17-38178866-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38178866
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38178866
    reference: chr 17
allele count: 2
allele frequency: 1.733072217119287e-5
allele num: 115402
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000440100
  ensembl transcript: ENST00000501516
  gene symbol: MED24
  hgvsc: ENST00000501516.3:c.2489+32G>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000348610
  ensembl transcript: ENST00000356271
  gene symbol: MED24
  hgvsc: ENST00000356271.3:c.2393+32G>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377686
  ensembl transcript: ENST00000394128
  gene symbol: MED24
  hgvsc: ENST00000394128.2:c.2432+32G>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377684
  ensembl transcript: ENST00000394126
  gene symbol: MED24
  hgvsc: ENST00000394126.1:c.2507+32G>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000439148
  ensembl transcript: ENST00000535508
  gene symbol: MED24
  hgvsc: ENST00000535508.2:c.*2055+32G>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000393464
  ensembl transcript: ENST00000422942
  gene symbol: MED24
  hgvsc: ENST00000422942.2:c.212+32G>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377685
  ensembl transcript: ENST00000394127
  gene symbol: MED24
  hgvsc: ENST00000394127.2:c.2393+32G>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000443344
  ensembl transcript: ENST00000535071
  gene symbol: MED24
  hgvsc: ENST00000535071.2:c.2282+32G>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl transcript: ENST00000492176
  gene symbol: MED24
  hgvsc: ENST00000492176.2:n.703+32G>A
  variant of: http://identifiers.org/hgnc/22963
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7468
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2566
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4342
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22997
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15308
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6417
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2124
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31995
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4014
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1254
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

17-38178867-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38178867
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38178867
    reference: chr 17
allele count: 3
allele frequency: 2.601456815816858e-5
allele num: 115320
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377684
  ensembl transcript: ENST00000394126
  gene symbol: MED24
  hgvsc: ENST00000394126.1:c.2507+31C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000439148
  ensembl transcript: ENST00000535508
  gene symbol: MED24
  hgvsc: ENST00000535508.2:c.*2055+31C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000443344
  ensembl transcript: ENST00000535071
  gene symbol: MED24
  hgvsc: ENST00000535071.2:c.2282+31C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl transcript: ENST00000492176
  gene symbol: MED24
  hgvsc: ENST00000492176.2:n.703+31C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000348610
  ensembl transcript: ENST00000356271
  gene symbol: MED24
  hgvsc: ENST00000356271.3:c.2393+31C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377686
  ensembl transcript: ENST00000394128
  gene symbol: MED24
  hgvsc: ENST00000394128.2:c.2432+31C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000440100
  ensembl transcript: ENST00000501516
  gene symbol: MED24
  hgvsc: ENST00000501516.3:c.2489+31C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377685
  ensembl transcript: ENST00000394127
  gene symbol: MED24
  hgvsc: ENST00000394127.2:c.2393+31C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000393464
  ensembl transcript: ENST00000422942
  gene symbol: MED24
  hgvsc: ENST00000422942.2:c.212+31C>T
  variant of: http://identifiers.org/hgnc/22963
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4541
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7028
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2547
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5623
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15680
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23679
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 854
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 282
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3186
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 601
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3993
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3210
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff

17-38178874-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38178874
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38178874
    reference: chr 17
allele count: 3
allele frequency: 2.58095598609725e-5
allele num: 116236
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000439148
  ensembl transcript: ENST00000535508
  gene symbol: MED24
  hgvsc: ENST00000535508.2:c.*2055+24C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377685
  ensembl transcript: ENST00000394127
  gene symbol: MED24
  hgvsc: ENST00000394127.2:c.2393+24C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000393464
  ensembl transcript: ENST00000422942
  gene symbol: MED24
  hgvsc: ENST00000422942.2:c.212+24C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377686
  ensembl transcript: ENST00000394128
  gene symbol: MED24
  hgvsc: ENST00000394128.2:c.2432+24C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000348610
  ensembl transcript: ENST00000356271
  gene symbol: MED24
  hgvsc: ENST00000356271.3:c.2393+24C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377684
  ensembl transcript: ENST00000394126
  gene symbol: MED24
  hgvsc: ENST00000394126.1:c.2507+24C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000443344
  ensembl transcript: ENST00000535071
  gene symbol: MED24
  hgvsc: ENST00000535071.2:c.2282+24C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000440100
  ensembl transcript: ENST00000501516
  gene symbol: MED24
  hgvsc: ENST00000501516.3:c.2489+24C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl transcript: ENST00000492176
  gene symbol: MED24
  hgvsc: ENST00000492176.2:n.703+24C>T
  variant of: http://identifiers.org/hgnc/22963
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3619
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5715
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16697
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26209
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2381
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4554
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 719
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1666
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 287
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2487
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 849
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: Other
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQ
site quality: ReadPosRankSum

17-38178876-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38178876
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38178876
    reference: chr 17
allele count: 1
allele frequency: 8.59017970655946e-6
allele num: 116412
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000443344
  ensembl transcript: ENST00000535071
  gene symbol: MED24
  hgvsc: ENST00000535071.2:c.2282+22G>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000440100
  ensembl transcript: ENST00000501516
  gene symbol: MED24
  hgvsc: ENST00000501516.3:c.2489+22G>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000393464
  ensembl transcript: ENST00000422942
  gene symbol: MED24
  hgvsc: ENST00000422942.2:c.212+22G>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377686
  ensembl transcript: ENST00000394128
  gene symbol: MED24
  hgvsc: ENST00000394128.2:c.2432+22G>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000348610
  ensembl transcript: ENST00000356271
  gene symbol: MED24
  hgvsc: ENST00000356271.3:c.2393+22G>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000439148
  ensembl transcript: ENST00000535508
  gene symbol: MED24
  hgvsc: ENST00000535508.2:c.*2055+22G>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377685
  ensembl transcript: ENST00000394127
  gene symbol: MED24
  hgvsc: ENST00000394127.2:c.2393+22G>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377684
  ensembl transcript: ENST00000394126
  gene symbol: MED24
  hgvsc: ENST00000394126.1:c.2507+22G>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl transcript: ENST00000492176
  gene symbol: MED24
  hgvsc: ENST00000492176.2:n.703+22G>A
  variant of: http://identifiers.org/hgnc/22963
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5284
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26466
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4659
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17219
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2279
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3262
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5199
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1559
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1353
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 484
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: DP

17-38178878-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38178878
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38178878
    reference: chr 17
allele count: 1
allele frequency: 8.572359284722342e-6
allele num: 116654
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000348610
  ensembl transcript: ENST00000356271
  gene symbol: MED24
  hgvsc: ENST00000356271.3:c.2393+20T>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377684
  ensembl transcript: ENST00000394126
  gene symbol: MED24
  hgvsc: ENST00000394126.1:c.2507+20T>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377685
  ensembl transcript: ENST00000394127
  gene symbol: MED24
  hgvsc: ENST00000394127.2:c.2393+20T>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000393464
  ensembl transcript: ENST00000422942
  gene symbol: MED24
  hgvsc: ENST00000422942.2:c.212+20T>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000439148
  ensembl transcript: ENST00000535508
  gene symbol: MED24
  hgvsc: ENST00000535508.2:c.*2055+20T>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000440100
  ensembl transcript: ENST00000501516
  gene symbol: MED24
  hgvsc: ENST00000501516.3:c.2489+20T>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377686
  ensembl transcript: ENST00000394128
  gene symbol: MED24
  hgvsc: ENST00000394128.2:c.2432+20T>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl transcript: ENST00000492176
  gene symbol: MED24
  hgvsc: ENST00000492176.2:n.703+20T>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000443344
  ensembl transcript: ENST00000535071
  gene symbol: MED24
  hgvsc: ENST00000535071.2:c.2282+20T>A
  variant of: http://identifiers.org/hgnc/22963
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27136
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2230
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4639
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4905
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2883
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17398
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 833
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 785
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 244
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1803
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQ

17-38178881-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38178881
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38178881
    reference: chr 17
allele count: 1
allele frequency: 8.552271483305966e-6
allele num: 116928
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000348610
  ensembl transcript: ENST00000356271
  gene symbol: MED24
  hgvsc: ENST00000356271.3:c.2393+17A>G
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000440100
  ensembl transcript: ENST00000501516
  gene symbol: MED24
  hgvsc: ENST00000501516.3:c.2489+17A>G
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377686
  ensembl transcript: ENST00000394128
  gene symbol: MED24
  hgvsc: ENST00000394128.2:c.2432+17A>G
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000443344
  ensembl transcript: ENST00000535071
  gene symbol: MED24
  hgvsc: ENST00000535071.2:c.2282+17A>G
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377685
  ensembl transcript: ENST00000394127
  gene symbol: MED24
  hgvsc: ENST00000394127.2:c.2393+17A>G
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000393464
  ensembl transcript: ENST00000422942
  gene symbol: MED24
  hgvsc: ENST00000422942.2:c.212+17A>G
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000439148
  ensembl transcript: ENST00000535508
  gene symbol: MED24
  hgvsc: ENST00000535508.2:c.*2055+17A>G
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl transcript: ENST00000492176
  gene symbol: MED24
  hgvsc: ENST00000492176.2:n.703+17A>G
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377684
  ensembl transcript: ENST00000394126
  gene symbol: MED24
  hgvsc: ENST00000394126.1:c.2507+17A>G
  variant of: http://identifiers.org/hgnc/22963
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4684
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28044
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17771
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2132
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2272
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4294
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 717
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1278
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 526
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1465
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 563
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: T
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

17-38178899-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38178899
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38178899
    reference: chr 17
allele count: 1
allele frequency: 8.457804015765346e-6
allele num: 118234
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377685
  ensembl transcript: ENST00000394127
  gene symbol: MED24
  hgvsc: ENST00000394127.2:c.2392A>G
  hgvsp: ENSP00000377685.2:p.Lys798Glu
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000348610
  ensembl transcript: ENST00000356271
  gene symbol: MED24
  hgvsc: ENST00000356271.3:c.2392A>G
  hgvsp: ENSP00000348610.3:p.Lys798Glu
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000393464
  ensembl transcript: ENST00000422942
  gene symbol: MED24
  hgvsc: ENST00000422942.2:c.211A>G
  hgvsp: ENSP00000393464.2:p.Lys71Glu
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377686
  ensembl transcript: ENST00000394128
  gene symbol: MED24
  hgvsc: ENST00000394128.2:c.2431A>G
  hgvsp: ENSP00000377686.2:p.Lys811Glu
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000443344
  ensembl transcript: ENST00000535071
  gene symbol: MED24
  hgvsc: ENST00000535071.2:c.2281A>G
  hgvsp: ENSP00000443344.2:p.Lys761Glu
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377684
  ensembl transcript: ENST00000394126
  gene symbol: MED24
  hgvsc: ENST00000394126.1:c.2506A>G
  hgvsp: ENSP00000377684.1:p.Lys836Glu
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000439148
  ensembl transcript: ENST00000535508
  gene symbol: MED24
  hgvsc: ENST00000535508.2:c.*2054A>G
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000008838
  ensembl transcript: ENST00000492176
  gene symbol: MED24
  hgvsc: ENST00000492176.2:n.702A>G
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000440100
  ensembl transcript: ENST00000501516
  gene symbol: MED24
  hgvsc: ENST00000501516.3:c.2488A>G
  hgvsp: ENSP00000440100.2:p.Lys830Glu
  variant of: http://identifiers.org/hgnc/22963
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1520
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2231
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4900
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 858
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30363
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1103
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19101
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 214
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Lys811Glu
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum

17-38178915-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38178915
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38178915
    reference: chr 17
allele count: 5
allele frequency: 4.202810839889718e-5
allele num: 118968
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000393464
  ensembl transcript: ENST00000422942
  gene symbol: MED24
  hgvsc: ENST00000422942.2:c.195G>A
  hgvsp: ENST00000422942.2:c.195G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008838
  ensembl transcript: ENST00000492176
  gene symbol: MED24
  hgvsc: ENST00000492176.2:n.686G>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000348610
  ensembl transcript: ENST00000356271
  gene symbol: MED24
  hgvsc: ENST00000356271.3:c.2376G>A
  hgvsp: ENST00000356271.3:c.2376G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000439148
  ensembl transcript: ENST00000535508
  gene symbol: MED24
  hgvsc: ENST00000535508.2:c.*2038G>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377686
  ensembl transcript: ENST00000394128
  gene symbol: MED24
  hgvsc: ENST00000394128.2:c.2415G>A
  hgvsp: ENST00000394128.2:c.2415G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377684
  ensembl transcript: ENST00000394126
  gene symbol: MED24
  hgvsc: ENST00000394126.1:c.2490G>A
  hgvsp: ENST00000394126.1:c.2490G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000440100
  ensembl transcript: ENST00000501516
  gene symbol: MED24
  hgvsc: ENST00000501516.3:c.2472G>A
  hgvsp: ENST00000501516.3:c.2472G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377685
  ensembl transcript: ENST00000394127
  gene symbol: MED24
  hgvsc: ENST00000394127.2:c.2376G>A
  hgvsp: ENST00000394127.2:c.2376G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000443344
  ensembl transcript: ENST00000535071
  gene symbol: MED24
  hgvsc: ENST00000535071.2:c.2265G>A
  hgvsp: ENST00000535071.2:c.2265G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22963
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29933
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5288
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20340
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1462
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 663
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 499
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 297
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Pro805Pro
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum

17-38178916-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38178916
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38178916
    reference: chr 17
allele count: 5
allele frequency: 4.201610056973833e-5
allele num: 119002
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000443344
  ensembl transcript: ENST00000535071
  gene symbol: MED24
  hgvsc: ENST00000535071.2:c.2264C>T
  hgvsp: ENSP00000443344.2:p.Pro755Leu
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377684
  ensembl transcript: ENST00000394126
  gene symbol: MED24
  hgvsc: ENST00000394126.1:c.2489C>T
  hgvsp: ENSP00000377684.1:p.Pro830Leu
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000393464
  ensembl transcript: ENST00000422942
  gene symbol: MED24
  hgvsc: ENST00000422942.2:c.194C>T
  hgvsp: ENSP00000393464.2:p.Pro65Leu
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000440100
  ensembl transcript: ENST00000501516
  gene symbol: MED24
  hgvsc: ENST00000501516.3:c.2471C>T
  hgvsp: ENSP00000440100.2:p.Pro824Leu
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377685
  ensembl transcript: ENST00000394127
  gene symbol: MED24
  hgvsc: ENST00000394127.2:c.2375C>T
  hgvsp: ENSP00000377685.2:p.Pro792Leu
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000348610
  ensembl transcript: ENST00000356271
  gene symbol: MED24
  hgvsc: ENST00000356271.3:c.2375C>T
  hgvsp: ENSP00000348610.3:p.Pro792Leu
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008838
  ensembl transcript: ENST00000492176
  gene symbol: MED24
  hgvsc: ENST00000492176.2:n.685C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377686
  ensembl transcript: ENST00000394128
  gene symbol: MED24
  hgvsc: ENST00000394128.2:c.2414C>T
  hgvsp: ENSP00000377686.2:p.Pro805Leu
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000439148
  ensembl transcript: ENST00000535508
  gene symbol: MED24
  hgvsc: ENST00000535508.2:c.*2037C>T
  variant of: http://identifiers.org/hgnc/22963
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29888
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1393
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5282
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20491
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1585
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 616
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 245
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Pro805Leu
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: Latino
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: QD
site quality: ClippingRankSum

17-38178916-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38178916
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38178916
    reference: chr 17
allele count: 1
allele frequency: 8.403220113947665e-6
allele num: 119002
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377685
  ensembl transcript: ENST00000394127
  gene symbol: MED24
  hgvsc: ENST00000394127.2:c.2375C>A
  hgvsp: ENSP00000377685.2:p.Pro792Gln
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000440100
  ensembl transcript: ENST00000501516
  gene symbol: MED24
  hgvsc: ENST00000501516.3:c.2471C>A
  hgvsp: ENSP00000440100.2:p.Pro824Gln
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000443344
  ensembl transcript: ENST00000535071
  gene symbol: MED24
  hgvsc: ENST00000535071.2:c.2264C>A
  hgvsp: ENSP00000443344.2:p.Pro755Gln
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377686
  ensembl transcript: ENST00000394128
  gene symbol: MED24
  hgvsc: ENST00000394128.2:c.2414C>A
  hgvsp: ENSP00000377686.2:p.Pro805Gln
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000439148
  ensembl transcript: ENST00000535508
  gene symbol: MED24
  hgvsc: ENST00000535508.2:c.*2037C>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000348610
  ensembl transcript: ENST00000356271
  gene symbol: MED24
  hgvsc: ENST00000356271.3:c.2375C>A
  hgvsp: ENSP00000348610.3:p.Pro792Gln
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000393464
  ensembl transcript: ENST00000422942
  gene symbol: MED24
  hgvsc: ENST00000422942.2:c.194C>A
  hgvsp: ENSP00000393464.2:p.Pro65Gln
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377684
  ensembl transcript: ENST00000394126
  gene symbol: MED24
  hgvsc: ENST00000394126.1:c.2489C>A
  hgvsp: ENSP00000377684.1:p.Pro830Gln
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008838
  ensembl transcript: ENST00000492176
  gene symbol: MED24
  hgvsc: ENST00000492176.2:n.685C>A
  variant of: http://identifiers.org/hgnc/22963
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5282
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1393
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20491
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29888
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 475
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 449
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1535
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 7.5e0
  variant carriers: 1
hgvs: p.Pro805Gln
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: East Asian
reference allele: G
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum

17-38178919-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38178919
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38178919
    reference: chr 17
allele count: 1
allele frequency: 8.377033524888167e-6
allele num: 119374
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000440100
  ensembl transcript: ENST00000501516
  gene symbol: MED24
  hgvsc: ENST00000501516.3:c.2468C>A
  hgvsp: ENSP00000440100.2:p.Pro823His
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008838
  ensembl transcript: ENST00000492176
  gene symbol: MED24
  hgvsc: ENST00000492176.2:n.682C>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377684
  ensembl transcript: ENST00000394126
  gene symbol: MED24
  hgvsc: ENST00000394126.1:c.2486C>A
  hgvsp: ENSP00000377684.1:p.Pro829His
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000443344
  ensembl transcript: ENST00000535071
  gene symbol: MED24
  hgvsc: ENST00000535071.2:c.2261C>A
  hgvsp: ENSP00000443344.2:p.Pro754His
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000439148
  ensembl transcript: ENST00000535508
  gene symbol: MED24
  hgvsc: ENST00000535508.2:c.*2034C>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377686
  ensembl transcript: ENST00000394128
  gene symbol: MED24
  hgvsc: ENST00000394128.2:c.2411C>A
  hgvsp: ENSP00000377686.2:p.Pro804His
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377685
  ensembl transcript: ENST00000394127
  gene symbol: MED24
  hgvsc: ENST00000394127.2:c.2372C>A
  hgvsp: ENSP00000377685.2:p.Pro791His
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000348610
  ensembl transcript: ENST00000356271
  gene symbol: MED24
  hgvsc: ENST00000356271.3:c.2372C>A
  hgvsp: ENSP00000348610.3:p.Pro791His
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000393464
  ensembl transcript: ENST00000422942
  gene symbol: MED24
  hgvsc: ENST00000422942.2:c.191C>A
  hgvsp: ENSP00000393464.2:p.Pro64His
  variant of: http://identifiers.org/hgnc/22963
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5209
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20711
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1342
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29970
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1002
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 380
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 286
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 747
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 497
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Pro804His
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum

17-38178920-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38178920
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38178920
    reference: chr 17
allele count: 1
allele frequency: 8.375770570892522e-6
allele num: 119392
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377686
  ensembl transcript: ENST00000394128
  gene symbol: MED24
  hgvsc: ENST00000394128.2:c.2410C>T
  hgvsp: ENSP00000377686.2:p.Pro804Ser
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000443344
  ensembl transcript: ENST00000535071
  gene symbol: MED24
  hgvsc: ENST00000535071.2:c.2260C>T
  hgvsp: ENSP00000443344.2:p.Pro754Ser
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000393464
  ensembl transcript: ENST00000422942
  gene symbol: MED24
  hgvsc: ENST00000422942.2:c.190C>T
  hgvsp: ENSP00000393464.2:p.Pro64Ser
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377685
  ensembl transcript: ENST00000394127
  gene symbol: MED24
  hgvsc: ENST00000394127.2:c.2371C>T
  hgvsp: ENSP00000377685.2:p.Pro791Ser
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377684
  ensembl transcript: ENST00000394126
  gene symbol: MED24
  hgvsc: ENST00000394126.1:c.2485C>T
  hgvsp: ENSP00000377684.1:p.Pro829Ser
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000440100
  ensembl transcript: ENST00000501516
  gene symbol: MED24
  hgvsc: ENST00000501516.3:c.2467C>T
  hgvsp: ENSP00000440100.2:p.Pro823Ser
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000348610
  ensembl transcript: ENST00000356271
  gene symbol: MED24
  hgvsc: ENST00000356271.3:c.2371C>T
  hgvsp: ENSP00000348610.3:p.Pro791Ser
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000439148
  ensembl transcript: ENST00000535508
  gene symbol: MED24
  hgvsc: ENST00000535508.2:c.*2033C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008838
  ensembl transcript: ENST00000492176
  gene symbol: MED24
  hgvsc: ENST00000492176.2:n.681C>T
  variant of: http://identifiers.org/hgnc/22963
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20775
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29950
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 957
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1320
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5218
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 548
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 185
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Pro804Ser
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: Other
population: Latino
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: QD

17-38178920-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38178920
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38178920
    reference: chr 17
allele count: 1
allele frequency: 8.375770570892522e-6
allele num: 119392
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377686
  ensembl transcript: ENST00000394128
  gene symbol: MED24
  hgvsc: ENST00000394128.2:c.2410C>A
  hgvsp: ENSP00000377686.2:p.Pro804Thr
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377685
  ensembl transcript: ENST00000394127
  gene symbol: MED24
  hgvsc: ENST00000394127.2:c.2371C>A
  hgvsp: ENSP00000377685.2:p.Pro791Thr
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000393464
  ensembl transcript: ENST00000422942
  gene symbol: MED24
  hgvsc: ENST00000422942.2:c.190C>A
  hgvsp: ENSP00000393464.2:p.Pro64Thr
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377684
  ensembl transcript: ENST00000394126
  gene symbol: MED24
  hgvsc: ENST00000394126.1:c.2485C>A
  hgvsp: ENSP00000377684.1:p.Pro829Thr
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000440100
  ensembl transcript: ENST00000501516
  gene symbol: MED24
  hgvsc: ENST00000501516.3:c.2467C>A
  hgvsp: ENSP00000440100.2:p.Pro823Thr
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000348610
  ensembl transcript: ENST00000356271
  gene symbol: MED24
  hgvsc: ENST00000356271.3:c.2371C>A
  hgvsp: ENSP00000348610.3:p.Pro791Thr
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000439148
  ensembl transcript: ENST00000535508
  gene symbol: MED24
  hgvsc: ENST00000535508.2:c.*2033C>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008838
  ensembl transcript: ENST00000492176
  gene symbol: MED24
  hgvsc: ENST00000492176.2:n.681C>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000443344
  ensembl transcript: ENST00000535071
  gene symbol: MED24
  hgvsc: ENST00000535071.2:c.2260C>A
  hgvsp: ENSP00000443344.2:p.Pro754Thr
  variant of: http://identifiers.org/hgnc/22963
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5218
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20775
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 957
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29950
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1320
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 249
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45580
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Pro804Thr
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: VQSLOD

17-38178925-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38178925
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38178925
    reference: chr 17
allele count: 1
allele frequency: 8.36050497450046e-6
allele num: 119610
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000439148
  ensembl transcript: ENST00000535508
  gene symbol: MED24
  hgvsc: ENST00000535508.2:c.*2028T>C
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000443344
  ensembl transcript: ENST00000535071
  gene symbol: MED24
  hgvsc: ENST00000535071.2:c.2255T>C
  hgvsp: ENSP00000443344.2:p.Met752Thr
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000440100
  ensembl transcript: ENST00000501516
  gene symbol: MED24
  hgvsc: ENST00000501516.3:c.2462T>C
  hgvsp: ENSP00000440100.2:p.Met821Thr
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377686
  ensembl transcript: ENST00000394128
  gene symbol: MED24
  hgvsc: ENST00000394128.2:c.2405T>C
  hgvsp: ENSP00000377686.2:p.Met802Thr
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377684
  ensembl transcript: ENST00000394126
  gene symbol: MED24
  hgvsc: ENST00000394126.1:c.2480T>C
  hgvsp: ENSP00000377684.1:p.Met827Thr
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377685
  ensembl transcript: ENST00000394127
  gene symbol: MED24
  hgvsc: ENST00000394127.2:c.2366T>C
  hgvsp: ENSP00000377685.2:p.Met789Thr
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008838
  ensembl transcript: ENST00000492176
  gene symbol: MED24
  hgvsc: ENST00000492176.2:n.676T>C
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000348610
  ensembl transcript: ENST00000356271
  gene symbol: MED24
  hgvsc: ENST00000356271.3:c.2366T>C
  hgvsp: ENSP00000348610.3:p.Met789Thr
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000393464
  ensembl transcript: ENST00000422942
  gene symbol: MED24
  hgvsc: ENST00000422942.2:c.185T>C
  hgvsp: ENSP00000393464.2:p.Met62Thr
  variant of: http://identifiers.org/hgnc/22963
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30044
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5213
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1211
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21005
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 866
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 367
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 740
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46124
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 345
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Met802Thr
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD

17-38178929-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38178929
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38178929
    reference: chr 17
allele count: 2
allele frequency: 1.671067143477825e-5
allele num: 119684
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377686
  ensembl transcript: ENST00000394128
  gene symbol: MED24
  hgvsc: ENST00000394128.2:c.2401C>G
  hgvsp: ENSP00000377686.2:p.Leu801Val
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377685
  ensembl transcript: ENST00000394127
  gene symbol: MED24
  hgvsc: ENST00000394127.2:c.2362C>G
  hgvsp: ENSP00000377685.2:p.Leu788Val
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008838
  ensembl transcript: ENST00000492176
  gene symbol: MED24
  hgvsc: ENST00000492176.2:n.672C>G
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377684
  ensembl transcript: ENST00000394126
  gene symbol: MED24
  hgvsc: ENST00000394126.1:c.2476C>G
  hgvsp: ENSP00000377684.1:p.Leu826Val
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000440100
  ensembl transcript: ENST00000501516
  gene symbol: MED24
  hgvsc: ENST00000501516.3:c.2458C>G
  hgvsp: ENSP00000440100.2:p.Leu820Val
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000439148
  ensembl transcript: ENST00000535508
  gene symbol: MED24
  hgvsc: ENST00000535508.2:c.*2024C>G
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000393464
  ensembl transcript: ENST00000422942
  gene symbol: MED24
  hgvsc: ENST00000422942.2:c.181C>G
  hgvsp: ENSP00000393464.2:p.Leu61Val
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000443344
  ensembl transcript: ENST00000535071
  gene symbol: MED24
  hgvsc: ENST00000535071.2:c.2251C>G
  hgvsp: ENSP00000443344.2:p.Leu751Val
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000348610
  ensembl transcript: ENST00000356271
  gene symbol: MED24
  hgvsc: ENST00000356271.3:c.2362C>G
  hgvsp: ENSP00000348610.3:p.Leu788Val
  variant of: http://identifiers.org/hgnc/22963
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5239
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 30022
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1139
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21143
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1277
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1466
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5996
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Leu801Val
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: InbreedingCoeff

17-38178930-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38178930
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38178930
    reference: chr 17
allele count: 1
allele frequency: 8.353241893178742e-6
allele num: 119714
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000348610
  ensembl transcript: ENST00000356271
  gene symbol: MED24
  hgvsc: ENST00000356271.3:c.2361C>G
  hgvsp: ENSP00000348610.3:p.Ser787Arg
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000440100
  ensembl transcript: ENST00000501516
  gene symbol: MED24
  hgvsc: ENST00000501516.3:c.2457C>G
  hgvsp: ENSP00000440100.2:p.Ser819Arg
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377686
  ensembl transcript: ENST00000394128
  gene symbol: MED24
  hgvsc: ENST00000394128.2:c.2400C>G
  hgvsp: ENSP00000377686.2:p.Ser800Arg
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000439148
  ensembl transcript: ENST00000535508
  gene symbol: MED24
  hgvsc: ENST00000535508.2:c.*2023C>G
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377685
  ensembl transcript: ENST00000394127
  gene symbol: MED24
  hgvsc: ENST00000394127.2:c.2361C>G
  hgvsp: ENSP00000377685.2:p.Ser787Arg
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008838
  ensembl transcript: ENST00000492176
  gene symbol: MED24
  hgvsc: ENST00000492176.2:n.671C>G
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000393464
  ensembl transcript: ENST00000422942
  gene symbol: MED24
  hgvsc: ENST00000422942.2:c.180C>G
  hgvsp: ENSP00000393464.2:p.Ser60Arg
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000443344
  ensembl transcript: ENST00000535071
  gene symbol: MED24
  hgvsc: ENST00000535071.2:c.2250C>G
  hgvsp: ENSP00000443344.2:p.Ser750Arg
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377684
  ensembl transcript: ENST00000394126
  gene symbol: MED24
  hgvsc: ENST00000394126.1:c.2475C>G
  hgvsp: ENSP00000377684.1:p.Ser825Arg
  variant of: http://identifiers.org/hgnc/22963
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21186
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 869
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1112
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29990
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5253
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 245
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 421
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1591
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ser800Arg
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: African
population: Other
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum

17-38178941-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38178941
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38178941
    reference: chr 17
allele count: 2
allele frequency: 1.667333600106709e-5
allele num: 119952
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000348610
  ensembl transcript: ENST00000356271
  gene symbol: MED24
  hgvsc: ENST00000356271.3:c.2350A>G
  hgvsp: ENSP00000348610.3:p.Lys784Glu
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377686
  ensembl transcript: ENST00000394128
  gene symbol: MED24
  hgvsc: ENST00000394128.2:c.2389A>G
  hgvsp: ENSP00000377686.2:p.Lys797Glu
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000443344
  ensembl transcript: ENST00000535071
  gene symbol: MED24
  hgvsc: ENST00000535071.2:c.2239A>G
  hgvsp: ENSP00000443344.2:p.Lys747Glu
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000393464
  ensembl transcript: ENST00000422942
  gene symbol: MED24
  hgvsc: ENST00000422942.2:c.169A>G
  hgvsp: ENSP00000393464.2:p.Lys57Glu
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000439148
  ensembl transcript: ENST00000535508
  gene symbol: MED24
  hgvsc: ENST00000535508.2:c.*2012A>G
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377685
  ensembl transcript: ENST00000394127
  gene symbol: MED24
  hgvsc: ENST00000394127.2:c.2350A>G
  hgvsp: ENSP00000377685.2:p.Lys784Glu
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008838
  ensembl transcript: ENST00000492176
  gene symbol: MED24
  hgvsc: ENST00000492176.2:n.660A>G
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377684
  ensembl transcript: ENST00000394126
  gene symbol: MED24
  hgvsc: ENST00000394126.1:c.2464A>G
  hgvsp: ENSP00000377684.1:p.Lys822Glu
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000440100
  ensembl transcript: ENST00000501516
  gene symbol: MED24
  hgvsc: ENST00000501516.3:c.2446A>G
  hgvsp: ENSP00000440100.2:p.Lys816Glu
  variant of: http://identifiers.org/hgnc/22963
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1048
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21642
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29484
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5321
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 313
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 402
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1164
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1575
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Lys797Glu
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: East Asian
reference allele: T
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum

17-38178943-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38178943
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38178943
    reference: chr 17
allele count: 2
allele frequency: 1.667361400583577e-5
allele num: 119950
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000348610
  ensembl transcript: ENST00000356271
  gene symbol: MED24
  hgvsc: ENST00000356271.3:c.2348C>T
  hgvsp: ENSP00000348610.3:p.Ser783Phe
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000393464
  ensembl transcript: ENST00000422942
  gene symbol: MED24
  hgvsc: ENST00000422942.2:c.167C>T
  hgvsp: ENSP00000393464.2:p.Ser56Phe
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377685
  ensembl transcript: ENST00000394127
  gene symbol: MED24
  hgvsc: ENST00000394127.2:c.2348C>T
  hgvsp: ENSP00000377685.2:p.Ser783Phe
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008838
  ensembl transcript: ENST00000492176
  gene symbol: MED24
  hgvsc: ENST00000492176.2:n.658C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000443344
  ensembl transcript: ENST00000535071
  gene symbol: MED24
  hgvsc: ENST00000535071.2:c.2237C>T
  hgvsp: ENSP00000443344.2:p.Ser746Phe
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377684
  ensembl transcript: ENST00000394126
  gene symbol: MED24
  hgvsc: ENST00000394126.1:c.2462C>T
  hgvsp: ENSP00000377684.1:p.Ser821Phe
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000440100
  ensembl transcript: ENST00000501516
  gene symbol: MED24
  hgvsc: ENST00000501516.3:c.2444C>T
  hgvsp: ENSP00000440100.2:p.Ser815Phe
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377686
  ensembl transcript: ENST00000394128
  gene symbol: MED24
  hgvsc: ENST00000394128.2:c.2387C>T
  hgvsp: ENSP00000377686.2:p.Ser796Phe
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000439148
  ensembl transcript: ENST00000535508
  gene symbol: MED24
  hgvsc: ENST00000535508.2:c.*2010C>T
  variant of: http://identifiers.org/hgnc/22963
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29388
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1011
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21681
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1096
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5341
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 379
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1162
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 238
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ser796Phe
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP

17-38178948-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38178948
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38178948
    reference: chr 17
allele count: 2
allele frequency: 1.666750004166875e-5
allele num: 119994
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377684
  ensembl transcript: ENST00000394126
  gene symbol: MED24
  hgvsc: ENST00000394126.1:c.2457C>G
  hgvsp: ENSP00000377684.1:p.Asp819Glu
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000440100
  ensembl transcript: ENST00000501516
  gene symbol: MED24
  hgvsc: ENST00000501516.3:c.2439C>G
  hgvsp: ENSP00000440100.2:p.Asp813Glu
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000348610
  ensembl transcript: ENST00000356271
  gene symbol: MED24
  hgvsc: ENST00000356271.3:c.2343C>G
  hgvsp: ENSP00000348610.3:p.Asp781Glu
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377686
  ensembl transcript: ENST00000394128
  gene symbol: MED24
  hgvsc: ENST00000394128.2:c.2382C>G
  hgvsp: ENSP00000377686.2:p.Asp794Glu
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000443344
  ensembl transcript: ENST00000535071
  gene symbol: MED24
  hgvsc: ENST00000535071.2:c.2232C>G
  hgvsp: ENSP00000443344.2:p.Asp744Glu
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000439148
  ensembl transcript: ENST00000535508
  gene symbol: MED24
  hgvsc: ENST00000535508.2:c.*2005C>G
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000393464
  ensembl transcript: ENST00000422942
  gene symbol: MED24
  hgvsc: ENST00000422942.2:c.162C>G
  hgvsp: ENSP00000393464.2:p.Asp54Glu
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377685
  ensembl transcript: ENST00000394127
  gene symbol: MED24
  hgvsc: ENST00000394127.2:c.2343C>G
  hgvsp: ENSP00000377685.2:p.Asp781Glu
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008838
  ensembl transcript: ENST00000492176
  gene symbol: MED24
  hgvsc: ENST00000492176.2:n.653C>G
  variant of: http://identifiers.org/hgnc/22963
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29107
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5314
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21857
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 444
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 243
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 600
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 450
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Asp794Glu
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
population: African
population: Latino
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

17-38178960-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38178960
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38178960
    reference: chr 17
allele count: 2
allele frequency: 1.66591700401486e-5
allele num: 120054
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008838
  ensembl transcript: ENST00000492176
  gene symbol: MED24
  hgvsc: ENST00000492176.2:n.641C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000443344
  ensembl transcript: ENST00000535071
  gene symbol: MED24
  hgvsc: ENST00000535071.2:c.2220C>T
  hgvsp: ENST00000535071.2:c.2220C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000440100
  ensembl transcript: ENST00000501516
  gene symbol: MED24
  hgvsc: ENST00000501516.3:c.2427C>T
  hgvsp: ENST00000501516.3:c.2427C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000439148
  ensembl transcript: ENST00000535508
  gene symbol: MED24
  hgvsc: ENST00000535508.2:c.*1993C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000393464
  ensembl transcript: ENST00000422942
  gene symbol: MED24
  hgvsc: ENST00000422942.2:c.150C>T
  hgvsp: ENST00000422942.2:c.150C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377685
  ensembl transcript: ENST00000394127
  gene symbol: MED24
  hgvsc: ENST00000394127.2:c.2331C>T
  hgvsp: ENST00000394127.2:c.2331C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000348610
  ensembl transcript: ENST00000356271
  gene symbol: MED24
  hgvsc: ENST00000356271.3:c.2331C>T
  hgvsp: ENST00000356271.3:c.2331C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377686
  ensembl transcript: ENST00000394128
  gene symbol: MED24
  hgvsc: ENST00000394128.2:c.2370C>T
  hgvsp: ENST00000394128.2:c.2370C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377684
  ensembl transcript: ENST00000394126
  gene symbol: MED24
  hgvsc: ENST00000394126.1:c.2445C>T
  hgvsp: ENST00000394126.1:c.2445C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22963
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 980
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1447
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5365
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 28632
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22160
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 464
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 525
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 532
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Gly790Gly
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum

17-38178965-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38178965
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38178965
    reference: chr 17
allele count: 5
allele frequency: 4.163335997868372e-5
allele num: 120096
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377685
  ensembl transcript: ENST00000394127
  gene symbol: MED24
  hgvsc: ENST00000394127.2:c.2326C>T
  hgvsp: ENSP00000377685.2:p.Pro776Ser
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000348610
  ensembl transcript: ENST00000356271
  gene symbol: MED24
  hgvsc: ENST00000356271.3:c.2326C>T
  hgvsp: ENSP00000348610.3:p.Pro776Ser
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000440100
  ensembl transcript: ENST00000501516
  gene symbol: MED24
  hgvsc: ENST00000501516.3:c.2422C>T
  hgvsp: ENSP00000440100.2:p.Pro808Ser
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377686
  ensembl transcript: ENST00000394128
  gene symbol: MED24
  hgvsc: ENST00000394128.2:c.2365C>T
  hgvsp: ENSP00000377686.2:p.Pro789Ser
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377684
  ensembl transcript: ENST00000394126
  gene symbol: MED24
  hgvsc: ENST00000394126.1:c.2440C>T
  hgvsp: ENSP00000377684.1:p.Pro814Ser
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000393464
  ensembl transcript: ENST00000422942
  gene symbol: MED24
  hgvsc: ENST00000422942.2:c.145C>T
  hgvsp: ENSP00000393464.2:p.Pro49Ser
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000439148
  ensembl transcript: ENST00000535508
  gene symbol: MED24
  hgvsc: ENST00000535508.2:c.*1988C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008838
  ensembl transcript: ENST00000492176
  gene symbol: MED24
  hgvsc: ENST00000492176.2:n.636C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000443344
  ensembl transcript: ENST00000535071
  gene symbol: MED24
  hgvsc: ENST00000535071.2:c.2215C>T
  hgvsp: ENSP00000443344.2:p.Pro739Ser
  variant of: http://identifiers.org/hgnc/22963
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28477
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1506
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5354
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22304
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 520
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 242
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Pro789Ser
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: DP

17-38178972-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38178972
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38178972
    reference: chr 17
allele count: 3
allele frequency: 2.497502497502498e-5
allele num: 120120
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000440100
  ensembl transcript: ENST00000501516
  gene symbol: MED24
  hgvsc: ENST00000501516.3:c.2415C>T
  hgvsp: ENST00000501516.3:c.2415C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377685
  ensembl transcript: ENST00000394127
  gene symbol: MED24
  hgvsc: ENST00000394127.2:c.2319C>T
  hgvsp: ENST00000394127.2:c.2319C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000348610
  ensembl transcript: ENST00000356271
  gene symbol: MED24
  hgvsc: ENST00000356271.3:c.2319C>T
  hgvsp: ENST00000356271.3:c.2319C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000443344
  ensembl transcript: ENST00000535071
  gene symbol: MED24
  hgvsc: ENST00000535071.2:c.2208C>T
  hgvsp: ENST00000535071.2:c.2208C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000393464
  ensembl transcript: ENST00000422942
  gene symbol: MED24
  hgvsc: ENST00000422942.2:c.138C>T
  hgvsp: ENST00000422942.2:c.138C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008838
  ensembl transcript: ENST00000492176
  gene symbol: MED24
  hgvsc: ENST00000492176.2:n.629C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377686
  ensembl transcript: ENST00000394128
  gene symbol: MED24
  hgvsc: ENST00000394128.2:c.2358C>T
  hgvsp: ENST00000394128.2:c.2358C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000439148
  ensembl transcript: ENST00000535508
  gene symbol: MED24
  hgvsc: ENST00000535508.2:c.*1981C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377684
  ensembl transcript: ENST00000394126
  gene symbol: MED24
  hgvsc: ENST00000394126.1:c.2433C>T
  hgvsp: ENST00000394126.1:c.2433C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22963
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 869
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22404
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28453
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1455
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5376
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 320
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 235
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 240
  bin: 8.75e1
  variant carriers: 0
hgvs: p.His786His
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum

17-38178981-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38178981
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38178981
    reference: chr 17
allele count: 4
allele frequency: 3.330114222917846e-5
allele num: 120116
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377684
  ensembl transcript: ENST00000394126
  gene symbol: MED24
  hgvsc: ENST00000394126.1:c.2424G>A
  hgvsp: ENST00000394126.1:c.2424G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000348610
  ensembl transcript: ENST00000356271
  gene symbol: MED24
  hgvsc: ENST00000356271.3:c.2310G>A
  hgvsp: ENST00000356271.3:c.2310G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008838
  ensembl transcript: ENST00000492176
  gene symbol: MED24
  hgvsc: ENST00000492176.2:n.620G>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377686
  ensembl transcript: ENST00000394128
  gene symbol: MED24
  hgvsc: ENST00000394128.2:c.2349G>A
  hgvsp: ENST00000394128.2:c.2349G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000440100
  ensembl transcript: ENST00000501516
  gene symbol: MED24
  hgvsc: ENST00000501516.3:c.2406G>A
  hgvsp: ENST00000501516.3:c.2406G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377685
  ensembl transcript: ENST00000394127
  gene symbol: MED24
  hgvsc: ENST00000394127.2:c.2310G>A
  hgvsp: ENST00000394127.2:c.2310G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000393464
  ensembl transcript: ENST00000422942
  gene symbol: MED24
  hgvsc: ENST00000422942.2:c.129G>A
  hgvsp: ENST00000422942.2:c.129G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000439148
  ensembl transcript: ENST00000535508
  gene symbol: MED24
  hgvsc: ENST00000535508.2:c.*1972G>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000443344
  ensembl transcript: ENST00000535071
  gene symbol: MED24
  hgvsc: ENST00000535071.2:c.2199G>A
  hgvsp: ENST00000535071.2:c.2199G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22963
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22812
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1406
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5445
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28063
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 432
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 351
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 284
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Leu783Leu
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

17-38178983-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38178983
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38178983
    reference: chr 17
allele count: 6
allele frequency: 4.99325910021471e-5
allele num: 120162
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377684
  ensembl transcript: ENST00000394126
  gene symbol: MED24
  hgvsc: ENST00000394126.1:c.2422C>T
  hgvsp: ENST00000394126.1:c.2422C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377685
  ensembl transcript: ENST00000394127
  gene symbol: MED24
  hgvsc: ENST00000394127.2:c.2308C>T
  hgvsp: ENST00000394127.2:c.2308C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377686
  ensembl transcript: ENST00000394128
  gene symbol: MED24
  hgvsc: ENST00000394128.2:c.2347C>T
  hgvsp: ENST00000394128.2:c.2347C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000439148
  ensembl transcript: ENST00000535508
  gene symbol: MED24
  hgvsc: ENST00000535508.2:c.*1970C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000393464
  ensembl transcript: ENST00000422942
  gene symbol: MED24
  hgvsc: ENST00000422942.2:c.127C>T
  hgvsp: ENST00000422942.2:c.127C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000440100
  ensembl transcript: ENST00000501516
  gene symbol: MED24
  hgvsc: ENST00000501516.3:c.2404C>T
  hgvsp: ENST00000501516.3:c.2404C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000443344
  ensembl transcript: ENST00000535071
  gene symbol: MED24
  hgvsc: ENST00000535071.2:c.2197C>T
  hgvsp: ENST00000535071.2:c.2197C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008838
  ensembl transcript: ENST00000492176
  gene symbol: MED24
  hgvsc: ENST00000492176.2:n.618C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000348610
  ensembl transcript: ENST00000356271
  gene symbol: MED24
  hgvsc: ENST00000356271.3:c.2308C>T
  hgvsp: ENST00000356271.3:c.2308C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22963
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1361
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28075
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5408
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22916
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1486
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 258
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Leu783Leu
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum

17-38179021-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38179021
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38179021
    reference: chr 17
allele count: 1
allele frequency: 8.318083513558476e-6
allele num: 120220
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377684
  ensembl transcript: ENST00000394126
  gene symbol: MED24
  hgvsc: ENST00000394126.1:c.2384C>G
  hgvsp: ENSP00000377684.1:p.Ser795Cys
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008838
  ensembl transcript: ENST00000492176
  gene symbol: MED24
  hgvsc: ENST00000492176.2:n.580C>G
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000348610
  ensembl transcript: ENST00000356271
  gene symbol: MED24
  hgvsc: ENST00000356271.3:c.2270C>G
  hgvsp: ENSP00000348610.3:p.Ser757Cys
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000393464
  ensembl transcript: ENST00000422942
  gene symbol: MED24
  hgvsc: ENST00000422942.2:c.89C>G
  hgvsp: ENSP00000393464.2:p.Ser30Cys
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000439148
  ensembl transcript: ENST00000535508
  gene symbol: MED24
  hgvsc: ENST00000535508.2:c.*1932C>G
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000443344
  ensembl transcript: ENST00000535071
  gene symbol: MED24
  hgvsc: ENST00000535071.2:c.2159C>G
  hgvsp: ENSP00000443344.2:p.Ser720Cys
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377686
  ensembl transcript: ENST00000394128
  gene symbol: MED24
  hgvsc: ENST00000394128.2:c.2309C>G
  hgvsp: ENSP00000377686.2:p.Ser770Cys
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377685
  ensembl transcript: ENST00000394127
  gene symbol: MED24
  hgvsc: ENST00000394127.2:c.2270C>G
  hgvsp: ENSP00000377685.2:p.Ser757Cys
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000440100
  ensembl transcript: ENST00000501516
  gene symbol: MED24
  hgvsc: ENST00000501516.3:c.2366C>G
  hgvsp: ENSP00000440100.2:p.Ser789Cys
  variant of: http://identifiers.org/hgnc/22963
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23714
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5484
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28406
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ser770Cys
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum

17-38179023-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38179023
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38179023
    reference: chr 17
allele count: 21
allele frequency: 1.746884722245329e-4
allele num: 120214
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008838
  ensembl transcript: ENST00000492176
  gene symbol: MED24
  hgvsc: ENST00000492176.2:n.578C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000348610
  ensembl transcript: ENST00000356271
  gene symbol: MED24
  hgvsc: ENST00000356271.3:c.2268C>T
  hgvsp: ENST00000356271.3:c.2268C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377685
  ensembl transcript: ENST00000394127
  gene symbol: MED24
  hgvsc: ENST00000394127.2:c.2268C>T
  hgvsp: ENST00000394127.2:c.2268C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000439148
  ensembl transcript: ENST00000535508
  gene symbol: MED24
  hgvsc: ENST00000535508.2:c.*1930C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377684
  ensembl transcript: ENST00000394126
  gene symbol: MED24
  hgvsc: ENST00000394126.1:c.2382C>T
  hgvsp: ENST00000394126.1:c.2382C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377686
  ensembl transcript: ENST00000394128
  gene symbol: MED24
  hgvsc: ENST00000394128.2:c.2307C>T
  hgvsp: ENST00000394128.2:c.2307C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000443344
  ensembl transcript: ENST00000535071
  gene symbol: MED24
  hgvsc: ENST00000535071.2:c.2157C>T
  hgvsp: ENST00000535071.2:c.2157C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000440100
  ensembl transcript: ENST00000501516
  gene symbol: MED24
  hgvsc: ENST00000501516.3:c.2364C>T
  hgvsp: ENST00000501516.3:c.2364C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000393464
  ensembl transcript: ENST00000422942
  gene symbol: MED24
  hgvsc: ENST00000422942.2:c.87C>T
  hgvsp: ENST00000422942.2:c.87C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22963
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23726
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28420
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5480
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 716
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 620
  bin: 9.75e1
  variant carriers: 21
genotype quality: GenotypeQuality
  all individuals: 251
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 210
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Tyr769Tyr
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum

17-38179038-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38179038
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38179038
    reference: chr 17
allele count: 2
allele frequency: 1.665806000233213e-5
allele num: 120062
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000348610
  ensembl transcript: ENST00000356271
  gene symbol: MED24
  hgvsc: ENST00000356271.3:c.2253A>G
  hgvsp: ENST00000356271.3:c.2253A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377684
  ensembl transcript: ENST00000394126
  gene symbol: MED24
  hgvsc: ENST00000394126.1:c.2367A>G
  hgvsp: ENST00000394126.1:c.2367A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000393464
  ensembl transcript: ENST00000422942
  gene symbol: MED24
  hgvsc: ENST00000422942.2:c.72A>G
  hgvsp: ENST00000422942.2:c.72A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000440100
  ensembl transcript: ENST00000501516
  gene symbol: MED24
  hgvsc: ENST00000501516.3:c.2349A>G
  hgvsp: ENST00000501516.3:c.2349A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377685
  ensembl transcript: ENST00000394127
  gene symbol: MED24
  hgvsc: ENST00000394127.2:c.2253A>G
  hgvsp: ENST00000394127.2:c.2253A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000443344
  ensembl transcript: ENST00000535071
  gene symbol: MED24
  hgvsc: ENST00000535071.2:c.2142A>G
  hgvsp: ENST00000535071.2:c.2142A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000439148
  ensembl transcript: ENST00000535508
  gene symbol: MED24
  hgvsc: ENST00000535508.2:c.*1915A>G
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377686
  ensembl transcript: ENST00000394128
  gene symbol: MED24
  hgvsc: ENST00000394128.2:c.2292A>G
  hgvsp: ENST00000394128.2:c.2292A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008838
  ensembl transcript: ENST00000492176
  gene symbol: MED24
  hgvsc: ENST00000492176.2:n.563A>G
  variant of: http://identifiers.org/hgnc/22963
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23877
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28256
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5456
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 952
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ala764Ala
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

17-38179042-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38179042
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38179042
    reference: chr 17
allele count: 3
allele frequency: 2.500583469476211e-5
allele num: 119972
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008838
  ensembl transcript: ENST00000492176
  gene symbol: MED24
  hgvsc: ENST00000492176.2:n.559G>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377686
  ensembl transcript: ENST00000394128
  gene symbol: MED24
  hgvsc: ENST00000394128.2:c.2288G>A
  hgvsp: ENSP00000377686.2:p.Arg763Gln
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000440100
  ensembl transcript: ENST00000501516
  gene symbol: MED24
  hgvsc: ENST00000501516.3:c.2345G>A
  hgvsp: ENSP00000440100.2:p.Arg782Gln
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000393464
  ensembl transcript: ENST00000422942
  gene symbol: MED24
  hgvsc: ENST00000422942.2:c.68G>A
  hgvsp: ENSP00000393464.2:p.Arg23Gln
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000443344
  ensembl transcript: ENST00000535071
  gene symbol: MED24
  hgvsc: ENST00000535071.2:c.2138G>A
  hgvsp: ENSP00000443344.2:p.Arg713Gln
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000348610
  ensembl transcript: ENST00000356271
  gene symbol: MED24
  hgvsc: ENST00000356271.3:c.2249G>A
  hgvsp: ENSP00000348610.3:p.Arg750Gln
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377684
  ensembl transcript: ENST00000394126
  gene symbol: MED24
  hgvsc: ENST00000394126.1:c.2363G>A
  hgvsp: ENSP00000377684.1:p.Arg788Gln
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377685
  ensembl transcript: ENST00000394127
  gene symbol: MED24
  hgvsc: ENST00000394127.2:c.2249G>A
  hgvsp: ENSP00000377685.2:p.Arg750Gln
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000439148
  ensembl transcript: ENST00000535508
  gene symbol: MED24
  hgvsc: ENST00000535508.2:c.*1911G>A
  variant of: http://identifiers.org/hgnc/22963
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5489
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 893
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23876
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28172
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1359
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Arg763Gln
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff

17-38179043-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38179043
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38179043
    reference: chr 17
allele count: 25
allele frequency: 2.084167000133387e-4
allele num: 119952
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377686
  ensembl transcript: ENST00000394128
  gene symbol: MED24
  hgvsc: ENST00000394128.2:c.2287C>T
  hgvsp: ENSP00000377686.2:p.Arg763Trp
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377684
  ensembl transcript: ENST00000394126
  gene symbol: MED24
  hgvsc: ENST00000394126.1:c.2362C>T
  hgvsp: ENSP00000377684.1:p.Arg788Trp
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000443344
  ensembl transcript: ENST00000535071
  gene symbol: MED24
  hgvsc: ENST00000535071.2:c.2137C>T
  hgvsp: ENSP00000443344.2:p.Arg713Trp
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000440100
  ensembl transcript: ENST00000501516
  gene symbol: MED24
  hgvsc: ENST00000501516.3:c.2344C>T
  hgvsp: ENSP00000440100.2:p.Arg782Trp
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000439148
  ensembl transcript: ENST00000535508
  gene symbol: MED24
  hgvsc: ENST00000535508.2:c.*1910C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000348610
  ensembl transcript: ENST00000356271
  gene symbol: MED24
  hgvsc: ENST00000356271.3:c.2248C>T
  hgvsp: ENSP00000348610.3:p.Arg750Trp
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377685
  ensembl transcript: ENST00000394127
  gene symbol: MED24
  hgvsc: ENST00000394127.2:c.2248C>T
  hgvsp: ENSP00000377685.2:p.Arg750Trp
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008838
  ensembl transcript: ENST00000492176
  gene symbol: MED24
  hgvsc: ENST00000492176.2:n.558C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000393464
  ensembl transcript: ENST00000422942
  gene symbol: MED24
  hgvsc: ENST00000422942.2:c.67C>T
  hgvsp: ENSP00000393464.2:p.Arg23Trp
  variant of: http://identifiers.org/hgnc/22963
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23895
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5491
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 28130
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48069
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1000
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg763Trp
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: DP

http://identifiers.org/exac.variant/17-38179047-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38179047
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38179047
    reference: chr 17
allele count: 1
allele frequency: 8.340005337603416e-6
allele num: 119904
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000443344
  ensembl transcript: ENST00000535071
  gene symbol: MED24
  hgvsc: ENST00000535071.2:c.2133G>T
  hgvsp: ENST00000535071.2:c.2133G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000393464
  ensembl transcript: ENST00000422942
  gene symbol: MED24
  hgvsc: ENST00000422942.2:c.63G>T
  hgvsp: ENST00000422942.2:c.63G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008838
  ensembl transcript: ENST00000492176
  gene symbol: MED24
  hgvsc: ENST00000492176.2:n.554G>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000439148
  ensembl transcript: ENST00000535508
  gene symbol: MED24
  hgvsc: ENST00000535508.2:c.*1906G>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377684
  ensembl transcript: ENST00000394126
  gene symbol: MED24
  hgvsc: ENST00000394126.1:c.2358G>T
  hgvsp: ENST00000394126.1:c.2358G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377685
  ensembl transcript: ENST00000394127
  gene symbol: MED24
  hgvsc: ENST00000394127.2:c.2244G>T
  hgvsp: ENST00000394127.2:c.2244G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000348610
  ensembl transcript: ENST00000356271
  gene symbol: MED24
  hgvsc: ENST00000356271.3:c.2244G>T
  hgvsp: ENST00000356271.3:c.2244G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000440100
  ensembl transcript: ENST00000501516
  gene symbol: MED24
  hgvsc: ENST00000501516.3:c.2340G>T
  hgvsp: ENST00000501516.3:c.2340G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377686
  ensembl transcript: ENST00000394128
  gene symbol: MED24
  hgvsc: ENST00000394128.2:c.2283G>T
  hgvsp: ENST00000394128.2:c.2283G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22963
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5449
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28018
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 869
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23856
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 240
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 683
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Thr761Thr
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum

17-38179047-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38179047
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38179047
    reference: chr 17
allele count: 336
allele frequency: 2.802241793434748e-3
allele num: 119904
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000443344
  ensembl transcript: ENST00000535071
  gene symbol: MED24
  hgvsc: ENST00000535071.2:c.2133G>A
  hgvsp: ENST00000535071.2:c.2133G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000348610
  ensembl transcript: ENST00000356271
  gene symbol: MED24
  hgvsc: ENST00000356271.3:c.2244G>A
  hgvsp: ENST00000356271.3:c.2244G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000440100
  ensembl transcript: ENST00000501516
  gene symbol: MED24
  hgvsc: ENST00000501516.3:c.2340G>A
  hgvsp: ENST00000501516.3:c.2340G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377684
  ensembl transcript: ENST00000394126
  gene symbol: MED24
  hgvsc: ENST00000394126.1:c.2358G>A
  hgvsp: ENST00000394126.1:c.2358G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377686
  ensembl transcript: ENST00000394128
  gene symbol: MED24
  hgvsc: ENST00000394128.2:c.2283G>A
  hgvsp: ENST00000394128.2:c.2283G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008838
  ensembl transcript: ENST00000492176
  gene symbol: MED24
  hgvsc: ENST00000492176.2:n.554G>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377685
  ensembl transcript: ENST00000394127
  gene symbol: MED24
  hgvsc: ENST00000394127.2:c.2244G>A
  hgvsp: ENST00000394127.2:c.2244G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000393464
  ensembl transcript: ENST00000422942
  gene symbol: MED24
  hgvsc: ENST00000422942.2:c.63G>A
  hgvsp: ENST00000422942.2:c.63G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000439148
  ensembl transcript: ENST00000535508
  gene symbol: MED24
  hgvsc: ENST00000535508.2:c.*1906G>A
  variant of: http://identifiers.org/hgnc/22963
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 5449
  bin: 3.25e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 869
  bin: 3.75e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 4.75e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 1.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 6.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 7.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 23856
  bin: 2.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 28018
  bin: 2.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 5.25e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.75e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 4.25e1
  variant carriers: 38
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48141
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Thr761Thr
num of homozygotes: 2
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD

17-38179048-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38179048
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38179048
    reference: chr 17
allele count: 8
allele frequency: 6.673896721448236e-5
allele num: 119870
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000439148
  ensembl transcript: ENST00000535508
  gene symbol: MED24
  hgvsc: ENST00000535508.2:c.*1905C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008838
  ensembl transcript: ENST00000492176
  gene symbol: MED24
  hgvsc: ENST00000492176.2:n.553C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377686
  ensembl transcript: ENST00000394128
  gene symbol: MED24
  hgvsc: ENST00000394128.2:c.2282C>T
  hgvsp: ENSP00000377686.2:p.Thr761Met
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377684
  ensembl transcript: ENST00000394126
  gene symbol: MED24
  hgvsc: ENST00000394126.1:c.2357C>T
  hgvsp: ENSP00000377684.1:p.Thr786Met
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000440100
  ensembl transcript: ENST00000501516
  gene symbol: MED24
  hgvsc: ENST00000501516.3:c.2339C>T
  hgvsp: ENSP00000440100.2:p.Thr780Met
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000348610
  ensembl transcript: ENST00000356271
  gene symbol: MED24
  hgvsc: ENST00000356271.3:c.2243C>T
  hgvsp: ENSP00000348610.3:p.Thr748Met
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000443344
  ensembl transcript: ENST00000535071
  gene symbol: MED24
  hgvsc: ENST00000535071.2:c.2132C>T
  hgvsp: ENSP00000443344.2:p.Thr711Met
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377685
  ensembl transcript: ENST00000394127
  gene symbol: MED24
  hgvsc: ENST00000394127.2:c.2243C>T
  hgvsp: ENSP00000377685.2:p.Thr748Met
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000393464
  ensembl transcript: ENST00000422942
  gene symbol: MED24
  hgvsc: ENST00000422942.2:c.62C>T
  hgvsp: ENSP00000393464.2:p.Thr21Met
  variant of: http://identifiers.org/hgnc/22963
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28002
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5504
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24004
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 581
  bin: 9.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 1450
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Thr761Met
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: Other
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD

17-38179049-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38179049
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38179049
    reference: chr 17
allele count: 1
allele frequency: 8.343345347750633e-6
allele num: 119856
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000348610
  ensembl transcript: ENST00000356271
  gene symbol: MED24
  hgvsc: ENST00000356271.3:c.2242A>G
  hgvsp: ENSP00000348610.3:p.Thr748Ala
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377684
  ensembl transcript: ENST00000394126
  gene symbol: MED24
  hgvsc: ENST00000394126.1:c.2356A>G
  hgvsp: ENSP00000377684.1:p.Thr786Ala
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377685
  ensembl transcript: ENST00000394127
  gene symbol: MED24
  hgvsc: ENST00000394127.2:c.2242A>G
  hgvsp: ENSP00000377685.2:p.Thr748Ala
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000439148
  ensembl transcript: ENST00000535508
  gene symbol: MED24
  hgvsc: ENST00000535508.2:c.*1904A>G
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000393464
  ensembl transcript: ENST00000422942
  gene symbol: MED24
  hgvsc: ENST00000422942.2:c.61A>G
  hgvsp: ENSP00000393464.2:p.Thr21Ala
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000443344
  ensembl transcript: ENST00000535071
  gene symbol: MED24
  hgvsc: ENST00000535071.2:c.2131A>G
  hgvsp: ENSP00000443344.2:p.Thr711Ala
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008838
  ensembl transcript: ENST00000492176
  gene symbol: MED24
  hgvsc: ENST00000492176.2:n.552A>G
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377686
  ensembl transcript: ENST00000394128
  gene symbol: MED24
  hgvsc: ENST00000394128.2:c.2281A>G
  hgvsp: ENSP00000377686.2:p.Thr761Ala
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000440100
  ensembl transcript: ENST00000501516
  gene symbol: MED24
  hgvsc: ENST00000501516.3:c.2338A>G
  hgvsp: ENSP00000440100.2:p.Thr780Ala
  variant of: http://identifiers.org/hgnc/22963
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24019
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27973
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5492
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Thr761Ala
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: DP

17-38179051-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38179051
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38179051
    reference: chr 17
allele count: 1
allele frequency: 8.347384764353328e-6
allele num: 119798
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377684
  ensembl transcript: ENST00000394126
  gene symbol: MED24
  hgvsc: ENST00000394126.1:c.2354A>G
  hgvsp: ENSP00000377684.1:p.His785Arg
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000348610
  ensembl transcript: ENST00000356271
  gene symbol: MED24
  hgvsc: ENST00000356271.3:c.2240A>G
  hgvsp: ENSP00000348610.3:p.His747Arg
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377686
  ensembl transcript: ENST00000394128
  gene symbol: MED24
  hgvsc: ENST00000394128.2:c.2279A>G
  hgvsp: ENSP00000377686.2:p.His760Arg
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000440100
  ensembl transcript: ENST00000501516
  gene symbol: MED24
  hgvsc: ENST00000501516.3:c.2336A>G
  hgvsp: ENSP00000440100.2:p.His779Arg
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008838
  ensembl transcript: ENST00000492176
  gene symbol: MED24
  hgvsc: ENST00000492176.2:n.550A>G
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000443344
  ensembl transcript: ENST00000535071
  gene symbol: MED24
  hgvsc: ENST00000535071.2:c.2129A>G
  hgvsp: ENSP00000443344.2:p.His710Arg
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000393464
  ensembl transcript: ENST00000422942
  gene symbol: MED24
  hgvsc: ENST00000422942.2:c.59A>G
  hgvsp: ENSP00000393464.2:p.His20Arg
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377685
  ensembl transcript: ENST00000394127
  gene symbol: MED24
  hgvsc: ENST00000394127.2:c.2240A>G
  hgvsp: ENSP00000377685.2:p.His747Arg
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000439148
  ensembl transcript: ENST00000535508
  gene symbol: MED24
  hgvsc: ENST00000535508.2:c.*1902A>G
  variant of: http://identifiers.org/hgnc/22963
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 854
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27910
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5485
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24002
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5751
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
hgvs: p.His760Arg
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

17-38179060-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38179060
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38179060
    reference: chr 17
allele count: 2
allele frequency: 1.673416111650323e-5
allele num: 119516
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377684
  ensembl transcript: ENST00000394126
  gene symbol: MED24
  hgvsc: ENST00000394126.1:c.2345G>A
  hgvsp: ENSP00000377684.1:p.Arg782Gln
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377686
  ensembl transcript: ENST00000394128
  gene symbol: MED24
  hgvsc: ENST00000394128.2:c.2270G>A
  hgvsp: ENSP00000377686.2:p.Arg757Gln
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000348610
  ensembl transcript: ENST00000356271
  gene symbol: MED24
  hgvsc: ENST00000356271.3:c.2231G>A
  hgvsp: ENSP00000348610.3:p.Arg744Gln
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377685
  ensembl transcript: ENST00000394127
  gene symbol: MED24
  hgvsc: ENST00000394127.2:c.2231G>A
  hgvsp: ENSP00000377685.2:p.Arg744Gln
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000440100
  ensembl transcript: ENST00000501516
  gene symbol: MED24
  hgvsc: ENST00000501516.3:c.2327G>A
  hgvsp: ENSP00000440100.2:p.Arg776Gln
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000439148
  ensembl transcript: ENST00000535508
  gene symbol: MED24
  hgvsc: ENST00000535508.2:c.*1893G>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008838
  ensembl transcript: ENST00000492176
  gene symbol: MED24
  hgvsc: ENST00000492176.2:n.541G>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000443344
  ensembl transcript: ENST00000535071
  gene symbol: MED24
  hgvsc: ENST00000535071.2:c.2120G>A
  hgvsp: ENSP00000443344.2:p.Arg707Gln
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000393464
  ensembl transcript: ENST00000422942
  gene symbol: MED24
  hgvsc: ENST00000422942.2:c.50G>A
  hgvsp: ENSP00000393464.2:p.Arg17Gln
  variant of: http://identifiers.org/hgnc/22963
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5504
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23930
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27604
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 858
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 676
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1435
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 236
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Arg757Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

17-38179061-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38179061
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38179061
    reference: chr 17
allele count: 2
allele frequency: 1.673836265336525e-5
allele num: 119486
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000348610
  ensembl transcript: ENST00000356271
  gene symbol: MED24
  hgvsc: ENST00000356271.3:c.2230C>T
  hgvsp: ENSP00000348610.3:p.Arg744Trp
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377686
  ensembl transcript: ENST00000394128
  gene symbol: MED24
  hgvsc: ENST00000394128.2:c.2269C>T
  hgvsp: ENSP00000377686.2:p.Arg757Trp
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008838
  ensembl transcript: ENST00000492176
  gene symbol: MED24
  hgvsc: ENST00000492176.2:n.540C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000439148
  ensembl transcript: ENST00000535508
  gene symbol: MED24
  hgvsc: ENST00000535508.2:c.*1892C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000393464
  ensembl transcript: ENST00000422942
  gene symbol: MED24
  hgvsc: ENST00000422942.2:c.49C>T
  hgvsp: ENSP00000393464.2:p.Arg17Trp
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377685
  ensembl transcript: ENST00000394127
  gene symbol: MED24
  hgvsc: ENST00000394127.2:c.2230C>T
  hgvsp: ENSP00000377685.2:p.Arg744Trp
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377684
  ensembl transcript: ENST00000394126
  gene symbol: MED24
  hgvsc: ENST00000394126.1:c.2344C>T
  hgvsp: ENSP00000377684.1:p.Arg782Trp
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000440100
  ensembl transcript: ENST00000501516
  gene symbol: MED24
  hgvsc: ENST00000501516.3:c.2326C>T
  hgvsp: ENSP00000440100.2:p.Arg776Trp
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000443344
  ensembl transcript: ENST00000535071
  gene symbol: MED24
  hgvsc: ENST00000535071.2:c.2119C>T
  hgvsp: ENSP00000443344.2:p.Arg707Trp
  variant of: http://identifiers.org/hgnc/22963
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23927
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27592
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5479
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 168
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 271
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Arg757Trp
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum

17-38179061-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38179061
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38179061
    reference: chr 17
allele count: 3
allele frequency: 2.510754398004787e-5
allele num: 119486
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000443344
  ensembl transcript: ENST00000535071
  gene symbol: MED24
  hgvsc: ENST00000535071.2:c.2119C>G
  hgvsp: ENSP00000443344.2:p.Arg707Gly
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000348610
  ensembl transcript: ENST00000356271
  gene symbol: MED24
  hgvsc: ENST00000356271.3:c.2230C>G
  hgvsp: ENSP00000348610.3:p.Arg744Gly
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000439148
  ensembl transcript: ENST00000535508
  gene symbol: MED24
  hgvsc: ENST00000535508.2:c.*1892C>G
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008838
  ensembl transcript: ENST00000492176
  gene symbol: MED24
  hgvsc: ENST00000492176.2:n.540C>G
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377684
  ensembl transcript: ENST00000394126
  gene symbol: MED24
  hgvsc: ENST00000394126.1:c.2344C>G
  hgvsp: ENSP00000377684.1:p.Arg782Gly
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377685
  ensembl transcript: ENST00000394127
  gene symbol: MED24
  hgvsc: ENST00000394127.2:c.2230C>G
  hgvsp: ENSP00000377685.2:p.Arg744Gly
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000393464
  ensembl transcript: ENST00000422942
  gene symbol: MED24
  hgvsc: ENST00000422942.2:c.49C>G
  hgvsp: ENSP00000393464.2:p.Arg17Gly
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000440100
  ensembl transcript: ENST00000501516
  gene symbol: MED24
  hgvsc: ENST00000501516.3:c.2326C>G
  hgvsp: ENSP00000440100.2:p.Arg776Gly
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377686
  ensembl transcript: ENST00000394128
  gene symbol: MED24
  hgvsc: ENST00000394128.2:c.2269C>G
  hgvsp: ENSP00000377686.2:p.Arg757Gly
  variant of: http://identifiers.org/hgnc/22963
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23927
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5479
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27592
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 168
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1307
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Arg757Gly
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD

17-38179061-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38179061
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38179061
    reference: chr 17
allele count: 1
allele frequency: 8.369181326682624e-6
allele num: 119486
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377686
  ensembl transcript: ENST00000394128
  gene symbol: MED24
  hgvsc: ENST00000394128.2:c.2269C>A
  hgvsp: ENST00000394128.2:c.2269C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008838
  ensembl transcript: ENST00000492176
  gene symbol: MED24
  hgvsc: ENST00000492176.2:n.540C>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000393464
  ensembl transcript: ENST00000422942
  gene symbol: MED24
  hgvsc: ENST00000422942.2:c.49C>A
  hgvsp: ENST00000422942.2:c.49C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377684
  ensembl transcript: ENST00000394126
  gene symbol: MED24
  hgvsc: ENST00000394126.1:c.2344C>A
  hgvsp: ENST00000394126.1:c.2344C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000439148
  ensembl transcript: ENST00000535508
  gene symbol: MED24
  hgvsc: ENST00000535508.2:c.*1892C>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377685
  ensembl transcript: ENST00000394127
  gene symbol: MED24
  hgvsc: ENST00000394127.2:c.2230C>A
  hgvsp: ENST00000394127.2:c.2230C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000440100
  ensembl transcript: ENST00000501516
  gene symbol: MED24
  hgvsc: ENST00000501516.3:c.2326C>A
  hgvsp: ENST00000501516.3:c.2326C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000443344
  ensembl transcript: ENST00000535071
  gene symbol: MED24
  hgvsc: ENST00000535071.2:c.2119C>A
  hgvsp: ENST00000535071.2:c.2119C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000348610
  ensembl transcript: ENST00000356271
  gene symbol: MED24
  hgvsc: ENST00000356271.3:c.2230C>A
  hgvsp: ENST00000356271.3:c.2230C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22963
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5479
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23927
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27592
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1307
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg757Arg
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: DP
site quality: ClippingRankSum

17-38179062-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38179062
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38179062
    reference: chr 17
allele count: 766
allele frequency: 6.412510254993554e-3
allele num: 119454
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377684
  ensembl transcript: ENST00000394126
  gene symbol: MED24
  hgvsc: ENST00000394126.1:c.2343G>A
  hgvsp: ENST00000394126.1:c.2343G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377685
  ensembl transcript: ENST00000394127
  gene symbol: MED24
  hgvsc: ENST00000394127.2:c.2229G>A
  hgvsp: ENST00000394127.2:c.2229G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377686
  ensembl transcript: ENST00000394128
  gene symbol: MED24
  hgvsc: ENST00000394128.2:c.2268G>A
  hgvsp: ENST00000394128.2:c.2268G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000439148
  ensembl transcript: ENST00000535508
  gene symbol: MED24
  hgvsc: ENST00000535508.2:c.*1891G>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000440100
  ensembl transcript: ENST00000501516
  gene symbol: MED24
  hgvsc: ENST00000501516.3:c.2325G>A
  hgvsp: ENST00000501516.3:c.2325G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000393464
  ensembl transcript: ENST00000422942
  gene symbol: MED24
  hgvsc: ENST00000422942.2:c.48G>A
  hgvsp: ENST00000422942.2:c.48G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008838
  ensembl transcript: ENST00000492176
  gene symbol: MED24
  hgvsc: ENST00000492176.2:n.539G>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000348610
  ensembl transcript: ENST00000356271
  gene symbol: MED24
  hgvsc: ENST00000356271.3:c.2229G>A
  hgvsp: ENST00000356271.3:c.2229G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000443344
  ensembl transcript: ENST00000535071
  gene symbol: MED24
  hgvsc: ENST00000535071.2:c.2118G>A
  hgvsp: ENST00000535071.2:c.2118G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22963
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 1.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 5419
  bin: 3.25e1
  variant carriers: 82
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 3.75e1
  variant carriers: 97
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 4.25e1
  variant carriers: 102
genotype depth: GenotypeDepth
  all individuals: 23774
  bin: 2.75e1
  variant carriers: 75
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 4.75e1
  variant carriers: 77
genotype depth: GenotypeDepth
  all individuals: 1032
  bin: 1.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 27379
  bin: 2.25e1
  variant carriers: 46
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 5.75e1
  variant carriers: 48
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.25e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 5.25e1
  variant carriers: 58
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1371
  bin: 7.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5559
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Thr756Thr
num of homozygotes: 30
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum

17-38179063-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38179063
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38179063
    reference: chr 17
allele count: 13
allele frequency: 1.089470684858034e-4
allele num: 119324
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000348610
  ensembl transcript: ENST00000356271
  gene symbol: MED24
  hgvsc: ENST00000356271.3:c.2228C>T
  hgvsp: ENSP00000348610.3:p.Thr743Met
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377686
  ensembl transcript: ENST00000394128
  gene symbol: MED24
  hgvsc: ENST00000394128.2:c.2267C>T
  hgvsp: ENSP00000377686.2:p.Thr756Met
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000440100
  ensembl transcript: ENST00000501516
  gene symbol: MED24
  hgvsc: ENST00000501516.3:c.2324C>T
  hgvsp: ENSP00000440100.2:p.Thr775Met
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000443344
  ensembl transcript: ENST00000535071
  gene symbol: MED24
  hgvsc: ENST00000535071.2:c.2117C>T
  hgvsp: ENSP00000443344.2:p.Thr706Met
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000439148
  ensembl transcript: ENST00000535508
  gene symbol: MED24
  hgvsc: ENST00000535508.2:c.*1890C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377685
  ensembl transcript: ENST00000394127
  gene symbol: MED24
  hgvsc: ENST00000394127.2:c.2228C>T
  hgvsp: ENSP00000377685.2:p.Thr743Met
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377684
  ensembl transcript: ENST00000394126
  gene symbol: MED24
  hgvsc: ENST00000394126.1:c.2342C>T
  hgvsp: ENSP00000377684.1:p.Thr781Met
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000393464
  ensembl transcript: ENST00000422942
  gene symbol: MED24
  hgvsc: ENST00000422942.2:c.47C>T
  hgvsp: ENSP00000393464.2:p.Thr16Met
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008838
  ensembl transcript: ENST00000492176
  gene symbol: MED24
  hgvsc: ENST00000492176.2:n.538C>T
  variant of: http://identifiers.org/hgnc/22963
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 24032
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27371
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1133
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5448
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 47890
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 301
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Thr756Met
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: European (Finnish)
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum

17-38179067-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38179067
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38179067
    reference: chr 17
allele count: 1
allele frequency: 8.395036854211791e-6
allele num: 119118
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000393464
  ensembl transcript: ENST00000422942
  gene symbol: MED24
  hgvsc: ENST00000422942.2:c.43G>A
  hgvsp: ENSP00000393464.2:p.Glu15Lys
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000439148
  ensembl transcript: ENST00000535508
  gene symbol: MED24
  hgvsc: ENST00000535508.2:c.*1886G>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377684
  ensembl transcript: ENST00000394126
  gene symbol: MED24
  hgvsc: ENST00000394126.1:c.2338G>A
  hgvsp: ENSP00000377684.1:p.Glu780Lys
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000443344
  ensembl transcript: ENST00000535071
  gene symbol: MED24
  hgvsc: ENST00000535071.2:c.2113G>A
  hgvsp: ENSP00000443344.2:p.Glu705Lys
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008838
  ensembl transcript: ENST00000492176
  gene symbol: MED24
  hgvsc: ENST00000492176.2:n.534G>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377685
  ensembl transcript: ENST00000394127
  gene symbol: MED24
  hgvsc: ENST00000394127.2:c.2224G>A
  hgvsp: ENSP00000377685.2:p.Glu742Lys
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000348610
  ensembl transcript: ENST00000356271
  gene symbol: MED24
  hgvsc: ENST00000356271.3:c.2224G>A
  hgvsp: ENSP00000348610.3:p.Glu742Lys
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377686
  ensembl transcript: ENST00000394128
  gene symbol: MED24
  hgvsc: ENST00000394128.2:c.2263G>A
  hgvsp: ENSP00000377686.2:p.Glu755Lys
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000440100
  ensembl transcript: ENST00000501516
  gene symbol: MED24
  hgvsc: ENST00000501516.3:c.2320G>A
  hgvsp: ENSP00000440100.2:p.Glu774Lys
  variant of: http://identifiers.org/hgnc/22963
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5415
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1372
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23992
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27080
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 196
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1371
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 615
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Glu755Lys
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: DP

17-38179074-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38179074
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38179074
    reference: chr 17
allele count: 99
allele frequency: 8.347526939746033e-4
allele num: 118598
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000439148
  ensembl transcript: ENST00000535508
  gene symbol: MED24
  hgvsc: ENST00000535508.2:c.*1879G>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000348610
  ensembl transcript: ENST00000356271
  gene symbol: MED24
  hgvsc: ENST00000356271.3:c.2217G>A
  hgvsp: ENST00000356271.3:c.2217G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377686
  ensembl transcript: ENST00000394128
  gene symbol: MED24
  hgvsc: ENST00000394128.2:c.2256G>A
  hgvsp: ENST00000394128.2:c.2256G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008838
  ensembl transcript: ENST00000492176
  gene symbol: MED24
  hgvsc: ENST00000492176.2:n.527G>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000440100
  ensembl transcript: ENST00000501516
  gene symbol: MED24
  hgvsc: ENST00000501516.3:c.2313G>A
  hgvsp: ENST00000501516.3:c.2313G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377684
  ensembl transcript: ENST00000394126
  gene symbol: MED24
  hgvsc: ENST00000394126.1:c.2331G>A
  hgvsp: ENST00000394126.1:c.2331G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000393464
  ensembl transcript: ENST00000422942
  gene symbol: MED24
  hgvsc: ENST00000422942.2:c.36G>A
  hgvsp: ENST00000422942.2:c.36G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377685
  ensembl transcript: ENST00000394127
  gene symbol: MED24
  hgvsc: ENST00000394127.2:c.2217G>A
  hgvsp: ENST00000394127.2:c.2217G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000443344
  ensembl transcript: ENST00000535071
  gene symbol: MED24
  hgvsc: ENST00000535071.2:c.2106G>A
  hgvsp: ENST00000535071.2:c.2106G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22963
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 5395
  bin: 3.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 3.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 1.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 4.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 2012
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 4.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 26303
  bin: 2.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 5.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 23687
  bin: 2.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1311
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 5.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 484
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 285
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46693
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 535
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Leu752Leu
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/17-38179086-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38179086
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38179086
    reference: chr 17
allele count: 6
allele frequency: 5.127241031600895e-5
allele num: 117022
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377686
  ensembl transcript: ENST00000394128
  gene symbol: MED24
  hgvsc: ENST00000394128.2:c.2251-7G>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl transcript: ENST00000492176
  gene symbol: MED24
  hgvsc: ENST00000492176.2:n.522-7G>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000439148
  ensembl transcript: ENST00000535508
  gene symbol: MED24
  hgvsc: ENST00000535508.2:c.*1874-7G>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377685
  ensembl transcript: ENST00000394127
  gene symbol: MED24
  hgvsc: ENST00000394127.2:c.2212-7G>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000348610
  ensembl transcript: ENST00000356271
  gene symbol: MED24
  hgvsc: ENST00000356271.3:c.2212-7G>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000393464
  ensembl transcript: ENST00000422942
  gene symbol: MED24
  hgvsc: ENST00000422942.2:c.31-7G>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000443344
  ensembl transcript: ENST00000535071
  gene symbol: MED24
  hgvsc: ENST00000535071.2:c.2101-7G>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000440100
  ensembl transcript: ENST00000501516
  gene symbol: MED24
  hgvsc: ENST00000501516.3:c.2308-7G>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377684
  ensembl transcript: ENST00000394126
  gene symbol: MED24
  hgvsc: ENST00000394126.1:c.2326-7G>T
  variant of: http://identifiers.org/hgnc/22963
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2020
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5179
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22171
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4276
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24367
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1330
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43085
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1232
  bin: 7.25e1
  variant carriers: 0
hgvs: c.2251-7G>T
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: Other
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

17-38179086-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38179086
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38179086
    reference: chr 17
allele count: 7
allele frequency: 5.981781203534378e-5
allele num: 117022
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377684
  ensembl transcript: ENST00000394126
  gene symbol: MED24
  hgvsc: ENST00000394126.1:c.2326-7G>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000393464
  ensembl transcript: ENST00000422942
  gene symbol: MED24
  hgvsc: ENST00000422942.2:c.31-7G>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000439148
  ensembl transcript: ENST00000535508
  gene symbol: MED24
  hgvsc: ENST00000535508.2:c.*1874-7G>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000443344
  ensembl transcript: ENST00000535071
  gene symbol: MED24
  hgvsc: ENST00000535071.2:c.2101-7G>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000348610
  ensembl transcript: ENST00000356271
  gene symbol: MED24
  hgvsc: ENST00000356271.3:c.2212-7G>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377685
  ensembl transcript: ENST00000394127
  gene symbol: MED24
  hgvsc: ENST00000394127.2:c.2212-7G>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000440100
  ensembl transcript: ENST00000501516
  gene symbol: MED24
  hgvsc: ENST00000501516.3:c.2308-7G>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377686
  ensembl transcript: ENST00000394128
  gene symbol: MED24
  hgvsc: ENST00000394128.2:c.2251-7G>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl transcript: ENST00000492176
  gene symbol: MED24
  hgvsc: ENST00000492176.2:n.522-7G>A
  variant of: http://identifiers.org/hgnc/22963
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24367
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1330
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2020
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4276
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22171
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5179
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 391
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 625
  bin: 3.75e1
  variant carriers: 0
hgvs: c.2251-7G>A
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum

17-38179087-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38179087
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38179087
    reference: chr 17
allele count: 4
allele frequency: 3.427650859483453e-5
allele num: 116698
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000440100
  ensembl transcript: ENST00000501516
  gene symbol: MED24
  hgvsc: ENST00000501516.3:c.2308-8C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000443344
  ensembl transcript: ENST00000535071
  gene symbol: MED24
  hgvsc: ENST00000535071.2:c.2101-8C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000393464
  ensembl transcript: ENST00000422942
  gene symbol: MED24
  hgvsc: ENST00000422942.2:c.31-8C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377684
  ensembl transcript: ENST00000394126
  gene symbol: MED24
  hgvsc: ENST00000394126.1:c.2326-8C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377685
  ensembl transcript: ENST00000394127
  gene symbol: MED24
  hgvsc: ENST00000394127.2:c.2212-8C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377686
  ensembl transcript: ENST00000394128
  gene symbol: MED24
  hgvsc: ENST00000394128.2:c.2251-8C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000439148
  ensembl transcript: ENST00000535508
  gene symbol: MED24
  hgvsc: ENST00000535508.2:c.*1874-8C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl transcript: ENST00000492176
  gene symbol: MED24
  hgvsc: ENST00000492176.2:n.522-8C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000348610
  ensembl transcript: ENST00000356271
  gene symbol: MED24
  hgvsc: ENST00000356271.3:c.2212-8C>T
  variant of: http://identifiers.org/hgnc/22963
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21890
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2154
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24007
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5130
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4735
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1424
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1112
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 1.75e1
  variant carriers: 0
hgvs: c.2251-8C>T
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ReadPosRankSum

17-38179092-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38179092
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38179092
    reference: chr 17
allele count: 4
allele frequency: 3.448454230391227e-5
allele num: 115994
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377684
  ensembl transcript: ENST00000394126
  gene symbol: MED24
  hgvsc: ENST00000394126.1:c.2326-13T>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000348610
  ensembl transcript: ENST00000356271
  gene symbol: MED24
  hgvsc: ENST00000356271.3:c.2212-13T>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000393464
  ensembl transcript: ENST00000422942
  gene symbol: MED24
  hgvsc: ENST00000422942.2:c.31-13T>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl transcript: ENST00000492176
  gene symbol: MED24
  hgvsc: ENST00000492176.2:n.522-13T>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000439148
  ensembl transcript: ENST00000535508
  gene symbol: MED24
  hgvsc: ENST00000535508.2:c.*1874-13T>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377686
  ensembl transcript: ENST00000394128
  gene symbol: MED24
  hgvsc: ENST00000394128.2:c.2251-13T>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000443344
  ensembl transcript: ENST00000535071
  gene symbol: MED24
  hgvsc: ENST00000535071.2:c.2101-13T>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377685
  ensembl transcript: ENST00000394127
  gene symbol: MED24
  hgvsc: ENST00000394127.2:c.2212-13T>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000440100
  ensembl transcript: ENST00000501516
  gene symbol: MED24
  hgvsc: ENST00000501516.3:c.2308-13T>A
  variant of: http://identifiers.org/hgnc/22963
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22657
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1861
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21145
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6240
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4924
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2509
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 291
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 454
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 4705
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40433
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 560
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum

17-38179096-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38179096
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38179096
    reference: chr 17
allele count: 8
allele frequency: 6.952169076751947e-5
allele num: 115072
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000439148
  ensembl transcript: ENST00000535508
  gene symbol: MED24
  hgvsc: ENST00000535508.2:c.*1874-17C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000348610
  ensembl transcript: ENST00000356271
  gene symbol: MED24
  hgvsc: ENST00000356271.3:c.2212-17C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000443344
  ensembl transcript: ENST00000535071
  gene symbol: MED24
  hgvsc: ENST00000535071.2:c.2101-17C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl transcript: ENST00000492176
  gene symbol: MED24
  hgvsc: ENST00000492176.2:n.522-17C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000393464
  ensembl transcript: ENST00000422942
  gene symbol: MED24
  hgvsc: ENST00000422942.2:c.31-17C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377684
  ensembl transcript: ENST00000394126
  gene symbol: MED24
  hgvsc: ENST00000394126.1:c.2326-17C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000440100
  ensembl transcript: ENST00000501516
  gene symbol: MED24
  hgvsc: ENST00000501516.3:c.2308-17C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377686
  ensembl transcript: ENST00000394128
  gene symbol: MED24
  hgvsc: ENST00000394128.2:c.2251-17C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377685
  ensembl transcript: ENST00000394127
  gene symbol: MED24
  hgvsc: ENST00000394127.2:c.2212-17C>T
  variant of: http://identifiers.org/hgnc/22963
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8158
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2864
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19927
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4773
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2646
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20915
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 233
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 533
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 321
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 201
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: ClippingRankSum

17-38179098-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38179098
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38179098
    reference: chr 17
allele count: 1
allele frequency: 8.729507481187912e-6
allele num: 114554
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377684
  ensembl transcript: ENST00000394126
  gene symbol: MED24
  hgvsc: ENST00000394126.1:c.2326-19C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000348610
  ensembl transcript: ENST00000356271
  gene symbol: MED24
  hgvsc: ENST00000356271.3:c.2212-19C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl transcript: ENST00000492176
  gene symbol: MED24
  hgvsc: ENST00000492176.2:n.522-19C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377685
  ensembl transcript: ENST00000394127
  gene symbol: MED24
  hgvsc: ENST00000394127.2:c.2212-19C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377686
  ensembl transcript: ENST00000394128
  gene symbol: MED24
  hgvsc: ENST00000394128.2:c.2251-19C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000439148
  ensembl transcript: ENST00000535508
  gene symbol: MED24
  hgvsc: ENST00000535508.2:c.*1874-19C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000443344
  ensembl transcript: ENST00000535071
  gene symbol: MED24
  hgvsc: ENST00000535071.2:c.2101-19C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000393464
  ensembl transcript: ENST00000422942
  gene symbol: MED24
  hgvsc: ENST00000422942.2:c.31-19C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000440100
  ensembl transcript: ENST00000501516
  gene symbol: MED24
  hgvsc: ENST00000501516.3:c.2308-19C>T
  variant of: http://identifiers.org/hgnc/22963
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9538
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3097
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19126
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4667
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3286
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19543
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 447
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34978
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2337
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2943
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 242
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 548
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: Other
reference allele: G
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

17-38179103-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38179103
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38179103
    reference: chr 17
allele count: 10
allele frequency: 8.799563541648335e-5
allele num: 113642
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377685
  ensembl transcript: ENST00000394127
  gene symbol: MED24
  hgvsc: ENST00000394127.2:c.2212-24A>G
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000439148
  ensembl transcript: ENST00000535508
  gene symbol: MED24
  hgvsc: ENST00000535508.2:c.*1874-24A>G
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000348610
  ensembl transcript: ENST00000356271
  gene symbol: MED24
  hgvsc: ENST00000356271.3:c.2212-24A>G
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000443344
  ensembl transcript: ENST00000535071
  gene symbol: MED24
  hgvsc: ENST00000535071.2:c.2101-24A>G
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl transcript: ENST00000492176
  gene symbol: MED24
  hgvsc: ENST00000492176.2:n.522-24A>G
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377686
  ensembl transcript: ENST00000394128
  gene symbol: MED24
  hgvsc: ENST00000394128.2:c.2251-24A>G
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377684
  ensembl transcript: ENST00000394126
  gene symbol: MED24
  hgvsc: ENST00000394126.1:c.2326-24A>G
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000393464
  ensembl transcript: ENST00000422942
  gene symbol: MED24
  hgvsc: ENST00000422942.2:c.31-24A>G
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000440100
  ensembl transcript: ENST00000501516
  gene symbol: MED24
  hgvsc: ENST00000501516.3:c.2308-24A>G
  variant of: http://identifiers.org/hgnc/22963
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3467
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17586
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17329
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4201
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11922
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4682
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3980
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 411
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 533
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 968
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 586
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2333
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP

17-38179112-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38179112
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38179112
    reference: chr 17
allele count: 1
allele frequency: 8.99733678831066e-6
allele num: 111144
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000439148
  ensembl transcript: ENST00000535508
  gene symbol: MED24
  hgvsc: ENST00000535508.2:c.*1874-33G>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000440100
  ensembl transcript: ENST00000501516
  gene symbol: MED24
  hgvsc: ENST00000501516.3:c.2308-33G>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377684
  ensembl transcript: ENST00000394126
  gene symbol: MED24
  hgvsc: ENST00000394126.1:c.2326-33G>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377685
  ensembl transcript: ENST00000394127
  gene symbol: MED24
  hgvsc: ENST00000394127.2:c.2212-33G>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000393464
  ensembl transcript: ENST00000422942
  gene symbol: MED24
  hgvsc: ENST00000422942.2:c.31-33G>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000348610
  ensembl transcript: ENST00000356271
  gene symbol: MED24
  hgvsc: ENST00000356271.3:c.2212-33G>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000443344
  ensembl transcript: ENST00000535071
  gene symbol: MED24
  hgvsc: ENST00000535071.2:c.2101-33G>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377686
  ensembl transcript: ENST00000394128
  gene symbol: MED24
  hgvsc: ENST00000394128.2:c.2251-33G>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl transcript: ENST00000492176
  gene symbol: MED24
  hgvsc: ENST00000492176.2:n.522-33G>A
  variant of: http://identifiers.org/hgnc/22963
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12174
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16164
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4153
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12318
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3248
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10913
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 395
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 501
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1524
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 822
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1609
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP

17-38179113-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38179113
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38179113
    reference: chr 17
allele count: 2
allele frequency: 1.803881953964933e-5
allele num: 110872
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl transcript: ENST00000492176
  gene symbol: MED24
  hgvsc: ENST00000492176.2:n.522-34T>C
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377684
  ensembl transcript: ENST00000394126
  gene symbol: MED24
  hgvsc: ENST00000394126.1:c.2326-34T>C
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000440100
  ensembl transcript: ENST00000501516
  gene symbol: MED24
  hgvsc: ENST00000501516.3:c.2308-34T>C
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000439148
  ensembl transcript: ENST00000535508
  gene symbol: MED24
  hgvsc: ENST00000535508.2:c.*1874-34T>C
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000443344
  ensembl transcript: ENST00000535071
  gene symbol: MED24
  hgvsc: ENST00000535071.2:c.2101-34T>C
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000348610
  ensembl transcript: ENST00000356271
  gene symbol: MED24
  hgvsc: ENST00000356271.3:c.2212-34T>C
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377685
  ensembl transcript: ENST00000394127
  gene symbol: MED24
  hgvsc: ENST00000394127.2:c.2212-34T>C
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000393464
  ensembl transcript: ENST00000422942
  gene symbol: MED24
  hgvsc: ENST00000422942.2:c.31-34T>C
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377686
  ensembl transcript: ENST00000394128
  gene symbol: MED24
  hgvsc: ENST00000394128.2:c.2251-34T>C
  variant of: http://identifiers.org/hgnc/22963
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3144
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11689
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11693
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4251
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16335
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11839
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 870
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11180
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7248
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 410
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 721
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4499
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum

17-38179115-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38179115
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38179115
    reference: chr 17
allele count: 2
allele frequency: 1.811495752042462e-5
allele num: 110406
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377684
  ensembl transcript: ENST00000394126
  gene symbol: MED24
  hgvsc: ENST00000394126.1:c.2326-36C>G
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000440100
  ensembl transcript: ENST00000501516
  gene symbol: MED24
  hgvsc: ENST00000501516.3:c.2308-36C>G
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377686
  ensembl transcript: ENST00000394128
  gene symbol: MED24
  hgvsc: ENST00000394128.2:c.2251-36C>G
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000439148
  ensembl transcript: ENST00000535508
  gene symbol: MED24
  hgvsc: ENST00000535508.2:c.*1874-36C>G
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000443344
  ensembl transcript: ENST00000535071
  gene symbol: MED24
  hgvsc: ENST00000535071.2:c.2101-36C>G
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377685
  ensembl transcript: ENST00000394127
  gene symbol: MED24
  hgvsc: ENST00000394127.2:c.2212-36C>G
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000348610
  ensembl transcript: ENST00000356271
  gene symbol: MED24
  hgvsc: ENST00000356271.3:c.2212-36C>G
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000393464
  ensembl transcript: ENST00000422942
  gene symbol: MED24
  hgvsc: ENST00000422942.2:c.31-36C>G
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl transcript: ENST00000492176
  gene symbol: MED24
  hgvsc: ENST00000492176.2:n.522-36C>G
  variant of: http://identifiers.org/hgnc/22963
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11082
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2994
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13052
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4426
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16476
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10872
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 834
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 442
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4627
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 482
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11236
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 851
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum

17-38179117-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38179117
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38179117
    reference: chr 17
allele count: 1
allele frequency: 9.108629515603082e-6
allele num: 109786
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000393464
  ensembl transcript: ENST00000422942
  gene symbol: MED24
  hgvsc: ENST00000422942.2:c.31-38C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000443344
  ensembl transcript: ENST00000535071
  gene symbol: MED24
  hgvsc: ENST00000535071.2:c.2101-38C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377686
  ensembl transcript: ENST00000394128
  gene symbol: MED24
  hgvsc: ENST00000394128.2:c.2251-38C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl transcript: ENST00000492176
  gene symbol: MED24
  hgvsc: ENST00000492176.2:n.522-38C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000348610
  ensembl transcript: ENST00000356271
  gene symbol: MED24
  hgvsc: ENST00000356271.3:c.2212-38C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377685
  ensembl transcript: ENST00000394127
  gene symbol: MED24
  hgvsc: ENST00000394127.2:c.2212-38C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000439148
  ensembl transcript: ENST00000535508
  gene symbol: MED24
  hgvsc: ENST00000535508.2:c.*1874-38C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000440100
  ensembl transcript: ENST00000501516
  gene symbol: MED24
  hgvsc: ENST00000501516.3:c.2308-38C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377684
  ensembl transcript: ENST00000394126
  gene symbol: MED24
  hgvsc: ENST00000394126.1:c.2326-38C>T
  variant of: http://identifiers.org/hgnc/22963
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9987
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14498
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4667
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2759
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10487
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16482
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1005
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7913
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 516
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 432
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 185
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Other
population: Latino
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQ

17-38179117-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38179117
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38179117
    reference: chr 17
allele count: 1
allele frequency: 9.108629515603082e-6
allele num: 109786
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377686
  ensembl transcript: ENST00000394128
  gene symbol: MED24
  hgvsc: ENST00000394128.2:c.2251-38C>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000348610
  ensembl transcript: ENST00000356271
  gene symbol: MED24
  hgvsc: ENST00000356271.3:c.2212-38C>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000393464
  ensembl transcript: ENST00000422942
  gene symbol: MED24
  hgvsc: ENST00000422942.2:c.31-38C>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000443344
  ensembl transcript: ENST00000535071
  gene symbol: MED24
  hgvsc: ENST00000535071.2:c.2101-38C>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000439148
  ensembl transcript: ENST00000535508
  gene symbol: MED24
  hgvsc: ENST00000535508.2:c.*1874-38C>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377684
  ensembl transcript: ENST00000394126
  gene symbol: MED24
  hgvsc: ENST00000394126.1:c.2326-38C>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000440100
  ensembl transcript: ENST00000501516
  gene symbol: MED24
  hgvsc: ENST00000501516.3:c.2308-38C>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377685
  ensembl transcript: ENST00000394127
  gene symbol: MED24
  hgvsc: ENST00000394127.2:c.2212-38C>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl transcript: ENST00000492176
  gene symbol: MED24
  hgvsc: ENST00000492176.2:n.522-38C>A
  variant of: http://identifiers.org/hgnc/22963
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14498
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2759
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10487
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16482
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4667
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9987
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11105
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 516
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7913
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2686
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 684
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP

17-38179120-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38179120
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38179120
    reference: chr 17
allele count: 3
allele frequency: 2.776852160390981e-5
allele num: 108036
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377685
  ensembl transcript: ENST00000394127
  gene symbol: MED24
  hgvsc: ENST00000394127.2:c.2212-41G>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000393464
  ensembl transcript: ENST00000422942
  gene symbol: MED24
  hgvsc: ENST00000422942.2:c.31-41G>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000443344
  ensembl transcript: ENST00000535071
  gene symbol: MED24
  hgvsc: ENST00000535071.2:c.2101-41G>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000439148
  ensembl transcript: ENST00000535508
  gene symbol: MED24
  hgvsc: ENST00000535508.2:c.*1874-41G>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377684
  ensembl transcript: ENST00000394126
  gene symbol: MED24
  hgvsc: ENST00000394126.1:c.2326-41G>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000348610
  ensembl transcript: ENST00000356271
  gene symbol: MED24
  hgvsc: ENST00000356271.3:c.2212-41G>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377686
  ensembl transcript: ENST00000394128
  gene symbol: MED24
  hgvsc: ENST00000394128.2:c.2251-41G>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl transcript: ENST00000492176
  gene symbol: MED24
  hgvsc: ENST00000492176.2:n.522-41G>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000440100
  ensembl transcript: ENST00000501516
  gene symbol: MED24
  hgvsc: ENST00000501516.3:c.2308-41G>A
  variant of: http://identifiers.org/hgnc/22963
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2443
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8365
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16284
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5209
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16603
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9926
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10641
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12861
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 824
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 449
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 4842
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 785
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: QD

17-38179121-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38179121
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38179121
    reference: chr 17
allele count: 2
allele frequency: 1.871993111065351e-5
allele num: 106838
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000440100
  ensembl transcript: ENST00000501516
  gene symbol: MED24
  hgvsc: ENST00000501516.3:c.2308-42C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377686
  ensembl transcript: ENST00000394128
  gene symbol: MED24
  hgvsc: ENST00000394128.2:c.2251-42C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377685
  ensembl transcript: ENST00000394127
  gene symbol: MED24
  hgvsc: ENST00000394127.2:c.2212-42C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000439148
  ensembl transcript: ENST00000535508
  gene symbol: MED24
  hgvsc: ENST00000535508.2:c.*1874-42C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000443344
  ensembl transcript: ENST00000535071
  gene symbol: MED24
  hgvsc: ENST00000535071.2:c.2101-42C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377684
  ensembl transcript: ENST00000394126
  gene symbol: MED24
  hgvsc: ENST00000394126.1:c.2326-42C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000393464
  ensembl transcript: ENST00000422942
  gene symbol: MED24
  hgvsc: ENST00000422942.2:c.31-42C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000348610
  ensembl transcript: ENST00000356271
  gene symbol: MED24
  hgvsc: ENST00000356271.3:c.2212-42C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl transcript: ENST00000492176
  gene symbol: MED24
  hgvsc: ENST00000492176.2:n.522-42C>T
  variant of: http://identifiers.org/hgnc/22963
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 841
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16918
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2256
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10434
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5619
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7510
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16080
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 301
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1725
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1258
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 181
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4218
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10160
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQ

17-38179131-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38179131
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38179131
    reference: chr 17
allele count: 2
allele frequency: 1.926448207439943e-5
allele num: 103818
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl transcript: ENST00000492176
  gene symbol: MED24
  hgvsc: ENST00000492176.2:n.522-52C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000393464
  ensembl transcript: ENST00000422942
  gene symbol: MED24
  hgvsc: ENST00000422942.2:c.31-52C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000439148
  ensembl transcript: ENST00000535508
  gene symbol: MED24
  hgvsc: ENST00000535508.2:c.*1874-52C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000348610
  ensembl transcript: ENST00000356271
  gene symbol: MED24
  hgvsc: ENST00000356271.3:c.2212-52C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000440100
  ensembl transcript: ENST00000501516
  gene symbol: MED24
  hgvsc: ENST00000501516.3:c.2308-52C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377685
  ensembl transcript: ENST00000394127
  gene symbol: MED24
  hgvsc: ENST00000394127.2:c.2212-52C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000443344
  ensembl transcript: ENST00000535071
  gene symbol: MED24
  hgvsc: ENST00000535071.2:c.2101-52C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377684
  ensembl transcript: ENST00000394126
  gene symbol: MED24
  hgvsc: ENST00000394126.1:c.2326-52C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377686
  ensembl transcript: ENST00000394128
  gene symbol: MED24
  hgvsc: ENST00000394128.2:c.2251-52C>T
  variant of: http://identifiers.org/hgnc/22963
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1882
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6748
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15589
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16364
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5706
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12531
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3104
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 747
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 236
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4820
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1599
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 819
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/17-38179338-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38179338
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38179338
    reference: chr 17
allele count: 1
allele frequency: 8.98876404494382e-6
allele num: 111250
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377685
  ensembl transcript: ENST00000394127
  gene symbol: MED24
  hgvsc: ENST00000394127.2:c.2211+46T>G
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377684
  ensembl transcript: ENST00000394126
  gene symbol: MED24
  hgvsc: ENST00000394126.1:c.2325+46T>G
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000440100
  ensembl transcript: ENST00000501516
  gene symbol: MED24
  hgvsc: ENST00000501516.3:c.2307+46T>G
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000348610
  ensembl transcript: ENST00000356271
  gene symbol: MED24
  hgvsc: ENST00000356271.3:c.2211+46T>G
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl transcript: ENST00000492176
  gene symbol: MED24
  hgvsc: ENST00000492176.2:n.521+46T>G
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000393464
  ensembl transcript: ENST00000422942
  gene symbol: MED24
  hgvsc: ENST00000422942.2:c.30+46T>G
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000439148
  ensembl transcript: ENST00000535508
  gene symbol: MED24
  hgvsc: ENST00000535508.2:c.*1873+46T>G
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000443344
  ensembl transcript: ENST00000535071
  gene symbol: MED24
  hgvsc: ENST00000535071.2:c.2100+46T>G
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377686
  ensembl transcript: ENST00000394128
  gene symbol: MED24
  hgvsc: ENST00000394128.2:c.2250+46T>G
  variant of: http://identifiers.org/hgnc/22963
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4601
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3867
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5205
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13837
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2177
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8340
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12307
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7001
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2363
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2493
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2100
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14015
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6533
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

17-38179340-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38179340
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38179340
    reference: chr 17
allele count: 1
allele frequency: 8.981498113885396e-6
allele num: 111340
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000443344
  ensembl transcript: ENST00000535071
  gene symbol: MED24
  hgvsc: ENST00000535071.2:c.2100+44C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000439148
  ensembl transcript: ENST00000535508
  gene symbol: MED24
  hgvsc: ENST00000535508.2:c.*1873+44C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377685
  ensembl transcript: ENST00000394127
  gene symbol: MED24
  hgvsc: ENST00000394127.2:c.2211+44C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377686
  ensembl transcript: ENST00000394128
  gene symbol: MED24
  hgvsc: ENST00000394128.2:c.2250+44C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl transcript: ENST00000492176
  gene symbol: MED24
  hgvsc: ENST00000492176.2:n.521+44C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000348610
  ensembl transcript: ENST00000356271
  gene symbol: MED24
  hgvsc: ENST00000356271.3:c.2211+44C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377684
  ensembl transcript: ENST00000394126
  gene symbol: MED24
  hgvsc: ENST00000394126.1:c.2325+44C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000393464
  ensembl transcript: ENST00000422942
  gene symbol: MED24
  hgvsc: ENST00000422942.2:c.30+44C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000440100
  ensembl transcript: ENST00000501516
  gene symbol: MED24
  hgvsc: ENST00000501516.3:c.2307+44C>T
  variant of: http://identifiers.org/hgnc/22963
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3869
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8410
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5172
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12452
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14484
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6178
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4622
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2178
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1315
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 517
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6430
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 15219
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6643
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD

17-38179342-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38179342
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38179342
    reference: chr 17
allele count: 1
allele frequency: 8.969897025582147e-6
allele num: 111484
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377686
  ensembl transcript: ENST00000394128
  gene symbol: MED24
  hgvsc: ENST00000394128.2:c.2250+42C>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000393464
  ensembl transcript: ENST00000422942
  gene symbol: MED24
  hgvsc: ENST00000422942.2:c.30+42C>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000439148
  ensembl transcript: ENST00000535508
  gene symbol: MED24
  hgvsc: ENST00000535508.2:c.*1873+42C>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000443344
  ensembl transcript: ENST00000535071
  gene symbol: MED24
  hgvsc: ENST00000535071.2:c.2100+42C>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000348610
  ensembl transcript: ENST00000356271
  gene symbol: MED24
  hgvsc: ENST00000356271.3:c.2211+42C>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl transcript: ENST00000492176
  gene symbol: MED24
  hgvsc: ENST00000492176.2:n.521+42C>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377685
  ensembl transcript: ENST00000394127
  gene symbol: MED24
  hgvsc: ENST00000394127.2:c.2211+42C>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000440100
  ensembl transcript: ENST00000501516
  gene symbol: MED24
  hgvsc: ENST00000501516.3:c.2307+42C>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377684
  ensembl transcript: ENST00000394126
  gene symbol: MED24
  hgvsc: ENST00000394126.1:c.2325+42C>A
  variant of: http://identifiers.org/hgnc/22963
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3878
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12574
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5119
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15075
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8499
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5453
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4620
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2182
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6688
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16036
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1021
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2378
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2124
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 591
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: South Asian
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

http://identifiers.org/exac.variant/17-38179343-A-AC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38179343
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38179344
    reference: chr 17
allele count: 1
allele frequency: 8.969092507220119e-6
allele num: 111494
alternate allele: AC
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377686
  ensembl transcript: ENST00000394128
  gene symbol: MED24
  hgvsc: ENST00000394128.2:c.2250+40dupG
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000439148
  ensembl transcript: ENST00000535508
  gene symbol: MED24
  hgvsc: ENST00000535508.2:c.*1873+40dupG
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000393464
  ensembl transcript: ENST00000422942
  gene symbol: MED24
  hgvsc: ENST00000422942.2:c.30+40dupG
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000440100
  ensembl transcript: ENST00000501516
  gene symbol: MED24
  hgvsc: ENST00000501516.3:c.2307+40dupG
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl transcript: ENST00000492176
  gene symbol: MED24
  hgvsc: ENST00000492176.2:n.521+40dupG
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000348610
  ensembl transcript: ENST00000356271
  gene symbol: MED24
  hgvsc: ENST00000356271.3:c.2211+40dupG
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000443344
  ensembl transcript: ENST00000535071
  gene symbol: MED24
  hgvsc: ENST00000535071.2:c.2100+40dupG
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377685
  ensembl transcript: ENST00000394127
  gene symbol: MED24
  hgvsc: ENST00000394127.2:c.2211+40dupG
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377684
  ensembl transcript: ENST00000394126
  gene symbol: MED24
  hgvsc: ENST00000394126.1:c.2325+40dupG
  variant of: http://identifiers.org/hgnc/22963
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8526
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 908
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5089
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3889
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15244
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2180
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5237
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4622
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12631
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 726
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2255
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16125
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1574
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6704
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: A
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP

17-38179348-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38179348
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38179348
    reference: chr 17
allele count: 2
allele frequency: 1.789933414476982e-5
allele num: 111736
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377686
  ensembl transcript: ENST00000394128
  gene symbol: MED24
  hgvsc: ENST00000394128.2:c.2250+36T>C
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl transcript: ENST00000492176
  gene symbol: MED24
  hgvsc: ENST00000492176.2:n.521+36T>C
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000348610
  ensembl transcript: ENST00000356271
  gene symbol: MED24
  hgvsc: ENST00000356271.3:c.2211+36T>C
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000443344
  ensembl transcript: ENST00000535071
  gene symbol: MED24
  hgvsc: ENST00000535071.2:c.2100+36T>C
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377684
  ensembl transcript: ENST00000394126
  gene symbol: MED24
  hgvsc: ENST00000394126.1:c.2325+36T>C
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000439148
  ensembl transcript: ENST00000535508
  gene symbol: MED24
  hgvsc: ENST00000535508.2:c.*1873+36T>C
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000393464
  ensembl transcript: ENST00000422942
  gene symbol: MED24
  hgvsc: ENST00000422942.2:c.30+36T>C
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377685
  ensembl transcript: ENST00000394127
  gene symbol: MED24
  hgvsc: ENST00000394127.2:c.2211+36T>C
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000440100
  ensembl transcript: ENST00000501516
  gene symbol: MED24
  hgvsc: ENST00000501516.3:c.2307+36T>C
  variant of: http://identifiers.org/hgnc/22963
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4867
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2185
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12944
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16189
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3931
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4135
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4646
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8684
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6448
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 410
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2150
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 409
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1058
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2084
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: DP

17-38179350-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38179350
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38179350
    reference: chr 17
allele count: 25
allele frequency: 2.235416145069566e-4
allele num: 111836
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000439148
  ensembl transcript: ENST00000535508
  gene symbol: MED24
  hgvsc: ENST00000535508.2:c.*1873+34G>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000393464
  ensembl transcript: ENST00000422942
  gene symbol: MED24
  hgvsc: ENST00000422942.2:c.30+34G>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000348610
  ensembl transcript: ENST00000356271
  gene symbol: MED24
  hgvsc: ENST00000356271.3:c.2211+34G>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377685
  ensembl transcript: ENST00000394127
  gene symbol: MED24
  hgvsc: ENST00000394127.2:c.2211+34G>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377684
  ensembl transcript: ENST00000394126
  gene symbol: MED24
  hgvsc: ENST00000394126.1:c.2325+34G>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000443344
  ensembl transcript: ENST00000535071
  gene symbol: MED24
  hgvsc: ENST00000535071.2:c.2100+34G>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl transcript: ENST00000492176
  gene symbol: MED24
  hgvsc: ENST00000492176.2:n.521+34G>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377686
  ensembl transcript: ENST00000394128
  gene symbol: MED24
  hgvsc: ENST00000394128.2:c.2250+34G>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000440100
  ensembl transcript: ENST00000501516
  gene symbol: MED24
  hgvsc: ENST00000501516.3:c.2307+34G>A
  variant of: http://identifiers.org/hgnc/22963
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16284
  bin: 2.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8805
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3828
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4661
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2189
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3890
  bin: 7.5e0
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 13199
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4795
  bin: 1.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4156
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1349
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1719
  bin: 8.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 3391
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 593
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 16953
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum

17-38179354-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38179354
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38179354
    reference: chr 17
allele count: 1
allele frequency: 8.914244963451595e-6
allele num: 112180
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000440100
  ensembl transcript: ENST00000501516
  gene symbol: MED24
  hgvsc: ENST00000501516.3:c.2307+30C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377686
  ensembl transcript: ENST00000394128
  gene symbol: MED24
  hgvsc: ENST00000394128.2:c.2250+30C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000443344
  ensembl transcript: ENST00000535071
  gene symbol: MED24
  hgvsc: ENST00000535071.2:c.2100+30C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377684
  ensembl transcript: ENST00000394126
  gene symbol: MED24
  hgvsc: ENST00000394126.1:c.2325+30C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000393464
  ensembl transcript: ENST00000422942
  gene symbol: MED24
  hgvsc: ENST00000422942.2:c.30+30C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000439148
  ensembl transcript: ENST00000535508
  gene symbol: MED24
  hgvsc: ENST00000535508.2:c.*1873+30C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000348610
  ensembl transcript: ENST00000356271
  gene symbol: MED24
  hgvsc: ENST00000356271.3:c.2211+30C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377685
  ensembl transcript: ENST00000394127
  gene symbol: MED24
  hgvsc: ENST00000394127.2:c.2211+30C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl transcript: ENST00000492176
  gene symbol: MED24
  hgvsc: ENST00000492176.2:n.521+30C>T
  variant of: http://identifiers.org/hgnc/22963
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17076
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8939
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2195
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4505
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3927
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3020
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13467
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4671
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6973
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4316
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3459
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 235
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1733
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum

17-38179356-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38179356
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38179356
    reference: chr 17
allele count: 3
allele frequency: 2.674178135919561e-5
allele num: 112184
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377686
  ensembl transcript: ENST00000394128
  gene symbol: MED24
  hgvsc: ENST00000394128.2:c.2250+28G>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377685
  ensembl transcript: ENST00000394127
  gene symbol: MED24
  hgvsc: ENST00000394127.2:c.2211+28G>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377684
  ensembl transcript: ENST00000394126
  gene symbol: MED24
  hgvsc: ENST00000394126.1:c.2325+28G>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000393464
  ensembl transcript: ENST00000422942
  gene symbol: MED24
  hgvsc: ENST00000422942.2:c.30+28G>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000440100
  ensembl transcript: ENST00000501516
  gene symbol: MED24
  hgvsc: ENST00000501516.3:c.2307+28G>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000348610
  ensembl transcript: ENST00000356271
  gene symbol: MED24
  hgvsc: ENST00000356271.3:c.2211+28G>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000439148
  ensembl transcript: ENST00000535508
  gene symbol: MED24
  hgvsc: ENST00000535508.2:c.*1873+28G>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl transcript: ENST00000492176
  gene symbol: MED24
  hgvsc: ENST00000492176.2:n.521+28G>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000443344
  ensembl transcript: ENST00000535071
  gene symbol: MED24
  hgvsc: ENST00000535071.2:c.2100+28G>A
  variant of: http://identifiers.org/hgnc/22963
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2205
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2868
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17134
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9062
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 13629
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4388
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4690
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3874
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 461
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 759
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 904
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 234
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3467
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 625
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQRankSum

17-38179357-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38179357
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38179357
    reference: chr 17
allele count: 4
allele frequency: 3.556124535481233e-5
allele num: 112482
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000439148
  ensembl transcript: ENST00000535508
  gene symbol: MED24
  hgvsc: ENST00000535508.2:c.*1873+27C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000440100
  ensembl transcript: ENST00000501516
  gene symbol: MED24
  hgvsc: ENST00000501516.3:c.2307+27C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377685
  ensembl transcript: ENST00000394127
  gene symbol: MED24
  hgvsc: ENST00000394127.2:c.2211+27C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl transcript: ENST00000492176
  gene symbol: MED24
  hgvsc: ENST00000492176.2:n.521+27C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377686
  ensembl transcript: ENST00000394128
  gene symbol: MED24
  hgvsc: ENST00000394128.2:c.2250+27C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000393464
  ensembl transcript: ENST00000422942
  gene symbol: MED24
  hgvsc: ENST00000422942.2:c.30+27C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000443344
  ensembl transcript: ENST00000535071
  gene symbol: MED24
  hgvsc: ENST00000535071.2:c.2100+27C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377684
  ensembl transcript: ENST00000394126
  gene symbol: MED24
  hgvsc: ENST00000394126.1:c.2325+27C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000348610
  ensembl transcript: ENST00000356271
  gene symbol: MED24
  hgvsc: ENST00000356271.3:c.2211+27C>T
  variant of: http://identifiers.org/hgnc/22963
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17430
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9136
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13728
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2208
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4258
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2568
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4704
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3884
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 742
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1573
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 574
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3537
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: African
reference allele: G
site quality: MQ
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

http://identifiers.org/exac.variant/17-38179362-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38179362
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38179362
    reference: chr 17
allele count: 51
allele frequency: 4.610794684024953e-4
allele num: 110610
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000393464
  ensembl transcript: ENST00000422942
  gene symbol: MED24
  hgvsc: ENST00000422942.2:c.30+22T>G
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000440100
  ensembl transcript: ENST00000501516
  gene symbol: MED24
  hgvsc: ENST00000501516.3:c.2307+22T>G
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377685
  ensembl transcript: ENST00000394127
  gene symbol: MED24
  hgvsc: ENST00000394127.2:c.2211+22T>G
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000443344
  ensembl transcript: ENST00000535071
  gene symbol: MED24
  hgvsc: ENST00000535071.2:c.2100+22T>G
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377684
  ensembl transcript: ENST00000394126
  gene symbol: MED24
  hgvsc: ENST00000394126.1:c.2325+22T>G
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000348610
  ensembl transcript: ENST00000356271
  gene symbol: MED24
  hgvsc: ENST00000356271.3:c.2211+22T>G
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000439148
  ensembl transcript: ENST00000535508
  gene symbol: MED24
  hgvsc: ENST00000535508.2:c.*1873+22T>G
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl transcript: ENST00000492176
  gene symbol: MED24
  hgvsc: ENST00000492176.2:n.521+22T>G
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377686
  ensembl transcript: ENST00000394128
  gene symbol: MED24
  hgvsc: ENST00000394128.2:c.2250+22T>G
  variant of: http://identifiers.org/hgnc/22963
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.95to100.00
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2340
  bin: 4.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17578
  bin: 2.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3659
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2213
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4869
  bin: 3.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3622
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 5.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9402
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1114
  bin: 4.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 14207
  bin: 2.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 952
  bin: 2.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1321
  bin: 3.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 3452
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4245
  bin: 2.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1339
  bin: 2.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 305
  bin: 1.75e1
  variant carriers: 4
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: A
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum

17-38179374-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38179374
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38179374
    reference: chr 17
allele count: 6361
allele frequency: 5.478991886165136e-2
allele num: 116098
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000443344
  ensembl transcript: ENST00000535071
  gene symbol: MED24
  hgvsc: ENST00000535071.2:c.2100+10C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000393464
  ensembl transcript: ENST00000422942
  gene symbol: MED24
  hgvsc: ENST00000422942.2:c.30+10C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377685
  ensembl transcript: ENST00000394127
  gene symbol: MED24
  hgvsc: ENST00000394127.2:c.2211+10C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000439148
  ensembl transcript: ENST00000535508
  gene symbol: MED24
  hgvsc: ENST00000535508.2:c.*1873+10C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377684
  ensembl transcript: ENST00000394126
  gene symbol: MED24
  hgvsc: ENST00000394126.1:c.2325+10C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl transcript: ENST00000492176
  gene symbol: MED24
  hgvsc: ENST00000492176.2:n.521+10C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000440100
  ensembl transcript: ENST00000501516
  gene symbol: MED24
  hgvsc: ENST00000501516.3:c.2307+10C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377686
  ensembl transcript: ENST00000394128
  gene symbol: MED24
  hgvsc: ENST00000394128.2:c.2250+10C>T
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000348610
  ensembl transcript: ENST00000356271
  gene symbol: MED24
  hgvsc: ENST00000356271.3:c.2211+10C>T
  variant of: http://identifiers.org/hgnc/22963
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1514
  bin: 4.75e1
  variant carriers: 456
genotype depth: GenotypeDepth
  all individuals: 14652
  bin: 2.75e1
  variant carriers: 856
genotype depth: GenotypeDepth
  all individuals: 5526
  bin: 3.75e1
  variant carriers: 880
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 5.25e1
  variant carriers: 339
genotype depth: GenotypeDepth
  all individuals: 2415
  bin: 1.25e1
  variant carriers: 240
genotype depth: GenotypeDepth
  all individuals: 10049
  bin: 3.25e1
  variant carriers: 898
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 6.25e1
  variant carriers: 131
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 6.75e1
  variant carriers: 83
genotype depth: GenotypeDepth
  all individuals: 2882
  bin: 4.25e1
  variant carriers: 655
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1574
  bin: 1.75e1
  variant carriers: 464
genotype depth: GenotypeDepth
  all individuals: 17264
  bin: 2.25e1
  variant carriers: 686
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.25e1
  variant carriers: 72
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 5.75e1
  variant carriers: 198
genotype depth: GenotypeDepth
  all individuals: 2450
  bin: 7.5e0
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.25e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.75e1
  variant carriers: 40
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 9.75e1
  variant carriers: 73
genotype quality: GenotypeQuality
  all individuals: 11699
  bin: 9.75e1
  variant carriers: 5924
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 1.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 1630
  bin: 8.75e1
  variant carriers: 13
genotype quality: GenotypeQuality
  all individuals: 2875
  bin: 2.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3369
  bin: 8.25e1
  variant carriers: 25
genotype quality: GenotypeQuality
  all individuals: 2008
  bin: 9.25e1
  variant carriers: 28
num of homozygotes: 229
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: South Asian
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ

17-38179376-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38179376
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38179376
    reference: chr 17
allele count: 2
allele frequency: 1.71609006040637e-5
allele num: 116544
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377685
  ensembl transcript: ENST00000394127
  gene symbol: MED24
  hgvsc: ENST00000394127.2:c.2211+8G>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000443344
  ensembl transcript: ENST00000535071
  gene symbol: MED24
  hgvsc: ENST00000535071.2:c.2100+8G>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377686
  ensembl transcript: ENST00000394128
  gene symbol: MED24
  hgvsc: ENST00000394128.2:c.2250+8G>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000439148
  ensembl transcript: ENST00000535508
  gene symbol: MED24
  hgvsc: ENST00000535508.2:c.*1873+8G>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl transcript: ENST00000492176
  gene symbol: MED24
  hgvsc: ENST00000492176.2:n.521+8G>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000440100
  ensembl transcript: ENST00000501516
  gene symbol: MED24
  hgvsc: ENST00000501516.3:c.2307+8G>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000393464
  ensembl transcript: ENST00000422942
  gene symbol: MED24
  hgvsc: ENST00000422942.2:c.30+8G>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377684
  ensembl transcript: ENST00000394126
  gene symbol: MED24
  hgvsc: ENST00000394126.1:c.2325+8G>A
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000348610
  ensembl transcript: ENST00000356271
  gene symbol: MED24
  hgvsc: ENST00000356271.3:c.2211+8G>A
  variant of: http://identifiers.org/hgnc/22963
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17634
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5512
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2231
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2834
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10296
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1443
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1442
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2248
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15167
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 344
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3781
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7986
  bin: 6.75e1
  variant carriers: 0
hgvs: c.2250+8G>A
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: InbreedingCoeff

17-38179380-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38179380
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 38179380
    reference: chr 17
allele count: 1
allele frequency: 8.519919571959241e-6
allele num: 117372
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377684
  ensembl transcript: ENST00000394126
  gene symbol: MED24
  hgvsc: ENST00000394126.1:c.2325+4C>G
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000348610
  ensembl transcript: ENST00000356271
  gene symbol: MED24
  hgvsc: ENST00000356271.3:c.2211+4C>G
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377685
  ensembl transcript: ENST00000394127
  gene symbol: MED24
  hgvsc: ENST00000394127.2:c.2211+4C>G
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000377686
  ensembl transcript: ENST00000394128
  gene symbol: MED24
  hgvsc: ENST00000394128.2:c.2250+4C>G
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000440100
  ensembl transcript: ENST00000501516
  gene symbol: MED24
  hgvsc: ENST00000501516.3:c.2307+4C>G
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl transcript: ENST00000492176
  gene symbol: MED24
  hgvsc: ENST00000492176.2:n.521+4C>G
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000443344
  ensembl transcript: ENST00000535071
  gene symbol: MED24
  hgvsc: ENST00000535071.2:c.2100+4C>G
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000393464
  ensembl transcript: ENST00000422942
  gene symbol: MED24
  hgvsc: ENST00000422942.2:c.30+4C>G
  variant of: http://identifiers.org/hgnc/22963
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000008838
  ensembl protein: ENSP00000439148
  ensembl transcript: ENST00000535508
  gene symbol: MED24
  hgvsc: ENST00000535508.2:c.*1873+4C>G
  variant of: http://identifiers.org/hgnc/22963
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1917
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1876
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15376
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10391
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5530
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1443
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18347
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1114
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2836
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
hgvs: c.2250+4C>G
num of homozygotes: 0
reference allele: G

GenotypeQuality
all individuals: 235
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 689
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1601
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2020
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3370
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 602
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 282
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 243
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1282
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3501
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1360
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4877
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 801
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11056
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9538
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 838
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5696
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.195886151638364e-4
allele num: 8362
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63918
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.252344629235963e-5
allele num: 15994
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.5e0

DP
type: SiteQuality
SIO_000300: 1.331745e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 1.03e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.24e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 2.098e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.36e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.305e0

QD
type: SiteQuality
SIO_000300: 1.483e1

GenotypeQuality
all individuals: 1734
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 224
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 991
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1284
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 180
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 694
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33634
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 245
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 400
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1348
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1457
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2063
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4903
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9550
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.066183136899366e-5
allele num: 11030
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5694
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8348
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.130282351468102e-5
allele num: 63892
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15970
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.6e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 7.02e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.06e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.8e-2

DP
type: SiteQuality
SIO_000300: 1.345303e6

QD
type: SiteQuality
SIO_000300: 8.51e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.06e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

GenotypeQuality
all individuals: 124
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 857
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1429
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1351
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2249
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 750
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37046
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3616
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 239
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1037
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 603
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 5205
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64334
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11132
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8416
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16066
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 3.09981401115933e-4
allele num: 9678
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 846
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -2.376e0

MQRankSum
type: SiteQuality
SIO_000300: 7.12e-1

FS
type: SiteQuality
SIO_000300: 1.377e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.639999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.514e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

DP
type: SiteQuality
SIO_000300: 1.375473e6

QD
type: SiteQuality
SIO_000300: 3.091e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.19e-1

GenotypeQuality
all individuals: 241
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 599
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 713
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 854
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38176
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1414
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2037
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 779
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2286
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3447
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 287
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 972
bin: 4.75e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5774
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11140
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8434
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.225874735400324e-5
allele num: 16062
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9712
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64438
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.95e-1

FS
type: SiteQuality
SIO_000300: 4.506e0

VQSLOD
type: SiteQuality
SIO_000300: -1.62e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 3.9e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.829e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

QD
type: SiteQuality
SIO_000300: 1.755e1

MQRankSum
type: SiteQuality
SIO_000300: 3.9e-2

DP
type: SiteQuality
SIO_000300: 1.38732e6

GenotypeQuality
all individuals: 47
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1443
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38708
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 657
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 721
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 875
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2060
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1375
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1442
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 599
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3273
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5343
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 287
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5794
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11172
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9752
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16086
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.549474728067185e-5
allele num: 64538
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8460
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.51e0

MQRankSum
type: SiteQuality
SIO_000300: 5.71e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.54e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.97e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.71e-1

QD
type: SiteQuality
SIO_000300: 1.262e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.394524e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 3123
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40778
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1437
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1756
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5395
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 306
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 600
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 12
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 244
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1386
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 289
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 666
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11196
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16110
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9794
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.546312045770837e-5
allele num: 64670
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5826
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8476
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

DP
type: SiteQuality
SIO_000300: 1.40765e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.72e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.28e-1

MQ
type: SiteQuality
SIO_000300: 5.948e1

MQRankSum
type: SiteQuality
SIO_000300: 9.07e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.36e0

QD
type: SiteQuality
SIO_000300: 1.351e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.19e-1

GenotypeQuality
all individuals: 342
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 897
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 629
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 490
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44485
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1497
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 249
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 603
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2170
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 291
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5631
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1420
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 724
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 733
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 223
bin: 4.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8548
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16246
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5954
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11306
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.996001599360256e-5
allele num: 10004
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65314
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -7.9e-1

DP
type: SiteQuality
SIO_000300: 1.452787e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.33e0

QD
type: SiteQuality
SIO_000300: 1.014e1

VQSLOD
type: SiteQuality
SIO_000300: 5.26e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.53e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.8e-2

GenotypeQuality
all individuals: 43
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1415
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1603
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 501
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 606
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 527
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44994
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6060
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.045808966861598e-5
allele num: 65664
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10110
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11362
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.838235294117647e-4
allele num: 16320
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -5.1e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -9.59e-1

VQSLOD
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SIO_000300: 1.04e0

MQ
type: SiteQuality
SIO_000300: 5.953e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

DP
type: SiteQuality
SIO_000300: 1.481441e6

QD
type: SiteQuality
SIO_000300: 1.144e1

FS
type: SiteQuality
SIO_000300: 3.566e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.68e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.1e-2

GenotypeQuality
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bin: 3.75e1
variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 4

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.091246878235975e-5
allele num: 65668
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16328
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10104
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 864
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.795074758135444e-5
allele num: 11370
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 3.61e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.070000000000001e-1

FS
type: SiteQuality
SIO_000300: 1.83e0

VQSLOD
type: SiteQuality
SIO_000300: 1.15e-1

ReadPosRankSum
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SIO_000300: 5.2e-1

InbreedingCoeff
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SIO_000300: 5.999999999999999e-4

DP
type: SiteQuality
SIO_000300: 1.484657e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 7.88e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.21e-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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variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11370
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16328
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.522811719558994e-5
allele num: 65668
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10104
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 864
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 7.88e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.21e-1

FS
type: SiteQuality
SIO_000300: 1.83e0

MQRankSum
type: SiteQuality
SIO_000300: 3.61e-1

DP
type: SiteQuality
SIO_000300: 1.484657e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.15e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.2e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.070000000000001e-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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bin: 5.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6094
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16356
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10156
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11400
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8604
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.517496737382015e-5
allele num: 65898
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.483231e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

QD
type: SiteQuality
SIO_000300: 1.283e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.16e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.8e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.06e-1

FS
type: SiteQuality
SIO_000300: 8.047000000000001e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.24e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.03e-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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bin: 7.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.51758885482745e-5
allele num: 65894
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6098
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16362
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 868
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.26e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.379999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.199999999999999e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -3.61e-1

FS
type: SiteQuality
SIO_000300: 5.369e0

VQSLOD
type: SiteQuality
SIO_000300: -1.067e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

DP
type: SiteQuality
SIO_000300: 1.484266e6

QD
type: SiteQuality
SIO_000300: 5.99e0

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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bin: 9.25e1
variant carriers: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6098
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16362
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.51758885482745e-5
allele num: 65894
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11404
num of homozygotes: 0

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

East Asian
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allele count: 0
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ClippingRankSum
type: SiteQuality
SIO_000300: 7.199999999999999e-2

ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 5.369e0

QD
type: SiteQuality
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BaseQRankSum
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MQRankSum
type: SiteQuality
SIO_000300: -3.61e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.484266e6

VQSLOD
type: SiteQuality
SIO_000300: -1.067e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.514692517418964e-5
allele num: 66020
num of homozygotes: 0

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

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6134
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.26e-1

InbreedingCoeff
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FS
type: SiteQuality
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VQSLOD
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MQ
type: SiteQuality
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MQRankSum
type: SiteQuality
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DP
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ClippingRankSum
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SIO_000300: 1.18e0

BaseQRankSum
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QD
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SIO_000300: 7.1e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

South Asian
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African
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East Asian
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European (Finnish)
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European (Non-Finnish)
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allele count: 2
allele frequency: 3.028375882014476e-5
allele num: 66042
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Other
type: Population
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Latino
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allele frequency: 0.0e0
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MQRankSum
type: SiteQuality
SIO_000300: 1.64e0

BaseQRankSum
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ReadPosRankSum
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VQSLOD
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FS
type: SiteQuality
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ClippingRankSum
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DP
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MQ
type: SiteQuality
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QD
type: SiteQuality
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InbreedingCoeff
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SIO_000300: -4.0e-4

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 336
bin: 3.75e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6160
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.514004542013626e-5
allele num: 66050
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8608
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16388
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10206
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 874
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.163e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.42e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

DP
type: SiteQuality
SIO_000300: 1.492089e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.01e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.04e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.2e-2

QD
type: SiteQuality
SIO_000300: 9.66e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.16e0

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

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

GenotypeQuality
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 284
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 603
bin: 9.75e1
variant carriers: 2

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.023980162690133e-5
allele num: 66138
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6220
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16414
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 1.51e0

QD
type: SiteQuality
SIO_000300: 1.222e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.49e-1

FS
type: SiteQuality
SIO_000300: 6.67e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.610000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 8.2e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.496873e6

MQRankSum
type: SiteQuality
SIO_000300: 3.01e-1

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
all individuals: 729
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 242
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10232
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.744287458573173e-4
allele num: 11466
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66126
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6228
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.162e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.93e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 1.37e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -2.66e-1

QD
type: SiteQuality
SIO_000300: 1.682e1

VQSLOD
type: SiteQuality
SIO_000300: 1.47e0

DP
type: SiteQuality
SIO_000300: 1.497496e6

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1415
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 718
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.511898642315019e-5
allele num: 66142
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6250
num of homozygotes: 0

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

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

African
type: Population
allele count: 1
allele frequency: 9.777082518576456e-5
allele num: 10228
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.18e0

MQRankSum
type: SiteQuality
SIO_000300: 1.45e0

DP
type: SiteQuality
SIO_000300: 1.497594e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.096e0

FS
type: SiteQuality
SIO_000300: 8.159999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.94e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 1.1e0

QD
type: SiteQuality
SIO_000300: 1.379e1

GenotypeQuality
all individuals: 243
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 706
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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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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 496
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1522
bin: 7.25e1
variant carriers: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 874
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10238
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.022243713733075e-5
allele num: 66176
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16414
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.126e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.39e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.48e-1

DP
type: SiteQuality
SIO_000300: 1.500053e6

QD
type: SiteQuality
SIO_000300: 1.124e1

FS
type: SiteQuality
SIO_000300: 4.432e0

MQRankSum
type: SiteQuality
SIO_000300: -4.75e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.12e-1

GenotypeQuality
all individuals: 1385
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5892
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 18
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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: 703
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variant carriers: 0

GenotypeQuality
all individuals: 331
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GenotypeQuality
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GenotypeQuality
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variant carriers: 5

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 572
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1077
bin: 2.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10224
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.553326484983986e-5
allele num: 66196
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 874
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6294
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 9.57e-1

MQ
type: SiteQuality
SIO_000300: 5.933e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.8e-2

MQRankSum
type: SiteQuality
SIO_000300: 7.78e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.43e-1

QD
type: SiteQuality
SIO_000300: 1.151e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.604e0

DP
type: SiteQuality
SIO_000300: 1.500946e6

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

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

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

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 282
bin: 9.25e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10226
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16422
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 874
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6318
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11474
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.532132821705895e-5
allele num: 66194
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.34e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 9.47e-1

DP
type: SiteQuality
SIO_000300: 1.502399e6

FS
type: SiteQuality
SIO_000300: 5.91e-1

QD
type: SiteQuality
SIO_000300: 1.153e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.067e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.45e-1

MQ
type: SiteQuality
SIO_000300: 5.962e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.11e-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: 4

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 282
bin: 9.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8604
num of homozygotes: 0

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

Other
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: 16426
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11478
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.045583701106342e-5
allele num: 66164
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.506948e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
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FS
type: SiteQuality
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BaseQRankSum
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ClippingRankSum
type: SiteQuality
SIO_000300: 9.72e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.14e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.473e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 242
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variant carriers: 0

GenotypeQuality
all individuals: 484
bin: 3.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16428
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8610
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10232
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6354
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 880
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.067553271875472e-5
allele num: 66170
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.4e0

MQ
type: SiteQuality
SIO_000300: 5.953e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

FS
type: SiteQuality
SIO_000300: 7.069e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.181e0

MQRankSum
type: SiteQuality
SIO_000300: 4.54e-1

DP
type: SiteQuality
SIO_000300: 1.507634e6

QD
type: SiteQuality
SIO_000300: 1.427e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.84e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.29e-1

GenotypeQuality
all individuals: 717
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 826
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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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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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
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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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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1491
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 249
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11508
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8610
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 880
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6446
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16442
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66116
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.786651008025054e-5
allele num: 10218
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.58e-1

MQ
type: SiteQuality
SIO_000300: 5.963e1

VQSLOD
type: SiteQuality
SIO_000300: -5.2e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 1.083e1

DP
type: SiteQuality
SIO_000300: 1.519546e6

MQRankSum
type: SiteQuality
SIO_000300: 1.92e0

FS
type: SiteQuality
SIO_000300: 3.495e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.27e-1

GenotypeQuality
all individuals: 203
bin: 2.75e1
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
all individuals: 1383
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 880
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.792401096748923e-5
allele num: 10212
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8610
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 18
allele frequency: 2.722817208204756e-4
allele num: 66108
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 2
allele frequency: 3.10077519379845e-4
allele num: 6450
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16442
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.520185e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.63e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.69e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.89e0

QD
type: SiteQuality
SIO_000300: 1.198e1

MQRankSum
type: SiteQuality
SIO_000300: 2.4e-2

FS
type: SiteQuality
SIO_000300: 1.739e0

MQ
type: SiteQuality
SIO_000300: 5.962e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.243e0

GenotypeQuality
all individuals: 707
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 2

GenotypeQuality
all individuals: 48174
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 4.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16436
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.692628650904033e-5
allele num: 11504
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8596
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10200
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6462
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.515472979116782e-5
allele num: 65986
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.74e-1

QD
type: SiteQuality
SIO_000300: 1.767e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -3.79e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.99e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.9e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.27e-1

DP
type: SiteQuality
SIO_000300: 1.519025e6

GenotypeQuality
all individuals: 48132
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 100
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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
all individuals: 984
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
all individuals: 707
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variant carriers: 0

GenotypeQuality
all individuals: 179
bin: 5.25e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8590
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16426
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.550694739396881e-5
allele num: 65924
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6472
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11494
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10188
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.24e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.824e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.7e-2

QD
type: SiteQuality
SIO_000300: 2.127e1

FS
type: SiteQuality
SIO_000300: 1.896e0

DP
type: SiteQuality
SIO_000300: 1.519528e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.87e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.6e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

GenotypeQuality
all individuals: 247
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 19
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 188
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GenotypeQuality
all individuals: 189
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 207
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GenotypeQuality
all individuals: 132
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GenotypeQuality
all individuals: 30
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GenotypeQuality
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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: 1471
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variant carriers: 0

GenotypeQuality
all individuals: 623
bin: 9.75e1
variant carriers: 25

European (Non-Finnish)
type: Population
allele count: 24
allele frequency: 3.640997633351538e-4
allele num: 65916
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6466
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.089392278650591e-5
allele num: 16422
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10188
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -4.33e-1

MQ
type: SiteQuality
SIO_000300: 5.965e1

MQRankSum
type: SiteQuality
SIO_000300: 2.3e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.14e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.338e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.32e-1

FS
type: SiteQuality
SIO_000300: 1.89e0

QD
type: SiteQuality
SIO_000300: 1.223e1

DP
type: SiteQuality
SIO_000300: 1.519759e6

GenotypeQuality
all individuals: 181
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
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GenotypeQuality
all individuals: 1329
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GenotypeQuality
all individuals: 14
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variant carriers: 0

GenotypeQuality
all individuals: 26
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GenotypeQuality
all individuals: 1445
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variant carriers: 0

GenotypeQuality
all individuals: 8
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GenotypeQuality
all individuals: 273
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 885
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 4.75e1
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GenotypeQuality
all individuals: 206
bin: 3.25e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8584
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6466
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10186
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.517957436473481e-5
allele num: 65878
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16420
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.65e-1

QD
type: SiteQuality
SIO_000300: 1.248e1

MQRankSum
type: SiteQuality
SIO_000300: 2.48e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.3e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -5.7e-2

FS
type: SiteQuality
SIO_000300: 1.185e0

MQ
type: SiteQuality
SIO_000300: 5.975e1

DP
type: SiteQuality
SIO_000300: 1.52731e6

VQSLOD
type: SiteQuality
SIO_000300: 5.07e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.07e-1

GenotypeQuality
all individuals: 57
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1021
bin: 2.25e1
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GenotypeQuality
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GenotypeQuality
all individuals: 240
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GenotypeQuality
all individuals: 38
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GenotypeQuality
all individuals: 115
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GenotypeQuality
all individuals: 26
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GenotypeQuality
all individuals: 1329
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GenotypeQuality
all individuals: 14
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GenotypeQuality
all individuals: 273
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GenotypeQuality
all individuals: 139
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1445
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GenotypeQuality
all individuals: 885
bin: 9.75e1
variant carriers: 332

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16420
num of homozygotes: 0

Latino
type: Population
allele count: 16
allele frequency: 1.392272885485555e-3
allele num: 11492
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8584
num of homozygotes: 0

African
type: Population
allele count: 306
allele frequency: 3.004123306499117e-2
allele num: 10186
num of homozygotes: 2

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6466
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 13
allele frequency: 1.973344667415526e-4
allele num: 65878
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.138952164009112e-3
allele num: 878
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.07e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.7e-2

QD
type: SiteQuality
SIO_000300: 1.248e1

DP
type: SiteQuality
SIO_000300: 1.52731e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.3e-3

FS
type: SiteQuality
SIO_000300: 1.185e0

MQRankSum
type: SiteQuality
SIO_000300: 2.48e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.65e-1

MQ
type: SiteQuality
SIO_000300: 5.975e1

VQSLOD
type: SiteQuality
SIO_000300: 5.07e0

GenotypeQuality
all individuals: 76
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 271
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GenotypeQuality
all individuals: 52
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GenotypeQuality
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GenotypeQuality
all individuals: 216
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GenotypeQuality
all individuals: 25
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
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GenotypeQuality
all individuals: 1334
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GenotypeQuality
all individuals: 690
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GenotypeQuality
all individuals: 111
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GenotypeQuality
all individuals: 182
bin: 2.75e1
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GenotypeQuality
all individuals: 12
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 4.75e1
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GenotypeQuality
all individuals: 240
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1059
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5766
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 4
allele frequency: 4.659832246039142e-4
allele num: 8584
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.089392278650591e-5
allele num: 16422
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6470
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.51846452866861e-5
allele num: 65856
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.966181675186787e-4
allele num: 10172
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 1.517643e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.131e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.55e-1

FS
type: SiteQuality
SIO_000300: 2.687e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.35e-1

QD
type: SiteQuality
SIO_000300: 1.143e1

VQSLOD
type: SiteQuality
SIO_000300: 1.96e0

GenotypeQuality
all individuals: 694
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 7.5e0
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1452
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48297
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 221
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 272
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1338
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1098
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5762
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 240
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 574
bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16418
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6472
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.706251088281386e-5
allele num: 11486
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10174
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 880
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65844
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.436e0

VQSLOD
type: SiteQuality
SIO_000300: -8.421999999999999e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 7.39e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.44e0

MQ
type: SiteQuality
SIO_000300: 5.925e1

QD
type: SiteQuality
SIO_000300: 8.42e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.177e0

DP
type: SiteQuality
SIO_000300: 1.516743e6

GenotypeQuality
all individuals: 232
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1340
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 242
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 574
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 122
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1140
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 53
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48183
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 691
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 272
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1453
bin: 7.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 880
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65800
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.545595054095827e-4
allele num: 6470
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10168
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11486
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16414
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -7.41e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.26e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.06e-1

FS
type: SiteQuality
SIO_000300: 2.769e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -9.216e-1

DP
type: SiteQuality
SIO_000300: 1.51577e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.56e-1

QD
type: SiteQuality
SIO_000300: 6.47e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 123
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 163
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 47867
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1310
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1379
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 271
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 271
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 243
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 573
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 169
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5663
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65616
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.709284096847239e-5
allele num: 11482
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10132
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8570
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.104260774020266e-5
allele num: 16382
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.51194e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.47e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -8.84e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.65e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.11e0

QD
type: SiteQuality
SIO_000300: 1.034e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.57e0

GenotypeQuality
all individuals: 141
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 273
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 676
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 576
bin: 9.75e1
variant carriers: 2

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

GenotypeQuality
all individuals: 246
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1431
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1417
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47859
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 234
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5661
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1307
bin: 7.75e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 2
allele frequency: 1.221747098350641e-4
allele num: 16370
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65616
num of homozygotes: 0

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: 7.72e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.72e-1

FS
type: SiteQuality
SIO_000300: 3.623e0

QD
type: SiteQuality
SIO_000300: 1.079e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.43e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.36e-1

MQ
type: SiteQuality
SIO_000300: 5.945e1

DP
type: SiteQuality
SIO_000300: 1.510515e6

ClippingRankSum
type: SiteQuality
SIO_000300: -7.54e-1

GenotypeQuality
all individuals: 47859
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 234
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 246
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 271
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 273
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 1417
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5661
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1431
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 576
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 676
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 4.25e1
variant carriers: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.57205559619605e-5
allele num: 65616
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16370
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.623e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.43e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.54e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

DP
type: SiteQuality
SIO_000300: 1.510515e6

BaseQRankSum
type: SiteQuality
SIO_000300: -7.36e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.72e-1

QD
type: SiteQuality
SIO_000300: 1.079e1

MQ
type: SiteQuality
SIO_000300: 5.945e1

VQSLOD
type: SiteQuality
SIO_000300: 7.72e-1

GenotypeQuality
all individuals: 676
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 246
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 271
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 576
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1431
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47859
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5661
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 234
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1417
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 168
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 273
bin: 3.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.166316771635176e-4
allele num: 8574
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65616
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16370
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -7.36e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.72e-1

FS
type: SiteQuality
SIO_000300: 3.623e0

VQSLOD
type: SiteQuality
SIO_000300: 7.72e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.43e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

QD
type: SiteQuality
SIO_000300: 1.079e1

MQ
type: SiteQuality
SIO_000300: 5.945e1

DP
type: SiteQuality
SIO_000300: 1.510515e6

ClippingRankSum
type: SiteQuality
SIO_000300: -7.54e-1

GenotypeQuality
all individuals: 55
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 214
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 134
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 624
bin: 8.25e1
variant carriers: 3

GenotypeQuality
all individuals: 49
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 272
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 248
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 107
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 5.75e1
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GenotypeQuality
all individuals: 1462
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1235
bin: 7.75e1
variant carriers: 2

GenotypeQuality
all individuals: 47598
bin: 6.25e1
variant carriers: 3

GenotypeQuality
all individuals: 244
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1194
bin: 9.75e1
variant carriers: 724

Latino
type: Population
allele count: 29
allele frequency: 2.526132404181185e-3
allele num: 11480
num of homozygotes: 0

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

African
type: Population
allele count: 719
allele frequency: 7.106147459972327e-2
allele num: 10118
num of homozygotes: 30

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6446
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.141552511415525e-3
allele num: 876
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 14
allele frequency: 2.134081278009817e-4
allele num: 65602
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.833965032400049e-4
allele num: 16358
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.98e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.79e0

DP
type: SiteQuality
SIO_000300: 1.521136e6

FS
type: SiteQuality
SIO_000300: 5.89e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.47e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.21e-2

QD
type: SiteQuality
SIO_000300: 1.306e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.38e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.34e-1

GenotypeQuality
all individuals: 187
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 53
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1379
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 265
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1595
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 491
bin: 9.75e1
variant carriers: 13

GenotypeQuality
all individuals: 1231
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 626
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 194
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 251
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5621
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 215
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 13
allele frequency: 1.132798884628791e-3
allele num: 11476
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65540
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16346
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10078
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6442
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8566
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.610000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.175e1

MQ
type: SiteQuality
SIO_000300: 5.943e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.17e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.99e-1

DP
type: SiteQuality
SIO_000300: 1.505577e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

VQSLOD
type: SiteQuality
SIO_000300: 3.34e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.11e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 3.25e1
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 213
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GenotypeQuality
all individuals: 1216
bin: 7.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10066
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.133464180569185e-5
allele num: 16304
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8562
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65410
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6430
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.807e0

MQRankSum
type: SiteQuality
SIO_000300: -1.018e0

VQSLOD
type: SiteQuality
SIO_000300: -5.371e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.36e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.29e-1

MQ
type: SiteQuality
SIO_000300: 5.938e1

QD
type: SiteQuality
SIO_000300: 1.645e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-3

DP
type: SiteQuality
SIO_000300: 1.500472e6

GenotypeQuality
all individuals: 16
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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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bin: 9.75e1
variant carriers: 97

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16192
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.738203425375742e-5
allele num: 11444
num of homozygotes: 0

African
type: Population
allele count: 96
allele frequency: 9.609609609609609e-3
allele num: 9990
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.141552511415525e-3
allele num: 876
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8542
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.53477807109092e-5
allele num: 65156
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.196e0

QD
type: SiteQuality
SIO_000300: 1.117e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.1e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.368e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.57e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.000000000000001e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.64e0

DP
type: SiteQuality
SIO_000300: 1.488962e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

GenotypeQuality
all individuals: 206
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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
all individuals: 1133
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64390
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8470
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9766
num of homozygotes: 0

Latino
type: Population
allele count: 6
allele frequency: 5.274261603375527e-4
allele num: 11376
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15848
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.925e1

VQSLOD
type: SiteQuality
SIO_000300: 1.46e0

MQRankSum
type: SiteQuality
SIO_000300: 8.99e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.97e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-3

DP
type: SiteQuality
SIO_000300: 1.43969e6

FS
type: SiteQuality
SIO_000300: 1.32e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.16e0

QD
type: SiteQuality
SIO_000300: 1.171e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.37e-1

GenotypeQuality
all individuals: 39
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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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variant carriers: 7

GenotypeQuality
all individuals: 288
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GenotypeQuality
all individuals: 1133
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.309944472488642e-5
allele num: 15848
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11376
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64390
num of homozygotes: 0

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

East Asian
type: Population
allele count: 2
allele frequency: 2.361275088547816e-4
allele num: 8470
num of homozygotes: 0

African
type: Population
allele count: 4
allele frequency: 4.095842719639566e-4
allele num: 9766
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-3

FS
type: SiteQuality
SIO_000300: 1.32e0

QD
type: SiteQuality
SIO_000300: 1.171e1

MQRankSum
type: SiteQuality
SIO_000300: 8.99e-1

DP
type: SiteQuality
SIO_000300: 1.43969e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.16e0

VQSLOD
type: SiteQuality
SIO_000300: 1.46e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.37e-1

MQ
type: SiteQuality
SIO_000300: 5.925e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.97e-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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9730
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.802816901408451e-5
allele num: 11360
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6298
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.366863905325444e-4
allele num: 8450
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 854
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64214
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.332320162107397e-5
allele num: 15792
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.18e-1

QD
type: SiteQuality
SIO_000300: 1.133e1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.59e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.3e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 2.96e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.71e-1

DP
type: SiteQuality
SIO_000300: 1.430445e6

FS
type: SiteQuality
SIO_000300: 2.747e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.67e-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
all individuals: 45
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8404
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9624
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.262917266862904e-5
allele num: 63868
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15668
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11316
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.413e0

FS
type: SiteQuality
SIO_000300: 9.868e0

QD
type: SiteQuality
SIO_000300: 1.148e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.05e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.55e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.091e-1

MQ
type: SiteQuality
SIO_000300: 5.943e1

DP
type: SiteQuality
SIO_000300: 1.400683e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

MQRankSum
type: SiteQuality
SIO_000300: 2.63e-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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bin: 6.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9480
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8328
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11264
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15516
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.26151129052605e-4
allele num: 63416
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6224
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.35e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

QD
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 4.1e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.21e0

MQRankSum
type: SiteQuality
SIO_000300: 1.12e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 4.753e0

DP
type: SiteQuality
SIO_000300: 1.363583e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.570000000000001e-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
all individuals: 414
bin: 4.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63164
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15438
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6200
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.903133903133904e-5
allele num: 11232
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: 8272
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 8.43e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

DP
type: SiteQuality
SIO_000300: 1.336845e6

FS
type: SiteQuality
SIO_000300: 1.775e0

VQSLOD
type: SiteQuality
SIO_000300: -4.837e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.21e-1

MQRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 2.2e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 8.19e-1

GenotypeQuality
all individuals: 459
bin: 9.75e1
variant carriers: 10

GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
all individuals: 241
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GenotypeQuality
all individuals: 148
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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bin: 2.25e1
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GenotypeQuality
all individuals: 526
bin: 4.75e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11192
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.21921482565228e-4
allele num: 8202
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6170
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15344
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 834
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 9
allele frequency: 1.437102800753681e-4
allele num: 62626
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.951e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.05e0

FS
type: SiteQuality
SIO_000300: 2.357e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.94e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.57e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

MQRankSum
type: SiteQuality
SIO_000300: 2.11e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.18e-1

QD
type: SiteQuality
SIO_000300: 1.179e1

DP
type: SiteQuality
SIO_000300: 1.284639e6

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 2.75e1
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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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bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11094
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61276
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8060
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.133272892112421e-4
allele num: 8824
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14986
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6096
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.244e0

QD
type: SiteQuality
SIO_000300: 1.473e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.8e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.658e0

MQ
type: SiteQuality
SIO_000300: 5.817e1

VQSLOD
type: SiteQuality
SIO_000300: -1.387e0

MQRankSum
type: SiteQuality
SIO_000300: 4.61e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.1e-3

DP
type: SiteQuality
SIO_000300: 1.158511e6

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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bin: 9.75e1
variant carriers: 2

Latino
type: Population
allele count: 2
allele frequency: 1.805706031058144e-4
allele num: 11076
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14964
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6070
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61130
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8042
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8776
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 814
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.739e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.16e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.64e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.147517e6

MQRankSum
type: SiteQuality
SIO_000300: 1.42e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.7e-1

QD
type: SiteQuality
SIO_000300: 1.123e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.72e0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 814
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14896
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11042
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.285366975491162e-5
allele num: 60876
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6058
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8744
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7976
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.623e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.5e-3

FS
type: SiteQuality
SIO_000300: 6.974e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.110000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.508e0

VQSLOD
type: SiteQuality
SIO_000300: 5.07e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.929999999999999e-1

DP
type: SiteQuality
SIO_000300: 1.130125e6

ClippingRankSum
type: SiteQuality
SIO_000300: 9.07e-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
all individuals: 4744
bin: 2.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60564
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7942
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.765899864682003e-5
allele num: 14780
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6042
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11026
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.679999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 5.33e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.06e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.47e-1

QD
type: SiteQuality
SIO_000300: 1.09e1

DP
type: SiteQuality
SIO_000300: 1.111534e6

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.29e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14780
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.069472156720479e-5
allele num: 11026
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6042
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60564
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7942
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.33e-1

QD
type: SiteQuality
SIO_000300: 1.09e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 8.47e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.06e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.29e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.679999999999999e-1

DP
type: SiteQuality
SIO_000300: 1.111534e6

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.894649751792609e-5
allele num: 14504
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.191043353978085e-4
allele num: 8396
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.676389727083752e-5
allele num: 59652
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5962
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10914
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.9e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.75e0

MQRankSum
type: SiteQuality
SIO_000300: 2.01e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.86e0

VQSLOD
type: SiteQuality
SIO_000300: 7.26e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.792e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.082326e6

QD
type: SiteQuality
SIO_000300: 1.252e1

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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bin: 6.75e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.390635065947852e-5
allele num: 58986
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
allele num: 14312
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5886
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.26e-1

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 6.71e0

BaseQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -3.48e-1

MQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 2.822e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.3e-3

DP
type: SiteQuality
SIO_000300: 1.069114e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 5584
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10596
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.495632642874969e-4
allele num: 8014
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13870
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5730
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7424
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 57402
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 782
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.045859e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.8e-2

VQSLOD
type: SiteQuality
SIO_000300: -9.79e-2

QD
type: SiteQuality
SIO_000300: 9.49e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.340000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.172e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.776e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 2.027e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.2e-3

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 1

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

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9990
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.572277601333291e-5
allele num: 63602
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 788
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6170
num of homozygotes: 0

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 10832
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.911e1

DP
type: SiteQuality
SIO_000300: 1.50725e6

QD
type: SiteQuality
SIO_000300: 1.008e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.56e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.28e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.6e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.2e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-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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variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9996
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 63618
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8542
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6182
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.19793966151582e-5
allele num: 10872
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.457e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.513784e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.97e0

VQSLOD
type: SiteQuality
SIO_000300: -3.581e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 2.093e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.52e0

MQRankSum
type: SiteQuality
SIO_000300: 2.51e-1

QD
type: SiteQuality
SIO_000300: 1.788e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
all individuals: 1990
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variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8558
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10012
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.570055893989826e-5
allele num: 63692
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6190
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11338
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 788
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10906
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.51941e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.67e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 9.146000000000001e0

MQRankSum
type: SiteQuality
SIO_000300: -5.72e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.589e0

VQSLOD
type: SiteQuality
SIO_000300: 2.73e-1

QD
type: SiteQuality
SIO_000300: 1.473e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.07e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
all individuals: 998
bin: 5.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6184
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11338
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10934
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 788
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10026
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.570647735125966e-5
allele num: 63668
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.36e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.67e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.09e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.1e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.53e0

FS
type: SiteQuality
SIO_000300: 1.407e0

DP
type: SiteQuality
SIO_000300: 1.521574e6

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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bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11044
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6202
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11340
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.991238550378335e-4
allele num: 10044
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8566
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63746
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.09e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
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MQRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -4.27e-1

VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.01e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.535136e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 26

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10054
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.568381430363864e-5
allele num: 63760
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11346
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6198
num of homozygotes: 0

East Asian
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: 24
allele frequency: 2.159438545978046e-3
allele num: 11114
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BaseQRankSum
type: SiteQuality
SIO_000300: -1.34e-1

MQRankSum
type: SiteQuality
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FS
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MQ
type: SiteQuality
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VQSLOD
type: SiteQuality
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DP
type: SiteQuality
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QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 8.1e-3

ReadPosRankSum
type: SiteQuality
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ClippingRankSum
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SIO_000300: -2.31e-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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bin: 2.75e1
variant carriers: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 11278
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 8.802816901408451e-5
allele num: 11360
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6222
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 63874
num of homozygotes: 0

African
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allele frequency: 0.0e0
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Other
type: Population
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allele frequency: 0.0e0
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VQSLOD
type: SiteQuality
SIO_000300: 6.850000000000001e-1

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

European (Non-Finnish)
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allele count: 3
allele frequency: 4.69792351780513e-5
allele num: 63858
num of homozygotes: 0

Other
type: Population
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 11300
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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African
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East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11358
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
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ClippingRankSum
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DP
type: SiteQuality
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ReadPosRankSum
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MQ
type: SiteQuality
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BaseQRankSum
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VQSLOD
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QD
type: SiteQuality
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FS
type: SiteQuality
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1836
bin: 3.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.129106952875649e-5
allele num: 63916
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.704735376044568e-5
allele num: 11488
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.791981712678038e-5
allele num: 11374
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6236
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10088
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 6.117e0

DP
type: SiteQuality
SIO_000300: 1.566596e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.04e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.36e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.67e0

MQRankSum
type: SiteQuality
SIO_000300: 5.96e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.93e-1

QD
type: SiteQuality
SIO_000300: 1.203e1

GenotypeQuality
all individuals: 639
bin: 4.25e1
variant carriers: 7

GenotypeQuality
all individuals: 679
bin: 4.75e1
variant carriers: 2

GenotypeQuality
all individuals: 4349
bin: 7.75e1
variant carriers: 2

GenotypeQuality
all individuals: 430
bin: 7.5e0
variant carriers: 3

GenotypeQuality
all individuals: 1724
bin: 8.75e1
variant carriers: 2

GenotypeQuality
all individuals: 690
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 19341
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 7026
bin: 6.75e1
variant carriers: 5

GenotypeQuality
all individuals: 356
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3514
bin: 7.25e1
variant carriers: 4

GenotypeQuality
all individuals: 1604
bin: 3.25e1
variant carriers: 2

GenotypeQuality
all individuals: 6314
bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 295
bin: 1.25e1
variant carriers: 3

GenotypeQuality
all individuals: 2128
bin: 9.25e1
variant carriers: 1

Latino
type: Population
allele count: 3
allele frequency: 2.652989034311992e-4
allele num: 11308
num of homozygotes: 0

African
type: Population
allele count: 6
allele frequency: 6.091370558375635e-4
allele num: 9850
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11892
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 9
allele frequency: 1.603706343549537e-3
allele num: 5612
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 32
allele frequency: 5.107904482186183e-4
allele num: 62648
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.288659793814433e-3
allele num: 776
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8524
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.58e0

DP
type: SiteQuality
SIO_000300: 1.597094e6

MQRankSum
type: SiteQuality
SIO_000300: 1.98e-1

FS
type: SiteQuality
SIO_000300: 3.68294e2

VQSLOD
type: SiteQuality
SIO_000300: -6.263e2

ClippingRankSum
type: SiteQuality
SIO_000300: 2.89e0

QD
type: SiteQuality
SIO_000300: 4.4e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.0e-3

MQ
type: SiteQuality
SIO_000300: 5.959e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.853e0

GenotypeQuality
all individuals: 317
bin: 4.25e1
variant carriers: 12

GenotypeQuality
all individuals: 50
bin: 1.75e1
variant carriers: 3

GenotypeQuality
all individuals: 700
bin: 3.75e1
variant carriers: 15

GenotypeQuality
all individuals: 114
bin: 7.5e0
variant carriers: 2

GenotypeQuality
all individuals: 20042
bin: 6.25e1
variant carriers: 15

GenotypeQuality
all individuals: 7174
bin: 6.75e1
variant carriers: 17

GenotypeQuality
all individuals: 4274
bin: 7.75e1
variant carriers: 35

GenotypeQuality
all individuals: 426
bin: 5.25e1
variant carriers: 15

GenotypeQuality
all individuals: 50
bin: 2.5e0
variant carriers: 2

GenotypeQuality
all individuals: 751
bin: 2.75e1
variant carriers: 7

GenotypeQuality
all individuals: 414
bin: 4.75e1
variant carriers: 18

GenotypeQuality
all individuals: 299
bin: 5.75e1
variant carriers: 13

GenotypeQuality
all individuals: 944
bin: 3.25e1
variant carriers: 14

GenotypeQuality
all individuals: 3517
bin: 7.25e1
variant carriers: 12

East Asian
type: Population
allele count: 11
allele frequency: 1.277584204413473e-3
allele num: 8610
num of homozygotes: 0

Latino
type: Population
allele count: 242
allele frequency: 2.116124519062609e-2
allele num: 11436
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 4717
allele frequency: 7.245775729646697e-2
allele num: 65100
num of homozygotes: 182

European (Finnish)
type: Population
allele count: 346
allele frequency: 5.419799498746867e-2
allele num: 6384
num of homozygotes: 11

African
type: Population
allele count: 112
allele frequency: 1.092256680319875e-2
allele num: 10254
num of homozygotes: 0

Other
type: Population
allele count: 41
allele frequency: 4.789719626168224e-2
allele num: 856
num of homozygotes: 1

South Asian
type: Population
allele count: 892
allele frequency: 6.628027938772477e-2
allele num: 13458
num of homozygotes: 34

QD
type: SiteQuality
SIO_000300: 1.306e1

MQRankSum
type: SiteQuality
SIO_000300: 6.7e-2

DP
type: SiteQuality
SIO_000300: 1.7098e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.39e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.56e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.819e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.12e-1

FS
type: SiteQuality
SIO_000300: 1.818e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.71e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 2700
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4784
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 57
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 588
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 927
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21673
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 515
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3925
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2312
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 718
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1868
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 705
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 318
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7329
bin: 9.75e1
variant carriers: 2

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

South Asian
type: Population
allele count: 1
allele frequency: 7.312079555425563e-5
allele num: 13676
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.531815814466469e-5
allele num: 65282
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10272
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 5.01e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.83e-1

QD
type: SiteQuality
SIO_000300: 9.529999999999999e0

VQSLOD
type: SiteQuality
SIO_000300: 2.65e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.79e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.79e-1

DP
type: SiteQuality
SIO_000300: 1.696324e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4