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000260408
  ensembl transcript: ENST00000260408
  gene symbol: ADAM10
  hgvsc: ENST00000260408.3:c.207-8897C>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000379444
  ensembl transcript: ENST00000396140
  gene symbol: ADAM10
  hgvsc: ENST00000396140.2:c.56-50381C>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000453952
  ensembl transcript: ENST00000559053
  gene symbol: ADAM10
  hgvsc: ENST00000559053.1:c.56-50381C>A
  variant of: http://identifiers.org/hgnc/188
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 7570
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1616
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13876
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12558
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5263
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1476
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15715
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1223
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

15-58983418-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58983418
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 58983418
    reference: chr 15
allele count: 8
allele frequency: 9.021606748161847e-5
allele num: 88676
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000558733
  gene symbol: ADAM10
  hgvsc: ENST00000558733.1:n.443-8905T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452704
  ensembl transcript: ENST00000558004
  gene symbol: ADAM10
  hgvsc: ENST00000558004.1:c.331+7061T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452639
  ensembl transcript: ENST00000561288
  gene symbol: ADAM10
  hgvsc: ENST00000561288.1:c.55+58261T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000386056
  ensembl transcript: ENST00000402627
  gene symbol: ADAM10
  hgvsc: ENST00000402627.1:c.56-50389T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000561149
  gene symbol: ADAM10
  hgvsc: ENST00000561149.1:n.467-8905T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000560608
  gene symbol: ADAM10
  hgvsc: ENST00000560608.1:n.464-11937T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000497846
  gene symbol: ADAM10
  hgvsc: ENST00000497846.1:n.324-8905T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000379444
  ensembl transcript: ENST00000396140
  gene symbol: ADAM10
  hgvsc: ENST00000396140.2:c.56-50389T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000260408
  ensembl transcript: ENST00000260408
  gene symbol: ADAM10
  hgvsc: ENST00000260408.3:c.207-8905T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000391930
  ensembl transcript: ENST00000439637
  gene symbol: ADAM10
  hgvsc: ENST00000439637.1:c.207-8905T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000453952
  ensembl transcript: ENST00000559053
  gene symbol: ADAM10
  hgvsc: ENST00000559053.1:c.56-50389T>C
  variant of: http://identifiers.org/hgnc/188
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7865
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5002
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15841
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1619
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11786
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1663
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14286
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1964
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: South Asian
reference allele: A
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

15-58983421-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58983421
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 58983421
    reference: chr 15
allele count: 8
allele frequency: 9.05961224859576e-5
allele num: 88304
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000391930
  ensembl transcript: ENST00000439637
  gene symbol: ADAM10
  hgvsc: ENST00000439637.1:c.207-8908A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000497846
  gene symbol: ADAM10
  hgvsc: ENST00000497846.1:n.324-8908A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000560608
  gene symbol: ADAM10
  hgvsc: ENST00000560608.1:n.464-11940A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452639
  ensembl transcript: ENST00000561288
  gene symbol: ADAM10
  hgvsc: ENST00000561288.1:c.55+58258A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000561149
  gene symbol: ADAM10
  hgvsc: ENST00000561149.1:n.467-8908A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000386056
  ensembl transcript: ENST00000402627
  gene symbol: ADAM10
  hgvsc: ENST00000402627.1:c.56-50392A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452704
  ensembl transcript: ENST00000558004
  gene symbol: ADAM10
  hgvsc: ENST00000558004.1:c.331+7058A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000260408
  ensembl transcript: ENST00000260408
  gene symbol: ADAM10
  hgvsc: ENST00000260408.3:c.207-8908A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000453952
  ensembl transcript: ENST00000559053
  gene symbol: ADAM10
  hgvsc: ENST00000559053.1:c.56-50392A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000379444
  ensembl transcript: ENST00000396140
  gene symbol: ADAM10
  hgvsc: ENST00000396140.2:c.56-50392A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000558733
  gene symbol: ADAM10
  hgvsc: ENST00000558733.1:n.443-8908A>G
  variant of: http://identifiers.org/hgnc/188
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4973
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1719
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14350
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11724
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15845
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1625
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7819
  bin: 1.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 309
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: European (Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ

15-58983423-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58983423
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 58983423
    reference: chr 15
allele count: 1
allele frequency: 1.137345889631955e-5
allele num: 87924
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452639
  ensembl transcript: ENST00000561288
  gene symbol: ADAM10
  hgvsc: ENST00000561288.1:c.55+58256T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000453952
  ensembl transcript: ENST00000559053
  gene symbol: ADAM10
  hgvsc: ENST00000559053.1:c.56-50394T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000558733
  gene symbol: ADAM10
  hgvsc: ENST00000558733.1:n.443-8910T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000560608
  gene symbol: ADAM10
  hgvsc: ENST00000560608.1:n.464-11942T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000391930
  ensembl transcript: ENST00000439637
  gene symbol: ADAM10
  hgvsc: ENST00000439637.1:c.207-8910T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000379444
  ensembl transcript: ENST00000396140
  gene symbol: ADAM10
  hgvsc: ENST00000396140.2:c.56-50394T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000561149
  gene symbol: ADAM10
  hgvsc: ENST00000561149.1:n.467-8910T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000260408
  ensembl transcript: ENST00000260408
  gene symbol: ADAM10
  hgvsc: ENST00000260408.3:c.207-8910T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000497846
  gene symbol: ADAM10
  hgvsc: ENST00000497846.1:n.324-8910T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452704
  ensembl transcript: ENST00000558004
  gene symbol: ADAM10
  hgvsc: ENST00000558004.1:c.331+7056T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000386056
  ensembl transcript: ENST00000402627
  gene symbol: ADAM10
  hgvsc: ENST00000402627.1:c.56-50394T>C
  variant of: http://identifiers.org/hgnc/188
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1624
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4974
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1745
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15873
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7803
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14318
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11706
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1001
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
reference allele: A
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum

15-58983424-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58983424
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 58983424
    reference: chr 15
allele count: 3
allele frequency: 3.421142661648991e-5
allele num: 87690
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000379444
  ensembl transcript: ENST00000396140
  gene symbol: ADAM10
  hgvsc: ENST00000396140.2:c.56-50395G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000386056
  ensembl transcript: ENST00000402627
  gene symbol: ADAM10
  hgvsc: ENST00000402627.1:c.56-50395G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000558733
  gene symbol: ADAM10
  hgvsc: ENST00000558733.1:n.443-8911G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000560608
  gene symbol: ADAM10
  hgvsc: ENST00000560608.1:n.464-11943G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452704
  ensembl transcript: ENST00000558004
  gene symbol: ADAM10
  hgvsc: ENST00000558004.1:c.331+7055G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000561149
  gene symbol: ADAM10
  hgvsc: ENST00000561149.1:n.467-8911G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000260408
  ensembl transcript: ENST00000260408
  gene symbol: ADAM10
  hgvsc: ENST00000260408.3:c.207-8911G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000391930
  ensembl transcript: ENST00000439637
  gene symbol: ADAM10
  hgvsc: ENST00000439637.1:c.207-8911G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000497846
  gene symbol: ADAM10
  hgvsc: ENST00000497846.1:n.324-8911G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452639
  ensembl transcript: ENST00000561288
  gene symbol: ADAM10
  hgvsc: ENST00000561288.1:c.55+58255G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000453952
  ensembl transcript: ENST00000559053
  gene symbol: ADAM10
  hgvsc: ENST00000559053.1:c.56-50395G>A
  variant of: http://identifiers.org/hgnc/188
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5015
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11582
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7846
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15879
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1642
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1779
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14285
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1802
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff

15-58983425-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58983425
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 58983425
    reference: chr 15
allele count: 47198
allele frequency: 5.150820674000349e-1
allele num: 91632
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452639
  ensembl transcript: ENST00000561288
  gene symbol: ADAM10
  hgvsc: ENST00000561288.1:c.55+58254C>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000497846
  gene symbol: ADAM10
  hgvsc: ENST00000497846.1:n.324-8912C>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000379444
  ensembl transcript: ENST00000396140
  gene symbol: ADAM10
  hgvsc: ENST00000396140.2:c.56-50396C>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000260408
  ensembl transcript: ENST00000260408
  gene symbol: ADAM10
  hgvsc: ENST00000260408.3:c.207-8912C>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000558733
  gene symbol: ADAM10
  hgvsc: ENST00000558733.1:n.443-8912C>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000391930
  ensembl transcript: ENST00000439637
  gene symbol: ADAM10
  hgvsc: ENST00000439637.1:c.207-8912C>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000560608
  gene symbol: ADAM10
  hgvsc: ENST00000560608.1:n.464-11944C>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000561149
  gene symbol: ADAM10
  hgvsc: ENST00000561149.1:n.467-8912C>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000386056
  ensembl transcript: ENST00000402627
  gene symbol: ADAM10
  hgvsc: ENST00000402627.1:c.56-50396C>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452704
  ensembl transcript: ENST00000558004
  gene symbol: ADAM10
  hgvsc: ENST00000558004.1:c.331+7054C>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000453952
  ensembl transcript: ENST00000559053
  gene symbol: ADAM10
  hgvsc: ENST00000559053.1:c.56-50396C>G
  variant of: http://identifiers.org/hgnc/188
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 3.75e1
  variant carriers: 471
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 4.25e1
  variant carriers: 311
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 7.75e1
  variant carriers: 239
genotype depth: GenotypeDepth
  all individuals: 4285
  bin: 2.75e1
  variant carriers: 2650
genotype depth: GenotypeDepth
  all individuals: 11801
  bin: 7.5e0
  variant carriers: 3995
genotype depth: GenotypeDepth
  all individuals: 10612
  bin: 1.75e1
  variant carriers: 9498
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 9.25e1
  variant carriers: 310
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 5.75e1
  variant carriers: 154
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 6.25e1
  variant carriers: 155
genotype depth: GenotypeDepth
  all individuals: 1423
  bin: 2.5e0
  variant carriers: 203
genotype depth: GenotypeDepth
  all individuals: 1477
  bin: 3.25e1
  variant carriers: 1114
genotype depth: GenotypeDepth
  all individuals: 8606
  bin: 2.25e1
  variant carriers: 5527
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 8.25e1
  variant carriers: 241
genotype depth: GenotypeDepth
  all individuals: 15232
  bin: 1.25e1
  variant carriers: 9873
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 4.75e1
  variant carriers: 186
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 6.75e1
  variant carriers: 180
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 5.25e1
  variant carriers: 153
genotype depth: GenotypeDepth
  all individuals: 3801
  bin: 9.75e1
  variant carriers: 3741
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.25e1
  variant carriers: 202
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 8.75e1
  variant carriers: 321
genotype quality: GenotypeQuality
  all individuals: 2159
  bin: 3.25e1
  variant carriers: 1340
num of homozygotes: 12344
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP

15-58983425-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58983425
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 58983425
    reference: chr 15
allele count: 4
allele frequency: 4.365287235900122e-5
allele num: 91632
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000558733
  gene symbol: ADAM10
  hgvsc: ENST00000558733.1:n.443-8912C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000497846
  gene symbol: ADAM10
  hgvsc: ENST00000497846.1:n.324-8912C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000561149
  gene symbol: ADAM10
  hgvsc: ENST00000561149.1:n.467-8912C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000260408
  ensembl transcript: ENST00000260408
  gene symbol: ADAM10
  hgvsc: ENST00000260408.3:c.207-8912C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000560608
  gene symbol: ADAM10
  hgvsc: ENST00000560608.1:n.464-11944C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000379444
  ensembl transcript: ENST00000396140
  gene symbol: ADAM10
  hgvsc: ENST00000396140.2:c.56-50396C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000391930
  ensembl transcript: ENST00000439637
  gene symbol: ADAM10
  hgvsc: ENST00000439637.1:c.207-8912C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000386056
  ensembl transcript: ENST00000402627
  gene symbol: ADAM10
  hgvsc: ENST00000402627.1:c.56-50396C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452639
  ensembl transcript: ENST00000561288
  gene symbol: ADAM10
  hgvsc: ENST00000561288.1:c.55+58254C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452704
  ensembl transcript: ENST00000558004
  gene symbol: ADAM10
  hgvsc: ENST00000558004.1:c.331+7054C>T
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000453952
  ensembl transcript: ENST00000559053
  gene symbol: ADAM10
  hgvsc: ENST00000559053.1:c.56-50396C>T
  variant of: http://identifiers.org/hgnc/188
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8606
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1423
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11801
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1477
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15232
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3801
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10612
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4285
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1488
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ

15-58983426-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58983426
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 58983426
    reference: chr 15
allele count: 1
allele frequency: 1.314716941442507e-5
allele num: 76062
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452704
  ensembl transcript: ENST00000558004
  gene symbol: ADAM10
  hgvsc: ENST00000558004.1:c.331+7053A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000260408
  ensembl transcript: ENST00000260408
  gene symbol: ADAM10
  hgvsc: ENST00000260408.3:c.207-8913A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000561149
  gene symbol: ADAM10
  hgvsc: ENST00000561149.1:n.467-8913A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000453952
  ensembl transcript: ENST00000559053
  gene symbol: ADAM10
  hgvsc: ENST00000559053.1:c.56-50397A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452639
  ensembl transcript: ENST00000561288
  gene symbol: ADAM10
  hgvsc: ENST00000561288.1:c.55+58253A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000560608
  gene symbol: ADAM10
  hgvsc: ENST00000560608.1:n.464-11945A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000379444
  ensembl transcript: ENST00000396140
  gene symbol: ADAM10
  hgvsc: ENST00000396140.2:c.56-50397A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000497846
  gene symbol: ADAM10
  hgvsc: ENST00000497846.1:n.324-8913A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000391930
  ensembl transcript: ENST00000439637
  gene symbol: ADAM10
  hgvsc: ENST00000439637.1:c.207-8913A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000558733
  gene symbol: ADAM10
  hgvsc: ENST00000558733.1:n.443-8913A>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000386056
  ensembl transcript: ENST00000402627
  gene symbol: ADAM10
  hgvsc: ENST00000402627.1:c.56-50397A>G
  variant of: http://identifiers.org/hgnc/188
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17347
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19720
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6426
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2563
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4292
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1019
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3142
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: Latino
population: East Asian
population: European (Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP

15-58983429-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58983429
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 58983429
    reference: chr 15
allele count: 1
allele frequency: 1.342858677552774e-5
allele num: 74468
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000497846
  gene symbol: ADAM10
  hgvsc: ENST00000497846.1:n.324-8916G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452639
  ensembl transcript: ENST00000561288
  gene symbol: ADAM10
  hgvsc: ENST00000561288.1:c.55+58250G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000560608
  gene symbol: ADAM10
  hgvsc: ENST00000560608.1:n.464-11948G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000379444
  ensembl transcript: ENST00000396140
  gene symbol: ADAM10
  hgvsc: ENST00000396140.2:c.56-50400G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000386056
  ensembl transcript: ENST00000402627
  gene symbol: ADAM10
  hgvsc: ENST00000402627.1:c.56-50400G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000453952
  ensembl transcript: ENST00000559053
  gene symbol: ADAM10
  hgvsc: ENST00000559053.1:c.56-50400G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000260408
  ensembl transcript: ENST00000260408
  gene symbol: ADAM10
  hgvsc: ENST00000260408.3:c.207-8916G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000561149
  gene symbol: ADAM10
  hgvsc: ENST00000561149.1:n.467-8916G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452704
  ensembl transcript: ENST00000558004
  gene symbol: ADAM10
  hgvsc: ENST00000558004.1:c.331+7050G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000558733
  gene symbol: ADAM10
  hgvsc: ENST00000558733.1:n.443-8916G>A
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000391930
  ensembl transcript: ENST00000439637
  gene symbol: ADAM10
  hgvsc: ENST00000439637.1:c.207-8916G>A
  variant of: http://identifiers.org/hgnc/188
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2896
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5842
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3939
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3139
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20105
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17605
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 254
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

15-58983431-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58983431
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 58983431
    reference: chr 15
allele count: 1
allele frequency: 1.36035913481159e-5
allele num: 73510
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000386056
  ensembl transcript: ENST00000402627
  gene symbol: ADAM10
  hgvsc: ENST00000402627.1:c.56-50402G>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000453952
  ensembl transcript: ENST00000559053
  gene symbol: ADAM10
  hgvsc: ENST00000559053.1:c.56-50402G>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000560608
  gene symbol: ADAM10
  hgvsc: ENST00000560608.1:n.464-11950G>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000391930
  ensembl transcript: ENST00000439637
  gene symbol: ADAM10
  hgvsc: ENST00000439637.1:c.207-8918G>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000497846
  gene symbol: ADAM10
  hgvsc: ENST00000497846.1:n.324-8918G>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000558733
  gene symbol: ADAM10
  hgvsc: ENST00000558733.1:n.443-8918G>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000260408
  ensembl transcript: ENST00000260408
  gene symbol: ADAM10
  hgvsc: ENST00000260408.3:c.207-8918G>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452639
  ensembl transcript: ENST00000561288
  gene symbol: ADAM10
  hgvsc: ENST00000561288.1:c.55+58248G>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000561149
  gene symbol: ADAM10
  hgvsc: ENST00000561149.1:n.467-8918G>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452704
  ensembl transcript: ENST00000558004
  gene symbol: ADAM10
  hgvsc: ENST00000558004.1:c.331+7048G>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000379444
  ensembl transcript: ENST00000396140
  gene symbol: ADAM10
  hgvsc: ENST00000396140.2:c.56-50402G>C
  variant of: http://identifiers.org/hgnc/188
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17795
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 975
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20293
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3752
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3137
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3141
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5415
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7871
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: VQSLOD

http://identifiers.org/exac.variant/15-58983436-C-CCA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58983436
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 58983438
    reference: chr 15
allele count: 1
allele frequency: 1.43000143000143e-5
allele num: 69930
alternate allele: CCA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000386056
  ensembl transcript: ENST00000402627
  gene symbol: ADAM10
  hgvsc: ENST00000402627.1:c.56-50409_56-50408dupTG
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000561149
  gene symbol: ADAM10
  hgvsc: ENST00000561149.1:n.467-8925_467-8924dupTG
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000497846
  gene symbol: ADAM10
  hgvsc: ENST00000497846.1:n.324-8925_324-8924dupTG
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000260408
  ensembl transcript: ENST00000260408
  gene symbol: ADAM10
  hgvsc: ENST00000260408.3:c.207-8925_207-8924dupTG
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000391930
  ensembl transcript: ENST00000439637
  gene symbol: ADAM10
  hgvsc: ENST00000439637.1:c.207-8925_207-8924dupTG
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000558733
  gene symbol: ADAM10
  hgvsc: ENST00000558733.1:n.443-8925_443-8924dupTG
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452704
  ensembl transcript: ENST00000558004
  gene symbol: ADAM10
  hgvsc: ENST00000558004.1:c.331+7041_331+7042dupTG
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000560608
  gene symbol: ADAM10
  hgvsc: ENST00000560608.1:n.464-11957_464-11956dupTG
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452639
  ensembl transcript: ENST00000561288
  gene symbol: ADAM10
  hgvsc: ENST00000561288.1:c.55+58241_55+58242dupTG
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000379444
  ensembl transcript: ENST00000396140
  gene symbol: ADAM10
  hgvsc: ENST00000396140.2:c.56-50409_56-50408dupTG
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000453952
  ensembl transcript: ENST00000559053
  gene symbol: ADAM10
  hgvsc: ENST00000559053.1:c.56-50409_56-50408dupTG
  variant of: http://identifiers.org/hgnc/188
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3128
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3088
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4660
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21111
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3958
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17634
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 379
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: African
population: South Asian
reference allele: C
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

15-58983438-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58983438
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 58983438
    reference: chr 15
allele count: 2
allele frequency: 2.888170055452865e-5
allele num: 69248
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452704
  ensembl transcript: ENST00000558004
  gene symbol: ADAM10
  hgvsc: ENST00000558004.1:c.331+7041T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000497846
  gene symbol: ADAM10
  hgvsc: ENST00000497846.1:n.324-8925T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000561149
  gene symbol: ADAM10
  hgvsc: ENST00000561149.1:n.467-8925T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000560608
  gene symbol: ADAM10
  hgvsc: ENST00000560608.1:n.464-11957T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000558733
  gene symbol: ADAM10
  hgvsc: ENST00000558733.1:n.443-8925T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000260408
  ensembl transcript: ENST00000260408
  gene symbol: ADAM10
  hgvsc: ENST00000260408.3:c.207-8925T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000386056
  ensembl transcript: ENST00000402627
  gene symbol: ADAM10
  hgvsc: ENST00000402627.1:c.56-50409T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000391930
  ensembl transcript: ENST00000439637
  gene symbol: ADAM10
  hgvsc: ENST00000439637.1:c.207-8925T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000379444
  ensembl transcript: ENST00000396140
  gene symbol: ADAM10
  hgvsc: ENST00000396140.2:c.56-50409T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452639
  ensembl transcript: ENST00000561288
  gene symbol: ADAM10
  hgvsc: ENST00000561288.1:c.55+58241T>C
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000453952
  ensembl transcript: ENST00000559053
  gene symbol: ADAM10
  hgvsc: ENST00000559053.1:c.56-50409T>C
  variant of: http://identifiers.org/hgnc/188
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21381
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2995
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17482
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4652
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4117
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2968
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 301
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/15-58983441-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 58983441
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 58983441
    reference: chr 15
allele count: 1
allele frequency: 1.474491300501327e-5
allele num: 67820
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000560608
  gene symbol: ADAM10
  hgvsc: ENST00000560608.1:n.464-11960T>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000379444
  ensembl transcript: ENST00000396140
  gene symbol: ADAM10
  hgvsc: ENST00000396140.2:c.56-50412T>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000558733
  gene symbol: ADAM10
  hgvsc: ENST00000558733.1:n.443-8928T>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000260408
  ensembl transcript: ENST00000260408
  gene symbol: ADAM10
  hgvsc: ENST00000260408.3:c.207-8928T>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000561149
  gene symbol: ADAM10
  hgvsc: ENST00000561149.1:n.467-8928T>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000386056
  ensembl transcript: ENST00000402627
  gene symbol: ADAM10
  hgvsc: ENST00000402627.1:c.56-50412T>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452639
  ensembl transcript: ENST00000561288
  gene symbol: ADAM10
  hgvsc: ENST00000561288.1:c.55+58238T>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl transcript: ENST00000497846
  gene symbol: ADAM10
  hgvsc: ENST00000497846.1:n.324-8928T>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000452704
  ensembl transcript: ENST00000558004
  gene symbol: ADAM10
  hgvsc: ENST00000558004.1:c.331+7038T>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000391930
  ensembl transcript: ENST00000439637
  gene symbol: ADAM10
  hgvsc: ENST00000439637.1:c.207-8928T>G
  variant of: http://identifiers.org/hgnc/188
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137845
  ensembl protein: ENSP00000453952
  ensembl transcript: ENST00000559053
  gene symbol: ADAM10
  hgvsc: ENST00000559053.1:c.56-50412T>G
  variant of: http://identifiers.org/hgnc/188
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21737
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2773
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2919
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4507
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17174
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4502
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1515
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
reference allele: A

GenotypeQuality
all individuals: 4169
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4954
bin: 7.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66540
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.626492106276473e-5
allele num: 10388
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.474635163307853e-4
allele num: 8634
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.439277e6

QD
type: SiteQuality
SIO_000300: 1.189e1

VQSLOD
type: SiteQuality
SIO_000300: 4.39e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.82e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 4.5e-1

MQ
type: SiteQuality
SIO_000300: 5.969e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.72e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.07e-1

GenotypeQuality
all individuals: 10
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11392
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3373
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34270
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2181
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3503
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1065
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 813
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 14
bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10368
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8636
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11544
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16502
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500915558490679e-5
allele num: 66626
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 2.035164e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.9e0

VQSLOD
type: SiteQuality
SIO_000300: -8.290999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.43e-1

MQ
type: SiteQuality
SIO_000300: 5.9e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.2e0

QD
type: SiteQuality
SIO_000300: 9.359999999999999e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.26e0

GenotypeQuality
all individuals: 4
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 27
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 818
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3833
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3499
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 2176
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11362
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1063
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11542
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10372
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501095799933952e-5
allele num: 66618
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16502
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.86e-1

MQ
type: SiteQuality
SIO_000300: 5.985e1

FS
type: SiteQuality
SIO_000300: 1.6472e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.799e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.44e0

QD
type: SiteQuality
SIO_000300: 1.534e1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.13e-1

DP
type: SiteQuality
SIO_000300: 2.035366e6

VQSLOD
type: SiteQuality
SIO_000300: -2.452e0

GenotypeQuality
all individuals: 4
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34274
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3822
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2175
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3353
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 116
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 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: 1.501005673801447e-5
allele num: 66622
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 1.011e0

MQ
type: SiteQuality
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VQSLOD
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QD
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SIO_000300: 1.511e1

ClippingRankSum
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ReadPosRankSum
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DP
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InbreedingCoeff
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SIO_000300: -2.0e-4

BaseQRankSum
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SIO_000300: 4.37e0

MQRankSum
type: SiteQuality
SIO_000300: 8.61e-1

GenotypeQuality
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variant carriers: 0

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

South Asian
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allele frequency: 0.0e0
allele num: 16502
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66630
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
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East Asian
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allele frequency: 1.156336725254394e-4
allele num: 8648
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

MQ
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SIO_000300: 5.967e1

VQSLOD
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InbreedingCoeff
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QD
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ClippingRankSum
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FS
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BaseQRankSum
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DP
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MQRankSum
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ReadPosRankSum
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SIO_000300: 3.6e-1

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.500915558490679e-5
allele num: 66626
num of homozygotes: 0

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

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

DP
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InbreedingCoeff
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MQ
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ClippingRankSum
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SIO_000300: -6.26e-1

ReadPosRankSum
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FS
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VQSLOD
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MQRankSum
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BaseQRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11542
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

East Asian
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allele count: 7
allele frequency: 8.094357076780758e-4
allele num: 8648
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66626
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.11e-1

VQSLOD
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InbreedingCoeff
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DP
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FS
type: SiteQuality
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BaseQRankSum
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MQ
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SIO_000300: 5.974e1

MQRankSum
type: SiteQuality
SIO_000300: 4.1e-2

QD
type: SiteQuality
SIO_000300: 1.244e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.97e-1

GenotypeQuality
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variant carriers: 0

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

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

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

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.50105073551486e-5
allele num: 66620
num of homozygotes: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 1.501140867058965e-5
allele num: 66616
num of homozygotes: 0

African
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South Asian
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Other
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East Asian
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allele num: 8644
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InbreedingCoeff
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ClippingRankSum
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FS
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BaseQRankSum
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ReadPosRankSum
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MQRankSum
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VQSLOD
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MQ
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DP
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
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allele frequency: 9.646922631680494e-5
allele num: 10366
num of homozygotes: 0

Latino
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allele count: 0
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num of homozygotes: 0

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

East Asian
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num of homozygotes: 0

South Asian
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BaseQRankSum
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MQRankSum
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FS
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DP
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MQ
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ClippingRankSum
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VQSLOD
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ReadPosRankSum
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InbreedingCoeff
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele num: 11548
num of homozygotes: 0

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

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 1.501276084671971e-5
allele num: 66610
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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South Asian
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DP
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BaseQRankSum
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QD
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ClippingRankSum
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ReadPosRankSum
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FS
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MQRankSum
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VQSLOD
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MQ
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InbreedingCoeff
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SIO_000300: -2.0e-4

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
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allele frequency: 0.0e0
allele num: 10296
num of homozygotes: 0

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

Latino
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allele frequency: 1.038781163434903e-3
allele num: 11552
num of homozygotes: 0

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

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

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8644
num of homozygotes: 0

European (Finnish)
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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 frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
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allele num: 66576
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Other
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Latino
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VQSLOD
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MQRankSum
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DP
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BaseQRankSum
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ReadPosRankSum
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InbreedingCoeff
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FS
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
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allele num: 10014
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66280
num of homozygotes: 0

East Asian
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num of homozygotes: 0

Latino
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QD
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FS
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BaseQRankSum
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VQSLOD
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ClippingRankSum
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InbreedingCoeff
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ReadPosRankSum
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MQ
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DP
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

Latino
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South Asian
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Other
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African
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East Asian
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European (Non-Finnish)
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FS
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VQSLOD
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QD
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DP
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InbreedingCoeff
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ClippingRankSum
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MQ
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MQRankSum
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BaseQRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Latino
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European (Finnish)
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European (Non-Finnish)
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allele num: 66164
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South Asian
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African
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Other
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BaseQRankSum
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InbreedingCoeff
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MQRankSum
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FS
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QD
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VQSLOD
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ReadPosRankSum
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DP
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MQ
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
type: Population
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num of homozygotes: 0

VQSLOD
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DP
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ClippingRankSum
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MQRankSum
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ReadPosRankSum
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MQ
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SIO_000300: 5.919e1

FS
type: SiteQuality
SIO_000300: 9.156000000000001e0

QD
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SIO_000300: 1.762e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.805e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

GenotypeQuality
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variant carriers: 0

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

African
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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: 896
num of homozygotes: 0

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

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

South Asian
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allele count: 1
allele frequency: 6.088650754992694e-5
allele num: 16424
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66084
num of homozygotes: 0

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

InbreedingCoeff
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MQ
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QD
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VQSLOD
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DP
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FS
type: SiteQuality
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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SIO_000300: -1.174e0

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
allele num: 9828
num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.517358582180141e-5
allele num: 65904
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 8546
num of homozygotes: 0

QD
type: SiteQuality
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DP
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MQ
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BaseQRankSum
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SIO_000300: -1.218e0

ReadPosRankSum
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SIO_000300: -1.738e0

ClippingRankSum
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SIO_000300: 1.16e0

FS
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VQSLOD
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SIO_000300: -2.308e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.2e-3

MQRankSum
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SIO_000300: 2.33e-1

GenotypeQuality
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variant carriers: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6532
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11342
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9610
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.540215014015957e-5
allele num: 64926
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
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num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.780061e6

FS
type: SiteQuality
SIO_000300: 2.144e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.04e-1

QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 3.78e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.32e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.6e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.3e-3

VQSLOD
type: SiteQuality
SIO_000300: 7.33e-1

GenotypeQuality
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variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11204
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6458
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele frequency: 9.600614439324117e-5
allele num: 62496
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.707e0

InbreedingCoeff
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SIO_000300: -3.1e-3

BaseQRankSum
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DP
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ReadPosRankSum
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QD
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MQRankSum
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VQSLOD
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ClippingRankSum
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MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

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

South Asian
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Other
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num of homozygotes: 0

European (Non-Finnish)
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allele num: 57504
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Latino
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allele frequency: 0.0e0
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African
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num of homozygotes: 0

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

European (Finnish)
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allele frequency: 0.0e0
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FS
type: SiteQuality
SIO_000300: 1.53477e2

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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num of homozygotes: 0

East Asian
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num of homozygotes: 0

South Asian
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Latino
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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BaseQRankSum
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SIO_000300: 6.66e-1

FS
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MQ
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VQSLOD
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ClippingRankSum
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QD
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InbreedingCoeff
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ReadPosRankSum
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DP
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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Other
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num of homozygotes: 0

East Asian
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Latino
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South Asian
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allele num: 10244
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 56404
num of homozygotes: 0

FS
type: SiteQuality
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BaseQRankSum
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InbreedingCoeff
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ClippingRankSum
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DP
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MQ
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MQRankSum
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VQSLOD
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QD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 2769
bin: 6.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6296
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10230
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10210
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.290322580645161e-4
allele num: 7750
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56190
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7420
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 730
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.187711e6

QD
type: SiteQuality
SIO_000300: 1.57e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.34e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.025e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-3

MQ
type: SiteQuality
SIO_000300: 5.682e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.62e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.36e0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1985
bin: 9.75e1
variant carriers: 5

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10210
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.552524068350563e-5
allele num: 56298
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7450
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 728
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6310
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.56871307474955e-4
allele num: 7786
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.66183574879227e-5
allele num: 10350
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.59e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.6e-3

DP
type: SiteQuality
SIO_000300: 1.188053e6

FS
type: SiteQuality
SIO_000300: 4.051e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.53e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.12e-1

QD
type: SiteQuality
SIO_000300: 1.424e1

MQRankSum
type: SiteQuality
SIO_000300: -4.1e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.590000000000001e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 785
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5264
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 163
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6316
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.883239171374765e-4
allele num: 10620
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56314
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7484
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10204
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 734
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.6e-3

FS
type: SiteQuality
SIO_000300: 4.314e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.06e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.58e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.03e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.0e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.58e-1

DP
type: SiteQuality
SIO_000300: 1.189541e6

QD
type: SiteQuality
SIO_000300: 1.389e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 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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variant carriers: 4

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 349
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GenotypeQuality
all individuals: 19766
bin: 6.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 734
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6320
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7480
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 8.875319511502414e-5
allele num: 56336
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7764
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.875e1

VQSLOD
type: SiteQuality
SIO_000300: -2.035e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.41e-1

FS
type: SiteQuality
SIO_000300: 1.4069e1

QD
type: SiteQuality
SIO_000300: 1.079e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.5e-3

DP
type: SiteQuality
SIO_000300: 1.189398e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.2e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.43e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.12e-1

GenotypeQuality
all individuals: 200
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variant carriers: 0

GenotypeQuality
all individuals: 1982
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variant carriers: 2

GenotypeQuality
all individuals: 4881
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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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1725
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 8.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7740
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7458
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.444519506840061e-5
allele num: 11842
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6268
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 740
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.789420943382721e-5
allele num: 55884
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.197582e6

MQRankSum
type: SiteQuality
SIO_000300: -6.1e-2

QD
type: SiteQuality
SIO_000300: 1.292e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.06e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.3e-3

FS
type: SiteQuality
SIO_000300: 6.329e0

VQSLOD
type: SiteQuality
SIO_000300: 8.94e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.91e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 161
bin: 9.25e1
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GenotypeQuality
all individuals: 1705
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GenotypeQuality
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GenotypeQuality
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6240
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10072
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7724
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 736
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7440
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12576
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.793528947557213e-5
allele num: 55756
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.854e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.1e-3

DP
type: SiteQuality
SIO_000300: 1.205939e6

ClippingRankSum
type: SiteQuality
SIO_000300: 4.08e-1

VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 2.15e-1

MQ
type: SiteQuality
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QD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 1.84e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12684
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10084
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 740
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7462
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 55802
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6244
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.09e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

ClippingRankSum
type: SiteQuality
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FS
type: SiteQuality
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MQRankSum
type: SiteQuality
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VQSLOD
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MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 3.86e0

DP
type: SiteQuality
SIO_000300: 1.208027e6

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10068
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6238
num of homozygotes: 0

East 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: 736
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 1.291655902867476e-4
allele num: 7742
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 55822
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.827e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.3e-3

ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.987e0

MQRankSum
type: SiteQuality
SIO_000300: -2.549e0

QD
type: SiteQuality
SIO_000300: 1.485e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.88e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.63e-1

DP
type: SiteQuality
SIO_000300: 1.211379e6

GenotypeQuality
all individuals: 188
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1328
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4567
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 770
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1804
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2834
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1996
bin: 9.75e1
variant carriers: 16

GenotypeQuality
all individuals: 377
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1544
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 617
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 166
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1628
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 322
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3508
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 12408
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21797
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 407
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3233
bin: 3.75e1
variant carriers: 0

Latino
type: Population
allele count: 18
allele frequency: 1.788908765652952e-3
allele num: 10062
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7708
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13094
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 740
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.794108148839212e-5
allele num: 55738
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7452
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6232
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.213753e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-3

FS
type: SiteQuality
SIO_000300: 7.271e0

MQRankSum
type: SiteQuality
SIO_000300: 3.12e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.5e-1

QD
type: SiteQuality
SIO_000300: 8.609999999999999e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.04e-1

VQSLOD
type: SiteQuality
SIO_000300: -8.14e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.161e0

GenotypeQuality
all individuals: 2600
bin: 3.25e1
variant carriers: 281

GenotypeQuality
all individuals: 15895
bin: 6.25e1
variant carriers: 268

GenotypeQuality
all individuals: 389
bin: 8.25e1
variant carriers: 208

GenotypeQuality
all individuals: 1217
bin: 7.5e0
variant carriers: 83

GenotypeQuality
all individuals: 636
bin: 7.25e1
variant carriers: 167

GenotypeQuality
all individuals: 454
bin: 1.75e1
variant carriers: 154

GenotypeQuality
all individuals: 337
bin: 1.25e1
variant carriers: 95

GenotypeQuality
all individuals: 2288
bin: 2.75e1
variant carriers: 140

GenotypeQuality
all individuals: 9130
bin: 2.25e1
variant carriers: 166

GenotypeQuality
all individuals: 892
bin: 5.75e1
variant carriers: 173

GenotypeQuality
all individuals: 1219
bin: 4.75e1
variant carriers: 344

GenotypeQuality
all individuals: 850
bin: 4.25e1
variant carriers: 171

GenotypeQuality
all individuals: 292
bin: 8.75e1
variant carriers: 224

GenotypeQuality
all individuals: 2057
bin: 6.75e1
variant carriers: 220

GenotypeQuality
all individuals: 1313
bin: 5.25e1
variant carriers: 289

GenotypeQuality
all individuals: 1826
bin: 3.75e1
variant carriers: 322

GenotypeQuality
all individuals: 598
bin: 7.75e1
variant carriers: 215

GenotypeQuality
all individuals: 331
bin: 9.25e1
variant carriers: 260

GenotypeQuality
all individuals: 16880
bin: 9.75e1
variant carriers: 15815

European (Non-Finnish)
type: Population
allele count: 9302
allele frequency: 1.664340669171587e-1
allele num: 55890
num of homozygotes: 637

Other
type: Population
allele count: 127
allele frequency: 1.688829787234042e-1
allele num: 752
num of homozygotes: 12

African
type: Population
allele count: 1557
allele frequency: 2.010588842975207e-1
allele num: 7744
num of homozygotes: 142

South Asian
type: Population
allele count: 2364
allele frequency: 1.692439862542955e-1
allele num: 13968
num of homozygotes: 200

East Asian
type: Population
allele count: 3198
allele frequency: 4.269692923898532e-1
allele num: 7490
num of homozygotes: 614

Latino
type: Population
allele count: 2644
allele frequency: 2.641358641358642e-1
allele num: 10010
num of homozygotes: 314

European (Finnish)
type: Population
allele count: 1166
allele frequency: 1.884292178409825e-1
allele num: 6188
num of homozygotes: 114

FS
type: SiteQuality
SIO_000300: 5.25e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.59e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.83e-2

DP
type: SiteQuality
SIO_000300: 1.267002e6

QD
type: SiteQuality
SIO_000300: 1.533e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.7e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.4e-2

MQRankSum
type: SiteQuality
SIO_000300: 5.2e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.36e0

GenotypeQuality
all individuals: 1582
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1481
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 203
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2549
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1949
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14233
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1343
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 665
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 757
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1962
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 144
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4627
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18134
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 361
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 429
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 777
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3148
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2063
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14048
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6090
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9840
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.846108403485453e-5
allele num: 54168
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7078
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 750
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7444
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.41e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.63e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.51e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.99e-1

FS
type: SiteQuality
SIO_000300: 3.834e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.1e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.23e-1

QD
type: SiteQuality
SIO_000300: 1.075e1

DP
type: SiteQuality
SIO_000300: 1.189595e6

GenotypeQuality
all individuals: 482
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14331
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3857
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3134
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1914
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1367
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1645
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4576
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 714
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 353
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 698
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 285
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19157
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2461
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1837
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 637
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1961
bin: 9.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9754
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7404
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7036
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.85336199866558e-5
allele num: 53956
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6076
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14022
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 750
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.12e0

DP
type: SiteQuality
SIO_000300: 1.192357e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.4e-3

FS
type: SiteQuality
SIO_000300: 3.224e0

MQRankSum
type: SiteQuality
SIO_000300: 3.15e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.507e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.071e0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.0e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 3.44e0

GenotypeQuality
all individuals: 2461
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 755
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1367
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1914
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1645
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 19157
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14331
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1837
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3134
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 285
bin: 2.5e0
variant carriers: 1

GenotypeQuality
all individuals: 4576
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1961
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3857
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 698
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 482
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 353
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 637
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7036
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6076
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14022
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 750
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9754
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.350621285791464e-4
allele num: 7404
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 53956
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.15e-1

FS
type: SiteQuality
SIO_000300: 3.224e0

DP
type: SiteQuality
SIO_000300: 1.192357e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.071e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.12e0

VQSLOD
type: SiteQuality
SIO_000300: -2.507e0

QD
type: SiteQuality
SIO_000300: 3.44e0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.0e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 375
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3066
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 446
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3854
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 623
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4540
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1669
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2513
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 737
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 237
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 658
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1979
bin: 9.75e1
variant carriers: 19

GenotypeQuality
all individuals: 1552
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1796
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14509
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1313
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 541
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6986
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7408
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9776
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 2.118344866544273e-4
allele num: 14162
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6082
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 16
allele frequency: 2.967138936280692e-4
allele num: 53924
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.326259946949602e-3
allele num: 754
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.21e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.04e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.38e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.13e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.2e-3

VQSLOD
type: SiteQuality
SIO_000300: 3.98e0

DP
type: SiteQuality
SIO_000300: 1.192062e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.44e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.44e-1

GenotypeQuality
all individuals: 2503
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1683
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1356
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1595
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 379
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3901
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 687
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1807
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3109
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14622
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 449
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18904
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 207
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1962
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1021
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 656
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 734
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14168
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 53806
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7002
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 754
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9756
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7386
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6052
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.233e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.187627e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.8e-3

VQSLOD
type: SiteQuality
SIO_000300: 3.9e0

GenotypeQuality
all individuals: 1795
bin: 4.75e1
variant carriers: 8

GenotypeQuality
all individuals: 940
bin: 1.75e1
variant carriers: 6

GenotypeQuality
all individuals: 4421
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 3049
bin: 3.75e1
variant carriers: 6

GenotypeQuality
all individuals: 3854
bin: 2.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1399
bin: 4.25e1
variant carriers: 4

GenotypeQuality
all individuals: 14918
bin: 2.25e1
variant carriers: 4

GenotypeQuality
all individuals: 146
bin: 8.75e1
variant carriers: 2

GenotypeQuality
all individuals: 355
bin: 8.25e1
variant carriers: 3

GenotypeQuality
all individuals: 1084
bin: 2.5e0
variant carriers: 1

GenotypeQuality
all individuals: 2281
bin: 6.75e1
variant carriers: 3

GenotypeQuality
all individuals: 874
bin: 5.75e1
variant carriers: 6

GenotypeQuality
all individuals: 683
bin: 1.25e1
variant carriers: 3

GenotypeQuality
all individuals: 152
bin: 9.25e1
variant carriers: 2

GenotypeQuality
all individuals: 604
bin: 7.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1357
bin: 5.25e1
variant carriers: 4

GenotypeQuality
all individuals: 660
bin: 7.25e1
variant carriers: 2

GenotypeQuality
all individuals: 1865
bin: 9.75e1
variant carriers: 20

GenotypeQuality
all individuals: 18355
bin: 6.25e1
variant carriers: 2

European (Finnish)
type: Population
allele count: 44
allele frequency: 8.026267785479753e-3
allele num: 5482
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 7040
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.466275659824047e-4
allele num: 6820
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 23
allele frequency: 4.431770010405025e-4
allele num: 51898
num of homozygotes: 0

Other
type: Population
allele count: 3
allele frequency: 4.166666666666667e-3
allele num: 720
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9552
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14302
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.05743e2

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.399999999999999e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 2.71e-1

QD
type: SiteQuality
SIO_000300: 8.4e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.922e2

MQ
type: SiteQuality
SIO_000300: 5.948e1

MQRankSum
type: SiteQuality
SIO_000300: 8.599999999999999e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.5e-2

DP
type: SiteQuality
SIO_000300: 1.174279e6

BaseQRankSum
type: SiteQuality
SIO_000300: -4.008e0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 744
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5956
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14334
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7284
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 53054
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6904
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.03777501037775e-4
allele num: 9636
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.86e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
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SIO_000300: -2.572e0

VQSLOD
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SIO_000300: -1.938e0

MQ
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SIO_000300: 5.878e1

MQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.169432e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.021e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.5e-3

QD
type: SiteQuality
SIO_000300: 8.24e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 9

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: 5.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5948
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.318615077421542e-4
allele num: 53086
num of homozygotes: 0

African
type: Population
allele count: 5
allele frequency: 6.870019236053861e-4
allele num: 7278
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14350
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 744
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6922
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.036699149906697e-4
allele num: 9646
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.168267e6

VQSLOD
type: SiteQuality
SIO_000300: -5.579e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.84e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.5e-3

QD
type: SiteQuality
SIO_000300: 6.92e0

MQRankSum
type: SiteQuality
SIO_000300: 2.82e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.25e-1

FS
type: SiteQuality
SIO_000300: 6.004e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.46e-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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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7190
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.83626807841332e-5
allele num: 52134
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9554
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14332
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5898
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6816
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 746
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.62e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.43e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.5e-3

DP
type: SiteQuality
SIO_000300: 1.152558e6

FS
type: SiteQuality
SIO_000300: 7.793e0

MQRankSum
type: SiteQuality
SIO_000300: 1.35e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.76e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.43e-1

QD
type: SiteQuality
SIO_000300: 1.227e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 442
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1431
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.94984986156066e-5
allele num: 51286
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14378
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7140
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9452
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 738
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6710
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5872
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -8.798e0

DP
type: SiteQuality
SIO_000300: 1.143987e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.92e0

MQRankSum
type: SiteQuality
SIO_000300: -8.95e-1

FS
type: SiteQuality
SIO_000300: 8.8011e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.96e-1

QD
type: SiteQuality
SIO_000300: 1.91e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.79e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.4e-3

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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GenotypeQuality
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variant carriers: 212

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 451
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variant carriers: 4

GenotypeQuality
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bin: 8.75e1
variant carriers: 3

Other
type: Population
allele count: 1
allele frequency: 1.351351351351351e-3
allele num: 740
num of homozygotes: 0

Latino
type: Population
allele count: 5
allele frequency: 5.285412262156448e-4
allele num: 9460
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 51196
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5868
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6710
num of homozygotes: 0

African
type: Population
allele count: 203
allele frequency: 2.847124824684432e-2
allele num: 7130
num of homozygotes: 3

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14370
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.235e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.98e-1

DP
type: SiteQuality
SIO_000300: 1.142357e6

VQSLOD
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SIO_000300: 2.36e0

MQRankSum
type: SiteQuality
SIO_000300: 2.48e-1

ClippingRankSum
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SIO_000300: -2.03e-1

FS
type: SiteQuality
SIO_000300: 5.017e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
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SIO_000300: 1.74e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.1e-3

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1978
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9364
num of homozygotes: 0

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

European (Finnish)
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: 736
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.982789388111195e-5
allele num: 50434
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7072
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
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BaseQRankSum
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InbreedingCoeff
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MQ
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ReadPosRankSum
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MQRankSum
type: SiteQuality
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ClippingRankSum
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DP
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.296e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 3.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 732
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5804
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.996087668170386e-5
allele num: 50098
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14252
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9344
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7052
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6544
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -9.475e0

DP
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 6.69e-1

MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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BaseQRankSum
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FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 6.4e-3

ReadPosRankSum
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MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

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: 2.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 2102
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1181
bin: 5.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14192
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.005615724027276e-5
allele num: 49860
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6558
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9262
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 720
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7002
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5776
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.135644e6

MQRankSum
type: SiteQuality
SIO_000300: 2.18e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.29e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.499e0

QD
type: SiteQuality
SIO_000300: 1.31e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.07e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.9e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.07e-1

GenotypeQuality
all individuals: 18515
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1991
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2690
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variant carriers: 0

GenotypeQuality
all individuals: 192
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9314
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.060152499293985e-5
allele num: 14164
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5812
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6586
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 49670
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7016
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 724
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.56e0

MQRankSum
type: SiteQuality
SIO_000300: 3.02e-1

VQSLOD
type: SiteQuality
SIO_000300: -9.581e1

DP
type: SiteQuality
SIO_000300: 1.127982e6

FS
type: SiteQuality
SIO_000300: 1.41496e2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.82e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 2.493e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.87e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1026
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6566
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5780
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14084
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6960
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 724
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9256
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.034587995930824e-5
allele num: 49150
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.120259e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.51e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.11e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 8.43e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.68e0

QD
type: SiteQuality
SIO_000300: 1.194e1

VQSLOD
type: SiteQuality
SIO_000300: 4.4e-1

GenotypeQuality
all individuals: 795
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 519
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2002
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variant carriers: 7

GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
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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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2681
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1718
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 204
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GenotypeQuality
all individuals: 1068
bin: 5.25e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6946
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6538
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5764
num of homozygotes: 0

South Asian
type: Population
allele count: 7
allele frequency: 4.990731498645373e-4
allele num: 14026
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9214
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 722
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 48904
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.13e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.5e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.58e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.629999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.5e-1

DP
type: SiteQuality
SIO_000300: 1.115752e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 3.332e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.3e-3

QD
type: SiteQuality
SIO_000300: 1.563e1

GenotypeQuality
all individuals: 1705
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 872
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 917
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 198
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GenotypeQuality
all individuals: 204
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6494
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 710
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6942
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9164
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13948
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.066884378487867e-5
allele num: 48382
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5736
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.891e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.18e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -5.36e-1

QD
type: SiteQuality
SIO_000300: 3.05e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.2e-3

DP
type: SiteQuality
SIO_000300: 1.106894e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.89e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.0e-1

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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bin: 7.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.113718030014796e-5
allele num: 47310
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7096
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9050
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5688
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6494
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 676
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13758
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.085878e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.5e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.53e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.6e-2

InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -3.243e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.452e0

QD
type: SiteQuality
SIO_000300: 3.424e1

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

GenotypeQuality
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GenotypeQuality
all individuals: 20105
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1997
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 496
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 704
bin: 7.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 676
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5668
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6502
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7122
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13744
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47312
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.107665042091272e-4
allele num: 9028
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.819e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.843e1

MQRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -2.89e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.29e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.89e-1

DP
type: SiteQuality
SIO_000300: 1.084438e6

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 3.75e1
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GenotypeQuality
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variant carriers: 8

GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 5288
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 499
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6456
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7118
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.15898786648819e-5
allele num: 46318
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 662
num of homozygotes: 0

Latino
type: Population
allele count: 7
allele frequency: 7.838745800671892e-4
allele num: 8930
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5578
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13614
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.166e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.75e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 8.44e-1

DP
type: SiteQuality
SIO_000300: 1.069521e6

MQRankSum
type: SiteQuality
SIO_000300: -1.82e-1

QD
type: SiteQuality
SIO_000300: 1.138e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.4e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.9e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.65e-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: 9

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 8918
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6416
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 8.694518106333956e-5
allele num: 46006
num of homozygotes: 0

African
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allele count: 1
allele frequency: 1.395478649176668e-4
allele num: 7166
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 13558
num of homozygotes: 0

European (Finnish)
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allele count: 3
allele frequency: 5.374417771408098e-4
allele num: 5582
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.01e0

DP
type: SiteQuality
SIO_000300: 1.067878e6

InbreedingCoeff
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SIO_000300: -5.6e-3

FS
type: SiteQuality
SIO_000300: 2.14e0

ClippingRankSum
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SIO_000300: 4.01e-1

VQSLOD
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ReadPosRankSum
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SIO_000300: -8.3e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.2e-2

QD
type: SiteQuality
SIO_000300: 1.557e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 654
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5560
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8852
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.185123678000175e-5
allele num: 45764
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 13522
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 7190
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6382
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.067481e6

MQRankSum
type: SiteQuality
SIO_000300: 7.24e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.463e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.86e-1

MQ
type: SiteQuality
SIO_000300: 5.862e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.04e-1

QD
type: SiteQuality
SIO_000300: 1.976e1

FS
type: SiteQuality
SIO_000300: 2.146e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.9e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.27e0

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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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 212
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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6422
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.131733816206428e-4
allele num: 8836
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5548
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.394831677946735e-5
allele num: 45508
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 654
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7222
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13500
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -4.21e-1

QD
type: SiteQuality
SIO_000300: 1.431e1

MQ
type: SiteQuality
SIO_000300: 5.89e1

VQSLOD
type: SiteQuality
SIO_000300: 5.31e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.0e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.44e-1

DP
type: SiteQuality
SIO_000300: 1.067406e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.2e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.6e-3

GenotypeQuality
all individuals: 1309
bin: 6.75e1
variant carriers: 869

GenotypeQuality
all individuals: 5245
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variant carriers: 1118

GenotypeQuality
all individuals: 1608
bin: 2.75e1
variant carriers: 640

GenotypeQuality
all individuals: 779
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variant carriers: 698

GenotypeQuality
all individuals: 1545
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GenotypeQuality
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variant carriers: 1459

GenotypeQuality
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GenotypeQuality
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variant carriers: 528

GenotypeQuality
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variant carriers: 866

GenotypeQuality
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variant carriers: 276

GenotypeQuality
all individuals: 1889
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variant carriers: 1528

GenotypeQuality
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variant carriers: 766

GenotypeQuality
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variant carriers: 605

GenotypeQuality
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variant carriers: 24290

GenotypeQuality
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variant carriers: 613

GenotypeQuality
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variant carriers: 577

GenotypeQuality
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variant carriers: 479

GenotypeQuality
all individuals: 1007
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variant carriers: 910

GenotypeQuality
all individuals: 1717
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variant carriers: 1622

Latino
type: Population
allele count: 5709
allele frequency: 6.28606033913235e-1
allele num: 9082
num of homozygotes: 1647

European (Finnish)
type: Population
allele count: 2920
allele frequency: 5.20870495897253e-1
allele num: 5606
num of homozygotes: 709

East Asian
type: Population
allele count: 6087
allele frequency: 8.60961810466761e-1
allele num: 7070
num of homozygotes: 2594

Other
type: Population
allele count: 308
allele frequency: 4.610778443113773e-1
allele num: 668
num of homozygotes: 66

European (Non-Finnish)
type: Population
allele count: 18184
allele frequency: 3.875202455033672e-1
allele num: 46924
num of homozygotes: 2858

African
type: Population
allele count: 6437
allele frequency: 7.688724319159101e-1
allele num: 8372
num of homozygotes: 2422

South Asian
type: Population
allele count: 7553
allele frequency: 5.429906542056074e-1
allele num: 13910
num of homozygotes: 2048

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.341e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.1e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.89e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.42e0

QD
type: SiteQuality
SIO_000300: 2.186e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.16e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.83e-1

DP
type: SiteQuality
SIO_000300: 1.497417e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7070
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.189072609633358e-5
allele num: 13910
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8372
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 668
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9082
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.783803068141277e-4
allele num: 5606
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.262211235188816e-5
allele num: 46924
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.89e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.341e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.1e-2

DP
type: SiteQuality
SIO_000300: 1.497417e6

BaseQRankSum
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SIO_000300: 1.16e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 2.186e1

VQSLOD
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SIO_000300: 6.42e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.83e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 388
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 40334
num of homozygotes: 0

South Asian
type: Population
allele count: 0
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allele num: 12052
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 590
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.975503753457131e-4
allele num: 5062
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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BaseQRankSum
type: SiteQuality
SIO_000300: -2.3e0

InbreedingCoeff
type: SiteQuality
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MQRankSum
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VQSLOD
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FS
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QD
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ReadPosRankSum
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MQ
type: SiteQuality
SIO_000300: 5.901e1

ClippingRankSum
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SIO_000300: -1.268e0

DP
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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 176
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GenotypeQuality
all individuals: 317
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6476
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11902
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 39434
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.562011871290222e-4
allele num: 6402
num of homozygotes: 0

East 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: 580
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BaseQRankSum
type: SiteQuality
SIO_000300: -1.826e0

MQ
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.037e1

ReadPosRankSum
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DP
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FS
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VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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InbreedingCoeff
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SIO_000300: -8.500000000000001e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 2.34e-1

GenotypeQuality
all individuals: 279
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GenotypeQuality
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GenotypeQuality
all individuals: 176
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1469
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3391
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 362
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5222
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3777
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 492
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 263
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1087
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28593
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1189
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1528
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 370
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 395
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 316
bin: 7.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 578
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4888
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11808
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4686
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.571884162337328e-5
allele num: 38882
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6394
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6274
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.999999999999999e-3

MQRankSum
type: SiteQuality
SIO_000300: -1.054e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.312e0

DP
type: SiteQuality
SIO_000300: 1.07602e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.52e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.855e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.272e1

VQSLOD
type: SiteQuality
SIO_000300: 1.74e-1

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

GenotypeQuality
all individuals: 294
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 302
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 436
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 347
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 408
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3867
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3499
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2157
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27935
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 471
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 212
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1522
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1543
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4272
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 903
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6396
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5221
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 281
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4534
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.714293469409913e-5
allele num: 36842
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4574
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 554
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5840
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6130
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11456
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.845e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.69e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.05e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.72e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.95e-1

FS
type: SiteQuality
SIO_000300: 4.706e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.74e-1

DP
type: SiteQuality
SIO_000300: 1.045131e6

GenotypeQuality
all individuals: 28228
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 427
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 890
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5223
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 3462
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3863
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1491
bin: 3.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 299
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4452
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 175
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6502
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1980
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 344
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 280
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 322
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1567
bin: 1.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 554
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5718
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4510
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11404
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6082
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4526
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 5.486366379546826e-5
allele num: 36454
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.65e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.08e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.57e0

MQRankSum
type: SiteQuality
SIO_000300: 1.34e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.408e0

FS
type: SiteQuality
SIO_000300: 1.6872e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.039699e6

QD
type: SiteQuality
SIO_000300: 7.66e0

GenotypeQuality
all individuals: 149
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 368
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1705
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5220
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2198
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 290
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4852
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 329
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3884
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 396
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 297
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 295
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27775
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 346
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 280
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6161
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 879
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3494
bin: 3.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4390
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5526
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11274
num of homozygotes: 0