http://identifiers.org/exac.variant/2-71789062-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71789062
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 71789062
    reference: chr 2
allele count: 1
allele frequency: 8.967001434720229e-6
allele num: 111520
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000407046
  ensembl transcript: ENST00000413539
  gene symbol: DYSF
  hgvsc: ENST00000413539.2:c.2436C>A
  hgvsp: ENST00000413539.2:c.2436C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000258104
  ensembl transcript: ENST00000258104
  gene symbol: DYSF
  hgvsc: ENST00000258104.3:c.2343C>A
  hgvsp: ENST00000258104.3:c.2343C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386285
  ensembl transcript: ENST00000409744
  gene symbol: DYSF
  hgvsc: ENST00000409744.1:c.2304C>A
  hgvsp: ENST00000409744.1:c.2304C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386881
  ensembl transcript: ENST00000410020
  gene symbol: DYSF
  hgvsc: ENST00000410020.3:c.2397C>A
  hgvsp: ENST00000410020.3:c.2397C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000387137
  ensembl transcript: ENST00000409762
  gene symbol: DYSF
  hgvsc: ENST00000409762.1:c.2394C>A
  hgvsp: ENST00000409762.1:c.2394C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386683
  ensembl transcript: ENST00000409651
  gene symbol: DYSF
  hgvsc: ENST00000409651.1:c.2439C>A
  hgvsp: ENST00000409651.1:c.2439C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386617
  ensembl transcript: ENST00000410041
  gene symbol: DYSF
  hgvsc: ENST00000410041.1:c.2397C>A
  hgvsp: ENST00000410041.1:c.2397C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000377678
  ensembl transcript: ENST00000394120
  gene symbol: DYSF
  hgvsc: ENST00000394120.2:c.2346C>A
  hgvsp: ENST00000394120.2:c.2346C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000398305
  ensembl transcript: ENST00000429174
  gene symbol: DYSF
  hgvsc: ENST00000429174.2:c.2343C>A
  hgvsp: ENST00000429174.2:c.2343C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386547
  ensembl transcript: ENST00000409582
  gene symbol: DYSF
  hgvsc: ENST00000409582.3:c.2394C>A
  hgvsp: ENST00000409582.3:c.2394C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386512
  ensembl transcript: ENST00000409366
  gene symbol: DYSF
  hgvsc: ENST00000409366.1:c.2346C>A
  hgvsp: ENST00000409366.1:c.2346C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4733
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1096
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7079
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22402
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12997
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1657
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4956
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala799Ala
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP

2-71789065-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71789065
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 71789065
    reference: chr 2
allele count: 2
allele frequency: 1.823652776511352e-5
allele num: 109670
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000258104
  ensembl transcript: ENST00000258104
  gene symbol: DYSF
  hgvsc: ENST00000258104.3:c.2346G>A
  hgvsp: ENST00000258104.3:c.2346G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386881
  ensembl transcript: ENST00000410020
  gene symbol: DYSF
  hgvsc: ENST00000410020.3:c.2400G>A
  hgvsp: ENST00000410020.3:c.2400G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000387137
  ensembl transcript: ENST00000409762
  gene symbol: DYSF
  hgvsc: ENST00000409762.1:c.2397G>A
  hgvsp: ENST00000409762.1:c.2397G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386547
  ensembl transcript: ENST00000409582
  gene symbol: DYSF
  hgvsc: ENST00000409582.3:c.2397G>A
  hgvsp: ENST00000409582.3:c.2397G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000398305
  ensembl transcript: ENST00000429174
  gene symbol: DYSF
  hgvsc: ENST00000429174.2:c.2346G>A
  hgvsp: ENST00000429174.2:c.2346G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000377678
  ensembl transcript: ENST00000394120
  gene symbol: DYSF
  hgvsc: ENST00000394120.2:c.2349G>A
  hgvsp: ENST00000394120.2:c.2349G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386512
  ensembl transcript: ENST00000409366
  gene symbol: DYSF
  hgvsc: ENST00000409366.1:c.2349G>A
  hgvsp: ENST00000409366.1:c.2349G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386683
  ensembl transcript: ENST00000409651
  gene symbol: DYSF
  hgvsc: ENST00000409651.1:c.2442G>A
  hgvsp: ENST00000409651.1:c.2442G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386617
  ensembl transcript: ENST00000410041
  gene symbol: DYSF
  hgvsc: ENST00000410041.1:c.2400G>A
  hgvsp: ENST00000410041.1:c.2400G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386285
  ensembl transcript: ENST00000409744
  gene symbol: DYSF
  hgvsc: ENST00000409744.1:c.2307G>A
  hgvsp: ENST00000409744.1:c.2307G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000407046
  ensembl transcript: ENST00000413539
  gene symbol: DYSF
  hgvsc: ENST00000413539.2:c.2439G>A
  hgvsp: ENST00000413539.2:c.2439G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2002
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8698
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1096
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12271
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20655
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5593
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4588
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu800Leu
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQ

2-71789067-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71789067
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 71789067
    reference: chr 2
allele count: 13
allele frequency: 1.190890602957073e-4
allele num: 109162
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386617
  ensembl transcript: ENST00000410041
  gene symbol: DYSF
  hgvsc: ENST00000410041.1:c.2402C>T
  hgvsp: ENSP00000386617.1:p.Ala801Val
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000398305
  ensembl transcript: ENST00000429174
  gene symbol: DYSF
  hgvsc: ENST00000429174.2:c.2348C>T
  hgvsp: ENSP00000398305.2:p.Ala783Val
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000407046
  ensembl transcript: ENST00000413539
  gene symbol: DYSF
  hgvsc: ENST00000413539.2:c.2441C>T
  hgvsp: ENSP00000407046.2:p.Ala814Val
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000258104
  ensembl transcript: ENST00000258104
  gene symbol: DYSF
  hgvsc: ENST00000258104.3:c.2348C>T
  hgvsp: ENSP00000258104.3:p.Ala783Val
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000377678
  ensembl transcript: ENST00000394120
  gene symbol: DYSF
  hgvsc: ENST00000394120.2:c.2351C>T
  hgvsp: ENSP00000377678.2:p.Ala784Val
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386881
  ensembl transcript: ENST00000410020
  gene symbol: DYSF
  hgvsc: ENST00000410020.3:c.2402C>T
  hgvsp: ENSP00000386881.3:p.Ala801Val
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386285
  ensembl transcript: ENST00000409744
  gene symbol: DYSF
  hgvsc: ENST00000409744.1:c.2309C>T
  hgvsp: ENSP00000386285.1:p.Ala770Val
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386547
  ensembl transcript: ENST00000409582
  gene symbol: DYSF
  hgvsc: ENST00000409582.3:c.2399C>T
  hgvsp: ENSP00000386547.3:p.Ala800Val
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386683
  ensembl transcript: ENST00000409651
  gene symbol: DYSF
  hgvsc: ENST00000409651.1:c.2444C>T
  hgvsp: ENSP00000386683.1:p.Ala815Val
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000387137
  ensembl transcript: ENST00000409762
  gene symbol: DYSF
  hgvsc: ENST00000409762.1:c.2399C>T
  hgvsp: ENSP00000387137.1:p.Ala800Val
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386512
  ensembl transcript: ENST00000409366
  gene symbol: DYSF
  hgvsc: ENST00000409366.1:c.2351C>T
  hgvsp: ENSP00000386512.1:p.Ala784Val
  variant of: http://identifiers.org/hgnc/3097
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5818
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12293
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 20164
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9082
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2057
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4394
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1096
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala801Val
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: BaseQRankSum

2-71789076-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71789076
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 71789076
    reference: chr 2
allele count: 1
allele frequency: 9.588830929733047e-6
allele num: 104288
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386881
  ensembl transcript: ENST00000410020
  gene symbol: DYSF
  hgvsc: ENST00000410020.3:c.2409+2T>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386617
  ensembl transcript: ENST00000410041
  gene symbol: DYSF
  hgvsc: ENST00000410041.1:c.2409+2T>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386512
  ensembl transcript: ENST00000409366
  gene symbol: DYSF
  hgvsc: ENST00000409366.1:c.2358+2T>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386683
  ensembl transcript: ENST00000409651
  gene symbol: DYSF
  hgvsc: ENST00000409651.1:c.2451+2T>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000407046
  ensembl transcript: ENST00000413539
  gene symbol: DYSF
  hgvsc: ENST00000413539.2:c.2448+2T>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000258104
  ensembl transcript: ENST00000258104
  gene symbol: DYSF
  hgvsc: ENST00000258104.3:c.2355+2T>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000398305
  ensembl transcript: ENST00000429174
  gene symbol: DYSF
  hgvsc: ENST00000429174.2:c.2355+2T>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000387137
  ensembl transcript: ENST00000409762
  gene symbol: DYSF
  hgvsc: ENST00000409762.1:c.2406+2T>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000377678
  ensembl transcript: ENST00000394120
  gene symbol: DYSF
  hgvsc: ENST00000394120.2:c.2358+2T>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386547
  ensembl transcript: ENST00000409582
  gene symbol: DYSF
  hgvsc: ENST00000409582.3:c.2406+2T>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386285
  ensembl transcript: ENST00000409744
  gene symbol: DYSF
  hgvsc: ENST00000409744.1:c.2316+2T>A
  variant of: http://identifiers.org/hgnc/3097
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7972
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10285
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3405
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15617
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13346
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3112
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1096
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 741
  bin: 5.25e1
  variant carriers: 0
hgvs: c.2409+2T>A
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: Latino
reference allele: T
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff

2-71789088-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71789088
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 71789088
    reference: chr 2
allele count: 65
allele frequency: 6.590955181504766e-4
allele num: 98620
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386285
  ensembl transcript: ENST00000409744
  gene symbol: DYSF
  hgvsc: ENST00000409744.1:c.2316+14G>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000407046
  ensembl transcript: ENST00000413539
  gene symbol: DYSF
  hgvsc: ENST00000413539.2:c.2448+14G>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386881
  ensembl transcript: ENST00000410020
  gene symbol: DYSF
  hgvsc: ENST00000410020.3:c.2409+14G>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000398305
  ensembl transcript: ENST00000429174
  gene symbol: DYSF
  hgvsc: ENST00000429174.2:c.2355+14G>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386617
  ensembl transcript: ENST00000410041
  gene symbol: DYSF
  hgvsc: ENST00000410041.1:c.2409+14G>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000377678
  ensembl transcript: ENST00000394120
  gene symbol: DYSF
  hgvsc: ENST00000394120.2:c.2358+14G>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000387137
  ensembl transcript: ENST00000409762
  gene symbol: DYSF
  hgvsc: ENST00000409762.1:c.2406+14G>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386512
  ensembl transcript: ENST00000409366
  gene symbol: DYSF
  hgvsc: ENST00000409366.1:c.2358+14G>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000258104
  ensembl transcript: ENST00000258104
  gene symbol: DYSF
  hgvsc: ENST00000258104.3:c.2355+14G>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386547
  ensembl transcript: ENST00000409582
  gene symbol: DYSF
  hgvsc: ENST00000409582.3:c.2406+14G>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386683
  ensembl transcript: ENST00000409651
  gene symbol: DYSF
  hgvsc: ENST00000409651.1:c.2451+14G>A
  variant of: http://identifiers.org/hgnc/3097
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19314
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10223
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10260
  bin: 2.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1096
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4202
  bin: 1.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 7066
  bin: 2.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2279
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 952
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: Latino
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum

2-71789090-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71789090
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 71789090
    reference: chr 2
allele count: 2
allele frequency: 2.048844451729225e-5
allele num: 97616
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386683
  ensembl transcript: ENST00000409651
  gene symbol: DYSF
  hgvsc: ENST00000409651.1:c.2451+16G>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000377678
  ensembl transcript: ENST00000394120
  gene symbol: DYSF
  hgvsc: ENST00000394120.2:c.2358+16G>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386547
  ensembl transcript: ENST00000409582
  gene symbol: DYSF
  hgvsc: ENST00000409582.3:c.2406+16G>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000258104
  ensembl transcript: ENST00000258104
  gene symbol: DYSF
  hgvsc: ENST00000258104.3:c.2355+16G>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386285
  ensembl transcript: ENST00000409744
  gene symbol: DYSF
  hgvsc: ENST00000409744.1:c.2316+16G>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386512
  ensembl transcript: ENST00000409366
  gene symbol: DYSF
  hgvsc: ENST00000409366.1:c.2358+16G>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386881
  ensembl transcript: ENST00000410020
  gene symbol: DYSF
  hgvsc: ENST00000410020.3:c.2409+16G>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386617
  ensembl transcript: ENST00000410041
  gene symbol: DYSF
  hgvsc: ENST00000410041.1:c.2409+16G>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000407046
  ensembl transcript: ENST00000413539
  gene symbol: DYSF
  hgvsc: ENST00000413539.2:c.2448+16G>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000387137
  ensembl transcript: ENST00000409762
  gene symbol: DYSF
  hgvsc: ENST00000409762.1:c.2406+16G>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000398305
  ensembl transcript: ENST00000429174
  gene symbol: DYSF
  hgvsc: ENST00000429174.2:c.2355+16G>T
  variant of: http://identifiers.org/hgnc/3097
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20489
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2118
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1096
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9260
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10586
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4443
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6317
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 955
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 346
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum

2-71789091-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71789091
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 71789091
    reference: chr 2
allele count: 1
allele frequency: 1.029526829469176e-5
allele num: 97132
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386617
  ensembl transcript: ENST00000410041
  gene symbol: DYSF
  hgvsc: ENST00000410041.1:c.2409+17G>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000398305
  ensembl transcript: ENST00000429174
  gene symbol: DYSF
  hgvsc: ENST00000429174.2:c.2355+17G>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386285
  ensembl transcript: ENST00000409744
  gene symbol: DYSF
  hgvsc: ENST00000409744.1:c.2316+17G>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386683
  ensembl transcript: ENST00000409651
  gene symbol: DYSF
  hgvsc: ENST00000409651.1:c.2451+17G>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000258104
  ensembl transcript: ENST00000258104
  gene symbol: DYSF
  hgvsc: ENST00000258104.3:c.2355+17G>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000377678
  ensembl transcript: ENST00000394120
  gene symbol: DYSF
  hgvsc: ENST00000394120.2:c.2358+17G>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000387137
  ensembl transcript: ENST00000409762
  gene symbol: DYSF
  hgvsc: ENST00000409762.1:c.2406+17G>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386881
  ensembl transcript: ENST00000410020
  gene symbol: DYSF
  hgvsc: ENST00000410020.3:c.2409+17G>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000407046
  ensembl transcript: ENST00000413539
  gene symbol: DYSF
  hgvsc: ENST00000413539.2:c.2448+17G>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386547
  ensembl transcript: ENST00000409582
  gene symbol: DYSF
  hgvsc: ENST00000409582.3:c.2406+17G>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386512
  ensembl transcript: ENST00000409366
  gene symbol: DYSF
  hgvsc: ENST00000409366.1:c.2358+17G>T
  variant of: http://identifiers.org/hgnc/3097
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21065
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10752
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5935
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2016
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1055
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4636
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8713
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1096
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: Other
population: South Asian
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum

2-71789095-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71789095
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 71789095
    reference: chr 2
allele count: 4
allele frequency: 4.3122035360069e-5
allele num: 92760
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000258104
  ensembl transcript: ENST00000258104
  gene symbol: DYSF
  hgvsc: ENST00000258104.3:c.2355+21C>G
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000377678
  ensembl transcript: ENST00000394120
  gene symbol: DYSF
  hgvsc: ENST00000394120.2:c.2358+21C>G
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000398305
  ensembl transcript: ENST00000429174
  gene symbol: DYSF
  hgvsc: ENST00000429174.2:c.2355+21C>G
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000407046
  ensembl transcript: ENST00000413539
  gene symbol: DYSF
  hgvsc: ENST00000413539.2:c.2448+21C>G
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386512
  ensembl transcript: ENST00000409366
  gene symbol: DYSF
  hgvsc: ENST00000409366.1:c.2358+21C>G
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386285
  ensembl transcript: ENST00000409744
  gene symbol: DYSF
  hgvsc: ENST00000409744.1:c.2316+21C>G
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000387137
  ensembl transcript: ENST00000409762
  gene symbol: DYSF
  hgvsc: ENST00000409762.1:c.2406+21C>G
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386617
  ensembl transcript: ENST00000410041
  gene symbol: DYSF
  hgvsc: ENST00000410041.1:c.2409+21C>G
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386683
  ensembl transcript: ENST00000409651
  gene symbol: DYSF
  hgvsc: ENST00000409651.1:c.2451+21C>G
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386881
  ensembl transcript: ENST00000410020
  gene symbol: DYSF
  hgvsc: ENST00000410020.3:c.2409+21C>G
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386547
  ensembl transcript: ENST00000409582
  gene symbol: DYSF
  hgvsc: ENST00000409582.3:c.2406+21C>G
  variant of: http://identifiers.org/hgnc/3097
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1687
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6061
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3983
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5430
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11931
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23744
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1096
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1454
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2783
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

2-71789096-TTTC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71789096
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 71789093
    reference: chr 2
allele count: 2
allele frequency: 2.156752792994867e-5
allele num: 92732
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000387137
  ensembl transcript: ENST00000409762
  gene symbol: DYSF
  hgvsc: ENST00000409762.1:c.2406+30_2406+32delTCT
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386617
  ensembl transcript: ENST00000410041
  gene symbol: DYSF
  hgvsc: ENST00000410041.1:c.2409+30_2409+32delTCT
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386683
  ensembl transcript: ENST00000409651
  gene symbol: DYSF
  hgvsc: ENST00000409651.1:c.2451+30_2451+32delTCT
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386285
  ensembl transcript: ENST00000409744
  gene symbol: DYSF
  hgvsc: ENST00000409744.1:c.2316+30_2316+32delTCT
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000398305
  ensembl transcript: ENST00000429174
  gene symbol: DYSF
  hgvsc: ENST00000429174.2:c.2355+30_2355+32delTCT
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386881
  ensembl transcript: ENST00000410020
  gene symbol: DYSF
  hgvsc: ENST00000410020.3:c.2409+30_2409+32delTCT
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386547
  ensembl transcript: ENST00000409582
  gene symbol: DYSF
  hgvsc: ENST00000409582.3:c.2406+30_2406+32delTCT
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000258104
  ensembl transcript: ENST00000258104
  gene symbol: DYSF
  hgvsc: ENST00000258104.3:c.2355+30_2355+32delTCT
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000377678
  ensembl transcript: ENST00000394120
  gene symbol: DYSF
  hgvsc: ENST00000394120.2:c.2358+30_2358+32delTCT
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386512
  ensembl transcript: ENST00000409366
  gene symbol: DYSF
  hgvsc: ENST00000409366.1:c.2358+30_2358+32delTCT
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000407046
  ensembl transcript: ENST00000413539
  gene symbol: DYSF
  hgvsc: ENST00000413539.2:c.2448+30_2448+32delTCT
  variant of: http://identifiers.org/hgnc/3097
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4003
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1432
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23738
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12069
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6059
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5305
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1096
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5882
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Other
population: South Asian
population: Latino
reference allele: TTTC
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff

2-71789101-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71789101
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 71789101
    reference: chr 2
allele count: 1
allele frequency: 1.113164280784558e-5
allele num: 89834
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386285
  ensembl transcript: ENST00000409744
  gene symbol: DYSF
  hgvsc: ENST00000409744.1:c.2316+27T>C
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000387137
  ensembl transcript: ENST00000409762
  gene symbol: DYSF
  hgvsc: ENST00000409762.1:c.2406+27T>C
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000377678
  ensembl transcript: ENST00000394120
  gene symbol: DYSF
  hgvsc: ENST00000394120.2:c.2358+27T>C
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386547
  ensembl transcript: ENST00000409582
  gene symbol: DYSF
  hgvsc: ENST00000409582.3:c.2406+27T>C
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386512
  ensembl transcript: ENST00000409366
  gene symbol: DYSF
  hgvsc: ENST00000409366.1:c.2358+27T>C
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000258104
  ensembl transcript: ENST00000258104
  gene symbol: DYSF
  hgvsc: ENST00000258104.3:c.2355+27T>C
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000407046
  ensembl transcript: ENST00000413539
  gene symbol: DYSF
  hgvsc: ENST00000413539.2:c.2448+27T>C
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386683
  ensembl transcript: ENST00000409651
  gene symbol: DYSF
  hgvsc: ENST00000409651.1:c.2451+27T>C
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386617
  ensembl transcript: ENST00000410041
  gene symbol: DYSF
  hgvsc: ENST00000410041.1:c.2409+27T>C
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386881
  ensembl transcript: ENST00000410020
  gene symbol: DYSF
  hgvsc: ENST00000410020.3:c.2409+27T>C
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000398305
  ensembl transcript: ENST00000429174
  gene symbol: DYSF
  hgvsc: ENST00000429174.2:c.2355+27T>C
  variant of: http://identifiers.org/hgnc/3097
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12942
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1096
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24240
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2360
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3003
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6728
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1032
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4008
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 813
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: QD
site quality: DP

2-71789104-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71789104
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 71789104
    reference: chr 2
allele count: 42
allele frequency: 4.766119697691836e-4
allele num: 88122
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000258104
  ensembl transcript: ENST00000258104
  gene symbol: DYSF
  hgvsc: ENST00000258104.3:c.2355+30T>G
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386617
  ensembl transcript: ENST00000410041
  gene symbol: DYSF
  hgvsc: ENST00000410041.1:c.2409+30T>G
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000398305
  ensembl transcript: ENST00000429174
  gene symbol: DYSF
  hgvsc: ENST00000429174.2:c.2355+30T>G
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386547
  ensembl transcript: ENST00000409582
  gene symbol: DYSF
  hgvsc: ENST00000409582.3:c.2406+30T>G
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386683
  ensembl transcript: ENST00000409651
  gene symbol: DYSF
  hgvsc: ENST00000409651.1:c.2451+30T>G
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386285
  ensembl transcript: ENST00000409744
  gene symbol: DYSF
  hgvsc: ENST00000409744.1:c.2316+30T>G
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000377678
  ensembl transcript: ENST00000394120
  gene symbol: DYSF
  hgvsc: ENST00000394120.2:c.2358+30T>G
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000407046
  ensembl transcript: ENST00000413539
  gene symbol: DYSF
  hgvsc: ENST00000413539.2:c.2448+30T>G
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000387137
  ensembl transcript: ENST00000409762
  gene symbol: DYSF
  hgvsc: ENST00000409762.1:c.2406+30T>G
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386881
  ensembl transcript: ENST00000410020
  gene symbol: DYSF
  hgvsc: ENST00000410020.3:c.2409+30T>G
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386512
  ensembl transcript: ENST00000409366
  gene symbol: DYSF
  hgvsc: ENST00000409366.1:c.2358+30T>G
  variant of: http://identifiers.org/hgnc/3097
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2590
  bin: 2.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7404
  bin: 1.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2638
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13518
  bin: 7.5e0
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1096
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23990
  bin: 1.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3286
  bin: 2.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 250
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: MQ

2-71789109-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71789109
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 71789109
    reference: chr 2
allele count: 3
allele frequency: 3.568369968598344e-5
allele num: 84072
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386881
  ensembl transcript: ENST00000410020
  gene symbol: DYSF
  hgvsc: ENST00000410020.3:c.2409+35T>G
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000377678
  ensembl transcript: ENST00000394120
  gene symbol: DYSF
  hgvsc: ENST00000394120.2:c.2358+35T>G
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000407046
  ensembl transcript: ENST00000413539
  gene symbol: DYSF
  hgvsc: ENST00000413539.2:c.2448+35T>G
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386512
  ensembl transcript: ENST00000409366
  gene symbol: DYSF
  hgvsc: ENST00000409366.1:c.2358+35T>G
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386617
  ensembl transcript: ENST00000410041
  gene symbol: DYSF
  hgvsc: ENST00000410041.1:c.2409+35T>G
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000398305
  ensembl transcript: ENST00000429174
  gene symbol: DYSF
  hgvsc: ENST00000429174.2:c.2355+35T>G
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386547
  ensembl transcript: ENST00000409582
  gene symbol: DYSF
  hgvsc: ENST00000409582.3:c.2406+35T>G
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386683
  ensembl transcript: ENST00000409651
  gene symbol: DYSF
  hgvsc: ENST00000409651.1:c.2451+35T>G
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000387137
  ensembl transcript: ENST00000409762
  gene symbol: DYSF
  hgvsc: ENST00000409762.1:c.2406+35T>G
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386285
  ensembl transcript: ENST00000409744
  gene symbol: DYSF
  hgvsc: ENST00000409744.1:c.2316+35T>G
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000258104
  ensembl transcript: ENST00000258104
  gene symbol: DYSF
  hgvsc: ENST00000258104.3:c.2355+35T>G
  variant of: http://identifiers.org/hgnc/3097
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2231
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23023
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2278
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1096
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3043
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14933
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8166
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3696
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: FS

2-71789110-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71789110
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 71789110
    reference: chr 2
allele count: 3
allele frequency: 3.659250585480094e-5
allele num: 81984
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386512
  ensembl transcript: ENST00000409366
  gene symbol: DYSF
  hgvsc: ENST00000409366.1:c.2358+36C>G
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386547
  ensembl transcript: ENST00000409582
  gene symbol: DYSF
  hgvsc: ENST00000409582.3:c.2406+36C>G
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386881
  ensembl transcript: ENST00000410020
  gene symbol: DYSF
  hgvsc: ENST00000410020.3:c.2409+36C>G
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000387137
  ensembl transcript: ENST00000409762
  gene symbol: DYSF
  hgvsc: ENST00000409762.1:c.2406+36C>G
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000258104
  ensembl transcript: ENST00000258104
  gene symbol: DYSF
  hgvsc: ENST00000258104.3:c.2355+36C>G
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000377678
  ensembl transcript: ENST00000394120
  gene symbol: DYSF
  hgvsc: ENST00000394120.2:c.2358+36C>G
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386285
  ensembl transcript: ENST00000409744
  gene symbol: DYSF
  hgvsc: ENST00000409744.1:c.2316+36C>G
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386617
  ensembl transcript: ENST00000410041
  gene symbol: DYSF
  hgvsc: ENST00000410041.1:c.2409+36C>G
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000407046
  ensembl transcript: ENST00000413539
  gene symbol: DYSF
  hgvsc: ENST00000413539.2:c.2448+36C>G
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000398305
  ensembl transcript: ENST00000429174
  gene symbol: DYSF
  hgvsc: ENST00000429174.2:c.2355+36C>G
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386683
  ensembl transcript: ENST00000409651
  gene symbol: DYSF
  hgvsc: ENST00000409651.1:c.2451+36C>G
  variant of: http://identifiers.org/hgnc/3097
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22292
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8670
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2089
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3163
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1851
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15661
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1096
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1105
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: African
population: South Asian
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD

2-71789113-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71789113
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 71789113
    reference: chr 2
allele count: 1
allele frequency: 1.235422020162087e-5
allele num: 80944
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386683
  ensembl transcript: ENST00000409651
  gene symbol: DYSF
  hgvsc: ENST00000409651.1:c.2451+39C>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386881
  ensembl transcript: ENST00000410020
  gene symbol: DYSF
  hgvsc: ENST00000410020.3:c.2409+39C>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000407046
  ensembl transcript: ENST00000413539
  gene symbol: DYSF
  hgvsc: ENST00000413539.2:c.2448+39C>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000377678
  ensembl transcript: ENST00000394120
  gene symbol: DYSF
  hgvsc: ENST00000394120.2:c.2358+39C>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000387137
  ensembl transcript: ENST00000409762
  gene symbol: DYSF
  hgvsc: ENST00000409762.1:c.2406+39C>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386547
  ensembl transcript: ENST00000409582
  gene symbol: DYSF
  hgvsc: ENST00000409582.3:c.2406+39C>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000258104
  ensembl transcript: ENST00000258104
  gene symbol: DYSF
  hgvsc: ENST00000258104.3:c.2355+39C>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386285
  ensembl transcript: ENST00000409744
  gene symbol: DYSF
  hgvsc: ENST00000409744.1:c.2316+39C>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386617
  ensembl transcript: ENST00000410041
  gene symbol: DYSF
  hgvsc: ENST00000410041.1:c.2409+39C>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000398305
  ensembl transcript: ENST00000429174
  gene symbol: DYSF
  hgvsc: ENST00000429174.2:c.2355+39C>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386512
  ensembl transcript: ENST00000409366
  gene symbol: DYSF
  hgvsc: ENST00000409366.1:c.2358+39C>T
  variant of: http://identifiers.org/hgnc/3097
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3218
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21900
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8592
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16272
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1096
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2127
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1669
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff

2-71789114-TG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71789114
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 71789113
    reference: chr 2
allele count: 1
allele frequency: 1.243595483261205e-5
allele num: 80412
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386512
  ensembl transcript: ENST00000409366
  gene symbol: DYSF
  hgvsc: ENST00000409366.1:c.2358+41delG
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386617
  ensembl transcript: ENST00000410041
  gene symbol: DYSF
  hgvsc: ENST00000410041.1:c.2409+41delG
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386683
  ensembl transcript: ENST00000409651
  gene symbol: DYSF
  hgvsc: ENST00000409651.1:c.2451+41delG
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386547
  ensembl transcript: ENST00000409582
  gene symbol: DYSF
  hgvsc: ENST00000409582.3:c.2406+41delG
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000377678
  ensembl transcript: ENST00000394120
  gene symbol: DYSF
  hgvsc: ENST00000394120.2:c.2358+41delG
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386881
  ensembl transcript: ENST00000410020
  gene symbol: DYSF
  hgvsc: ENST00000410020.3:c.2409+41delG
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000258104
  ensembl transcript: ENST00000258104
  gene symbol: DYSF
  hgvsc: ENST00000258104.3:c.2355+41delG
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000398305
  ensembl transcript: ENST00000429174
  gene symbol: DYSF
  hgvsc: ENST00000429174.2:c.2355+41delG
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000407046
  ensembl transcript: ENST00000413539
  gene symbol: DYSF
  hgvsc: ENST00000413539.2:c.2448+41delG
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000387137
  ensembl transcript: ENST00000409762
  gene symbol: DYSF
  hgvsc: ENST00000409762.1:c.2406+41delG
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386285
  ensembl transcript: ENST00000409744
  gene symbol: DYSF
  hgvsc: ENST00000409744.1:c.2316+41delG
  variant of: http://identifiers.org/hgnc/3097
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8637
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16599
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21637
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2105
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3245
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1096
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1574
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2522
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: TG
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD

2-71789123-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71789123
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 71789123
    reference: chr 2
allele count: 1
allele frequency: 1.357920751744928e-5
allele num: 73642
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386285
  ensembl transcript: ENST00000409744
  gene symbol: DYSF
  hgvsc: ENST00000409744.1:c.2316+49G>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000258104
  ensembl transcript: ENST00000258104
  gene symbol: DYSF
  hgvsc: ENST00000258104.3:c.2355+49G>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386683
  ensembl transcript: ENST00000409651
  gene symbol: DYSF
  hgvsc: ENST00000409651.1:c.2451+49G>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386881
  ensembl transcript: ENST00000410020
  gene symbol: DYSF
  hgvsc: ENST00000410020.3:c.2409+49G>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000387137
  ensembl transcript: ENST00000409762
  gene symbol: DYSF
  hgvsc: ENST00000409762.1:c.2406+49G>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386512
  ensembl transcript: ENST00000409366
  gene symbol: DYSF
  hgvsc: ENST00000409366.1:c.2358+49G>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000398305
  ensembl transcript: ENST00000429174
  gene symbol: DYSF
  hgvsc: ENST00000429174.2:c.2355+49G>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000407046
  ensembl transcript: ENST00000413539
  gene symbol: DYSF
  hgvsc: ENST00000413539.2:c.2448+49G>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386547
  ensembl transcript: ENST00000409582
  gene symbol: DYSF
  hgvsc: ENST00000409582.3:c.2406+49G>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000377678
  ensembl transcript: ENST00000394120
  gene symbol: DYSF
  hgvsc: ENST00000394120.2:c.2358+49G>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386617
  ensembl transcript: ENST00000410041
  gene symbol: DYSF
  hgvsc: ENST00000410041.1:c.2409+49G>A
  variant of: http://identifiers.org/hgnc/3097
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2599
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19162
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3349
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1096
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19526
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8270
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff

2-71791137-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71791137
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 71791137
    reference: chr 2
allele count: 3
allele frequency: 2.549979600163199e-5
allele num: 117648
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386617
  ensembl transcript: ENST00000410041
  gene symbol: DYSF
  hgvsc: ENST00000410041.1:c.2410-51C>G
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000258104
  ensembl transcript: ENST00000258104
  gene symbol: DYSF
  hgvsc: ENST00000258104.3:c.2356-51C>G
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000407046
  ensembl transcript: ENST00000413539
  gene symbol: DYSF
  hgvsc: ENST00000413539.2:c.2449-51C>G
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386285
  ensembl transcript: ENST00000409744
  gene symbol: DYSF
  hgvsc: ENST00000409744.1:c.2317-51C>G
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000387137
  ensembl transcript: ENST00000409762
  gene symbol: DYSF
  hgvsc: ENST00000409762.1:c.2407-51C>G
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000398305
  ensembl transcript: ENST00000429174
  gene symbol: DYSF
  hgvsc: ENST00000429174.2:c.2356-51C>G
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386512
  ensembl transcript: ENST00000409366
  gene symbol: DYSF
  hgvsc: ENST00000409366.1:c.2359-51C>G
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386547
  ensembl transcript: ENST00000409582
  gene symbol: DYSF
  hgvsc: ENST00000409582.3:c.2407-51C>G
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386683
  ensembl transcript: ENST00000409651
  gene symbol: DYSF
  hgvsc: ENST00000409651.1:c.2452-51C>G
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386881
  ensembl transcript: ENST00000410020
  gene symbol: DYSF
  hgvsc: ENST00000410020.3:c.2410-51C>G
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000377678
  ensembl transcript: ENST00000394120
  gene symbol: DYSF
  hgvsc: ENST00000394120.2:c.2359-51C>G
  variant of: http://identifiers.org/hgnc/3097
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2484
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2138
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1152
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4719
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1368
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5527
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8826
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1921
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12930
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3299
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13601
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 251
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum

2-71791137-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71791137
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 71791137
    reference: chr 2
allele count: 258
allele frequency: 2.192982456140351e-3
allele num: 117648
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386617
  ensembl transcript: ENST00000410041
  gene symbol: DYSF
  hgvsc: ENST00000410041.1:c.2410-51C>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386285
  ensembl transcript: ENST00000409744
  gene symbol: DYSF
  hgvsc: ENST00000409744.1:c.2317-51C>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000387137
  ensembl transcript: ENST00000409762
  gene symbol: DYSF
  hgvsc: ENST00000409762.1:c.2407-51C>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000398305
  ensembl transcript: ENST00000429174
  gene symbol: DYSF
  hgvsc: ENST00000429174.2:c.2356-51C>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000377678
  ensembl transcript: ENST00000394120
  gene symbol: DYSF
  hgvsc: ENST00000394120.2:c.2359-51C>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000258104
  ensembl transcript: ENST00000258104
  gene symbol: DYSF
  hgvsc: ENST00000258104.3:c.2356-51C>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386512
  ensembl transcript: ENST00000409366
  gene symbol: DYSF
  hgvsc: ENST00000409366.1:c.2359-51C>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386547
  ensembl transcript: ENST00000409582
  gene symbol: DYSF
  hgvsc: ENST00000409582.3:c.2407-51C>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386683
  ensembl transcript: ENST00000409651
  gene symbol: DYSF
  hgvsc: ENST00000409651.1:c.2452-51C>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386881
  ensembl transcript: ENST00000410020
  gene symbol: DYSF
  hgvsc: ENST00000410020.3:c.2410-51C>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000407046
  ensembl transcript: ENST00000413539
  gene symbol: DYSF
  hgvsc: ENST00000413539.2:c.2449-51C>T
  variant of: http://identifiers.org/hgnc/3097
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13601
  bin: 3.25e1
  variant carriers: 44
genotype depth: GenotypeDepth
  all individuals: 12930
  bin: 2.75e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1152
  bin: 7.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 4719
  bin: 2.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 5527
  bin: 4.25e1
  variant carriers: 40
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2484
  bin: 1.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1921
  bin: 1.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1368
  bin: 5.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3299
  bin: 4.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 2138
  bin: 5.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 8826
  bin: 3.75e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 6.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 251
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 1
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: DP

2-71791138-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71791138
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 71791138
    reference: chr 2
allele count: 8
allele frequency: 6.746158905773026e-5
allele num: 118586
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000398305
  ensembl transcript: ENST00000429174
  gene symbol: DYSF
  hgvsc: ENST00000429174.2:c.2356-50G>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386512
  ensembl transcript: ENST00000409366
  gene symbol: DYSF
  hgvsc: ENST00000409366.1:c.2359-50G>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386285
  ensembl transcript: ENST00000409744
  gene symbol: DYSF
  hgvsc: ENST00000409744.1:c.2317-50G>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386547
  ensembl transcript: ENST00000409582
  gene symbol: DYSF
  hgvsc: ENST00000409582.3:c.2407-50G>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386881
  ensembl transcript: ENST00000410020
  gene symbol: DYSF
  hgvsc: ENST00000410020.3:c.2410-50G>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000377678
  ensembl transcript: ENST00000394120
  gene symbol: DYSF
  hgvsc: ENST00000394120.2:c.2359-50G>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000407046
  ensembl transcript: ENST00000413539
  gene symbol: DYSF
  hgvsc: ENST00000413539.2:c.2449-50G>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000258104
  ensembl transcript: ENST00000258104
  gene symbol: DYSF
  hgvsc: ENST00000258104.3:c.2356-50G>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000387137
  ensembl transcript: ENST00000409762
  gene symbol: DYSF
  hgvsc: ENST00000409762.1:c.2407-50G>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386617
  ensembl transcript: ENST00000410041
  gene symbol: DYSF
  hgvsc: ENST00000410041.1:c.2410-50G>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386683
  ensembl transcript: ENST00000409651
  gene symbol: DYSF
  hgvsc: ENST00000409651.1:c.2452-50G>A
  variant of: http://identifiers.org/hgnc/3097
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1878
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4997
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13150
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1985
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1366
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1092
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13739
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2136
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 932
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8859
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5510
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3287
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 638
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum

2-71791142-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71791142
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 71791142
    reference: chr 2
allele count: 1
allele frequency: 8.409155888931868e-6
allele num: 118918
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000377678
  ensembl transcript: ENST00000394120
  gene symbol: DYSF
  hgvsc: ENST00000394120.2:c.2359-46G>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386683
  ensembl transcript: ENST00000409651
  gene symbol: DYSF
  hgvsc: ENST00000409651.1:c.2452-46G>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000407046
  ensembl transcript: ENST00000413539
  gene symbol: DYSF
  hgvsc: ENST00000413539.2:c.2449-46G>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000398305
  ensembl transcript: ENST00000429174
  gene symbol: DYSF
  hgvsc: ENST00000429174.2:c.2356-46G>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386881
  ensembl transcript: ENST00000410020
  gene symbol: DYSF
  hgvsc: ENST00000410020.3:c.2410-46G>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000258104
  ensembl transcript: ENST00000258104
  gene symbol: DYSF
  hgvsc: ENST00000258104.3:c.2356-46G>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000387137
  ensembl transcript: ENST00000409762
  gene symbol: DYSF
  hgvsc: ENST00000409762.1:c.2407-46G>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386512
  ensembl transcript: ENST00000409366
  gene symbol: DYSF
  hgvsc: ENST00000409366.1:c.2359-46G>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386285
  ensembl transcript: ENST00000409744
  gene symbol: DYSF
  hgvsc: ENST00000409744.1:c.2317-46G>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386617
  ensembl transcript: ENST00000410041
  gene symbol: DYSF
  hgvsc: ENST00000410041.1:c.2410-46G>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386547
  ensembl transcript: ENST00000409582
  gene symbol: DYSF
  hgvsc: ENST00000409582.3:c.2407-46G>A
  variant of: http://identifiers.org/hgnc/3097
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3291
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1616
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13831
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2134
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1363
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5855
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1077
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8858
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 931
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13440
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5497
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1092
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: African
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

2-71791146-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71791146
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 71791146
    reference: chr 2
allele count: 1
allele frequency: 8.387854386847844e-6
allele num: 119220
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386617
  ensembl transcript: ENST00000410041
  gene symbol: DYSF
  hgvsc: ENST00000410041.1:c.2410-42G>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386285
  ensembl transcript: ENST00000409744
  gene symbol: DYSF
  hgvsc: ENST00000409744.1:c.2317-42G>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000398305
  ensembl transcript: ENST00000429174
  gene symbol: DYSF
  hgvsc: ENST00000429174.2:c.2356-42G>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386881
  ensembl transcript: ENST00000410020
  gene symbol: DYSF
  hgvsc: ENST00000410020.3:c.2410-42G>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386683
  ensembl transcript: ENST00000409651
  gene symbol: DYSF
  hgvsc: ENST00000409651.1:c.2452-42G>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000258104
  ensembl transcript: ENST00000258104
  gene symbol: DYSF
  hgvsc: ENST00000258104.3:c.2356-42G>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000407046
  ensembl transcript: ENST00000413539
  gene symbol: DYSF
  hgvsc: ENST00000413539.2:c.2449-42G>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000387137
  ensembl transcript: ENST00000409762
  gene symbol: DYSF
  hgvsc: ENST00000409762.1:c.2407-42G>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000377678
  ensembl transcript: ENST00000394120
  gene symbol: DYSF
  hgvsc: ENST00000394120.2:c.2359-42G>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386547
  ensembl transcript: ENST00000409582
  gene symbol: DYSF
  hgvsc: ENST00000409582.3:c.2407-42G>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386512
  ensembl transcript: ENST00000409366
  gene symbol: DYSF
  hgvsc: ENST00000409366.1:c.2359-42G>T
  variant of: http://identifiers.org/hgnc/3097
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1277
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3291
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5501
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8876
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2133
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13975
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1362
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13630
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 954
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6498
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
population: African
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff

2-71791147-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71791147
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 71791147
    reference: chr 2
allele count: 1
allele frequency: 8.379139294811638e-6
allele num: 119344
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386617
  ensembl transcript: ENST00000410041
  gene symbol: DYSF
  hgvsc: ENST00000410041.1:c.2410-41G>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000258104
  ensembl transcript: ENST00000258104
  gene symbol: DYSF
  hgvsc: ENST00000258104.3:c.2356-41G>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000377678
  ensembl transcript: ENST00000394120
  gene symbol: DYSF
  hgvsc: ENST00000394120.2:c.2359-41G>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000387137
  ensembl transcript: ENST00000409762
  gene symbol: DYSF
  hgvsc: ENST00000409762.1:c.2407-41G>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000398305
  ensembl transcript: ENST00000429174
  gene symbol: DYSF
  hgvsc: ENST00000429174.2:c.2356-41G>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000407046
  ensembl transcript: ENST00000413539
  gene symbol: DYSF
  hgvsc: ENST00000413539.2:c.2449-41G>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386683
  ensembl transcript: ENST00000409651
  gene symbol: DYSF
  hgvsc: ENST00000409651.1:c.2452-41G>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386881
  ensembl transcript: ENST00000410020
  gene symbol: DYSF
  hgvsc: ENST00000410020.3:c.2410-41G>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386547
  ensembl transcript: ENST00000409582
  gene symbol: DYSF
  hgvsc: ENST00000409582.3:c.2407-41G>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386285
  ensembl transcript: ENST00000409744
  gene symbol: DYSF
  hgvsc: ENST00000409744.1:c.2317-41G>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386512
  ensembl transcript: ENST00000409366
  gene symbol: DYSF
  hgvsc: ENST00000409366.1:c.2359-41G>T
  variant of: http://identifiers.org/hgnc/3097
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 932
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1362
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2133
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6628
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3291
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1207
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13988
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5498
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13657
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8876
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4280
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum

2-71791149-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71791149
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 71791149
    reference: chr 2
allele count: 1
allele frequency: 8.36946150884652e-6
allele num: 119482
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386683
  ensembl transcript: ENST00000409651
  gene symbol: DYSF
  hgvsc: ENST00000409651.1:c.2452-39G>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000387137
  ensembl transcript: ENST00000409762
  gene symbol: DYSF
  hgvsc: ENST00000409762.1:c.2407-39G>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386285
  ensembl transcript: ENST00000409744
  gene symbol: DYSF
  hgvsc: ENST00000409744.1:c.2317-39G>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000377678
  ensembl transcript: ENST00000394120
  gene symbol: DYSF
  hgvsc: ENST00000394120.2:c.2359-39G>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386512
  ensembl transcript: ENST00000409366
  gene symbol: DYSF
  hgvsc: ENST00000409366.1:c.2359-39G>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000407046
  ensembl transcript: ENST00000413539
  gene symbol: DYSF
  hgvsc: ENST00000413539.2:c.2449-39G>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386547
  ensembl transcript: ENST00000409582
  gene symbol: DYSF
  hgvsc: ENST00000409582.3:c.2407-39G>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386881
  ensembl transcript: ENST00000410020
  gene symbol: DYSF
  hgvsc: ENST00000410020.3:c.2410-39G>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000258104
  ensembl transcript: ENST00000258104
  gene symbol: DYSF
  hgvsc: ENST00000258104.3:c.2356-39G>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000398305
  ensembl transcript: ENST00000429174
  gene symbol: DYSF
  hgvsc: ENST00000429174.2:c.2356-39G>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386617
  ensembl transcript: ENST00000410041
  gene symbol: DYSF
  hgvsc: ENST00000410041.1:c.2410-39G>A
  variant of: http://identifiers.org/hgnc/3097
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13825
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6636
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 932
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5517
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8902
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14025
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3293
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2132
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1362
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: MQ

2-71791151-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71791151
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 71791151
    reference: chr 2
allele count: 112
allele frequency: 9.365331549460658e-4
allele num: 119590
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000398305
  ensembl transcript: ENST00000429174
  gene symbol: DYSF
  hgvsc: ENST00000429174.2:c.2356-37G>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386683
  ensembl transcript: ENST00000409651
  gene symbol: DYSF
  hgvsc: ENST00000409651.1:c.2452-37G>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386617
  ensembl transcript: ENST00000410041
  gene symbol: DYSF
  hgvsc: ENST00000410041.1:c.2410-37G>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386512
  ensembl transcript: ENST00000409366
  gene symbol: DYSF
  hgvsc: ENST00000409366.1:c.2359-37G>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386285
  ensembl transcript: ENST00000409744
  gene symbol: DYSF
  hgvsc: ENST00000409744.1:c.2317-37G>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000377678
  ensembl transcript: ENST00000394120
  gene symbol: DYSF
  hgvsc: ENST00000394120.2:c.2359-37G>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386881
  ensembl transcript: ENST00000410020
  gene symbol: DYSF
  hgvsc: ENST00000410020.3:c.2410-37G>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000258104
  ensembl transcript: ENST00000258104
  gene symbol: DYSF
  hgvsc: ENST00000258104.3:c.2356-37G>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000407046
  ensembl transcript: ENST00000413539
  gene symbol: DYSF
  hgvsc: ENST00000413539.2:c.2449-37G>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386547
  ensembl transcript: ENST00000409582
  gene symbol: DYSF
  hgvsc: ENST00000409582.3:c.2407-37G>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000387137
  ensembl transcript: ENST00000409762
  gene symbol: DYSF
  hgvsc: ENST00000409762.1:c.2407-37G>A
  variant of: http://identifiers.org/hgnc/3097
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13859
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3294
  bin: 4.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 2140
  bin: 5.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 935
  bin: 6.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6751
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 980
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8900
  bin: 3.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 14055
  bin: 3.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1371
  bin: 5.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 5526
  bin: 4.25e1
  variant carriers: 19
genotype quality: GenotypeQuality
  all individuals: 7394
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

2-71791152-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71791152
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 71791152
    reference: chr 2
allele count: 1
allele frequency: 8.358548287333457e-6
allele num: 119638
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000398305
  ensembl transcript: ENST00000429174
  gene symbol: DYSF
  hgvsc: ENST00000429174.2:c.2356-36T>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386512
  ensembl transcript: ENST00000409366
  gene symbol: DYSF
  hgvsc: ENST00000409366.1:c.2359-36T>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000387137
  ensembl transcript: ENST00000409762
  gene symbol: DYSF
  hgvsc: ENST00000409762.1:c.2407-36T>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386881
  ensembl transcript: ENST00000410020
  gene symbol: DYSF
  hgvsc: ENST00000410020.3:c.2410-36T>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000258104
  ensembl transcript: ENST00000258104
  gene symbol: DYSF
  hgvsc: ENST00000258104.3:c.2356-36T>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000377678
  ensembl transcript: ENST00000394120
  gene symbol: DYSF
  hgvsc: ENST00000394120.2:c.2359-36T>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386285
  ensembl transcript: ENST00000409744
  gene symbol: DYSF
  hgvsc: ENST00000409744.1:c.2317-36T>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000407046
  ensembl transcript: ENST00000413539
  gene symbol: DYSF
  hgvsc: ENST00000413539.2:c.2449-36T>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386683
  ensembl transcript: ENST00000409651
  gene symbol: DYSF
  hgvsc: ENST00000409651.1:c.2452-36T>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386547
  ensembl transcript: ENST00000409582
  gene symbol: DYSF
  hgvsc: ENST00000409582.3:c.2407-36T>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386617
  ensembl transcript: ENST00000410041
  gene symbol: DYSF
  hgvsc: ENST00000410041.1:c.2410-36T>A
  variant of: http://identifiers.org/hgnc/3097
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1363
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13889
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6823
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 929
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2131
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3295
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5516
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8907
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14090
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7410
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: MQ
site quality: ReadPosRankSum

2-71791162-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71791162
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 71791162
    reference: chr 2
allele count: 1
allele frequency: 8.303854649328218e-6
allele num: 120426
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000258104
  ensembl transcript: ENST00000258104
  gene symbol: DYSF
  hgvsc: ENST00000258104.3:c.2356-26C>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000377678
  ensembl transcript: ENST00000394120
  gene symbol: DYSF
  hgvsc: ENST00000394120.2:c.2359-26C>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386512
  ensembl transcript: ENST00000409366
  gene symbol: DYSF
  hgvsc: ENST00000409366.1:c.2359-26C>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386881
  ensembl transcript: ENST00000410020
  gene symbol: DYSF
  hgvsc: ENST00000410020.3:c.2410-26C>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000387137
  ensembl transcript: ENST00000409762
  gene symbol: DYSF
  hgvsc: ENST00000409762.1:c.2407-26C>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000407046
  ensembl transcript: ENST00000413539
  gene symbol: DYSF
  hgvsc: ENST00000413539.2:c.2449-26C>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386683
  ensembl transcript: ENST00000409651
  gene symbol: DYSF
  hgvsc: ENST00000409651.1:c.2452-26C>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386547
  ensembl transcript: ENST00000409582
  gene symbol: DYSF
  hgvsc: ENST00000409582.3:c.2407-26C>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000398305
  ensembl transcript: ENST00000429174
  gene symbol: DYSF
  hgvsc: ENST00000429174.2:c.2356-26C>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386285
  ensembl transcript: ENST00000409744
  gene symbol: DYSF
  hgvsc: ENST00000409744.1:c.2317-26C>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386617
  ensembl transcript: ENST00000410041
  gene symbol: DYSF
  hgvsc: ENST00000410041.1:c.2410-26C>T
  variant of: http://identifiers.org/hgnc/3097
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 5531
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14278
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14271
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1364
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7246
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8931
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3303
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2131
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 570
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP

http://identifiers.org/exac.variant/2-71791163-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71791163
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 71791163
    reference: chr 2
allele count: 2
allele frequency: 1.660743348722888e-5
allele num: 120428
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000258104
  ensembl transcript: ENST00000258104
  gene symbol: DYSF
  hgvsc: ENST00000258104.3:c.2356-25A>C
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386617
  ensembl transcript: ENST00000410041
  gene symbol: DYSF
  hgvsc: ENST00000410041.1:c.2410-25A>C
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386881
  ensembl transcript: ENST00000410020
  gene symbol: DYSF
  hgvsc: ENST00000410020.3:c.2410-25A>C
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000377678
  ensembl transcript: ENST00000394120
  gene symbol: DYSF
  hgvsc: ENST00000394120.2:c.2359-25A>C
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000407046
  ensembl transcript: ENST00000413539
  gene symbol: DYSF
  hgvsc: ENST00000413539.2:c.2449-25A>C
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386683
  ensembl transcript: ENST00000409651
  gene symbol: DYSF
  hgvsc: ENST00000409651.1:c.2452-25A>C
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000398305
  ensembl transcript: ENST00000429174
  gene symbol: DYSF
  hgvsc: ENST00000429174.2:c.2356-25A>C
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386512
  ensembl transcript: ENST00000409366
  gene symbol: DYSF
  hgvsc: ENST00000409366.1:c.2359-25A>C
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000387137
  ensembl transcript: ENST00000409762
  gene symbol: DYSF
  hgvsc: ENST00000409762.1:c.2407-25A>C
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386547
  ensembl transcript: ENST00000409582
  gene symbol: DYSF
  hgvsc: ENST00000409582.3:c.2407-25A>C
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386285
  ensembl transcript: ENST00000409744
  gene symbol: DYSF
  hgvsc: ENST00000409744.1:c.2317-25A>C
  variant of: http://identifiers.org/hgnc/3097
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5531
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7206
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8939
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3305
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14307
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14335
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1364
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2134
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5079
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum

2-71791164-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71791164
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 71791164
    reference: chr 2
allele count: 5
allele frequency: 4.14586822772425e-5
allele num: 120602
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386617
  ensembl transcript: ENST00000410041
  gene symbol: DYSF
  hgvsc: ENST00000410041.1:c.2410-24C>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000398305
  ensembl transcript: ENST00000429174
  gene symbol: DYSF
  hgvsc: ENST00000429174.2:c.2356-24C>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000407046
  ensembl transcript: ENST00000413539
  gene symbol: DYSF
  hgvsc: ENST00000413539.2:c.2449-24C>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000387137
  ensembl transcript: ENST00000409762
  gene symbol: DYSF
  hgvsc: ENST00000409762.1:c.2407-24C>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386547
  ensembl transcript: ENST00000409582
  gene symbol: DYSF
  hgvsc: ENST00000409582.3:c.2407-24C>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386285
  ensembl transcript: ENST00000409744
  gene symbol: DYSF
  hgvsc: ENST00000409744.1:c.2317-24C>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386881
  ensembl transcript: ENST00000410020
  gene symbol: DYSF
  hgvsc: ENST00000410020.3:c.2410-24C>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386683
  ensembl transcript: ENST00000409651
  gene symbol: DYSF
  hgvsc: ENST00000409651.1:c.2452-24C>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386512
  ensembl transcript: ENST00000409366
  gene symbol: DYSF
  hgvsc: ENST00000409366.1:c.2359-24C>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000258104
  ensembl transcript: ENST00000258104
  gene symbol: DYSF
  hgvsc: ENST00000258104.3:c.2356-24C>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000377678
  ensembl transcript: ENST00000394120
  gene symbol: DYSF
  hgvsc: ENST00000394120.2:c.2359-24C>T
  variant of: http://identifiers.org/hgnc/3097
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14380
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3302
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14330
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5532
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7290
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2136
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8942
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1366
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18824
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum

2-71791165-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71791165
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 71791165
    reference: chr 2
allele count: 3
allele frequency: 2.485954357877989e-5
allele num: 120678
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000398305
  ensembl transcript: ENST00000429174
  gene symbol: DYSF
  hgvsc: ENST00000429174.2:c.2356-23C>G
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386683
  ensembl transcript: ENST00000409651
  gene symbol: DYSF
  hgvsc: ENST00000409651.1:c.2452-23C>G
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000407046
  ensembl transcript: ENST00000413539
  gene symbol: DYSF
  hgvsc: ENST00000413539.2:c.2449-23C>G
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386512
  ensembl transcript: ENST00000409366
  gene symbol: DYSF
  hgvsc: ENST00000409366.1:c.2359-23C>G
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386617
  ensembl transcript: ENST00000410041
  gene symbol: DYSF
  hgvsc: ENST00000410041.1:c.2410-23C>G
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386547
  ensembl transcript: ENST00000409582
  gene symbol: DYSF
  hgvsc: ENST00000409582.3:c.2407-23C>G
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000258104
  ensembl transcript: ENST00000258104
  gene symbol: DYSF
  hgvsc: ENST00000258104.3:c.2356-23C>G
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000387137
  ensembl transcript: ENST00000409762
  gene symbol: DYSF
  hgvsc: ENST00000409762.1:c.2407-23C>G
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386881
  ensembl transcript: ENST00000410020
  gene symbol: DYSF
  hgvsc: ENST00000410020.3:c.2410-23C>G
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386285
  ensembl transcript: ENST00000409744
  gene symbol: DYSF
  hgvsc: ENST00000409744.1:c.2317-23C>G
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000377678
  ensembl transcript: ENST00000394120
  gene symbol: DYSF
  hgvsc: ENST00000394120.2:c.2359-23C>G
  variant of: http://identifiers.org/hgnc/3097
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7333
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8945
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5539
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1365
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2133
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14339
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14399
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3302
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 14642
  bin: 9.75e1
  variant carriers: 3
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP

2-71791167-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71791167
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 71791167
    reference: chr 2
allele count: 1
allele frequency: 8.280613427842734e-6
allele num: 120764
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386285
  ensembl transcript: ENST00000409744
  gene symbol: DYSF
  hgvsc: ENST00000409744.1:c.2317-21C>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000407046
  ensembl transcript: ENST00000413539
  gene symbol: DYSF
  hgvsc: ENST00000413539.2:c.2449-21C>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386512
  ensembl transcript: ENST00000409366
  gene symbol: DYSF
  hgvsc: ENST00000409366.1:c.2359-21C>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000258104
  ensembl transcript: ENST00000258104
  gene symbol: DYSF
  hgvsc: ENST00000258104.3:c.2356-21C>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000377678
  ensembl transcript: ENST00000394120
  gene symbol: DYSF
  hgvsc: ENST00000394120.2:c.2359-21C>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000398305
  ensembl transcript: ENST00000429174
  gene symbol: DYSF
  hgvsc: ENST00000429174.2:c.2356-21C>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386617
  ensembl transcript: ENST00000410041
  gene symbol: DYSF
  hgvsc: ENST00000410041.1:c.2410-21C>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000387137
  ensembl transcript: ENST00000409762
  gene symbol: DYSF
  hgvsc: ENST00000409762.1:c.2407-21C>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386881
  ensembl transcript: ENST00000410020
  gene symbol: DYSF
  hgvsc: ENST00000410020.3:c.2410-21C>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386683
  ensembl transcript: ENST00000409651
  gene symbol: DYSF
  hgvsc: ENST00000409651.1:c.2452-21C>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386547
  ensembl transcript: ENST00000409582
  gene symbol: DYSF
  hgvsc: ENST00000409582.3:c.2407-21C>T
  variant of: http://identifiers.org/hgnc/3097
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3304
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2131
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1365
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7336
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14373
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5542
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8947
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14461
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD

2-71791168-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71791168
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 71791168
    reference: chr 2
allele count: 2
allele frequency: 1.65576620581174e-5
allele num: 120790
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386617
  ensembl transcript: ENST00000410041
  gene symbol: DYSF
  hgvsc: ENST00000410041.1:c.2410-20G>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000258104
  ensembl transcript: ENST00000258104
  gene symbol: DYSF
  hgvsc: ENST00000258104.3:c.2356-20G>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000387137
  ensembl transcript: ENST00000409762
  gene symbol: DYSF
  hgvsc: ENST00000409762.1:c.2407-20G>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000377678
  ensembl transcript: ENST00000394120
  gene symbol: DYSF
  hgvsc: ENST00000394120.2:c.2359-20G>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386512
  ensembl transcript: ENST00000409366
  gene symbol: DYSF
  hgvsc: ENST00000409366.1:c.2359-20G>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000398305
  ensembl transcript: ENST00000429174
  gene symbol: DYSF
  hgvsc: ENST00000429174.2:c.2356-20G>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386683
  ensembl transcript: ENST00000409651
  gene symbol: DYSF
  hgvsc: ENST00000409651.1:c.2452-20G>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386881
  ensembl transcript: ENST00000410020
  gene symbol: DYSF
  hgvsc: ENST00000410020.3:c.2410-20G>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000407046
  ensembl transcript: ENST00000413539
  gene symbol: DYSF
  hgvsc: ENST00000413539.2:c.2449-20G>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386547
  ensembl transcript: ENST00000409582
  gene symbol: DYSF
  hgvsc: ENST00000409582.3:c.2407-20G>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386285
  ensembl transcript: ENST00000409744
  gene symbol: DYSF
  hgvsc: ENST00000409744.1:c.2317-20G>A
  variant of: http://identifiers.org/hgnc/3097
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7333
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1367
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3309
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14507
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14388
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5540
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8947
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2132
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14643
  bin: 9.75e1
  variant carriers: 2
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: QD

http://identifiers.org/exac.variant/2-71791173-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71791173
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 71791173
    reference: chr 2
allele count: 2
allele frequency: 1.652455548945733e-5
allele num: 121032
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000387137
  ensembl transcript: ENST00000409762
  gene symbol: DYSF
  hgvsc: ENST00000409762.1:c.2407-15C>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386547
  ensembl transcript: ENST00000409582
  gene symbol: DYSF
  hgvsc: ENST00000409582.3:c.2407-15C>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386683
  ensembl transcript: ENST00000409651
  gene symbol: DYSF
  hgvsc: ENST00000409651.1:c.2452-15C>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386881
  ensembl transcript: ENST00000410020
  gene symbol: DYSF
  hgvsc: ENST00000410020.3:c.2410-15C>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386617
  ensembl transcript: ENST00000410041
  gene symbol: DYSF
  hgvsc: ENST00000410041.1:c.2410-15C>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000398305
  ensembl transcript: ENST00000429174
  gene symbol: DYSF
  hgvsc: ENST00000429174.2:c.2356-15C>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000377678
  ensembl transcript: ENST00000394120
  gene symbol: DYSF
  hgvsc: ENST00000394120.2:c.2359-15C>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386285
  ensembl transcript: ENST00000409744
  gene symbol: DYSF
  hgvsc: ENST00000409744.1:c.2317-15C>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000258104
  ensembl transcript: ENST00000258104
  gene symbol: DYSF
  hgvsc: ENST00000258104.3:c.2356-15C>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000407046
  ensembl transcript: ENST00000413539
  gene symbol: DYSF
  hgvsc: ENST00000413539.2:c.2449-15C>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386512
  ensembl transcript: ENST00000409366
  gene symbol: DYSF
  hgvsc: ENST00000409366.1:c.2359-15C>A
  variant of: http://identifiers.org/hgnc/3097
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14423
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5541
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14617
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1365
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2132
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3306
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8953
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7422
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 929
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3700
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: Other
population: European (Finnish)
population: South Asian
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum

http://identifiers.org/exac.variant/2-71791176-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71791176
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 71791176
    reference: chr 2
allele count: 1
allele frequency: 8.257911078813503e-6
allele num: 121096
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000387137
  ensembl transcript: ENST00000409762
  gene symbol: DYSF
  hgvsc: ENST00000409762.1:c.2407-12C>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000258104
  ensembl transcript: ENST00000258104
  gene symbol: DYSF
  hgvsc: ENST00000258104.3:c.2356-12C>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386617
  ensembl transcript: ENST00000410041
  gene symbol: DYSF
  hgvsc: ENST00000410041.1:c.2410-12C>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386547
  ensembl transcript: ENST00000409582
  gene symbol: DYSF
  hgvsc: ENST00000409582.3:c.2407-12C>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000377678
  ensembl transcript: ENST00000394120
  gene symbol: DYSF
  hgvsc: ENST00000394120.2:c.2359-12C>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000407046
  ensembl transcript: ENST00000413539
  gene symbol: DYSF
  hgvsc: ENST00000413539.2:c.2449-12C>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386881
  ensembl transcript: ENST00000410020
  gene symbol: DYSF
  hgvsc: ENST00000410020.3:c.2410-12C>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000398305
  ensembl transcript: ENST00000429174
  gene symbol: DYSF
  hgvsc: ENST00000429174.2:c.2356-12C>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386683
  ensembl transcript: ENST00000409651
  gene symbol: DYSF
  hgvsc: ENST00000409651.1:c.2452-12C>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386285
  ensembl transcript: ENST00000409744
  gene symbol: DYSF
  hgvsc: ENST00000409744.1:c.2317-12C>A
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386512
  ensembl transcript: ENST00000409366
  gene symbol: DYSF
  hgvsc: ENST00000409366.1:c.2359-12C>A
  variant of: http://identifiers.org/hgnc/3097
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3306
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14655
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1366
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14445
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8957
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7457
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5541
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2132
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5147
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff

2-71791185-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71791185
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 71791185
    reference: chr 2
allele count: 1
allele frequency: 8.248783304462591e-6
allele num: 121230
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000258104
  ensembl transcript: ENST00000258104
  gene symbol: DYSF
  hgvsc: ENST00000258104.3:c.2356-3C>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386683
  ensembl transcript: ENST00000409651
  gene symbol: DYSF
  hgvsc: ENST00000409651.1:c.2452-3C>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386547
  ensembl transcript: ENST00000409582
  gene symbol: DYSF
  hgvsc: ENST00000409582.3:c.2407-3C>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386285
  ensembl transcript: ENST00000409744
  gene symbol: DYSF
  hgvsc: ENST00000409744.1:c.2317-3C>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386617
  ensembl transcript: ENST00000410041
  gene symbol: DYSF
  hgvsc: ENST00000410041.1:c.2410-3C>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000377678
  ensembl transcript: ENST00000394120
  gene symbol: DYSF
  hgvsc: ENST00000394120.2:c.2359-3C>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386881
  ensembl transcript: ENST00000410020
  gene symbol: DYSF
  hgvsc: ENST00000410020.3:c.2410-3C>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000387137
  ensembl transcript: ENST00000409762
  gene symbol: DYSF
  hgvsc: ENST00000409762.1:c.2407-3C>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000407046
  ensembl transcript: ENST00000413539
  gene symbol: DYSF
  hgvsc: ENST00000413539.2:c.2449-3C>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386512
  ensembl transcript: ENST00000409366
  gene symbol: DYSF
  hgvsc: ENST00000409366.1:c.2359-3C>T
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000398305
  ensembl transcript: ENST00000429174
  gene symbol: DYSF
  hgvsc: ENST00000429174.2:c.2356-3C>T
  variant of: http://identifiers.org/hgnc/3097
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8961
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1366
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7507
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5542
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3307
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14711
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14478
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2132
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.2410-3C>T
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/2-71791188-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71791188
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 71791188
    reference: chr 2
allele count: 1
allele frequency: 8.247558722618106e-6
allele num: 121248
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386881
  ensembl transcript: ENST00000410020
  gene symbol: DYSF
  hgvsc: ENST00000410020.3:c.2410C>A
  hgvsp: ENSP00000386881.3:p.Pro804Thr
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386547
  ensembl transcript: ENST00000409582
  gene symbol: DYSF
  hgvsc: ENST00000409582.3:c.2407C>A
  hgvsp: ENSP00000386547.3:p.Pro803Thr
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386285
  ensembl transcript: ENST00000409744
  gene symbol: DYSF
  hgvsc: ENST00000409744.1:c.2317C>A
  hgvsp: ENSP00000386285.1:p.Pro773Thr
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386683
  ensembl transcript: ENST00000409651
  gene symbol: DYSF
  hgvsc: ENST00000409651.1:c.2452C>A
  hgvsp: ENSP00000386683.1:p.Pro818Thr
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386617
  ensembl transcript: ENST00000410041
  gene symbol: DYSF
  hgvsc: ENST00000410041.1:c.2410C>A
  hgvsp: ENSP00000386617.1:p.Pro804Thr
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000407046
  ensembl transcript: ENST00000413539
  gene symbol: DYSF
  hgvsc: ENST00000413539.2:c.2449C>A
  hgvsp: ENSP00000407046.2:p.Pro817Thr
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000387137
  ensembl transcript: ENST00000409762
  gene symbol: DYSF
  hgvsc: ENST00000409762.1:c.2407C>A
  hgvsp: ENSP00000387137.1:p.Pro803Thr
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000398305
  ensembl transcript: ENST00000429174
  gene symbol: DYSF
  hgvsc: ENST00000429174.2:c.2356C>A
  hgvsp: ENSP00000398305.2:p.Pro786Thr
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000258104
  ensembl transcript: ENST00000258104
  gene symbol: DYSF
  hgvsc: ENST00000258104.3:c.2356C>A
  hgvsp: ENSP00000258104.3:p.Pro786Thr
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000377678
  ensembl transcript: ENST00000394120
  gene symbol: DYSF
  hgvsc: ENST00000394120.2:c.2359C>A
  hgvsp: ENSP00000377678.2:p.Pro787Thr
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386512
  ensembl transcript: ENST00000409366
  gene symbol: DYSF
  hgvsc: ENST00000409366.1:c.2359C>A
  hgvsp: ENSP00000386512.1:p.Pro787Thr
  variant of: http://identifiers.org/hgnc/3097
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7496
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8965
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5545
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2134
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3309
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14736
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro804Thr
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum

2-71791189-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71791189
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 71791189
    reference: chr 2
allele count: 1
allele frequency: 8.246470510621453e-6
allele num: 121264
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000258104
  ensembl transcript: ENST00000258104
  gene symbol: DYSF
  hgvsc: ENST00000258104.3:c.2357C>T
  hgvsp: ENSP00000258104.3:p.Pro786Leu
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000377678
  ensembl transcript: ENST00000394120
  gene symbol: DYSF
  hgvsc: ENST00000394120.2:c.2360C>T
  hgvsp: ENSP00000377678.2:p.Pro787Leu
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386683
  ensembl transcript: ENST00000409651
  gene symbol: DYSF
  hgvsc: ENST00000409651.1:c.2453C>T
  hgvsp: ENSP00000386683.1:p.Pro818Leu
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386285
  ensembl transcript: ENST00000409744
  gene symbol: DYSF
  hgvsc: ENST00000409744.1:c.2318C>T
  hgvsp: ENSP00000386285.1:p.Pro773Leu
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000407046
  ensembl transcript: ENST00000413539
  gene symbol: DYSF
  hgvsc: ENST00000413539.2:c.2450C>T
  hgvsp: ENSP00000407046.2:p.Pro817Leu
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386512
  ensembl transcript: ENST00000409366
  gene symbol: DYSF
  hgvsc: ENST00000409366.1:c.2360C>T
  hgvsp: ENSP00000386512.1:p.Pro787Leu
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386881
  ensembl transcript: ENST00000410020
  gene symbol: DYSF
  hgvsc: ENST00000410020.3:c.2411C>T
  hgvsp: ENSP00000386881.3:p.Pro804Leu
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000387137
  ensembl transcript: ENST00000409762
  gene symbol: DYSF
  hgvsc: ENST00000409762.1:c.2408C>T
  hgvsp: ENSP00000387137.1:p.Pro803Leu
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386617
  ensembl transcript: ENST00000410041
  gene symbol: DYSF
  hgvsc: ENST00000410041.1:c.2411C>T
  hgvsp: ENSP00000386617.1:p.Pro804Leu
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000398305
  ensembl transcript: ENST00000429174
  gene symbol: DYSF
  hgvsc: ENST00000429174.2:c.2357C>T
  hgvsp: ENSP00000398305.2:p.Pro786Leu
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386547
  ensembl transcript: ENST00000409582
  gene symbol: DYSF
  hgvsc: ENST00000409582.3:c.2408C>T
  hgvsp: ENSP00000386547.3:p.Pro803Leu
  variant of: http://identifiers.org/hgnc/3097
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8964
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2132
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5544
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14742
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14483
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3309
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7495
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1366
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro804Leu
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ

2-71791199-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71791199
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 71791199
    reference: chr 2
allele count: 88
allele frequency: 7.253185632098643e-4
allele num: 121326
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386881
  ensembl transcript: ENST00000410020
  gene symbol: DYSF
  hgvsc: ENST00000410020.3:c.2421C>T
  hgvsp: ENST00000410020.3:c.2421C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386547
  ensembl transcript: ENST00000409582
  gene symbol: DYSF
  hgvsc: ENST00000409582.3:c.2418C>T
  hgvsp: ENST00000409582.3:c.2418C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000407046
  ensembl transcript: ENST00000413539
  gene symbol: DYSF
  hgvsc: ENST00000413539.2:c.2460C>T
  hgvsp: ENST00000413539.2:c.2460C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000258104
  ensembl transcript: ENST00000258104
  gene symbol: DYSF
  hgvsc: ENST00000258104.3:c.2367C>T
  hgvsp: ENST00000258104.3:c.2367C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000377678
  ensembl transcript: ENST00000394120
  gene symbol: DYSF
  hgvsc: ENST00000394120.2:c.2370C>T
  hgvsp: ENST00000394120.2:c.2370C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386683
  ensembl transcript: ENST00000409651
  gene symbol: DYSF
  hgvsc: ENST00000409651.1:c.2463C>T
  hgvsp: ENST00000409651.1:c.2463C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386512
  ensembl transcript: ENST00000409366
  gene symbol: DYSF
  hgvsc: ENST00000409366.1:c.2370C>T
  hgvsp: ENST00000409366.1:c.2370C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386617
  ensembl transcript: ENST00000410041
  gene symbol: DYSF
  hgvsc: ENST00000410041.1:c.2421C>T
  hgvsp: ENST00000410041.1:c.2421C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000398305
  ensembl transcript: ENST00000429174
  gene symbol: DYSF
  hgvsc: ENST00000429174.2:c.2367C>T
  hgvsp: ENST00000429174.2:c.2367C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386285
  ensembl transcript: ENST00000409744
  gene symbol: DYSF
  hgvsc: ENST00000409744.1:c.2328C>T
  hgvsp: ENST00000409744.1:c.2328C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000387137
  ensembl transcript: ENST00000409762
  gene symbol: DYSF
  hgvsc: ENST00000409762.1:c.2418C>T
  hgvsp: ENST00000409762.1:c.2418C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14769
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2133
  bin: 5.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1369
  bin: 5.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 5530
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 7.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7489
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8948
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 932
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 9.75e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 8.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 14484
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3298
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser807Ser
num of homozygotes: 2
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: FS

2-71791202-G-GC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71791202
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 71791203
    reference: chr 2
allele count: 1
allele frequency: 8.241033755274261e-6
allele num: 121344
alternate allele: GC
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000377678
  ensembl transcript: ENST00000394120
  gene symbol: DYSF
  hgvsc: ENST00000394120.2:c.2375dupC
  hgvsp: ENSP00000377678.2:p.Asp793GlyfsTer73
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386285
  ensembl transcript: ENST00000409744
  gene symbol: DYSF
  hgvsc: ENST00000409744.1:c.2333dupC
  hgvsp: ENSP00000386285.1:p.Asp779GlyfsTer73
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386881
  ensembl transcript: ENST00000410020
  gene symbol: DYSF
  hgvsc: ENST00000410020.3:c.2426dupC
  hgvsp: ENSP00000386881.3:p.Asp810GlyfsTer73
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000258104
  ensembl transcript: ENST00000258104
  gene symbol: DYSF
  hgvsc: ENST00000258104.3:c.2372dupC
  hgvsp: ENSP00000258104.3:p.Asp792GlyfsTer73
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386617
  ensembl transcript: ENST00000410041
  gene symbol: DYSF
  hgvsc: ENST00000410041.1:c.2426dupC
  hgvsp: ENSP00000386617.1:p.Asp810GlyfsTer73
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386547
  ensembl transcript: ENST00000409582
  gene symbol: DYSF
  hgvsc: ENST00000409582.3:c.2423dupC
  hgvsp: ENSP00000386547.3:p.Asp809GlyfsTer73
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000387137
  ensembl transcript: ENST00000409762
  gene symbol: DYSF
  hgvsc: ENST00000409762.1:c.2423dupC
  hgvsp: ENSP00000387137.1:p.Asp809GlyfsTer73
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000398305
  ensembl transcript: ENST00000429174
  gene symbol: DYSF
  hgvsc: ENST00000429174.2:c.2372dupC
  hgvsp: ENSP00000398305.2:p.Asp792GlyfsTer73
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386512
  ensembl transcript: ENST00000409366
  gene symbol: DYSF
  hgvsc: ENST00000409366.1:c.2375dupC
  hgvsp: ENSP00000386512.1:p.Asp793GlyfsTer73
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000407046
  ensembl transcript: ENST00000413539
  gene symbol: DYSF
  hgvsc: ENST00000413539.2:c.2465dupC
  hgvsp: ENSP00000407046.2:p.Asp823GlyfsTer73
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386683
  ensembl transcript: ENST00000409651
  gene symbol: DYSF
  hgvsc: ENST00000409651.1:c.2468dupC
  hgvsp: ENSP00000386683.1:p.Asp824GlyfsTer73
  variant of: http://identifiers.org/hgnc/3097
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3302
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14794
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1366
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14502
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5530
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8956
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2133
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7490
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 930
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp810GlyfsTer73
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD

2-71791202-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71791202
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 71791202
    reference: chr 2
allele count: 1
allele frequency: 8.241033755274261e-6
allele num: 121344
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000258104
  ensembl transcript: ENST00000258104
  gene symbol: DYSF
  hgvsc: ENST00000258104.3:c.2370G>T
  hgvsp: ENST00000258104.3:c.2370G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386617
  ensembl transcript: ENST00000410041
  gene symbol: DYSF
  hgvsc: ENST00000410041.1:c.2424G>T
  hgvsp: ENST00000410041.1:c.2424G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386285
  ensembl transcript: ENST00000409744
  gene symbol: DYSF
  hgvsc: ENST00000409744.1:c.2331G>T
  hgvsp: ENST00000409744.1:c.2331G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000407046
  ensembl transcript: ENST00000413539
  gene symbol: DYSF
  hgvsc: ENST00000413539.2:c.2463G>T
  hgvsp: ENST00000413539.2:c.2463G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386512
  ensembl transcript: ENST00000409366
  gene symbol: DYSF
  hgvsc: ENST00000409366.1:c.2373G>T
  hgvsp: ENST00000409366.1:c.2373G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000398305
  ensembl transcript: ENST00000429174
  gene symbol: DYSF
  hgvsc: ENST00000429174.2:c.2370G>T
  hgvsp: ENST00000429174.2:c.2370G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000377678
  ensembl transcript: ENST00000394120
  gene symbol: DYSF
  hgvsc: ENST00000394120.2:c.2373G>T
  hgvsp: ENST00000394120.2:c.2373G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000387137
  ensembl transcript: ENST00000409762
  gene symbol: DYSF
  hgvsc: ENST00000409762.1:c.2421G>T
  hgvsp: ENST00000409762.1:c.2421G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386683
  ensembl transcript: ENST00000409651
  gene symbol: DYSF
  hgvsc: ENST00000409651.1:c.2466G>T
  hgvsp: ENST00000409651.1:c.2466G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386547
  ensembl transcript: ENST00000409582
  gene symbol: DYSF
  hgvsc: ENST00000409582.3:c.2421G>T
  hgvsp: ENST00000409582.3:c.2421G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386881
  ensembl transcript: ENST00000410020
  gene symbol: DYSF
  hgvsc: ENST00000410020.3:c.2424G>T
  hgvsp: ENST00000410020.3:c.2424G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2133
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14502
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7490
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5530
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3302
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 930
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14794
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8956
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1366
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu808Leu
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: Other
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

2-71791205-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71791205
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 71791205
    reference: chr 2
allele count: 14
allele frequency: 1.1536876802637e-4
allele num: 121350
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000398305
  ensembl transcript: ENST00000429174
  gene symbol: DYSF
  hgvsc: ENST00000429174.2:c.2373G>A
  hgvsp: ENST00000429174.2:c.2373G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386683
  ensembl transcript: ENST00000409651
  gene symbol: DYSF
  hgvsc: ENST00000409651.1:c.2469G>A
  hgvsp: ENST00000409651.1:c.2469G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386617
  ensembl transcript: ENST00000410041
  gene symbol: DYSF
  hgvsc: ENST00000410041.1:c.2427G>A
  hgvsp: ENST00000410041.1:c.2427G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386547
  ensembl transcript: ENST00000409582
  gene symbol: DYSF
  hgvsc: ENST00000409582.3:c.2424G>A
  hgvsp: ENST00000409582.3:c.2424G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386285
  ensembl transcript: ENST00000409744
  gene symbol: DYSF
  hgvsc: ENST00000409744.1:c.2334G>A
  hgvsp: ENST00000409744.1:c.2334G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386881
  ensembl transcript: ENST00000410020
  gene symbol: DYSF
  hgvsc: ENST00000410020.3:c.2427G>A
  hgvsp: ENST00000410020.3:c.2427G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000258104
  ensembl transcript: ENST00000258104
  gene symbol: DYSF
  hgvsc: ENST00000258104.3:c.2373G>A
  hgvsp: ENST00000258104.3:c.2373G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000387137
  ensembl transcript: ENST00000409762
  gene symbol: DYSF
  hgvsc: ENST00000409762.1:c.2424G>A
  hgvsp: ENST00000409762.1:c.2424G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000407046
  ensembl transcript: ENST00000413539
  gene symbol: DYSF
  hgvsc: ENST00000413539.2:c.2466G>A
  hgvsp: ENST00000413539.2:c.2466G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386512
  ensembl transcript: ENST00000409366
  gene symbol: DYSF
  hgvsc: ENST00000409366.1:c.2376G>A
  hgvsp: ENST00000409366.1:c.2376G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000377678
  ensembl transcript: ENST00000394120
  gene symbol: DYSF
  hgvsc: ENST00000394120.2:c.2376G>A
  hgvsp: ENST00000394120.2:c.2376G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2135
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5530
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 930
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8957
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14506
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14800
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1367
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3300
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7478
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
hgvs: p.Pro809Pro
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ

2-71791211-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71791211
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 71791211
    reference: chr 2
allele count: 1
allele frequency: 8.239132584121543e-6
allele num: 121372
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000377678
  ensembl transcript: ENST00000394120
  gene symbol: DYSF
  hgvsc: ENST00000394120.2:c.2382C>T
  hgvsp: ENST00000394120.2:c.2382C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386881
  ensembl transcript: ENST00000410020
  gene symbol: DYSF
  hgvsc: ENST00000410020.3:c.2433C>T
  hgvsp: ENST00000410020.3:c.2433C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000407046
  ensembl transcript: ENST00000413539
  gene symbol: DYSF
  hgvsc: ENST00000413539.2:c.2472C>T
  hgvsp: ENST00000413539.2:c.2472C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386512
  ensembl transcript: ENST00000409366
  gene symbol: DYSF
  hgvsc: ENST00000409366.1:c.2382C>T
  hgvsp: ENST00000409366.1:c.2382C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386617
  ensembl transcript: ENST00000410041
  gene symbol: DYSF
  hgvsc: ENST00000410041.1:c.2433C>T
  hgvsp: ENST00000410041.1:c.2433C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000258104
  ensembl transcript: ENST00000258104
  gene symbol: DYSF
  hgvsc: ENST00000258104.3:c.2379C>T
  hgvsp: ENST00000258104.3:c.2379C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386285
  ensembl transcript: ENST00000409744
  gene symbol: DYSF
  hgvsc: ENST00000409744.1:c.2340C>T
  hgvsp: ENST00000409744.1:c.2340C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000398305
  ensembl transcript: ENST00000429174
  gene symbol: DYSF
  hgvsc: ENST00000429174.2:c.2379C>T
  hgvsp: ENST00000429174.2:c.2379C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000387137
  ensembl transcript: ENST00000409762
  gene symbol: DYSF
  hgvsc: ENST00000409762.1:c.2430C>T
  hgvsp: ENST00000409762.1:c.2430C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386547
  ensembl transcript: ENST00000409582
  gene symbol: DYSF
  hgvsc: ENST00000409582.3:c.2430C>T
  hgvsp: ENST00000409582.3:c.2430C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386683
  ensembl transcript: ENST00000409651
  gene symbol: DYSF
  hgvsc: ENST00000409651.1:c.2475C>T
  hgvsp: ENST00000409651.1:c.2475C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5530
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1366
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7485
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8958
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3301
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14812
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2132
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14512
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile811Ile
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum

2-71791212-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71791212
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 71791212
    reference: chr 2
allele count: 3
allele frequency: 2.471576866040534e-5
allele num: 121380
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386881
  ensembl transcript: ENST00000410020
  gene symbol: DYSF
  hgvsc: ENST00000410020.3:c.2434G>A
  hgvsp: ENSP00000386881.3:p.Val812Ile
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000258104
  ensembl transcript: ENST00000258104
  gene symbol: DYSF
  hgvsc: ENST00000258104.3:c.2380G>A
  hgvsp: ENSP00000258104.3:p.Val794Ile
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386512
  ensembl transcript: ENST00000409366
  gene symbol: DYSF
  hgvsc: ENST00000409366.1:c.2383G>A
  hgvsp: ENSP00000386512.1:p.Val795Ile
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386617
  ensembl transcript: ENST00000410041
  gene symbol: DYSF
  hgvsc: ENST00000410041.1:c.2434G>A
  hgvsp: ENSP00000386617.1:p.Val812Ile
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386547
  ensembl transcript: ENST00000409582
  gene symbol: DYSF
  hgvsc: ENST00000409582.3:c.2431G>A
  hgvsp: ENSP00000386547.3:p.Val811Ile
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000387137
  ensembl transcript: ENST00000409762
  gene symbol: DYSF
  hgvsc: ENST00000409762.1:c.2431G>A
  hgvsp: ENSP00000387137.1:p.Val811Ile
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386683
  ensembl transcript: ENST00000409651
  gene symbol: DYSF
  hgvsc: ENST00000409651.1:c.2476G>A
  hgvsp: ENSP00000386683.1:p.Val826Ile
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000398305
  ensembl transcript: ENST00000429174
  gene symbol: DYSF
  hgvsc: ENST00000429174.2:c.2380G>A
  hgvsp: ENSP00000398305.2:p.Val794Ile
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386285
  ensembl transcript: ENST00000409744
  gene symbol: DYSF
  hgvsc: ENST00000409744.1:c.2341G>A
  hgvsp: ENSP00000386285.1:p.Val781Ile
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000407046
  ensembl transcript: ENST00000413539
  gene symbol: DYSF
  hgvsc: ENST00000413539.2:c.2473G>A
  hgvsp: ENSP00000407046.2:p.Val825Ile
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000377678
  ensembl transcript: ENST00000394120
  gene symbol: DYSF
  hgvsc: ENST00000394120.2:c.2383G>A
  hgvsp: ENSP00000377678.2:p.Val795Ile
  variant of: http://identifiers.org/hgnc/3097
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5529
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7484
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14513
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8958
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3302
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2132
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1366
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14817
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val812Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Latino
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff

2-71791238-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71791238
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 71791238
    reference: chr 2
allele count: 1
allele frequency: 8.237775141689733e-6
allele num: 121392
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000398305
  ensembl transcript: ENST00000429174
  gene symbol: DYSF
  hgvsc: ENST00000429174.2:c.2406G>A
  hgvsp: ENST00000429174.2:c.2406G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000387137
  ensembl transcript: ENST00000409762
  gene symbol: DYSF
  hgvsc: ENST00000409762.1:c.2457G>A
  hgvsp: ENST00000409762.1:c.2457G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000377678
  ensembl transcript: ENST00000394120
  gene symbol: DYSF
  hgvsc: ENST00000394120.2:c.2409G>A
  hgvsp: ENST00000394120.2:c.2409G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386881
  ensembl transcript: ENST00000410020
  gene symbol: DYSF
  hgvsc: ENST00000410020.3:c.2460G>A
  hgvsp: ENST00000410020.3:c.2460G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000407046
  ensembl transcript: ENST00000413539
  gene symbol: DYSF
  hgvsc: ENST00000413539.2:c.2499G>A
  hgvsp: ENST00000413539.2:c.2499G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000258104
  ensembl transcript: ENST00000258104
  gene symbol: DYSF
  hgvsc: ENST00000258104.3:c.2406G>A
  hgvsp: ENST00000258104.3:c.2406G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386547
  ensembl transcript: ENST00000409582
  gene symbol: DYSF
  hgvsc: ENST00000409582.3:c.2457G>A
  hgvsp: ENST00000409582.3:c.2457G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386617
  ensembl transcript: ENST00000410041
  gene symbol: DYSF
  hgvsc: ENST00000410041.1:c.2460G>A
  hgvsp: ENST00000410041.1:c.2460G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386512
  ensembl transcript: ENST00000409366
  gene symbol: DYSF
  hgvsc: ENST00000409366.1:c.2409G>A
  hgvsp: ENST00000409366.1:c.2409G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386285
  ensembl transcript: ENST00000409744
  gene symbol: DYSF
  hgvsc: ENST00000409744.1:c.2367G>A
  hgvsp: ENST00000409744.1:c.2367G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386683
  ensembl transcript: ENST00000409651
  gene symbol: DYSF
  hgvsc: ENST00000409651.1:c.2502G>A
  hgvsp: ENST00000409651.1:c.2502G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7464
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3302
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14531
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 931
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2132
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14831
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1366
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8957
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys820Lys
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ

2-71791239-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71791239
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 71791239
    reference: chr 2
allele count: 5
allele frequency: 4.11868399808893e-5
allele num: 121398
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000377678
  ensembl transcript: ENST00000394120
  gene symbol: DYSF
  hgvsc: ENST00000394120.2:c.2410C>T
  hgvsp: ENSP00000377678.2:p.Arg804Cys
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386512
  ensembl transcript: ENST00000409366
  gene symbol: DYSF
  hgvsc: ENST00000409366.1:c.2410C>T
  hgvsp: ENSP00000386512.1:p.Arg804Cys
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386285
  ensembl transcript: ENST00000409744
  gene symbol: DYSF
  hgvsc: ENST00000409744.1:c.2368C>T
  hgvsp: ENSP00000386285.1:p.Arg790Cys
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000407046
  ensembl transcript: ENST00000413539
  gene symbol: DYSF
  hgvsc: ENST00000413539.2:c.2500C>T
  hgvsp: ENSP00000407046.2:p.Arg834Cys
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000387137
  ensembl transcript: ENST00000409762
  gene symbol: DYSF
  hgvsc: ENST00000409762.1:c.2458C>T
  hgvsp: ENSP00000387137.1:p.Arg820Cys
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386617
  ensembl transcript: ENST00000410041
  gene symbol: DYSF
  hgvsc: ENST00000410041.1:c.2461C>T
  hgvsp: ENSP00000386617.1:p.Arg821Cys
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000258104
  ensembl transcript: ENST00000258104
  gene symbol: DYSF
  hgvsc: ENST00000258104.3:c.2407C>T
  hgvsp: ENSP00000258104.3:p.Arg803Cys
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386683
  ensembl transcript: ENST00000409651
  gene symbol: DYSF
  hgvsc: ENST00000409651.1:c.2503C>T
  hgvsp: ENSP00000386683.1:p.Arg835Cys
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000398305
  ensembl transcript: ENST00000429174
  gene symbol: DYSF
  hgvsc: ENST00000429174.2:c.2407C>T
  hgvsp: ENSP00000398305.2:p.Arg803Cys
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386881
  ensembl transcript: ENST00000410020
  gene symbol: DYSF
  hgvsc: ENST00000410020.3:c.2461C>T
  hgvsp: ENSP00000386881.3:p.Arg821Cys
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386547
  ensembl transcript: ENST00000409582
  gene symbol: DYSF
  hgvsc: ENST00000409582.3:c.2458C>T
  hgvsp: ENSP00000386547.3:p.Arg820Cys
  variant of: http://identifiers.org/hgnc/3097
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 8957
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2131
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7462
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1366
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5529
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3302
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14530
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14834
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 930
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg821Cys
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS

2-71791240-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71791240
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 71791240
    reference: chr 2
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386881
  ensembl transcript: ENST00000410020
  gene symbol: DYSF
  hgvsc: ENST00000410020.3:c.2462G>A
  hgvsp: ENSP00000386881.3:p.Arg821His
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386512
  ensembl transcript: ENST00000409366
  gene symbol: DYSF
  hgvsc: ENST00000409366.1:c.2411G>A
  hgvsp: ENSP00000386512.1:p.Arg804His
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000258104
  ensembl transcript: ENST00000258104
  gene symbol: DYSF
  hgvsc: ENST00000258104.3:c.2408G>A
  hgvsp: ENSP00000258104.3:p.Arg803His
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386683
  ensembl transcript: ENST00000409651
  gene symbol: DYSF
  hgvsc: ENST00000409651.1:c.2504G>A
  hgvsp: ENSP00000386683.1:p.Arg835His
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000387137
  ensembl transcript: ENST00000409762
  gene symbol: DYSF
  hgvsc: ENST00000409762.1:c.2459G>A
  hgvsp: ENSP00000387137.1:p.Arg820His
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386285
  ensembl transcript: ENST00000409744
  gene symbol: DYSF
  hgvsc: ENST00000409744.1:c.2369G>A
  hgvsp: ENSP00000386285.1:p.Arg790His
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386617
  ensembl transcript: ENST00000410041
  gene symbol: DYSF
  hgvsc: ENST00000410041.1:c.2462G>A
  hgvsp: ENSP00000386617.1:p.Arg821His
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000377678
  ensembl transcript: ENST00000394120
  gene symbol: DYSF
  hgvsc: ENST00000394120.2:c.2411G>A
  hgvsp: ENSP00000377678.2:p.Arg804His
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386547
  ensembl transcript: ENST00000409582
  gene symbol: DYSF
  hgvsc: ENST00000409582.3:c.2459G>A
  hgvsp: ENSP00000386547.3:p.Arg820His
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000398305
  ensembl transcript: ENST00000429174
  gene symbol: DYSF
  hgvsc: ENST00000429174.2:c.2408G>A
  hgvsp: ENSP00000398305.2:p.Arg803His
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000407046
  ensembl transcript: ENST00000413539
  gene symbol: DYSF
  hgvsc: ENST00000413539.2:c.2501G>A
  hgvsp: ENSP00000407046.2:p.Arg834His
  variant of: http://identifiers.org/hgnc/3097
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5528
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2131
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3302
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7462
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14529
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1368
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8957
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 930
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg821His
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD

2-71791250-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71791250
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 71791250
    reference: chr 2
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386683
  ensembl transcript: ENST00000409651
  gene symbol: DYSF
  hgvsc: ENST00000409651.1:c.2514C>T
  hgvsp: ENST00000409651.1:c.2514C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000377678
  ensembl transcript: ENST00000394120
  gene symbol: DYSF
  hgvsc: ENST00000394120.2:c.2421C>T
  hgvsp: ENST00000394120.2:c.2421C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000398305
  ensembl transcript: ENST00000429174
  gene symbol: DYSF
  hgvsc: ENST00000429174.2:c.2418C>T
  hgvsp: ENST00000429174.2:c.2418C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000407046
  ensembl transcript: ENST00000413539
  gene symbol: DYSF
  hgvsc: ENST00000413539.2:c.2511C>T
  hgvsp: ENST00000413539.2:c.2511C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386617
  ensembl transcript: ENST00000410041
  gene symbol: DYSF
  hgvsc: ENST00000410041.1:c.2472C>T
  hgvsp: ENST00000410041.1:c.2472C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386285
  ensembl transcript: ENST00000409744
  gene symbol: DYSF
  hgvsc: ENST00000409744.1:c.2379C>T
  hgvsp: ENST00000409744.1:c.2379C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386881
  ensembl transcript: ENST00000410020
  gene symbol: DYSF
  hgvsc: ENST00000410020.3:c.2472C>T
  hgvsp: ENST00000410020.3:c.2472C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000387137
  ensembl transcript: ENST00000409762
  gene symbol: DYSF
  hgvsc: ENST00000409762.1:c.2469C>T
  hgvsp: ENST00000409762.1:c.2469C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000258104
  ensembl transcript: ENST00000258104
  gene symbol: DYSF
  hgvsc: ENST00000258104.3:c.2418C>T
  hgvsp: ENST00000258104.3:c.2418C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386512
  ensembl transcript: ENST00000409366
  gene symbol: DYSF
  hgvsc: ENST00000409366.1:c.2421C>T
  hgvsp: ENST00000409366.1:c.2421C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386547
  ensembl transcript: ENST00000409582
  gene symbol: DYSF
  hgvsc: ENST00000409582.3:c.2469C>T
  hgvsp: ENST00000409582.3:c.2469C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7425
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2132
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14529
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14835
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8968
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 930
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3307
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5537
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr824Tyr
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: Other
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum

2-71791255-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71791255
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 71791255
    reference: chr 2
allele count: 36
allele frequency: 2.966674358044632e-4
allele num: 121348
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000258104
  ensembl transcript: ENST00000258104
  gene symbol: DYSF
  hgvsc: ENST00000258104.3:c.2423G>A
  hgvsp: ENSP00000258104.3:p.Arg808Gln
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000398305
  ensembl transcript: ENST00000429174
  gene symbol: DYSF
  hgvsc: ENST00000429174.2:c.2423G>A
  hgvsp: ENSP00000398305.2:p.Arg808Gln
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000387137
  ensembl transcript: ENST00000409762
  gene symbol: DYSF
  hgvsc: ENST00000409762.1:c.2474G>A
  hgvsp: ENSP00000387137.1:p.Arg825Gln
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386683
  ensembl transcript: ENST00000409651
  gene symbol: DYSF
  hgvsc: ENST00000409651.1:c.2519G>A
  hgvsp: ENSP00000386683.1:p.Arg840Gln
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386512
  ensembl transcript: ENST00000409366
  gene symbol: DYSF
  hgvsc: ENST00000409366.1:c.2426G>A
  hgvsp: ENSP00000386512.1:p.Arg809Gln
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386285
  ensembl transcript: ENST00000409744
  gene symbol: DYSF
  hgvsc: ENST00000409744.1:c.2384G>A
  hgvsp: ENSP00000386285.1:p.Arg795Gln
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386547
  ensembl transcript: ENST00000409582
  gene symbol: DYSF
  hgvsc: ENST00000409582.3:c.2474G>A
  hgvsp: ENSP00000386547.3:p.Arg825Gln
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000407046
  ensembl transcript: ENST00000413539
  gene symbol: DYSF
  hgvsc: ENST00000413539.2:c.2516G>A
  hgvsp: ENSP00000407046.2:p.Arg839Gln
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386617
  ensembl transcript: ENST00000410041
  gene symbol: DYSF
  hgvsc: ENST00000410041.1:c.2477G>A
  hgvsp: ENSP00000386617.1:p.Arg826Gln
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386881
  ensembl transcript: ENST00000410020
  gene symbol: DYSF
  hgvsc: ENST00000410020.3:c.2477G>A
  hgvsp: ENSP00000386881.3:p.Arg826Gln
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000377678
  ensembl transcript: ENST00000394120
  gene symbol: DYSF
  hgvsc: ENST00000394120.2:c.2426G>A
  hgvsp: ENSP00000377678.2:p.Arg809Gln
  variant of: http://identifiers.org/hgnc/3097
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14845
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 930
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.75e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8959
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7401
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3291
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14529
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5523
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2128
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Arg826Gln
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: African
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: QD

http://identifiers.org/exac.variant/2-71791260-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71791260
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 71791260
    reference: chr 2
allele count: 3
allele frequency: 2.471169686985173e-5
allele num: 121400
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000387137
  ensembl transcript: ENST00000409762
  gene symbol: DYSF
  hgvsc: ENST00000409762.1:c.2479C>A
  hgvsp: ENSP00000387137.1:p.Pro827Thr
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386547
  ensembl transcript: ENST00000409582
  gene symbol: DYSF
  hgvsc: ENST00000409582.3:c.2479C>A
  hgvsp: ENSP00000386547.3:p.Pro827Thr
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386617
  ensembl transcript: ENST00000410041
  gene symbol: DYSF
  hgvsc: ENST00000410041.1:c.2482C>A
  hgvsp: ENSP00000386617.1:p.Pro828Thr
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000407046
  ensembl transcript: ENST00000413539
  gene symbol: DYSF
  hgvsc: ENST00000413539.2:c.2521C>A
  hgvsp: ENSP00000407046.2:p.Pro841Thr
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386285
  ensembl transcript: ENST00000409744
  gene symbol: DYSF
  hgvsc: ENST00000409744.1:c.2389C>A
  hgvsp: ENSP00000386285.1:p.Pro797Thr
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386881
  ensembl transcript: ENST00000410020
  gene symbol: DYSF
  hgvsc: ENST00000410020.3:c.2482C>A
  hgvsp: ENSP00000386881.3:p.Pro828Thr
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386683
  ensembl transcript: ENST00000409651
  gene symbol: DYSF
  hgvsc: ENST00000409651.1:c.2524C>A
  hgvsp: ENSP00000386683.1:p.Pro842Thr
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000398305
  ensembl transcript: ENST00000429174
  gene symbol: DYSF
  hgvsc: ENST00000429174.2:c.2428C>A
  hgvsp: ENSP00000398305.2:p.Pro810Thr
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000258104
  ensembl transcript: ENST00000258104
  gene symbol: DYSF
  hgvsc: ENST00000258104.3:c.2428C>A
  hgvsp: ENSP00000258104.3:p.Pro810Thr
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386512
  ensembl transcript: ENST00000409366
  gene symbol: DYSF
  hgvsc: ENST00000409366.1:c.2431C>A
  hgvsp: ENSP00000386512.1:p.Pro811Thr
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000377678
  ensembl transcript: ENST00000394120
  gene symbol: DYSF
  hgvsc: ENST00000394120.2:c.2431C>A
  hgvsp: ENSP00000377678.2:p.Pro811Thr
  variant of: http://identifiers.org/hgnc/3097
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2136
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14837
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7361
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3307
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14545
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 940
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5538
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8976
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1371
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Pro828Thr
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD

2-71791260-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71791260
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 71791260
    reference: chr 2
allele count: 4
allele frequency: 3.29489291598023e-5
allele num: 121400
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000387137
  ensembl transcript: ENST00000409762
  gene symbol: DYSF
  hgvsc: ENST00000409762.1:c.2479C>T
  hgvsp: ENSP00000387137.1:p.Pro827Ser
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386285
  ensembl transcript: ENST00000409744
  gene symbol: DYSF
  hgvsc: ENST00000409744.1:c.2389C>T
  hgvsp: ENSP00000386285.1:p.Pro797Ser
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386617
  ensembl transcript: ENST00000410041
  gene symbol: DYSF
  hgvsc: ENST00000410041.1:c.2482C>T
  hgvsp: ENSP00000386617.1:p.Pro828Ser
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386881
  ensembl transcript: ENST00000410020
  gene symbol: DYSF
  hgvsc: ENST00000410020.3:c.2482C>T
  hgvsp: ENSP00000386881.3:p.Pro828Ser
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000377678
  ensembl transcript: ENST00000394120
  gene symbol: DYSF
  hgvsc: ENST00000394120.2:c.2431C>T
  hgvsp: ENSP00000377678.2:p.Pro811Ser
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000398305
  ensembl transcript: ENST00000429174
  gene symbol: DYSF
  hgvsc: ENST00000429174.2:c.2428C>T
  hgvsp: ENSP00000398305.2:p.Pro810Ser
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386512
  ensembl transcript: ENST00000409366
  gene symbol: DYSF
  hgvsc: ENST00000409366.1:c.2431C>T
  hgvsp: ENSP00000386512.1:p.Pro811Ser
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386683
  ensembl transcript: ENST00000409651
  gene symbol: DYSF
  hgvsc: ENST00000409651.1:c.2524C>T
  hgvsp: ENSP00000386683.1:p.Pro842Ser
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000258104
  ensembl transcript: ENST00000258104
  gene symbol: DYSF
  hgvsc: ENST00000258104.3:c.2428C>T
  hgvsp: ENSP00000258104.3:p.Pro810Ser
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386547
  ensembl transcript: ENST00000409582
  gene symbol: DYSF
  hgvsc: ENST00000409582.3:c.2479C>T
  hgvsp: ENSP00000386547.3:p.Pro827Ser
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000407046
  ensembl transcript: ENST00000413539
  gene symbol: DYSF
  hgvsc: ENST00000413539.2:c.2521C>T
  hgvsp: ENSP00000407046.2:p.Pro841Ser
  variant of: http://identifiers.org/hgnc/3097
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 940
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8976
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14837
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2136
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3307
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5538
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14545
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7361
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1371
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro828Ser
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

2-71791262-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71791262
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 71791262
    reference: chr 2
allele count: 16
allele frequency: 1.31791374254555e-4
allele num: 121404
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000407046
  ensembl transcript: ENST00000413539
  gene symbol: DYSF
  hgvsc: ENST00000413539.2:c.2523C>T
  hgvsp: ENST00000413539.2:c.2523C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000377678
  ensembl transcript: ENST00000394120
  gene symbol: DYSF
  hgvsc: ENST00000394120.2:c.2433C>T
  hgvsp: ENST00000394120.2:c.2433C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000398305
  ensembl transcript: ENST00000429174
  gene symbol: DYSF
  hgvsc: ENST00000429174.2:c.2430C>T
  hgvsp: ENST00000429174.2:c.2430C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386683
  ensembl transcript: ENST00000409651
  gene symbol: DYSF
  hgvsc: ENST00000409651.1:c.2526C>T
  hgvsp: ENST00000409651.1:c.2526C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386285
  ensembl transcript: ENST00000409744
  gene symbol: DYSF
  hgvsc: ENST00000409744.1:c.2391C>T
  hgvsp: ENST00000409744.1:c.2391C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386617
  ensembl transcript: ENST00000410041
  gene symbol: DYSF
  hgvsc: ENST00000410041.1:c.2484C>T
  hgvsp: ENST00000410041.1:c.2484C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386881
  ensembl transcript: ENST00000410020
  gene symbol: DYSF
  hgvsc: ENST00000410020.3:c.2484C>T
  hgvsp: ENST00000410020.3:c.2484C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000387137
  ensembl transcript: ENST00000409762
  gene symbol: DYSF
  hgvsc: ENST00000409762.1:c.2481C>T
  hgvsp: ENST00000409762.1:c.2481C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000258104
  ensembl transcript: ENST00000258104
  gene symbol: DYSF
  hgvsc: ENST00000258104.3:c.2430C>T
  hgvsp: ENST00000258104.3:c.2430C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386512
  ensembl transcript: ENST00000409366
  gene symbol: DYSF
  hgvsc: ENST00000409366.1:c.2433C>T
  hgvsp: ENST00000409366.1:c.2433C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386547
  ensembl transcript: ENST00000409582
  gene symbol: DYSF
  hgvsc: ENST00000409582.3:c.2481C>T
  hgvsp: ENST00000409582.3:c.2481C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 940
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2137
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14545
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5539
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8974
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14838
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3308
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7357
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.75e1
  variant carriers: 10
genotype quality: GenotypeQuality
hgvs: p.Pro828Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
reference allele: C
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum

2-71791263-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71791263
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 71791263
    reference: chr 2
allele count: 10
allele frequency: 8.237096588194593e-5
allele num: 121402
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000377678
  ensembl transcript: ENST00000394120
  gene symbol: DYSF
  hgvsc: ENST00000394120.2:c.2434G>A
  hgvsp: ENSP00000377678.2:p.Ala812Thr
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386512
  ensembl transcript: ENST00000409366
  gene symbol: DYSF
  hgvsc: ENST00000409366.1:c.2434G>A
  hgvsp: ENSP00000386512.1:p.Ala812Thr
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386683
  ensembl transcript: ENST00000409651
  gene symbol: DYSF
  hgvsc: ENST00000409651.1:c.2527G>A
  hgvsp: ENSP00000386683.1:p.Ala843Thr
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386617
  ensembl transcript: ENST00000410041
  gene symbol: DYSF
  hgvsc: ENST00000410041.1:c.2485G>A
  hgvsp: ENSP00000386617.1:p.Ala829Thr
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386285
  ensembl transcript: ENST00000409744
  gene symbol: DYSF
  hgvsc: ENST00000409744.1:c.2392G>A
  hgvsp: ENSP00000386285.1:p.Ala798Thr
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000387137
  ensembl transcript: ENST00000409762
  gene symbol: DYSF
  hgvsc: ENST00000409762.1:c.2482G>A
  hgvsp: ENSP00000387137.1:p.Ala828Thr
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000258104
  ensembl transcript: ENST00000258104
  gene symbol: DYSF
  hgvsc: ENST00000258104.3:c.2431G>A
  hgvsp: ENSP00000258104.3:p.Ala811Thr
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386881
  ensembl transcript: ENST00000410020
  gene symbol: DYSF
  hgvsc: ENST00000410020.3:c.2485G>A
  hgvsp: ENSP00000386881.3:p.Ala829Thr
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000407046
  ensembl transcript: ENST00000413539
  gene symbol: DYSF
  hgvsc: ENST00000413539.2:c.2524G>A
  hgvsp: ENSP00000407046.2:p.Ala842Thr
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000398305
  ensembl transcript: ENST00000429174
  gene symbol: DYSF
  hgvsc: ENST00000429174.2:c.2431G>A
  hgvsp: ENSP00000398305.2:p.Ala811Thr
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386547
  ensembl transcript: ENST00000409582
  gene symbol: DYSF
  hgvsc: ENST00000409582.3:c.2482G>A
  hgvsp: ENSP00000386547.3:p.Ala828Thr
  variant of: http://identifiers.org/hgnc/3097
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3307
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1369
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5539
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8977
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14839
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14546
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7356
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2136
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
hgvs: p.Ala829Thr
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: South Asian
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum

2-71791278-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71791278
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 71791278
    reference: chr 2
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386683
  ensembl transcript: ENST00000409651
  gene symbol: DYSF
  hgvsc: ENST00000409651.1:c.2542T>C
  hgvsp: ENSP00000386683.1:p.Phe848Leu
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000387137
  ensembl transcript: ENST00000409762
  gene symbol: DYSF
  hgvsc: ENST00000409762.1:c.2497T>C
  hgvsp: ENSP00000387137.1:p.Phe833Leu
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386881
  ensembl transcript: ENST00000410020
  gene symbol: DYSF
  hgvsc: ENST00000410020.3:c.2500T>C
  hgvsp: ENSP00000386881.3:p.Phe834Leu
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386285
  ensembl transcript: ENST00000409744
  gene symbol: DYSF
  hgvsc: ENST00000409744.1:c.2407T>C
  hgvsp: ENSP00000386285.1:p.Phe803Leu
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000377678
  ensembl transcript: ENST00000394120
  gene symbol: DYSF
  hgvsc: ENST00000394120.2:c.2449T>C
  hgvsp: ENSP00000377678.2:p.Phe817Leu
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000398305
  ensembl transcript: ENST00000429174
  gene symbol: DYSF
  hgvsc: ENST00000429174.2:c.2446T>C
  hgvsp: ENSP00000398305.2:p.Phe816Leu
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000407046
  ensembl transcript: ENST00000413539
  gene symbol: DYSF
  hgvsc: ENST00000413539.2:c.2539T>C
  hgvsp: ENSP00000407046.2:p.Phe847Leu
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000258104
  ensembl transcript: ENST00000258104
  gene symbol: DYSF
  hgvsc: ENST00000258104.3:c.2446T>C
  hgvsp: ENSP00000258104.3:p.Phe816Leu
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386617
  ensembl transcript: ENST00000410041
  gene symbol: DYSF
  hgvsc: ENST00000410041.1:c.2500T>C
  hgvsp: ENSP00000386617.1:p.Phe834Leu
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386512
  ensembl transcript: ENST00000409366
  gene symbol: DYSF
  hgvsc: ENST00000409366.1:c.2449T>C
  hgvsp: ENSP00000386512.1:p.Phe817Leu
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386547
  ensembl transcript: ENST00000409582
  gene symbol: DYSF
  hgvsc: ENST00000409582.3:c.2497T>C
  hgvsp: ENSP00000386547.3:p.Phe833Leu
  variant of: http://identifiers.org/hgnc/3097
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14841
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14551
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8981
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1369
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2137
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3307
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7363
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe834Leu
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

2-71791284-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71791284
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 71791284
    reference: chr 2
allele count: 23
allele frequency: 1.894407379952228e-4
allele num: 121410
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386683
  ensembl transcript: ENST00000409651
  gene symbol: DYSF
  hgvsc: ENST00000409651.1:c.2548C>T
  hgvsp: ENSP00000386683.1:p.Arg850Trp
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000387137
  ensembl transcript: ENST00000409762
  gene symbol: DYSF
  hgvsc: ENST00000409762.1:c.2503C>T
  hgvsp: ENSP00000387137.1:p.Arg835Trp
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000258104
  ensembl transcript: ENST00000258104
  gene symbol: DYSF
  hgvsc: ENST00000258104.3:c.2452C>T
  hgvsp: ENSP00000258104.3:p.Arg818Trp
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386285
  ensembl transcript: ENST00000409744
  gene symbol: DYSF
  hgvsc: ENST00000409744.1:c.2413C>T
  hgvsp: ENSP00000386285.1:p.Arg805Trp
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386617
  ensembl transcript: ENST00000410041
  gene symbol: DYSF
  hgvsc: ENST00000410041.1:c.2506C>T
  hgvsp: ENSP00000386617.1:p.Arg836Trp
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000398305
  ensembl transcript: ENST00000429174
  gene symbol: DYSF
  hgvsc: ENST00000429174.2:c.2452C>T
  hgvsp: ENSP00000398305.2:p.Arg818Trp
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386512
  ensembl transcript: ENST00000409366
  gene symbol: DYSF
  hgvsc: ENST00000409366.1:c.2455C>T
  hgvsp: ENSP00000386512.1:p.Arg819Trp
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000407046
  ensembl transcript: ENST00000413539
  gene symbol: DYSF
  hgvsc: ENST00000413539.2:c.2545C>T
  hgvsp: ENSP00000407046.2:p.Arg849Trp
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386881
  ensembl transcript: ENST00000410020
  gene symbol: DYSF
  hgvsc: ENST00000410020.3:c.2506C>T
  hgvsp: ENSP00000386881.3:p.Arg836Trp
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386547
  ensembl transcript: ENST00000409582
  gene symbol: DYSF
  hgvsc: ENST00000409582.3:c.2503C>T
  hgvsp: ENSP00000386547.3:p.Arg835Trp
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000377678
  ensembl transcript: ENST00000394120
  gene symbol: DYSF
  hgvsc: ENST00000394120.2:c.2455C>T
  hgvsp: ENSP00000377678.2:p.Arg819Trp
  variant of: http://identifiers.org/hgnc/3097
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8979
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7352
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3304
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2133
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1369
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5536
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14845
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 9.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 937
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg836Trp
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum

2-71791285-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71791285
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 71791285
    reference: chr 2
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000258104
  ensembl transcript: ENST00000258104
  gene symbol: DYSF
  hgvsc: ENST00000258104.3:c.2453G>A
  hgvsp: ENSP00000258104.3:p.Arg818Gln
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000387137
  ensembl transcript: ENST00000409762
  gene symbol: DYSF
  hgvsc: ENST00000409762.1:c.2504G>A
  hgvsp: ENSP00000387137.1:p.Arg835Gln
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386512
  ensembl transcript: ENST00000409366
  gene symbol: DYSF
  hgvsc: ENST00000409366.1:c.2456G>A
  hgvsp: ENSP00000386512.1:p.Arg819Gln
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386683
  ensembl transcript: ENST00000409651
  gene symbol: DYSF
  hgvsc: ENST00000409651.1:c.2549G>A
  hgvsp: ENSP00000386683.1:p.Arg850Gln
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000377678
  ensembl transcript: ENST00000394120
  gene symbol: DYSF
  hgvsc: ENST00000394120.2:c.2456G>A
  hgvsp: ENSP00000377678.2:p.Arg819Gln
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386881
  ensembl transcript: ENST00000410020
  gene symbol: DYSF
  hgvsc: ENST00000410020.3:c.2507G>A
  hgvsp: ENSP00000386881.3:p.Arg836Gln
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000398305
  ensembl transcript: ENST00000429174
  gene symbol: DYSF
  hgvsc: ENST00000429174.2:c.2453G>A
  hgvsp: ENSP00000398305.2:p.Arg818Gln
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386547
  ensembl transcript: ENST00000409582
  gene symbol: DYSF
  hgvsc: ENST00000409582.3:c.2504G>A
  hgvsp: ENSP00000386547.3:p.Arg835Gln
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386285
  ensembl transcript: ENST00000409744
  gene symbol: DYSF
  hgvsc: ENST00000409744.1:c.2414G>A
  hgvsp: ENSP00000386285.1:p.Arg805Gln
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000407046
  ensembl transcript: ENST00000413539
  gene symbol: DYSF
  hgvsc: ENST00000413539.2:c.2546G>A
  hgvsp: ENSP00000407046.2:p.Arg849Gln
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386617
  ensembl transcript: ENST00000410041
  gene symbol: DYSF
  hgvsc: ENST00000410041.1:c.2507G>A
  hgvsp: ENSP00000386617.1:p.Arg836Gln
  variant of: http://identifiers.org/hgnc/3097
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7352
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14555
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1369
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5538
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3305
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2132
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8980
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 937
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg836Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: DP

2-71791287-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71791287
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 71791287
    reference: chr 2
allele count: 3
allele frequency: 2.471454698235381e-5
allele num: 121386
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000407046
  ensembl transcript: ENST00000413539
  gene symbol: DYSF
  hgvsc: ENST00000413539.2:c.2548C>T
  hgvsp: ENSP00000407046.2:p.Arg850Trp
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000258104
  ensembl transcript: ENST00000258104
  gene symbol: DYSF
  hgvsc: ENST00000258104.3:c.2455C>T
  hgvsp: ENSP00000258104.3:p.Arg819Trp
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386617
  ensembl transcript: ENST00000410041
  gene symbol: DYSF
  hgvsc: ENST00000410041.1:c.2509C>T
  hgvsp: ENSP00000386617.1:p.Arg837Trp
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386547
  ensembl transcript: ENST00000409582
  gene symbol: DYSF
  hgvsc: ENST00000409582.3:c.2506C>T
  hgvsp: ENSP00000386547.3:p.Arg836Trp
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386285
  ensembl transcript: ENST00000409744
  gene symbol: DYSF
  hgvsc: ENST00000409744.1:c.2416C>T
  hgvsp: ENSP00000386285.1:p.Arg806Trp
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386512
  ensembl transcript: ENST00000409366
  gene symbol: DYSF
  hgvsc: ENST00000409366.1:c.2458C>T
  hgvsp: ENSP00000386512.1:p.Arg820Trp
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000377678
  ensembl transcript: ENST00000394120
  gene symbol: DYSF
  hgvsc: ENST00000394120.2:c.2458C>T
  hgvsp: ENSP00000377678.2:p.Arg820Trp
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000398305
  ensembl transcript: ENST00000429174
  gene symbol: DYSF
  hgvsc: ENST00000429174.2:c.2455C>T
  hgvsp: ENSP00000398305.2:p.Arg819Trp
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000387137
  ensembl transcript: ENST00000409762
  gene symbol: DYSF
  hgvsc: ENST00000409762.1:c.2506C>T
  hgvsp: ENSP00000387137.1:p.Arg836Trp
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386881
  ensembl transcript: ENST00000410020
  gene symbol: DYSF
  hgvsc: ENST00000410020.3:c.2509C>T
  hgvsp: ENSP00000386881.3:p.Arg837Trp
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386683
  ensembl transcript: ENST00000409651
  gene symbol: DYSF
  hgvsc: ENST00000409651.1:c.2551C>T
  hgvsp: ENSP00000386683.1:p.Arg851Trp
  variant of: http://identifiers.org/hgnc/3097
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8977
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7350
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14547
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14847
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1369
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2133
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5539
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3303
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 937
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg837Trp
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum

2-71791288-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71791288
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 71791288
    reference: chr 2
allele count: 3
allele frequency: 2.471413978317461e-5
allele num: 121388
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386285
  ensembl transcript: ENST00000409744
  gene symbol: DYSF
  hgvsc: ENST00000409744.1:c.2417G>A
  hgvsp: ENSP00000386285.1:p.Arg806Gln
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386512
  ensembl transcript: ENST00000409366
  gene symbol: DYSF
  hgvsc: ENST00000409366.1:c.2459G>A
  hgvsp: ENSP00000386512.1:p.Arg820Gln
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000407046
  ensembl transcript: ENST00000413539
  gene symbol: DYSF
  hgvsc: ENST00000413539.2:c.2549G>A
  hgvsp: ENSP00000407046.2:p.Arg850Gln
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000258104
  ensembl transcript: ENST00000258104
  gene symbol: DYSF
  hgvsc: ENST00000258104.3:c.2456G>A
  hgvsp: ENSP00000258104.3:p.Arg819Gln
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000387137
  ensembl transcript: ENST00000409762
  gene symbol: DYSF
  hgvsc: ENST00000409762.1:c.2507G>A
  hgvsp: ENSP00000387137.1:p.Arg836Gln
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000398305
  ensembl transcript: ENST00000429174
  gene symbol: DYSF
  hgvsc: ENST00000429174.2:c.2456G>A
  hgvsp: ENSP00000398305.2:p.Arg819Gln
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386683
  ensembl transcript: ENST00000409651
  gene symbol: DYSF
  hgvsc: ENST00000409651.1:c.2552G>A
  hgvsp: ENSP00000386683.1:p.Arg851Gln
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386881
  ensembl transcript: ENST00000410020
  gene symbol: DYSF
  hgvsc: ENST00000410020.3:c.2510G>A
  hgvsp: ENSP00000386881.3:p.Arg837Gln
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000377678
  ensembl transcript: ENST00000394120
  gene symbol: DYSF
  hgvsc: ENST00000394120.2:c.2459G>A
  hgvsp: ENSP00000377678.2:p.Arg820Gln
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386617
  ensembl transcript: ENST00000410041
  gene symbol: DYSF
  hgvsc: ENST00000410041.1:c.2510G>A
  hgvsp: ENSP00000386617.1:p.Arg837Gln
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386547
  ensembl transcript: ENST00000409582
  gene symbol: DYSF
  hgvsc: ENST00000409582.3:c.2507G>A
  hgvsp: ENSP00000386547.3:p.Arg836Gln
  variant of: http://identifiers.org/hgnc/3097
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5539
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3304
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8976
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7350
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14849
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1369
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14547
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2132
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg837Gln
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: ReadPosRankSum

2-71791292-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71791292
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 71791292
    reference: chr 2
allele count: 73
allele frequency: 6.04815324197584e-4
allele num: 120698
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000387137
  ensembl transcript: ENST00000409762
  gene symbol: DYSF
  hgvsc: ENST00000409762.1:c.2511T>G
  hgvsp: ENST00000409762.1:c.2511T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000407046
  ensembl transcript: ENST00000413539
  gene symbol: DYSF
  hgvsc: ENST00000413539.2:c.2553T>G
  hgvsp: ENST00000413539.2:c.2553T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386285
  ensembl transcript: ENST00000409744
  gene symbol: DYSF
  hgvsc: ENST00000409744.1:c.2421T>G
  hgvsp: ENST00000409744.1:c.2421T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386881
  ensembl transcript: ENST00000410020
  gene symbol: DYSF
  hgvsc: ENST00000410020.3:c.2514T>G
  hgvsp: ENST00000410020.3:c.2514T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000258104
  ensembl transcript: ENST00000258104
  gene symbol: DYSF
  hgvsc: ENST00000258104.3:c.2460T>G
  hgvsp: ENST00000258104.3:c.2460T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386617
  ensembl transcript: ENST00000410041
  gene symbol: DYSF
  hgvsc: ENST00000410041.1:c.2514T>G
  hgvsp: ENST00000410041.1:c.2514T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000398305
  ensembl transcript: ENST00000429174
  gene symbol: DYSF
  hgvsc: ENST00000429174.2:c.2460T>G
  hgvsp: ENST00000429174.2:c.2460T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386512
  ensembl transcript: ENST00000409366
  gene symbol: DYSF
  hgvsc: ENST00000409366.1:c.2463T>G
  hgvsp: ENST00000409366.1:c.2463T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386683
  ensembl transcript: ENST00000409651
  gene symbol: DYSF
  hgvsc: ENST00000409651.1:c.2556T>G
  hgvsp: ENST00000409651.1:c.2556T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000377678
  ensembl transcript: ENST00000394120
  gene symbol: DYSF
  hgvsc: ENST00000394120.2:c.2463T>G
  hgvsp: ENST00000394120.2:c.2463T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386547
  ensembl transcript: ENST00000409582
  gene symbol: DYSF
  hgvsc: ENST00000409582.3:c.2511T>G
  hgvsp: ENST00000409582.3:c.2511T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14415
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 8.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 7.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 14606
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7093
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 9.75e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 6.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 5563
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1441
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3349
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 6.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 2186
  bin: 5.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
hgvs: p.Gly838Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: African
reference allele: T
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD

2-71791294-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71791294
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 71791294
    reference: chr 2
allele count: 1
allele frequency: 8.237775141689733e-6
allele num: 121392
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386683
  ensembl transcript: ENST00000409651
  gene symbol: DYSF
  hgvsc: ENST00000409651.1:c.2558C>T
  hgvsp: ENSP00000386683.1:p.Ala853Val
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000398305
  ensembl transcript: ENST00000429174
  gene symbol: DYSF
  hgvsc: ENST00000429174.2:c.2462C>T
  hgvsp: ENSP00000398305.2:p.Ala821Val
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386617
  ensembl transcript: ENST00000410041
  gene symbol: DYSF
  hgvsc: ENST00000410041.1:c.2516C>T
  hgvsp: ENSP00000386617.1:p.Ala839Val
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386881
  ensembl transcript: ENST00000410020
  gene symbol: DYSF
  hgvsc: ENST00000410020.3:c.2516C>T
  hgvsp: ENSP00000386881.3:p.Ala839Val
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386547
  ensembl transcript: ENST00000409582
  gene symbol: DYSF
  hgvsc: ENST00000409582.3:c.2513C>T
  hgvsp: ENSP00000386547.3:p.Ala838Val
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000377678
  ensembl transcript: ENST00000394120
  gene symbol: DYSF
  hgvsc: ENST00000394120.2:c.2465C>T
  hgvsp: ENSP00000377678.2:p.Ala822Val
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386512
  ensembl transcript: ENST00000409366
  gene symbol: DYSF
  hgvsc: ENST00000409366.1:c.2465C>T
  hgvsp: ENSP00000386512.1:p.Ala822Val
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000258104
  ensembl transcript: ENST00000258104
  gene symbol: DYSF
  hgvsc: ENST00000258104.3:c.2462C>T
  hgvsp: ENSP00000258104.3:p.Ala821Val
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386285
  ensembl transcript: ENST00000409744
  gene symbol: DYSF
  hgvsc: ENST00000409744.1:c.2423C>T
  hgvsp: ENSP00000386285.1:p.Ala808Val
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000387137
  ensembl transcript: ENST00000409762
  gene symbol: DYSF
  hgvsc: ENST00000409762.1:c.2513C>T
  hgvsp: ENSP00000387137.1:p.Ala838Val
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000407046
  ensembl transcript: ENST00000413539
  gene symbol: DYSF
  hgvsc: ENST00000413539.2:c.2555C>T
  hgvsp: ENSP00000407046.2:p.Ala852Val
  variant of: http://identifiers.org/hgnc/3097
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 5592
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14863
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2149
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14568
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7137
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8995
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3328
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1385
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala839Val
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: Latino
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum

2-71791306-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71791306
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 71791306
    reference: chr 2
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000377678
  ensembl transcript: ENST00000394120
  gene symbol: DYSF
  hgvsc: ENST00000394120.2:c.2477G>A
  hgvsp: ENSP00000377678.2:p.Gly826Asp
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000258104
  ensembl transcript: ENST00000258104
  gene symbol: DYSF
  hgvsc: ENST00000258104.3:c.2474G>A
  hgvsp: ENSP00000258104.3:p.Gly825Asp
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000407046
  ensembl transcript: ENST00000413539
  gene symbol: DYSF
  hgvsc: ENST00000413539.2:c.2567G>A
  hgvsp: ENSP00000407046.2:p.Gly856Asp
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386617
  ensembl transcript: ENST00000410041
  gene symbol: DYSF
  hgvsc: ENST00000410041.1:c.2528G>A
  hgvsp: ENSP00000386617.1:p.Gly843Asp
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000387137
  ensembl transcript: ENST00000409762
  gene symbol: DYSF
  hgvsc: ENST00000409762.1:c.2525G>A
  hgvsp: ENSP00000387137.1:p.Gly842Asp
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386881
  ensembl transcript: ENST00000410020
  gene symbol: DYSF
  hgvsc: ENST00000410020.3:c.2528G>A
  hgvsp: ENSP00000386881.3:p.Gly843Asp
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386285
  ensembl transcript: ENST00000409744
  gene symbol: DYSF
  hgvsc: ENST00000409744.1:c.2435G>A
  hgvsp: ENSP00000386285.1:p.Gly812Asp
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386547
  ensembl transcript: ENST00000409582
  gene symbol: DYSF
  hgvsc: ENST00000409582.3:c.2525G>A
  hgvsp: ENSP00000386547.3:p.Gly842Asp
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000398305
  ensembl transcript: ENST00000429174
  gene symbol: DYSF
  hgvsc: ENST00000429174.2:c.2474G>A
  hgvsp: ENSP00000398305.2:p.Gly825Asp
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386512
  ensembl transcript: ENST00000409366
  gene symbol: DYSF
  hgvsc: ENST00000409366.1:c.2477G>A
  hgvsp: ENSP00000386512.1:p.Gly826Asp
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386683
  ensembl transcript: ENST00000409651
  gene symbol: DYSF
  hgvsc: ENST00000409651.1:c.2570G>A
  hgvsp: ENSP00000386683.1:p.Gly857Asp
  variant of: http://identifiers.org/hgnc/3097
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7134
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14571
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8995
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2149
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5592
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14866
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1383
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly843Asp
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: African
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

2-71791307-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71791307
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 71791307
    reference: chr 2
allele count: 2
allele frequency: 1.647500741375333e-5
allele num: 121396
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000377678
  ensembl transcript: ENST00000394120
  gene symbol: DYSF
  hgvsc: ENST00000394120.2:c.2478C>T
  hgvsp: ENST00000394120.2:c.2478C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000387137
  ensembl transcript: ENST00000409762
  gene symbol: DYSF
  hgvsc: ENST00000409762.1:c.2526C>T
  hgvsp: ENST00000409762.1:c.2526C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000398305
  ensembl transcript: ENST00000429174
  gene symbol: DYSF
  hgvsc: ENST00000429174.2:c.2475C>T
  hgvsp: ENST00000429174.2:c.2475C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386512
  ensembl transcript: ENST00000409366
  gene symbol: DYSF
  hgvsc: ENST00000409366.1:c.2478C>T
  hgvsp: ENST00000409366.1:c.2478C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386285
  ensembl transcript: ENST00000409744
  gene symbol: DYSF
  hgvsc: ENST00000409744.1:c.2436C>T
  hgvsp: ENST00000409744.1:c.2436C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000407046
  ensembl transcript: ENST00000413539
  gene symbol: DYSF
  hgvsc: ENST00000413539.2:c.2568C>T
  hgvsp: ENST00000413539.2:c.2568C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386683
  ensembl transcript: ENST00000409651
  gene symbol: DYSF
  hgvsc: ENST00000409651.1:c.2571C>T
  hgvsp: ENST00000409651.1:c.2571C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000258104
  ensembl transcript: ENST00000258104
  gene symbol: DYSF
  hgvsc: ENST00000258104.3:c.2475C>T
  hgvsp: ENST00000258104.3:c.2475C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386881
  ensembl transcript: ENST00000410020
  gene symbol: DYSF
  hgvsc: ENST00000410020.3:c.2529C>T
  hgvsp: ENST00000410020.3:c.2529C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386547
  ensembl transcript: ENST00000409582
  gene symbol: DYSF
  hgvsc: ENST00000409582.3:c.2526C>T
  hgvsp: ENST00000409582.3:c.2526C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386617
  ensembl transcript: ENST00000410041
  gene symbol: DYSF
  hgvsc: ENST00000410041.1:c.2529C>T
  hgvsp: ENST00000410041.1:c.2529C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3328
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14867
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5592
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8995
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14568
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1383
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7136
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2149
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly843Gly
num of homozygotes: 0
population: Latino
population: Other
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

2-71791322-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71791322
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 71791322
    reference: chr 2
allele count: 3
allele frequency: 2.471536142096851e-5
allele num: 121382
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000377678
  ensembl transcript: ENST00000394120
  gene symbol: DYSF
  hgvsc: ENST00000394120.2:c.2493G>A
  hgvsp: ENST00000394120.2:c.2493G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386683
  ensembl transcript: ENST00000409651
  gene symbol: DYSF
  hgvsc: ENST00000409651.1:c.2586G>A
  hgvsp: ENST00000409651.1:c.2586G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386512
  ensembl transcript: ENST00000409366
  gene symbol: DYSF
  hgvsc: ENST00000409366.1:c.2493G>A
  hgvsp: ENST00000409366.1:c.2493G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000407046
  ensembl transcript: ENST00000413539
  gene symbol: DYSF
  hgvsc: ENST00000413539.2:c.2583G>A
  hgvsp: ENST00000413539.2:c.2583G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386881
  ensembl transcript: ENST00000410020
  gene symbol: DYSF
  hgvsc: ENST00000410020.3:c.2544G>A
  hgvsp: ENST00000410020.3:c.2544G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386547
  ensembl transcript: ENST00000409582
  gene symbol: DYSF
  hgvsc: ENST00000409582.3:c.2541G>A
  hgvsp: ENST00000409582.3:c.2541G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000258104
  ensembl transcript: ENST00000258104
  gene symbol: DYSF
  hgvsc: ENST00000258104.3:c.2490G>A
  hgvsp: ENST00000258104.3:c.2490G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386617
  ensembl transcript: ENST00000410041
  gene symbol: DYSF
  hgvsc: ENST00000410041.1:c.2544G>A
  hgvsp: ENST00000410041.1:c.2544G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386285
  ensembl transcript: ENST00000409744
  gene symbol: DYSF
  hgvsc: ENST00000409744.1:c.2451G>A
  hgvsp: ENST00000409744.1:c.2451G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000387137
  ensembl transcript: ENST00000409762
  gene symbol: DYSF
  hgvsc: ENST00000409762.1:c.2541G>A
  hgvsp: ENST00000409762.1:c.2541G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000398305
  ensembl transcript: ENST00000429174
  gene symbol: DYSF
  hgvsc: ENST00000429174.2:c.2490G>A
  hgvsp: ENST00000429174.2:c.2490G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3328
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1383
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7123
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8995
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14569
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5591
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14858
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2149
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 941
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys848Lys
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
population: Other
reference allele: G
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ReadPosRankSum

2-71791324-TACAG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71791324
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 71791320
    reference: chr 2
allele count: 1
allele frequency: 8.238861059847087e-6
allele num: 121376
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386547
  ensembl transcript: ENST00000409582
  gene symbol: DYSF
  hgvsc: ENST00000409582.3:c.2547_2550delGACA
  hgvsp: ENSP00000386547.3:p.Thr850SerfsTer3
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000387137
  ensembl transcript: ENST00000409762
  gene symbol: DYSF
  hgvsc: ENST00000409762.1:c.2547_2550delGACA
  hgvsp: ENSP00000387137.1:p.Thr850SerfsTer3
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386512
  ensembl transcript: ENST00000409366
  gene symbol: DYSF
  hgvsc: ENST00000409366.1:c.2499_2502delGACA
  hgvsp: ENSP00000386512.1:p.Thr834SerfsTer3
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000398305
  ensembl transcript: ENST00000429174
  gene symbol: DYSF
  hgvsc: ENST00000429174.2:c.2496_2499delGACA
  hgvsp: ENSP00000398305.2:p.Thr833SerfsTer3
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000258104
  ensembl transcript: ENST00000258104
  gene symbol: DYSF
  hgvsc: ENST00000258104.3:c.2496_2499delGACA
  hgvsp: ENSP00000258104.3:p.Thr833SerfsTer3
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386617
  ensembl transcript: ENST00000410041
  gene symbol: DYSF
  hgvsc: ENST00000410041.1:c.2550_2553delGACA
  hgvsp: ENSP00000386617.1:p.Thr851SerfsTer3
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386881
  ensembl transcript: ENST00000410020
  gene symbol: DYSF
  hgvsc: ENST00000410020.3:c.2550_2553delGACA
  hgvsp: ENSP00000386881.3:p.Thr851SerfsTer3
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386285
  ensembl transcript: ENST00000409744
  gene symbol: DYSF
  hgvsc: ENST00000409744.1:c.2457_2460delGACA
  hgvsp: ENSP00000386285.1:p.Thr820SerfsTer3
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386683
  ensembl transcript: ENST00000409651
  gene symbol: DYSF
  hgvsc: ENST00000409651.1:c.2592_2595delGACA
  hgvsp: ENSP00000386683.1:p.Thr865SerfsTer3
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000377678
  ensembl transcript: ENST00000394120
  gene symbol: DYSF
  hgvsc: ENST00000394120.2:c.2499_2502delGACA
  hgvsp: ENSP00000377678.2:p.Thr834SerfsTer3
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000407046
  ensembl transcript: ENST00000413539
  gene symbol: DYSF
  hgvsc: ENST00000413539.2:c.2589_2592delGACA
  hgvsp: ENSP00000407046.2:p.Thr864SerfsTer3
  variant of: http://identifiers.org/hgnc/3097
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 14569
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3328
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14854
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8996
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5592
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7121
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2149
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1382
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr851SerfsTer3
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: TACAG
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum

2-71791326-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71791326
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 71791326
    reference: chr 2
allele count: 3
allele frequency: 2.472024918011174e-5
allele num: 121358
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386547
  ensembl transcript: ENST00000409582
  gene symbol: DYSF
  hgvsc: ENST00000409582.3:c.2545C>T
  hgvsp: ENSP00000386547.3:p.Gln849Ter
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386285
  ensembl transcript: ENST00000409744
  gene symbol: DYSF
  hgvsc: ENST00000409744.1:c.2455C>T
  hgvsp: ENSP00000386285.1:p.Gln819Ter
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386881
  ensembl transcript: ENST00000410020
  gene symbol: DYSF
  hgvsc: ENST00000410020.3:c.2548C>T
  hgvsp: ENSP00000386881.3:p.Gln850Ter
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386512
  ensembl transcript: ENST00000409366
  gene symbol: DYSF
  hgvsc: ENST00000409366.1:c.2497C>T
  hgvsp: ENSP00000386512.1:p.Gln833Ter
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386683
  ensembl transcript: ENST00000409651
  gene symbol: DYSF
  hgvsc: ENST00000409651.1:c.2590C>T
  hgvsp: ENSP00000386683.1:p.Gln864Ter
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000258104
  ensembl transcript: ENST00000258104
  gene symbol: DYSF
  hgvsc: ENST00000258104.3:c.2494C>T
  hgvsp: ENSP00000258104.3:p.Gln832Ter
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000407046
  ensembl transcript: ENST00000413539
  gene symbol: DYSF
  hgvsc: ENST00000413539.2:c.2587C>T
  hgvsp: ENSP00000407046.2:p.Gln863Ter
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000387137
  ensembl transcript: ENST00000409762
  gene symbol: DYSF
  hgvsc: ENST00000409762.1:c.2545C>T
  hgvsp: ENSP00000387137.1:p.Gln849Ter
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000398305
  ensembl transcript: ENST00000429174
  gene symbol: DYSF
  hgvsc: ENST00000429174.2:c.2494C>T
  hgvsp: ENSP00000398305.2:p.Gln832Ter
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386617
  ensembl transcript: ENST00000410041
  gene symbol: DYSF
  hgvsc: ENST00000410041.1:c.2548C>T
  hgvsp: ENSP00000386617.1:p.Gln850Ter
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000377678
  ensembl transcript: ENST00000394120
  gene symbol: DYSF
  hgvsc: ENST00000394120.2:c.2497C>T
  hgvsp: ENSP00000377678.2:p.Gln833Ter
  variant of: http://identifiers.org/hgnc/3097
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8996
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7116
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1381
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5592
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 941
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2149
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14848
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14559
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3328
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln850Ter
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD

2-71791332-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71791332
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 71791332
    reference: chr 2
allele count: 3132
allele frequency: 2.581091772151899e-2
allele num: 121344
alternate allele: G
annotation: Annotation
  canonical: false
  clinical significance: benign&likely_benign
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000387137
  ensembl transcript: ENST00000409762
  gene symbol: DYSF
  hgvsc: ENST00000409762.1:c.2551A>G
  hgvsp: ENSP00000387137.1:p.Ile851Val
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: true
  clinical significance: benign&likely_benign
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386881
  ensembl transcript: ENST00000410020
  gene symbol: DYSF
  hgvsc: ENST00000410020.3:c.2554A>G
  hgvsp: ENSP00000386881.3:p.Ile852Val
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  clinical significance: benign&likely_benign
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386512
  ensembl transcript: ENST00000409366
  gene symbol: DYSF
  hgvsc: ENST00000409366.1:c.2503A>G
  hgvsp: ENSP00000386512.1:p.Ile835Val
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  clinical significance: benign&likely_benign
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000398305
  ensembl transcript: ENST00000429174
  gene symbol: DYSF
  hgvsc: ENST00000429174.2:c.2500A>G
  hgvsp: ENSP00000398305.2:p.Ile834Val
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  clinical significance: benign&likely_benign
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386683
  ensembl transcript: ENST00000409651
  gene symbol: DYSF
  hgvsc: ENST00000409651.1:c.2596A>G
  hgvsp: ENSP00000386683.1:p.Ile866Val
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  clinical significance: benign&likely_benign
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386617
  ensembl transcript: ENST00000410041
  gene symbol: DYSF
  hgvsc: ENST00000410041.1:c.2554A>G
  hgvsp: ENSP00000386617.1:p.Ile852Val
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  clinical significance: benign&likely_benign
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000258104
  ensembl transcript: ENST00000258104
  gene symbol: DYSF
  hgvsc: ENST00000258104.3:c.2500A>G
  hgvsp: ENSP00000258104.3:p.Ile834Val
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  clinical significance: benign&likely_benign
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386285
  ensembl transcript: ENST00000409744
  gene symbol: DYSF
  hgvsc: ENST00000409744.1:c.2461A>G
  hgvsp: ENSP00000386285.1:p.Ile821Val
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  clinical significance: benign&likely_benign
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000377678
  ensembl transcript: ENST00000394120
  gene symbol: DYSF
  hgvsc: ENST00000394120.2:c.2503A>G
  hgvsp: ENSP00000377678.2:p.Ile835Val
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  clinical significance: benign&likely_benign
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386547
  ensembl transcript: ENST00000409582
  gene symbol: DYSF
  hgvsc: ENST00000409582.3:c.2551A>G
  hgvsp: ENSP00000386547.3:p.Ile851Val
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  clinical significance: benign&likely_benign
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000407046
  ensembl transcript: ENST00000413539
  gene symbol: DYSF
  hgvsc: ENST00000413539.2:c.2593A>G
  hgvsp: ENSP00000407046.2:p.Ile865Val
  variant of: http://identifiers.org/hgnc/3097
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.75e1
  variant carriers: 128
genotype depth: GenotypeDepth
  all individuals: 1970
  bin: 5.25e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 8.25e1
  variant carriers: 137
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14072
  bin: 3.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 6762
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8539
  bin: 3.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 14397
  bin: 2.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 7.25e1
  variant carriers: 90
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 6.25e1
  variant carriers: 54
genotype depth: GenotypeDepth
  all individuals: 3070
  bin: 4.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 8.75e1
  variant carriers: 145
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1272
  bin: 5.75e1
  variant carriers: 37
genotype quality: GenotypeQuality
hgvs: p.Ile852Val
num of homozygotes: 82
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD

2-71791338-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71791338
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 71791338
    reference: chr 2
allele count: 2
allele frequency: 1.648723063986942e-5
allele num: 121306
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000387137
  ensembl transcript: ENST00000409762
  gene symbol: DYSF
  hgvsc: ENST00000409762.1:c.2557C>G
  hgvsp: ENSP00000387137.1:p.Leu853Val
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386285
  ensembl transcript: ENST00000409744
  gene symbol: DYSF
  hgvsc: ENST00000409744.1:c.2467C>G
  hgvsp: ENSP00000386285.1:p.Leu823Val
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000398305
  ensembl transcript: ENST00000429174
  gene symbol: DYSF
  hgvsc: ENST00000429174.2:c.2506C>G
  hgvsp: ENSP00000398305.2:p.Leu836Val
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386881
  ensembl transcript: ENST00000410020
  gene symbol: DYSF
  hgvsc: ENST00000410020.3:c.2560C>G
  hgvsp: ENSP00000386881.3:p.Leu854Val
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386683
  ensembl transcript: ENST00000409651
  gene symbol: DYSF
  hgvsc: ENST00000409651.1:c.2602C>G
  hgvsp: ENSP00000386683.1:p.Leu868Val
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000258104
  ensembl transcript: ENST00000258104
  gene symbol: DYSF
  hgvsc: ENST00000258104.3:c.2506C>G
  hgvsp: ENSP00000258104.3:p.Leu836Val
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386512
  ensembl transcript: ENST00000409366
  gene symbol: DYSF
  hgvsc: ENST00000409366.1:c.2509C>G
  hgvsp: ENSP00000386512.1:p.Leu837Val
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386617
  ensembl transcript: ENST00000410041
  gene symbol: DYSF
  hgvsc: ENST00000410041.1:c.2560C>G
  hgvsp: ENSP00000386617.1:p.Leu854Val
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000377678
  ensembl transcript: ENST00000394120
  gene symbol: DYSF
  hgvsc: ENST00000394120.2:c.2509C>G
  hgvsp: ENSP00000377678.2:p.Leu837Val
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000407046
  ensembl transcript: ENST00000413539
  gene symbol: DYSF
  hgvsc: ENST00000413539.2:c.2599C>G
  hgvsp: ENSP00000407046.2:p.Leu867Val
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386547
  ensembl transcript: ENST00000409582
  gene symbol: DYSF
  hgvsc: ENST00000409582.3:c.2557C>G
  hgvsp: ENSP00000386547.3:p.Leu853Val
  variant of: http://identifiers.org/hgnc/3097
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5482
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3232
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2053
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15054
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8966
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6833
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14823
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1327
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 929
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu854Val
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

2-71791340-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71791340
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 71791340
    reference: chr 2
allele count: 3
allele frequency: 2.473451619286327e-5
allele num: 121288
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000398305
  ensembl transcript: ENST00000429174
  gene symbol: DYSF
  hgvsc: ENST00000429174.2:c.2508G>C
  hgvsp: ENST00000429174.2:c.2508G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386881
  ensembl transcript: ENST00000410020
  gene symbol: DYSF
  hgvsc: ENST00000410020.3:c.2562G>C
  hgvsp: ENST00000410020.3:c.2562G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000407046
  ensembl transcript: ENST00000413539
  gene symbol: DYSF
  hgvsc: ENST00000413539.2:c.2601G>C
  hgvsp: ENST00000413539.2:c.2601G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386617
  ensembl transcript: ENST00000410041
  gene symbol: DYSF
  hgvsc: ENST00000410041.1:c.2562G>C
  hgvsp: ENST00000410041.1:c.2562G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386512
  ensembl transcript: ENST00000409366
  gene symbol: DYSF
  hgvsc: ENST00000409366.1:c.2511G>C
  hgvsp: ENST00000409366.1:c.2511G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000387137
  ensembl transcript: ENST00000409762
  gene symbol: DYSF
  hgvsc: ENST00000409762.1:c.2559G>C
  hgvsp: ENST00000409762.1:c.2559G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386547
  ensembl transcript: ENST00000409582
  gene symbol: DYSF
  hgvsc: ENST00000409582.3:c.2559G>C
  hgvsp: ENST00000409582.3:c.2559G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386285
  ensembl transcript: ENST00000409744
  gene symbol: DYSF
  hgvsc: ENST00000409744.1:c.2469G>C
  hgvsp: ENST00000409744.1:c.2469G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000377678
  ensembl transcript: ENST00000394120
  gene symbol: DYSF
  hgvsc: ENST00000394120.2:c.2511G>C
  hgvsp: ENST00000394120.2:c.2511G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386683
  ensembl transcript: ENST00000409651
  gene symbol: DYSF
  hgvsc: ENST00000409651.1:c.2604G>C
  hgvsp: ENST00000409651.1:c.2604G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000258104
  ensembl transcript: ENST00000258104
  gene symbol: DYSF
  hgvsc: ENST00000258104.3:c.2508G>C
  hgvsp: ENST00000258104.3:c.2508G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3097
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6827
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1327
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3232
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 929
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2052
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14822
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15047
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8963
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu854Leu
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD

2-71791349-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71791349
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 71791349
    reference: chr 2
allele count: 1
allele frequency: 8.248647221855616e-6
allele num: 121232
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000407046
  ensembl transcript: ENST00000413539
  gene symbol: DYSF
  hgvsc: ENST00000413539.2:c.2604+6T>C
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000387137
  ensembl transcript: ENST00000409762
  gene symbol: DYSF
  hgvsc: ENST00000409762.1:c.2562+6T>C
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386547
  ensembl transcript: ENST00000409582
  gene symbol: DYSF
  hgvsc: ENST00000409582.3:c.2562+6T>C
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386512
  ensembl transcript: ENST00000409366
  gene symbol: DYSF
  hgvsc: ENST00000409366.1:c.2514+6T>C
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000258104
  ensembl transcript: ENST00000258104
  gene symbol: DYSF
  hgvsc: ENST00000258104.3:c.2511+6T>C
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386881
  ensembl transcript: ENST00000410020
  gene symbol: DYSF
  hgvsc: ENST00000410020.3:c.2565+6T>C
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386617
  ensembl transcript: ENST00000410041
  gene symbol: DYSF
  hgvsc: ENST00000410041.1:c.2565+6T>C
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386285
  ensembl transcript: ENST00000409744
  gene symbol: DYSF
  hgvsc: ENST00000409744.1:c.2472+6T>C
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000398305
  ensembl transcript: ENST00000429174
  gene symbol: DYSF
  hgvsc: ENST00000429174.2:c.2511+6T>C
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000377678
  ensembl transcript: ENST00000394120
  gene symbol: DYSF
  hgvsc: ENST00000394120.2:c.2514+6T>C
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386683
  ensembl transcript: ENST00000409651
  gene symbol: DYSF
  hgvsc: ENST00000409651.1:c.2607+6T>C
  variant of: http://identifiers.org/hgnc/3097
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1327
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14813
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5481
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6793
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15026
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 929
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8961
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3230
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2052
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.2565+6T>C
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

2-71791363-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71791363
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 71791363
    reference: chr 2
allele count: 1
allele frequency: 8.257774694875225e-6
allele num: 121098
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386617
  ensembl transcript: ENST00000410041
  gene symbol: DYSF
  hgvsc: ENST00000410041.1:c.2565+20A>G
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386881
  ensembl transcript: ENST00000410020
  gene symbol: DYSF
  hgvsc: ENST00000410020.3:c.2565+20A>G
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386683
  ensembl transcript: ENST00000409651
  gene symbol: DYSF
  hgvsc: ENST00000409651.1:c.2607+20A>G
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000258104
  ensembl transcript: ENST00000258104
  gene symbol: DYSF
  hgvsc: ENST00000258104.3:c.2511+20A>G
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000377678
  ensembl transcript: ENST00000394120
  gene symbol: DYSF
  hgvsc: ENST00000394120.2:c.2514+20A>G
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000387137
  ensembl transcript: ENST00000409762
  gene symbol: DYSF
  hgvsc: ENST00000409762.1:c.2562+20A>G
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386285
  ensembl transcript: ENST00000409744
  gene symbol: DYSF
  hgvsc: ENST00000409744.1:c.2472+20A>G
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000407046
  ensembl transcript: ENST00000413539
  gene symbol: DYSF
  hgvsc: ENST00000413539.2:c.2604+20A>G
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386512
  ensembl transcript: ENST00000409366
  gene symbol: DYSF
  hgvsc: ENST00000409366.1:c.2514+20A>G
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000398305
  ensembl transcript: ENST00000429174
  gene symbol: DYSF
  hgvsc: ENST00000429174.2:c.2511+20A>G
  variant of: http://identifiers.org/hgnc/3097
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135636
  ensembl protein: ENSP00000386547
  ensembl transcript: ENST00000409582
  gene symbol: DYSF
  hgvsc: ENST00000409582.3:c.2562+20A>G
  variant of: http://identifiers.org/hgnc/3097
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5470
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8938
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1328
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3231
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6722
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14922
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2051
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14751
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
reference allele: A

GenotypeDepth
all individuals: 466
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1069
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9308
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 442
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31789
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 285
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 388
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 734
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1450
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5107
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 435
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6054
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 914
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 576
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1549
bin: 2.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8010
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9438
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5582
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.46790380609733e-5
allele num: 10562
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61676
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 806
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15446
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.87e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.69e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.95e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.43e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.398e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.99e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

DP
type: SiteQuality
SIO_000300: 1.6864e6

GenotypeDepth
all individuals: 328
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11221
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1875
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 413
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28781
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 995
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1779
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 812
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 881
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 900
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 852
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6053
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 442
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 327
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4686
bin: 6.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15254
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.295327225993541e-5
allele num: 60692
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5470
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10332
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7850
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.641437e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.44e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.7e-3

MQRankSum
type: SiteQuality
SIO_000300: 7.22e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.62e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.78e0

VQSLOD
type: SiteQuality
SIO_000300: 4.64e-1

FS
type: SiteQuality
SIO_000300: 4.407e0

QD
type: SiteQuality
SIO_000300: 1.564e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 559
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6060
bin: 9.75e1
variant carriers: 13

GenotypeQuality
all individuals: 332
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11719
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1832
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4569
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 511
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 389
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 224
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 804
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 717
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 915
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 939
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28831
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1951
bin: 2.75e1
variant carriers: 0

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

African
type: Population
allele count: 13
allele frequency: 1.411509229098806e-3
allele num: 9210
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5448
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60416
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10288
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7798
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15214
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 5.887e0

MQRankSum
type: SiteQuality
SIO_000300: 6.900000000000001e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.07e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.42e-1

QD
type: SiteQuality
SIO_000300: 1.159e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.9e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.42e0

DP
type: SiteQuality
SIO_000300: 1.62922e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.971e0

GenotypeQuality
all individuals: 932
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 502
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22202
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6040
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 419
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2825
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 764
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3651
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 315
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 650
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16403
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 250
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 397
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2751
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1386
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5094
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.743088334457182e-5
allele num: 14830
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 57796
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8770
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7322
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 748
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9728
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.71e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.25e-1

DP
type: SiteQuality
SIO_000300: 1.512255e6

VQSLOD
type: SiteQuality
SIO_000300: -9.07e-2

QD
type: SiteQuality
SIO_000300: 9.609999999999999e0

MQRankSum
type: SiteQuality
SIO_000300: 4.78e-1

FS
type: SiteQuality
SIO_000300: 7.183e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.059e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.7e-3

GenotypeQuality
all individuals: 251
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 520
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2008
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2275
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21617
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 463
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 295
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15082
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 491
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 426
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 502
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 122
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 301
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4359
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6096
bin: 9.75e1
variant carriers: 62

GenotypeQuality
all individuals: 4283
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 414
bin: 5.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6870
num of homozygotes: 0

African
type: Population
allele count: 64
allele frequency: 7.688611244593946e-3
allele num: 8324
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.828956031896993e-5
allele num: 54676
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14336
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4722
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8972
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.71e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.61e-1

QD
type: SiteQuality
SIO_000300: 1.476e1

FS
type: SiteQuality
SIO_000300: 2.61e0

VQSLOD
type: SiteQuality
SIO_000300: 2.24e0

MQRankSum
type: SiteQuality
SIO_000300: 2.0e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.0e-3

DP
type: SiteQuality
SIO_000300: 1.364521e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.5e-1

GenotypeQuality
all individuals: 6039
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2185
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1107
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 481
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 435
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 335
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 530
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 472
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4649
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 242
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 385
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22385
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2171
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4675
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13417
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 476
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8182
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6772
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.693989878467733e-5
allele num: 54142
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14276
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 718
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8866
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4660
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.922e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.09e0

VQSLOD
type: SiteQuality
SIO_000300: -6.827e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.7e0

FS
type: SiteQuality
SIO_000300: 7.454e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.4e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -8.37e-1

DP
type: SiteQuality
SIO_000300: 1.335959e6

QD
type: SiteQuality
SIO_000300: 1.265e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.53e-1

GenotypeQuality
all individuals: 362
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 496
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2122
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 431
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4858
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 347
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 234
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2292
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1218
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 22718
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4901
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6037
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 546
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 290
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 464
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12545
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.856114039646596e-5
allele num: 53876
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8798
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6724
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4644
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8150
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 714
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14226
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.691e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.89e0

DP
type: SiteQuality
SIO_000300: 1.32083e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.7e-3

QD
type: SiteQuality
SIO_000300: 7.65e0

MQ
type: SiteQuality
SIO_000300: 5.93e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.852e0

MQRankSum
type: SiteQuality
SIO_000300: -5.6e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.719e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.676e0

GenotypeQuality
all individuals: 282
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5452
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5918
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 616
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 281
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1284
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1975
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 669
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 732
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 434
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1029
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8040
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5984
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 176
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 491
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24143
bin: 2.25e1
variant carriers: 0

African
type: Population
allele count: 3
allele frequency: 3.896103896103896e-4
allele num: 7700
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6320
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 51634
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 678
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.198465963566635e-4
allele num: 8344
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4316
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13768
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.5e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.288e1

DP
type: SiteQuality
SIO_000300: 1.238613e6

FS
type: SiteQuality
SIO_000300: 1.0839e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.12e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.67e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.71e-1

VQSLOD
type: SiteQuality
SIO_000300: -8.004e-1

GenotypeQuality
all individuals: 170
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 609
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5985
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 24420
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1946
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5446
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 892
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 281
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 280
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 468
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 451
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 436
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 650
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 165
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8378
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1257
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 86
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2761
bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.936708370453577e-5
allele num: 51634
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6306
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.298026998961578e-4
allele num: 7704
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4322
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 680
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13750
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8336
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.8e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.76e0

QD
type: SiteQuality
SIO_000300: 1.054e1

MQ
type: SiteQuality
SIO_000300: 5.95e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.18e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.1e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.35e-1

DP
type: SiteQuality
SIO_000300: 1.23667e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.6e-3

GenotypeQuality
all individuals: 252
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 612
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 289
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1092
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 370
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5670
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23887
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6751
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2684
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1243
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5845
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 944
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3475
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5981
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 115
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 262
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7952
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 664
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13510
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.656177542232527e-4
allele num: 6038
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 50082
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4168
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.58e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.97e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.5e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.8e-2

MQRankSum
type: SiteQuality
SIO_000300: -5.28e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.8e-3

MQ
type: SiteQuality
SIO_000300: 5.911e1

FS
type: SiteQuality
SIO_000300: 5.579e0

QD
type: SiteQuality
SIO_000300: 6.72e0

DP
type: SiteQuality
SIO_000300: 1.183728e6

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

GenotypeQuality
all individuals: 1414
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 252
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3063
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 828
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3748
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23466
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4834
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1347
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 184
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 961
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6022
bin: 9.75e1
variant carriers: 47

GenotypeQuality
all individuals: 230
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5896
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 730
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6947
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 5.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7246
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5860
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 652
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7758
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13370
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4066
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 42
allele frequency: 8.541793776693106e-4
allele num: 49170
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.16346e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.38e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.6e-3

MQRankSum
type: SiteQuality
SIO_000300: -1.06e-1

FS
type: SiteQuality
SIO_000300: 7.63e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.5e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.41e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.65e-1

QD
type: SiteQuality
SIO_000300: 1.411e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 293
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2056
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 233
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3464
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7099
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 569
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1186
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22208
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4111
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 943
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2001
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5814
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 295
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 205
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5980
bin: 9.75e1
variant carriers: 3

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3836
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13024
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5488
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 4.131093362709997e-4
allele num: 7262
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6820
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 628
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47014
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -3.557e-1

DP
type: SiteQuality
SIO_000300: 1.130685e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.900000000000001e-3

MQ
type: SiteQuality
SIO_000300: 5.89e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.26e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.29e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.37e-1

QD
type: SiteQuality
SIO_000300: 1.328e1

MQRankSum
type: SiteQuality
SIO_000300: 1.03e-1

FS
type: SiteQuality
SIO_000300: 3.104e0

GenotypeQuality
all individuals: 4258
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2651
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5981
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 20898
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 518
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 379
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2322
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5789
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7162
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 253
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2897
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3945
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1294
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 388
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 230
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 202
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 6.543646119617851e-5
allele num: 45846
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6972
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3728
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 608
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6618
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12882
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5330
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.5e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.09e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.324e0

DP
type: SiteQuality
SIO_000300: 1.118274e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.22e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.417e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.5e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.72e0

GenotypeQuality
all individuals: 2483
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 455
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2692
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 195
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7138
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4027
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1133
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5743
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5979
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2624
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21069
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4246
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 356
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1314
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 228
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 481
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6846
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3702
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6528
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 606
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.923076923076923e-4
allele num: 5200
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12788
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 45274
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.1e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.453e0

VQSLOD
type: SiteQuality
SIO_000300: -1.776e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.453e0

DP
type: SiteQuality
SIO_000300: 1.110806e6

MQRankSum
type: SiteQuality
SIO_000300: 1.67e0

QD
type: SiteQuality
SIO_000300: 8.970000000000001e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.12e-2

GenotypeQuality
all individuals: 2606
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 376
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 191
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4251
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2864
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5978
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1347
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4080
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7187
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5765
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 367
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 225
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20736
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 476
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1190
bin: 4.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5186
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6780
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.851758793969849e-5
allele num: 12736
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6462
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3688
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44966
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 594
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.3e-1

QD
type: SiteQuality
SIO_000300: 1.337e1

DP
type: SiteQuality
SIO_000300: 1.10662e6

MQRankSum
type: SiteQuality
SIO_000300: 6.42e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.5e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.09e-2

FS
type: SiteQuality
SIO_000300: 1.895e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.095e0

MQ
type: SiteQuality
SIO_000300: 5.96e1

VQSLOD
type: SiteQuality
SIO_000300: 2.26e0

GenotypeQuality
all individuals: 812
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1440
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 963
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 396
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5554
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3602
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1689
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4271
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 213
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7153
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15001
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7512
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4317
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5981
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 935
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 224
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5918
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5896
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.424947863620932e-5
allele num: 41238
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12166
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3322
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 560
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.807e0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.22e-1

DP
type: SiteQuality
SIO_000300: 1.084099e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.88e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.129999999999999e-1

MQ
type: SiteQuality
SIO_000300: 5.855e1

MQRankSum
type: SiteQuality
SIO_000300: 1.14e0

QD
type: SiteQuality
SIO_000300: 1.055e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.35e-2

GenotypeQuality
all individuals: 4181
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 866
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3301
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3106
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14739
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 596
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 895
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 265
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 990
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4777
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 244
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 839
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 477
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2148
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1179
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13982
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 742
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6501
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 615
bin: 4.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.105107902499612e-5
allele num: 64410
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.028171910343409e-4
allele num: 9726
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6148
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 858
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.53e-2

QD
type: SiteQuality
SIO_000300: 1.203e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 5.57e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.8e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.78e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.564e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.047848e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.5e-2

GenotypeQuality
all individuals: 895
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 477
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 742
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 990
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 866
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14739
bin: 9.75e1
variant carriers: 250

GenotypeQuality
all individuals: 839
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 244
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4777
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 13982
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 3106
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 265
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 596
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3301
bin: 7.25e1
variant carriers: 2

GenotypeQuality
all individuals: 4181
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 6501
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1179
bin: 5.25e1
variant carriers: 2

GenotypeQuality
all individuals: 2148
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 615
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 245
allele frequency: 2.519021180341353e-2
allele num: 9726
num of homozygotes: 1

East Asian
type: Population
allele count: 1
allele frequency: 1.165229550221394e-4
allele num: 8582
num of homozygotes: 0

Latino
type: Population
allele count: 7
allele frequency: 6.125306265313265e-4
allele num: 11428
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6148
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.762769756249029e-5
allele num: 64410
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 858
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.564e0

MQRankSum
type: SiteQuality
SIO_000300: 2.78e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.53e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.203e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.5e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.8e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 5.57e0

DP
type: SiteQuality
SIO_000300: 2.047848e6

GenotypeQuality
all individuals: 810
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 173
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 819
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14779
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 817
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6860
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2180
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 386
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 892
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 530
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3434
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4243
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1066
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3147
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14605
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 4890
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.008471157724889e-4
allele num: 9916
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6344
num of homozygotes: 0

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

South Asian
type: Population
allele count: 4
allele frequency: 2.424242424242424e-4
allele num: 16500
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.62178400862733e-5
allele num: 64910
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.96e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.79e-1

DP
type: SiteQuality
SIO_000300: 2.054176e6

QD
type: SiteQuality
SIO_000300: 1.224e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.42e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 2.99e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.34e-1

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

GenotypeQuality
all individuals: 561
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4921
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 246
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16486
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 418
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 330
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14593
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1237
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3148
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 596
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7146
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4239
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3478
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2187
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65112
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6382
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.727526618956188e-5
allele num: 11458
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9976
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.3e0

MQ
type: SiteQuality
SIO_000300: 5.957e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.2e-2

FS
type: SiteQuality
SIO_000300: 2.143e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -4.273e0

DP
type: SiteQuality
SIO_000300: 2.064259e6

MQRankSum
type: SiteQuality
SIO_000300: -8.500000000000001e-2

QD
type: SiteQuality
SIO_000300: 1.229e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.58e-1

GenotypeQuality
all individuals: 17351
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1131
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3160
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 185
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 216
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 547
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14603
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 28
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3537
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 465
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2200
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4274
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4935
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7287
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.530877805333578e-5
allele num: 65322
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6428
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10018
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.935e0

MQRankSum
type: SiteQuality
SIO_000300: -1.436e0

DP
type: SiteQuality
SIO_000300: 2.07485e6

QD
type: SiteQuality
SIO_000300: 1.613e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.026e0

MQ
type: SiteQuality
SIO_000300: 5.928e1

VQSLOD
type: SiteQuality
SIO_000300: -9.981e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.51e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

GenotypeQuality
all individuals: 69
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 447
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17530
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 508
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 173
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1121
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4959
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 352
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2209
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7351
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3552
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3163
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14605
bin: 9.75e1
variant carriers: 1

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.529239050648397e-5
allele num: 65392
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6448
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.600000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -6.25e-1

DP
type: SiteQuality
SIO_000300: 2.076346e6

MQRankSum
type: SiteQuality
SIO_000300: 9.370000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.434e1

FS
type: SiteQuality
SIO_000300: 6.394e0

MQ
type: SiteQuality
SIO_000300: 5.957e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.82e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.86e-1

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

GenotypeQuality
all individuals: 406
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3577
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 17682
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7379
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3173
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4993
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1032
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4289
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2217
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14621
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 303
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 472
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10062
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6458
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: 1
allele frequency: 1.52699731248473e-5
allele num: 65488
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: 8620
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.47e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.234e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.43e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.095e0

QD
type: SiteQuality
SIO_000300: 5.53e0

DP
type: SiteQuality
SIO_000300: 2.080757e6

VQSLOD
type: SiteQuality
SIO_000300: -2.653e0

MQ
type: SiteQuality
SIO_000300: 5.893e1

GenotypeQuality
all individuals: 13
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 376
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14680
bin: 9.75e1
variant carriers: 113

GenotypeQuality
all individuals: 18
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2218
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17837
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 268
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 55
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3173
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4981
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 973
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 404
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4286
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3579
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

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

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

African
type: Population
allele count: 4
allele frequency: 3.965107057890563e-4
allele num: 10088
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 102
allele frequency: 1.555921654768442e-3
allele num: 65556
num of homozygotes: 0

Latino
type: Population
allele count: 5
allele frequency: 4.358437935843794e-4
allele num: 11472
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 5.41e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.165e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

DP
type: SiteQuality
SIO_000300: 2.084729e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.26e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.83e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.43e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.802e0

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

GenotypeQuality
all individuals: 118
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14606
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 17951
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3584
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 359
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4301
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2218
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3191
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 953
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 246
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5009
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 374
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 1.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.05766900896535e-5
allele num: 16508
num of homozygotes: 0

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65590
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -9.87e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.91e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -8.43e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.81e-1

DP
type: SiteQuality
SIO_000300: 2.084907e6

FS
type: SiteQuality
SIO_000300: 1.17e0

QD
type: SiteQuality
SIO_000300: 8.92e0

MQ
type: SiteQuality
SIO_000300: 5.952e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.98e-1

GenotypeQuality
all individuals: 172
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18698
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5072
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2230
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7560
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 3633
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4331
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14627
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3197
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 4.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6544
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.75800156128025e-5
allele num: 10248
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66092
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8642
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11500
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.51e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.4e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.659e0

MQ
type: SiteQuality
SIO_000300: 5.96e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.147e0

FS
type: SiteQuality
SIO_000300: 2.337e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.2e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 3.137e1

DP
type: SiteQuality
SIO_000300: 2.100972e6

GenotypeQuality
all individuals: 3197
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 524
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 178
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 21
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 126
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3635
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2229
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18618
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4333
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14631
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 7535
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 98
bin: 4.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8638
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10250
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.025627061208436e-5
allele num: 66102
num of homozygotes: 0

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.4e-2

QD
type: SiteQuality
SIO_000300: 1.112e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

FS
type: SiteQuality
SIO_000300: 4.905e0

MQRankSum
type: SiteQuality
SIO_000300: 4.59e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.78e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 8.32e-1

DP
type: SiteQuality
SIO_000300: 2.102756e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.5e0

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

GenotypeQuality
all individuals: 33
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4349
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14640
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 15
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5104
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3663
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 5.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 143
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 455
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7640
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2236
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3206
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 4.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10282
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 2
allele frequency: 3.049710277523635e-4
allele num: 6558
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66206
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.606882168925965e-4
allele num: 11508
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 8.67e-1

QD
type: SiteQuality
SIO_000300: 1.325e1

FS
type: SiteQuality
SIO_000300: 3.743e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -3.348e0

MQRankSum
type: SiteQuality
SIO_000300: -5.33e-1

DP
type: SiteQuality
SIO_000300: 2.104997e6

ClippingRankSum
type: SiteQuality
SIO_000300: -8.44e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.71e-1

GenotypeQuality
all individuals: 2235
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 13
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7646
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 416
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 2.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 97
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3207
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18893
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4356
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5097
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3667
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66254
num of homozygotes: 0

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

Latino
type: Population
allele count: 3
allele frequency: 2.605523710265763e-4
allele num: 11514
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10294
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.525e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.538e1

FS
type: SiteQuality
SIO_000300: 7.08e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.36e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.73e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.26e0

MQRankSum
type: SiteQuality
SIO_000300: 1.43e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 2.106123e6

GenotypeQuality
all individuals: 359
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 121
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2239
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5105
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18942
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3212
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3668
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4355
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7646
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14642
bin: 9.75e1
variant carriers: 1

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

African
type: Population
allele count: 1
allele frequency: 9.691800736576855e-5
allele num: 10318
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66310
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11514
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.2e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.1e-2

DP
type: SiteQuality
SIO_000300: 2.10805e6

MQRankSum
type: SiteQuality
SIO_000300: 1.69e0

QD
type: SiteQuality
SIO_000300: 1.217e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.8e-2

FS
type: SiteQuality
SIO_000300: 6.032e0

MQ
type: SiteQuality
SIO_000300: 5.958e1

VQSLOD
type: SiteQuality
SIO_000300: -9.41e-2

GenotypeQuality
all individuals: 62
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 313
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 18976
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3662
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3210
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5109
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2237
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7634
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4349
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.679048776254123e-5
allele num: 11522
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66322
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10336
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6550
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.32e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.65e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.97e-1

MQRankSum
type: SiteQuality
SIO_000300: -8.699999999999999e-2

FS
type: SiteQuality
SIO_000300: 2.255e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

DP
type: SiteQuality
SIO_000300: 2.109398e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.22e0

MQ
type: SiteQuality
SIO_000300: 5.89e1

QD
type: SiteQuality
SIO_000300: 1.008e1

GenotypeQuality
all individuals: 5137
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6
bin: 7.5e0
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2241
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19195
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3224
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7698
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 207
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4365
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14647
bin: 9.75e1
variant carriers: 2

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.008695128922586e-5
allele num: 66474
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11534
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10370
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 4.233e0

VQSLOD
type: SiteQuality
SIO_000300: -8.225e-1

MQ
type: SiteQuality
SIO_000300: 5.87e1

MQRankSum
type: SiteQuality
SIO_000300: 1.06e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.521e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

QD
type: SiteQuality
SIO_000300: 1.3e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.17e-1

DP
type: SiteQuality
SIO_000300: 2.112739e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.134e0

GenotypeQuality
all individuals: 46
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 7715
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4370
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 19277
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 19
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 168
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3229
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3713
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14647
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 46
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2240
bin: 8.75e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66530
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.184e0

DP
type: SiteQuality
SIO_000300: 2.114239e6

FS
type: SiteQuality
SIO_000300: 2.44e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.5e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.49e0

QD
type: SiteQuality
SIO_000300: 9.82e0

MQ
type: SiteQuality
SIO_000300: 5.972e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.206e0

MQRankSum
type: SiteQuality
SIO_000300: 6.43e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

GenotypeDepth
all individuals: 159
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 14
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7729
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14649
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2246
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 19399
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4367
bin: 8.25e1
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 100
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3722
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5156
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3230
bin: 9.25e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66614
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10390
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.155802126675913e-4
allele num: 8652
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.77e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.152e0

FS
type: SiteQuality
SIO_000300: 1.608e0

VQSLOD
type: SiteQuality
SIO_000300: 4.4e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.403e0

MQRankSum
type: SiteQuality
SIO_000300: -4.61e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.116546e6

QD
type: SiteQuality
SIO_000300: 1.17e1

GenotypeDepth
all individuals: 168
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 206
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1366
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14480
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3230
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5157
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3725
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14650
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 18
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7729
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19414
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4367
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2248
bin: 8.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10390
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500780405811022e-5
allele num: 66632
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.45e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.04e-1

DP
type: SiteQuality
SIO_000300: 2.117128e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.31e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 1.342e1

MQ
type: SiteQuality
SIO_000300: 5.963e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.628e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.42e-1

GenotypeDepth
all individuals: 928
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 168
bin: 8.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 361
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4368
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19420
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5160
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 16
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 5.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3230
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3724
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7737
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2247
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14651
bin: 9.75e1
variant carriers: 1

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66642
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10390
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.16e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.33e0

FS
type: SiteQuality
SIO_000300: 7.3e-1

QD
type: SiteQuality
SIO_000300: 1.31e1

VQSLOD
type: SiteQuality
SIO_000300: -9.299999999999999e-3

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.28e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.8e-2

DP
type: SiteQuality
SIO_000300: 2.117283e6

MQ
type: SiteQuality
SIO_000300: 5.916e1

GenotypeDepth
all individuals: 42
bin: 9.25e1
variant carriers: 4

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 5157
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3732
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14684
bin: 9.75e1
variant carriers: 86

GenotypeQuality
all individuals: 4
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 19455
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4363
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7751
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3227
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2248
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

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

South Asian
type: Population
allele count: 88
allele frequency: 5.329457364341085e-3
allele num: 16512
num of homozygotes: 2

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66682
num of homozygotes: 0

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.09e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.29e-1

QD
type: SiteQuality
SIO_000300: 1.25e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.72e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.01e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.21e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.744e0

DP
type: SiteQuality
SIO_000300: 2.122461e6

MQ
type: SiteQuality
SIO_000300: 5.968e1

FS
type: SiteQuality
SIO_000300: 5.649999999999999e-1

GenotypeDepth
all individuals: 366
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7757
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 39
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5160
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14646
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3233
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4369
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3739
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2248
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19475
bin: 6.25e1
variant carriers: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499295331194339e-5
allele num: 66698
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.55e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.128e0

MQRankSum
type: SiteQuality
SIO_000300: 4.21e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.985e1

DP
type: SiteQuality
SIO_000300: 2.119868e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.31e-1

QD
type: SiteQuality
SIO_000300: 1.245e1

VQSLOD
type: SiteQuality
SIO_000300: 5.26e0

GenotypeDepth
all individuals: 593
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5160
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 39
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7757
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2248
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 3.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 10
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4369
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3233
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14646
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 19475
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3739
bin: 7.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499295331194339e-5
allele num: 66698
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 5.26e0

QD
type: SiteQuality
SIO_000300: 1.245e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 4.21e-1

MQ
type: SiteQuality
SIO_000300: 5.985e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.31e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.128e0

DP
type: SiteQuality
SIO_000300: 2.119868e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.55e-1

GenotypeDepth
all individuals: 95
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5158
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 35
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7750
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4370
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2248
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3741
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3230
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 4.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 7
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19479
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14655
bin: 9.75e1
variant carriers: 14

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

African
type: Population
allele count: 1
allele frequency: 9.615384615384615e-5
allele num: 10400
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 2
allele frequency: 2.311604253351826e-4
allele num: 8652
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 11
allele frequency: 1.649076517150396e-4
allele num: 66704
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.55e0

DP
type: SiteQuality
SIO_000300: 2.120797e6

QD
type: SiteQuality
SIO_000300: 1.227e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.97e0

MQRankSum
type: SiteQuality
SIO_000300: 3.41e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

FS
type: SiteQuality
SIO_000300: 5.649999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.5e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.9e-1

MQ
type: SiteQuality
SIO_000300: 5.976e1

GenotypeDepth
all individuals: 930
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 23
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4375
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19500
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3748
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7751
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2249
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 14644
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3231
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5163
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.155802126675913e-4
allele num: 8652
num of homozygotes: 0

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66716
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.120304e6

MQRankSum
type: SiteQuality
SIO_000300: 1.41e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.42e-1

FS
type: SiteQuality
SIO_000300: 1.654e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 4.04e-1

QD
type: SiteQuality
SIO_000300: 1.155e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.506e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.0e-3

GenotypeDepth
all individuals: 931
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 18
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7751
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2249
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14645
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3746
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5162
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3231
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19501
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4375
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.997512064986062e-5
allele num: 66722
num of homozygotes: 0

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

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

African
type: Population
allele count: 1
allele frequency: 9.611687812379854e-5
allele num: 10404
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.929999999999999e-1

DP
type: SiteQuality
SIO_000300: 2.12049e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.92e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.77e-1

FS
type: SiteQuality
SIO_000300: 1.3214e1

QD
type: SiteQuality
SIO_000300: 1.462e1

VQSLOD
type: SiteQuality
SIO_000300: -7.441e-1

MQ
type: SiteQuality
SIO_000300: 5.963e1

MQRankSum
type: SiteQuality
SIO_000300: -1.56e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

GenotypeDepth
all individuals: 5529
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5171
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 7755
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3231
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 19511
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3744
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14645
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2249
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4377
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498621268433042e-5
allele num: 66728
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: 6.28e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.175e0

MQRankSum
type: SiteQuality
SIO_000300: 4.6e-1

FS
type: SiteQuality
SIO_000300: 5.049e0

DP
type: SiteQuality
SIO_000300: 2.12104e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.04e0

QD
type: SiteQuality
SIO_000300: 1.316e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.99e-1

MQ
type: SiteQuality
SIO_000300: 5.987e1

GenotypeDepth
all individuals: 367
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 14647
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 19511
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3230
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3745
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2249
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7754
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4376
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5169
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.75e1
variant carriers: 0

Latino
type: Population
allele count: 5
allele frequency: 4.320027648176948e-4
allele num: 11574
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66734
num of homozygotes: 0

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

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

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

DP
type: SiteQuality
SIO_000300: 2.121349e6

VQSLOD
type: SiteQuality
SIO_000300: 1.11e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.942e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.9e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.963e1

QD
type: SiteQuality
SIO_000300: 1.154e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.71e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.54e-1

FS
type: SiteQuality
SIO_000300: 5.54e-1

GenotypeDepth
all individuals: 14838
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4374
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3746
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2249
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3230
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5169
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7757
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14645
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 19515
bin: 6.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498486528606108e-5
allele num: 66734
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 7.66e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 4.558e0

QD
type: SiteQuality
SIO_000300: 1.066e1

DP
type: SiteQuality
SIO_000300: 2.120985e6

MQ
type: SiteQuality
SIO_000300: 5.944e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.325e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.58e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.24e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.9e-2

GenotypeDepth
all individuals: 1371
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2250
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3743
bin: 7.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 13
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4374
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3229
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5169
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19473
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7750
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14645
bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66734
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.964e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.005e0

VQSLOD
type: SiteQuality
SIO_000300: 1.35e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.4e-2

QD
type: SiteQuality
SIO_000300: 1.387e1

MQRankSum
type: SiteQuality
SIO_000300: 6.59e-1

DP
type: SiteQuality
SIO_000300: 2.121645e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.41e-1

GenotypeDepth
all individuals: 1370
bin: 5.75e1
variant carriers: 2

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

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

GenotypeQuality
all individuals: 25
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4370
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7751
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3740
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5170
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2251
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14646
bin: 9.75e1
variant carriers: 36

GenotypeQuality
all individuals: 19485
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3227
bin: 9.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 33
allele frequency: 4.947526236881559e-4
allele num: 66700
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

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

African
type: Population
allele count: 3
allele frequency: 2.884615384615385e-4
allele num: 10400
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 3.29e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.078e0

FS
type: SiteQuality
SIO_000300: 1.147e0

MQRankSum
type: SiteQuality
SIO_000300: 3.46e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.11e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 2.48e0

DP
type: SiteQuality
SIO_000300: 2.126927e6

MQ
type: SiteQuality
SIO_000300: 5.957e1

QD
type: SiteQuality
SIO_000300: 1.321e1

GenotypeDepth
all individuals: 177
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19453
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2254
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5175
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3741
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 11
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4379
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3234
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14683
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 7747
bin: 6.75e1
variant carriers: 0

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.495594317568783e-5
allele num: 66732
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 2.124108e6

QD
type: SiteQuality
SIO_000300: 1.173e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.23e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.31e0

MQ
type: SiteQuality
SIO_000300: 5.967e1

FS
type: SiteQuality
SIO_000300: 3.261e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.07e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 4.08e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.96e0

GenotypeDepth
all individuals: 177
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 3.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2254
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 19453
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3741
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3234
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14683
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 4
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7747
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5175
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4379
bin: 8.25e1
variant carriers: 0

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 5.994125756758376e-5
allele num: 66732
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -5.07e-1

DP
type: SiteQuality
SIO_000300: 2.124108e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.31e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 4.08e-1

FS
type: SiteQuality
SIO_000300: 3.261e0

VQSLOD
type: SiteQuality
SIO_000300: 1.96e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.23e0

QD
type: SiteQuality
SIO_000300: 1.173e1

MQ
type: SiteQuality
SIO_000300: 5.967e1

GenotypeDepth
all individuals: 1369
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3741
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7749
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5173
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2254
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19456
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3235
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4382
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14685
bin: 9.75e1
variant carriers: 16

GenotypeQuality
all individuals: 4
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 11
allele frequency: 1.648335181466719e-4
allele num: 66734
num of homozygotes: 0

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

Other
type: Population
allele count: 1
allele frequency: 1.101321585903084e-3
allele num: 908
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.49e0

QD
type: SiteQuality
SIO_000300: 1.434e1

MQRankSum
type: SiteQuality
SIO_000300: -8.9e-2

MQ
type: SiteQuality
SIO_000300: 5.959e1

VQSLOD
type: SiteQuality
SIO_000300: 1.97e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.21e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 2.124873e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.71e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.29e0

GenotypeDepth
all individuals: 97
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2255
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5174
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3740
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 19459
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7751
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14681
bin: 9.75e1
variant carriers: 10

GenotypeQuality
all individuals: 4378
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3236
bin: 9.25e1
variant carriers: 0

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

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

Other
type: Population
allele count: 2
allele frequency: 2.202643171806168e-3
allele num: 908
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.311604253351826e-4
allele num: 8652
num of homozygotes: 0

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.12e-1

QD
type: SiteQuality
SIO_000300: 1.242e1

MQ
type: SiteQuality
SIO_000300: 5.962e1

MQRankSum
type: SiteQuality
SIO_000300: -7.4e-2

DP
type: SiteQuality
SIO_000300: 2.124689e6

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.04e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.49e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.43e-1

GenotypeDepth
all individuals: 5537
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2258
bin: 8.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 3739
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5178
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7755
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4380
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3237
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14676
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 19472
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

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

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66738
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.037e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.301e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.76e0

FS
type: SiteQuality
SIO_000300: 7.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.911e1

DP
type: SiteQuality
SIO_000300: 2.124285e6

VQSLOD
type: SiteQuality
SIO_000300: -7.896e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.93e-1

QD
type: SiteQuality
SIO_000300: 1.291e1

GenotypeDepth
all individuals: 14549
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5175
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3739
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 4
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 14686
bin: 9.75e1
variant carriers: 23

GenotypeQuality
all individuals: 2
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19465
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2257
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3237
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4379
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7752
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 20
allele frequency: 1.211240310077519e-3
allele num: 16512
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.495190146543199e-5
allele num: 66738
num of homozygotes: 0

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

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

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

QD
type: SiteQuality
SIO_000300: 1.336e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.93e0

MQRankSum
type: SiteQuality
SIO_000300: 1.19e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.28e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.08e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.126003e6

MQ
type: SiteQuality
SIO_000300: 5.974e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.96e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.02e-1

GenotypeDepth
all individuals: 14853
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4380
bin: 8.25e1
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 2
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3740
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5178
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2258
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7754
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19476
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3237
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14670
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.4983967155144e-5
allele num: 66738
num of homozygotes: 0

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

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

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

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.55e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.621e0

MQ
type: SiteQuality
SIO_000300: 5.935e1

MQRankSum
type: SiteQuality
SIO_000300: 1.53e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.82e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.19e0

FS
type: SiteQuality
SIO_000300: 6.53e-1

QD
type: SiteQuality
SIO_000300: 1.348e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.124419e6

GenotypeDepth
all individuals: 600
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14669
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 2258
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3235
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4377
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5174
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7752
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19468
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3740
bin: 7.25e1
variant carriers: 0

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

African
type: Population
allele count: 3
allele frequency: 2.884615384615385e-4
allele num: 10400
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66728
num of homozygotes: 0

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.764e0

FS
type: SiteQuality
SIO_000300: 9.382e0

DP
type: SiteQuality
SIO_000300: 2.125737e6

MQRankSum
type: SiteQuality
SIO_000300: -6.57e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.026e0

MQ
type: SiteQuality
SIO_000300: 5.942e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.316e1

VQSLOD
type: SiteQuality
SIO_000300: -4.794e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.2e0

GenotypeDepth
all individuals: 599
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3235
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3740
bin: 7.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2258
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14668
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 4376
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7752
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19470
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5175
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.495729057395475e-5
allele num: 66730
num of homozygotes: 0

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

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 3.29e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.55e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.379999999999999e-1

DP
type: SiteQuality
SIO_000300: 2.125799e6

MQRankSum
type: SiteQuality
SIO_000300: 1.15e0

FS
type: SiteQuality
SIO_000300: 4.066e0

QD
type: SiteQuality
SIO_000300: 1.456e1

MQ
type: SiteQuality
SIO_000300: 5.983e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.29e0

GenotypeDepth
all individuals: 8917
bin: 3.75e1
variant carriers: 2

GenotypeQuality
all individuals: 65
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 3.75e1
variant carriers: 3

GenotypeQuality
all individuals: 243
bin: 2.5e0
variant carriers: 6

GenotypeQuality
all individuals: 5083
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 56
bin: 2.25e1
variant carriers: 10

GenotypeQuality
all individuals: 29
bin: 7.5e0
variant carriers: 4

GenotypeQuality
all individuals: 19164
bin: 6.25e1
variant carriers: 5

GenotypeQuality
all individuals: 66
bin: 4.25e1
variant carriers: 3

GenotypeQuality
all individuals: 51
bin: 3.25e1
variant carriers: 2

GenotypeQuality
all individuals: 4325
bin: 8.25e1
variant carriers: 4

GenotypeQuality
all individuals: 40
bin: 1.75e1
variant carriers: 7

GenotypeQuality
all individuals: 3657
bin: 7.25e1
variant carriers: 3

GenotypeQuality
all individuals: 2231
bin: 8.75e1
variant carriers: 3

GenotypeQuality
all individuals: 7614
bin: 6.75e1
variant carriers: 2

GenotypeQuality
all individuals: 41
bin: 1.25e1
variant carriers: 4

GenotypeQuality
all individuals: 14584
bin: 9.75e1
variant carriers: 20

GenotypeQuality
all individuals: 84
bin: 5.75e1
variant carriers: 5

GenotypeQuality
all individuals: 3209
bin: 9.25e1
variant carriers: 3

GenotypeQuality
all individuals: 44
bin: 2.75e1
variant carriers: 6

GenotypeQuality
all individuals: 65
bin: 4.75e1
variant carriers: 3

European (Non-Finnish)
type: Population
allele count: 11
allele frequency: 1.651453278885419e-4
allele num: 66608
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 62
allele frequency: 1.020408163265306e-2
allele num: 6076
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 884
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10392
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.938e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.95e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.528e2

FS
type: SiteQuality
SIO_000300: 1.82984e2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.0e-1

DP
type: SiteQuality
SIO_000300: 2.157174e6

BaseQRankSum
type: SiteQuality
SIO_000300: -5.073e0

MQRankSum
type: SiteQuality
SIO_000300: 2.64e-1

QD
type: SiteQuality
SIO_000300: 5.9e-1

GenotypeDepth
all individuals: 182
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7700
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3261
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3695
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14786
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19460
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2246
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4375
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5152
bin: 7.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.4983967155144e-5
allele num: 66738
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: -3.763e0

MQRankSum
type: SiteQuality
SIO_000300: -3.01e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.384e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 2.130859e6

FS
type: SiteQuality
SIO_000300: 3.657e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.747e0

QD
type: SiteQuality
SIO_000300: 3.08e0

MQ
type: SiteQuality
SIO_000300: 5.889e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.24e-1

GenotypeDepth
all individuals: 3328
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7702
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3261
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3698
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5151
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 16
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2246
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4376
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14782
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 19461
bin: 6.25e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.4983967155144e-5
allele num: 66738
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10394
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.08e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.72e-1

DP
type: SiteQuality
SIO_000300: 2.130488e6

BaseQRankSum
type: SiteQuality
SIO_000300: -6.482e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.939e1

VQSLOD
type: SiteQuality
SIO_000300: 5.590000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.138e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.0e-2

GenotypeDepth
all individuals: 607
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14782
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2246
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19462
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5152
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4376
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 7702
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3261
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3698
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 2
allele frequency: 1.727712508638562e-4
allele num: 11576
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10394
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66738
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -1.0e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.735e0

MQ
type: SiteQuality
SIO_000300: 5.938e1

DP
type: SiteQuality
SIO_000300: 2.130535e6

QD
type: SiteQuality
SIO_000300: 1.126e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.1e-2

VQSLOD
type: SiteQuality
SIO_000300: 8.400000000000001e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.245e0

GenotypeDepth
all individuals: 96
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 14780
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 4376
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 19445
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5150
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2246
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3261
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7699
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3696
bin: 7.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.495055439017081e-5
allele num: 66740
num of homozygotes: 0

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

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

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.964e1

QD
type: SiteQuality
SIO_000300: 1.139e1

MQRankSum
type: SiteQuality
SIO_000300: 3.57e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.587e0

VQSLOD
type: SiteQuality
SIO_000300: 1.55e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.57e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 2.167e0

DP
type: SiteQuality
SIO_000300: 2.130324e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.24e-1

GenotypeDepth
all individuals: 379
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7696
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4377
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2246
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 19444
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5150
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14778
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3696
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3262
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498351813005694e-5
allele num: 66740
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.034e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.02e-1

DP
type: SiteQuality
SIO_000300: 2.129948e6

FS
type: SiteQuality
SIO_000300: 1.0823e1

MQRankSum
type: SiteQuality
SIO_000300: -2.007e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.07e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.77e0

MQ
type: SiteQuality
SIO_000300: 5.668e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.72e-1

GenotypeDepth
all individuals: 380
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2246
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 4377
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14778
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 5
bin: 5.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 19423
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7692
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5150
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3262
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3695
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 2.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10356
num of homozygotes: 0

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

East Asian
type: Population
allele count: 3
allele frequency: 3.466605038132656e-4
allele num: 8654
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66738
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.946e1

MQRankSum
type: SiteQuality
SIO_000300: -1.292e0

FS
type: SiteQuality
SIO_000300: 2.147e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.22e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.304e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.12977e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.31e0

QD
type: SiteQuality
SIO_000300: 1.006e1

VQSLOD
type: SiteQuality
SIO_000300: -3.018e-1

GenotypeDepth
all individuals: 2269
bin: 9.75e1
variant carriers: 2119

GenotypeDepth
all individuals: 211
bin: 9.25e1
variant carriers: 176

GenotypeDepth
all individuals: 5194
bin: 4.25e1
variant carriers: 15

GenotypeDepth
all individuals: 624
bin: 6.75e1
variant carriers: 63

GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 3
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4174
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 87
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7439
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19052
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16273
bin: 9.75e1
variant carriers: 3049

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

GenotypeQuality
all individuals: 3543
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2092
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4961
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3065
bin: 9.25e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 227
allele frequency: 3.432113698215906e-2
allele num: 6614
num of homozygotes: 7

Other
type: Population
allele count: 18
allele frequency: 1.982378854625551e-2
allele num: 908
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1891
allele frequency: 2.83346818903773e-2
allele num: 66738
num of homozygotes: 28

African
type: Population
allele count: 896
allele frequency: 8.662026295436968e-2
allele num: 10344
num of homozygotes: 47

Latino
type: Population
allele count: 91
allele frequency: 7.862450319682046e-3
allele num: 11574
num of homozygotes: 0

South Asian
type: Population
allele count: 9
allele frequency: 5.450581395348837e-4
allele num: 16512
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.33e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.39e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.49e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.95e0

MQ
type: SiteQuality
SIO_000300: 5.951e1

DP
type: SiteQuality
SIO_000300: 2.358267e6

MQRankSum
type: SiteQuality
SIO_000300: 2.03e-1

FS
type: SiteQuality
SIO_000300: 1.292e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.51e-1

QD
type: SiteQuality
SIO_000300: 1.467e1

GenotypeDepth
all individuals: 387
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14147
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19969
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 126
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5194
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2182
bin: 8.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3233
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7771
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4373
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3684
bin: 7.25e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.44e-1

FS
type: SiteQuality
SIO_000300: 2.763e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.55e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.28e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.132889e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.01e-1

QD
type: SiteQuality
SIO_000300: 1.116e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.91e-1

GenotypeDepth
all individuals: 5483
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4372
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2182
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14147
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 5
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19953
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7769
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5194
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 136
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3233
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3684
bin: 7.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10292
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.592464569650881e-4
allele num: 11572
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.12e-1

FS
type: SiteQuality
SIO_000300: 3.367e0

DP
type: SiteQuality
SIO_000300: 2.132682e6

VQSLOD
type: SiteQuality
SIO_000300: 1.19e0

MQ
type: SiteQuality
SIO_000300: 5.967e1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.0e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.78e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.999999999999999e-3

QD
type: SiteQuality
SIO_000300: 1.412e1

GenotypeDepth
all individuals: 615
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3684
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2182
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5192
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3233
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19888
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7760
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4371
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14144
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10248
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66728
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.95e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 4.956e0

VQSLOD
type: SiteQuality
SIO_000300: 1.04e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.66e0

DP
type: SiteQuality
SIO_000300: 2.131299e6

MQRankSum
type: SiteQuality
SIO_000300: 6.56e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.3e-1

QD
type: SiteQuality
SIO_000300: 1.389e1

MQ
type: SiteQuality
SIO_000300: 5.972e1

GenotypeQuality
all individuals: 7723
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2182
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3228
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4369
bin: 8.25e1
variant carriers: 0