X-117053457-G-GA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117053457
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117053458
    reference: chr 0
allele count: 1
allele frequency: 1.14983499867769e-5
allele num: 86969
alternate allele: GA
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000443191
  ensembl transcript: ENST00000539496
  gene symbol: KLHL13
  hgvsc: ENST00000539496.1:c.579+26dupT
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360945
  ensembl transcript: ENST00000371878
  gene symbol: KLHL13
  hgvsc: ENST00000371878.1:c.417+26dupT
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360949
  ensembl transcript: ENST00000371882
  gene symbol: KLHL13
  hgvsc: ENST00000371882.1:c.417+26dupT
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000441029
  ensembl transcript: ENST00000540167
  gene symbol: KLHL13
  hgvsc: ENST00000540167.1:c.522+26dupT
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360943
  ensembl transcript: ENST00000371876
  gene symbol: KLHL13
  hgvsc: ENST00000371876.1:c.417+26dupT
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000440707
  ensembl transcript: ENST00000545703
  gene symbol: KLHL13
  hgvsc: ENST00000545703.1:c.444+26dupT
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000419803
  ensembl transcript: ENST00000469946
  gene symbol: KLHL13
  hgvsc: ENST00000469946.1:c.417+26dupT
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000262820
  ensembl transcript: ENST00000262820
  gene symbol: KLHL13
  hgvsc: ENST00000262820.3:c.570+26dupT
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000444450
  ensembl transcript: ENST00000541812
  gene symbol: KLHL13
  hgvsc: ENST00000541812.1:c.522+26dupT
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000412640
  ensembl transcript: ENST00000447671
  gene symbol: KLHL13
  hgvsc: ENST00000447671.2:c.417+26dupT
  variant of: http://identifiers.org/hgnc/22931
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 27039
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10497
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10866
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2613
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1354
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1397
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2085
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 747
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum

X-117053464-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117053464
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117053464
    reference: chr 0
allele count: 1
allele frequency: 1.149438499293095e-5
allele num: 86999
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000441029
  ensembl transcript: ENST00000540167
  gene symbol: KLHL13
  hgvsc: ENST00000540167.1:c.522+20G>C
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360943
  ensembl transcript: ENST00000371876
  gene symbol: KLHL13
  hgvsc: ENST00000371876.1:c.417+20G>C
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000443191
  ensembl transcript: ENST00000539496
  gene symbol: KLHL13
  hgvsc: ENST00000539496.1:c.579+20G>C
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000262820
  ensembl transcript: ENST00000262820
  gene symbol: KLHL13
  hgvsc: ENST00000262820.3:c.570+20G>C
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000412640
  ensembl transcript: ENST00000447671
  gene symbol: KLHL13
  hgvsc: ENST00000447671.2:c.417+20G>C
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000419803
  ensembl transcript: ENST00000469946
  gene symbol: KLHL13
  hgvsc: ENST00000469946.1:c.417+20G>C
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000440707
  ensembl transcript: ENST00000545703
  gene symbol: KLHL13
  hgvsc: ENST00000545703.1:c.444+20G>C
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360949
  ensembl transcript: ENST00000371882
  gene symbol: KLHL13
  hgvsc: ENST00000371882.1:c.417+20G>C
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000444450
  ensembl transcript: ENST00000541812
  gene symbol: KLHL13
  hgvsc: ENST00000541812.1:c.522+20G>C
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360945
  ensembl transcript: ENST00000371878
  gene symbol: KLHL13
  hgvsc: ENST00000371878.1:c.417+20G>C
  variant of: http://identifiers.org/hgnc/22931
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1398
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10959
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27078
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2618
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1355
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10515
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1886
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 748
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: DP

X-117053466-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117053466
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117053466
    reference: chr 0
allele count: 6
allele frequency: 6.895362868470953e-5
allele num: 87015
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000441029
  ensembl transcript: ENST00000540167
  gene symbol: KLHL13
  hgvsc: ENST00000540167.1:c.522+18C>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000412640
  ensembl transcript: ENST00000447671
  gene symbol: KLHL13
  hgvsc: ENST00000447671.2:c.417+18C>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000419803
  ensembl transcript: ENST00000469946
  gene symbol: KLHL13
  hgvsc: ENST00000469946.1:c.417+18C>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000440707
  ensembl transcript: ENST00000545703
  gene symbol: KLHL13
  hgvsc: ENST00000545703.1:c.444+18C>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000262820
  ensembl transcript: ENST00000262820
  gene symbol: KLHL13
  hgvsc: ENST00000262820.3:c.570+18C>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360943
  ensembl transcript: ENST00000371876
  gene symbol: KLHL13
  hgvsc: ENST00000371876.1:c.417+18C>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000443191
  ensembl transcript: ENST00000539496
  gene symbol: KLHL13
  hgvsc: ENST00000539496.1:c.579+18C>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360945
  ensembl transcript: ENST00000371878
  gene symbol: KLHL13
  hgvsc: ENST00000371878.1:c.417+18C>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000444450
  ensembl transcript: ENST00000541812
  gene symbol: KLHL13
  hgvsc: ENST00000541812.1:c.522+18C>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360949
  ensembl transcript: ENST00000371882
  gene symbol: KLHL13
  hgvsc: ENST00000371882.1:c.417+18C>G
  variant of: http://identifiers.org/hgnc/22931
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1397
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27096
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2617
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10514
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1357
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10979
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36466
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2093
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

X-117053475-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117053475
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117053475
    reference: chr 0
allele count: 3
allele frequency: 3.445780641604355e-5
allele num: 87063
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360943
  ensembl transcript: ENST00000371876
  gene symbol: KLHL13
  hgvsc: ENST00000371876.1:c.417+9T>C
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000441029
  ensembl transcript: ENST00000540167
  gene symbol: KLHL13
  hgvsc: ENST00000540167.1:c.522+9T>C
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000262820
  ensembl transcript: ENST00000262820
  gene symbol: KLHL13
  hgvsc: ENST00000262820.3:c.570+9T>C
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000443191
  ensembl transcript: ENST00000539496
  gene symbol: KLHL13
  hgvsc: ENST00000539496.1:c.579+9T>C
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360945
  ensembl transcript: ENST00000371878
  gene symbol: KLHL13
  hgvsc: ENST00000371878.1:c.417+9T>C
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000440707
  ensembl transcript: ENST00000545703
  gene symbol: KLHL13
  hgvsc: ENST00000545703.1:c.444+9T>C
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000419803
  ensembl transcript: ENST00000469946
  gene symbol: KLHL13
  hgvsc: ENST00000469946.1:c.417+9T>C
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000412640
  ensembl transcript: ENST00000447671
  gene symbol: KLHL13
  hgvsc: ENST00000447671.2:c.417+9T>C
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000444450
  ensembl transcript: ENST00000541812
  gene symbol: KLHL13
  hgvsc: ENST00000541812.1:c.522+9T>C
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360949
  ensembl transcript: ENST00000371882
  gene symbol: KLHL13
  hgvsc: ENST00000371882.1:c.417+9T>C
  variant of: http://identifiers.org/hgnc/22931
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27151
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11011
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2616
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1398
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10524
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1353
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2096
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7839
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: DP

X-117053499-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117053499
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117053499
    reference: chr 0
allele count: 11175
allele frequency: 1.276442637181889e-1
allele num: 87548
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000419803
  ensembl transcript: ENST00000469946
  gene symbol: KLHL13
  hgvsc: ENST00000469946.1:c.402G>A
  hgvsp: ENST00000469946.1:c.402G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000444450
  ensembl transcript: ENST00000541812
  gene symbol: KLHL13
  hgvsc: ENST00000541812.1:c.507G>A
  hgvsp: ENST00000541812.1:c.507G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360945
  ensembl transcript: ENST00000371878
  gene symbol: KLHL13
  hgvsc: ENST00000371878.1:c.402G>A
  hgvsp: ENST00000371878.1:c.402G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000262820
  ensembl transcript: ENST00000262820
  gene symbol: KLHL13
  hgvsc: ENST00000262820.3:c.555G>A
  hgvsp: ENST00000262820.3:c.555G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000440707
  ensembl transcript: ENST00000545703
  gene symbol: KLHL13
  hgvsc: ENST00000545703.1:c.429G>A
  hgvsp: ENST00000545703.1:c.429G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000441029
  ensembl transcript: ENST00000540167
  gene symbol: KLHL13
  hgvsc: ENST00000540167.1:c.507G>A
  hgvsp: ENST00000540167.1:c.507G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360949
  ensembl transcript: ENST00000371882
  gene symbol: KLHL13
  hgvsc: ENST00000371882.1:c.402G>A
  hgvsp: ENST00000371882.1:c.402G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000443191
  ensembl transcript: ENST00000539496
  gene symbol: KLHL13
  hgvsc: ENST00000539496.1:c.564G>A
  hgvsp: ENST00000539496.1:c.564G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360943
  ensembl transcript: ENST00000371876
  gene symbol: KLHL13
  hgvsc: ENST00000371876.1:c.402G>A
  hgvsp: ENST00000371876.1:c.402G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000412640
  ensembl transcript: ENST00000447671
  gene symbol: KLHL13
  hgvsc: ENST00000447671.2:c.402G>A
  hgvsp: ENST00000447671.2:c.402G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9867
  bin: 3.25e1
  variant carriers: 110
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 5.25e1
  variant carriers: 302
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 8.25e1
  variant carriers: 350
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 1.75e1
  variant carriers: 97
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 1.25e1
  variant carriers: 59
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 7.75e1
  variant carriers: 359
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 8.75e1
  variant carriers: 315
genotype depth: GenotypeDepth
  all individuals: 2097
  bin: 3.75e1
  variant carriers: 173
genotype depth: GenotypeDepth
  all individuals: 26552
  bin: 2.75e1
  variant carriers: 89
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 5.75e1
  variant carriers: 377
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.5e0
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 9.25e1
  variant carriers: 329
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 6.75e1
  variant carriers: 366
genotype depth: GenotypeDepth
  all individuals: 5297
  bin: 9.75e1
  variant carriers: 5129
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 6.25e1
  variant carriers: 369
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 7.25e1
  variant carriers: 375
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 4.25e1
  variant carriers: 212
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 4.75e1
  variant carriers: 332
genotype depth: GenotypeDepth
  all individuals: 10427
  bin: 2.25e1
  variant carriers: 99
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 6
hgvs: p.Val188Val
num of homozygotes: 1757
population: African
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: QD

X-117053503-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117053503
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117053503
    reference: chr 0
allele count: 2
allele frequency: 2.283417819792666e-5
allele num: 87588
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000262820
  ensembl transcript: ENST00000262820
  gene symbol: KLHL13
  hgvsc: ENST00000262820.3:c.551A>C
  hgvsp: ENSP00000262820.3:p.Lys184Thr
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360945
  ensembl transcript: ENST00000371878
  gene symbol: KLHL13
  hgvsc: ENST00000371878.1:c.398A>C
  hgvsp: ENSP00000360945.1:p.Lys133Thr
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000440707
  ensembl transcript: ENST00000545703
  gene symbol: KLHL13
  hgvsc: ENST00000545703.1:c.425A>C
  hgvsp: ENSP00000440707.1:p.Lys142Thr
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000419803
  ensembl transcript: ENST00000469946
  gene symbol: KLHL13
  hgvsc: ENST00000469946.1:c.398A>C
  hgvsp: ENSP00000419803.1:p.Lys133Thr
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000443191
  ensembl transcript: ENST00000539496
  gene symbol: KLHL13
  hgvsc: ENST00000539496.1:c.560A>C
  hgvsp: ENSP00000443191.1:p.Lys187Thr
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360949
  ensembl transcript: ENST00000371882
  gene symbol: KLHL13
  hgvsc: ENST00000371882.1:c.398A>C
  hgvsp: ENSP00000360949.1:p.Lys133Thr
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360943
  ensembl transcript: ENST00000371876
  gene symbol: KLHL13
  hgvsc: ENST00000371876.1:c.398A>C
  hgvsp: ENSP00000360943.1:p.Lys133Thr
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000444450
  ensembl transcript: ENST00000541812
  gene symbol: KLHL13
  hgvsc: ENST00000541812.1:c.503A>C
  hgvsp: ENSP00000444450.1:p.Lys168Thr
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000412640
  ensembl transcript: ENST00000447671
  gene symbol: KLHL13
  hgvsc: ENST00000447671.2:c.398A>C
  hgvsp: ENSP00000412640.2:p.Lys133Thr
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000441029
  ensembl transcript: ENST00000540167
  gene symbol: KLHL13
  hgvsc: ENST00000540167.1:c.503A>C
  hgvsp: ENSP00000441029.1:p.Lys168Thr
  variant of: http://identifiers.org/hgnc/22931
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30986
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2440
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11742
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11782
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Lys187Thr
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ

X-117053524-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117053524
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117053524
    reference: chr 0
allele count: 1
allele frequency: 1.141018473089079e-5
allele num: 87641
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000262820
  ensembl transcript: ENST00000262820
  gene symbol: KLHL13
  hgvsc: ENST00000262820.3:c.530T>G
  hgvsp: ENSP00000262820.3:p.Leu177Arg
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000419803
  ensembl transcript: ENST00000469946
  gene symbol: KLHL13
  hgvsc: ENST00000469946.1:c.377T>G
  hgvsp: ENSP00000419803.1:p.Leu126Arg
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000441029
  ensembl transcript: ENST00000540167
  gene symbol: KLHL13
  hgvsc: ENST00000540167.1:c.482T>G
  hgvsp: ENSP00000441029.1:p.Leu161Arg
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000443191
  ensembl transcript: ENST00000539496
  gene symbol: KLHL13
  hgvsc: ENST00000539496.1:c.539T>G
  hgvsp: ENSP00000443191.1:p.Leu180Arg
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000440707
  ensembl transcript: ENST00000545703
  gene symbol: KLHL13
  hgvsc: ENST00000545703.1:c.404T>G
  hgvsp: ENSP00000440707.1:p.Leu135Arg
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000412640
  ensembl transcript: ENST00000447671
  gene symbol: KLHL13
  hgvsc: ENST00000447671.2:c.377T>G
  hgvsp: ENSP00000412640.2:p.Leu126Arg
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000444450
  ensembl transcript: ENST00000541812
  gene symbol: KLHL13
  hgvsc: ENST00000541812.1:c.482T>G
  hgvsp: ENSP00000444450.1:p.Leu161Arg
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360943
  ensembl transcript: ENST00000371876
  gene symbol: KLHL13
  hgvsc: ENST00000371876.1:c.377T>G
  hgvsp: ENSP00000360943.1:p.Leu126Arg
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360949
  ensembl transcript: ENST00000371882
  gene symbol: KLHL13
  hgvsc: ENST00000371882.1:c.377T>G
  hgvsp: ENSP00000360949.1:p.Leu126Arg
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360945
  ensembl transcript: ENST00000371878
  gene symbol: KLHL13
  hgvsc: ENST00000371878.1:c.377T>G
  hgvsp: ENSP00000360945.1:p.Leu126Arg
  variant of: http://identifiers.org/hgnc/22931
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11859
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2439
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11743
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31055
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Leu180Arg
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: A
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum

X-117053527-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117053527
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117053527
    reference: chr 0
allele count: 2
allele frequency: 2.281984870440309e-5
allele num: 87643
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000262820
  ensembl transcript: ENST00000262820
  gene symbol: KLHL13
  hgvsc: ENST00000262820.3:c.527T>G
  hgvsp: ENSP00000262820.3:p.Ile176Ser
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000440707
  ensembl transcript: ENST00000545703
  gene symbol: KLHL13
  hgvsc: ENST00000545703.1:c.401T>G
  hgvsp: ENSP00000440707.1:p.Ile134Ser
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360943
  ensembl transcript: ENST00000371876
  gene symbol: KLHL13
  hgvsc: ENST00000371876.1:c.374T>G
  hgvsp: ENSP00000360943.1:p.Ile125Ser
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000419803
  ensembl transcript: ENST00000469946
  gene symbol: KLHL13
  hgvsc: ENST00000469946.1:c.374T>G
  hgvsp: ENSP00000419803.1:p.Ile125Ser
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000443191
  ensembl transcript: ENST00000539496
  gene symbol: KLHL13
  hgvsc: ENST00000539496.1:c.536T>G
  hgvsp: ENSP00000443191.1:p.Ile179Ser
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360945
  ensembl transcript: ENST00000371878
  gene symbol: KLHL13
  hgvsc: ENST00000371878.1:c.374T>G
  hgvsp: ENSP00000360945.1:p.Ile125Ser
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000444450
  ensembl transcript: ENST00000541812
  gene symbol: KLHL13
  hgvsc: ENST00000541812.1:c.479T>G
  hgvsp: ENSP00000444450.1:p.Ile160Ser
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000441029
  ensembl transcript: ENST00000540167
  gene symbol: KLHL13
  hgvsc: ENST00000540167.1:c.479T>G
  hgvsp: ENSP00000441029.1:p.Ile160Ser
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360949
  ensembl transcript: ENST00000371882
  gene symbol: KLHL13
  hgvsc: ENST00000371882.1:c.374T>G
  hgvsp: ENSP00000360949.1:p.Ile125Ser
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000412640
  ensembl transcript: ENST00000447671
  gene symbol: KLHL13
  hgvsc: ENST00000447671.2:c.374T>G
  hgvsp: ENSP00000412640.2:p.Ile125Ser
  variant of: http://identifiers.org/hgnc/22931
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31062
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11863
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11743
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2438
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ile179Ser
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD

X-117053531-GT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117053531
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117053530
    reference: chr 0
allele count: 1
allele frequency: 1.140940363047223e-5
allele num: 87647
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000443191
  ensembl transcript: ENST00000539496
  gene symbol: KLHL13
  hgvsc: ENST00000539496.1:c.531delA
  hgvsp: ENSP00000443191.1:p.Gln178ArgfsTer19
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000262820
  ensembl transcript: ENST00000262820
  gene symbol: KLHL13
  hgvsc: ENST00000262820.3:c.522delA
  hgvsp: ENSP00000262820.3:p.Gln175ArgfsTer19
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000441029
  ensembl transcript: ENST00000540167
  gene symbol: KLHL13
  hgvsc: ENST00000540167.1:c.474delA
  hgvsp: ENSP00000441029.1:p.Gln159ArgfsTer19
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000440707
  ensembl transcript: ENST00000545703
  gene symbol: KLHL13
  hgvsc: ENST00000545703.1:c.396delA
  hgvsp: ENSP00000440707.1:p.Gln133ArgfsTer19
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360949
  ensembl transcript: ENST00000371882
  gene symbol: KLHL13
  hgvsc: ENST00000371882.1:c.369delA
  hgvsp: ENSP00000360949.1:p.Gln124ArgfsTer19
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360943
  ensembl transcript: ENST00000371876
  gene symbol: KLHL13
  hgvsc: ENST00000371876.1:c.369delA
  hgvsp: ENSP00000360943.1:p.Gln124ArgfsTer19
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360945
  ensembl transcript: ENST00000371878
  gene symbol: KLHL13
  hgvsc: ENST00000371878.1:c.369delA
  hgvsp: ENSP00000360945.1:p.Gln124ArgfsTer19
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000412640
  ensembl transcript: ENST00000447671
  gene symbol: KLHL13
  hgvsc: ENST00000447671.2:c.369delA
  hgvsp: ENSP00000412640.2:p.Gln124ArgfsTer19
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000419803
  ensembl transcript: ENST00000469946
  gene symbol: KLHL13
  hgvsc: ENST00000469946.1:c.369delA
  hgvsp: ENSP00000419803.1:p.Gln124ArgfsTer19
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000444450
  ensembl transcript: ENST00000541812
  gene symbol: KLHL13
  hgvsc: ENST00000541812.1:c.474delA
  hgvsp: ENSP00000444450.1:p.Gln159ArgfsTer19
  variant of: http://identifiers.org/hgnc/22931
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31062
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11867
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2438
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11748
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 455
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Gln178ArgfsTer19
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: GT
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

X-117053532-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117053532
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117053532
    reference: chr 0
allele count: 2
allele frequency: 2.281880726094447e-5
allele num: 87647
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000412640
  ensembl transcript: ENST00000447671
  gene symbol: KLHL13
  hgvsc: ENST00000447671.2:c.369A>G
  hgvsp: ENST00000447671.2:c.369A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000443191
  ensembl transcript: ENST00000539496
  gene symbol: KLHL13
  hgvsc: ENST00000539496.1:c.531A>G
  hgvsp: ENST00000539496.1:c.531A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360949
  ensembl transcript: ENST00000371882
  gene symbol: KLHL13
  hgvsc: ENST00000371882.1:c.369A>G
  hgvsp: ENST00000371882.1:c.369A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000262820
  ensembl transcript: ENST00000262820
  gene symbol: KLHL13
  hgvsc: ENST00000262820.3:c.522A>G
  hgvsp: ENST00000262820.3:c.522A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360945
  ensembl transcript: ENST00000371878
  gene symbol: KLHL13
  hgvsc: ENST00000371878.1:c.369A>G
  hgvsp: ENST00000371878.1:c.369A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360943
  ensembl transcript: ENST00000371876
  gene symbol: KLHL13
  hgvsc: ENST00000371876.1:c.369A>G
  hgvsp: ENST00000371876.1:c.369A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000441029
  ensembl transcript: ENST00000540167
  gene symbol: KLHL13
  hgvsc: ENST00000540167.1:c.474A>G
  hgvsp: ENST00000540167.1:c.474A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000419803
  ensembl transcript: ENST00000469946
  gene symbol: KLHL13
  hgvsc: ENST00000469946.1:c.369A>G
  hgvsp: ENST00000469946.1:c.369A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000440707
  ensembl transcript: ENST00000545703
  gene symbol: KLHL13
  hgvsc: ENST00000545703.1:c.396A>G
  hgvsp: ENST00000545703.1:c.396A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000444450
  ensembl transcript: ENST00000541812
  gene symbol: KLHL13
  hgvsc: ENST00000541812.1:c.474A>G
  hgvsp: ENST00000541812.1:c.474A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11746
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11866
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2437
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31067
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2035
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Leu177Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: T
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: QD

X-117053553-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117053553
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117053553
    reference: chr 0
allele count: 1
allele frequency: 1.140628029793204e-5
allele num: 87671
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000412640
  ensembl transcript: ENST00000447671
  gene symbol: KLHL13
  hgvsc: ENST00000447671.2:c.348G>C
  hgvsp: ENST00000447671.2:c.348G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360943
  ensembl transcript: ENST00000371876
  gene symbol: KLHL13
  hgvsc: ENST00000371876.1:c.348G>C
  hgvsp: ENST00000371876.1:c.348G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000444450
  ensembl transcript: ENST00000541812
  gene symbol: KLHL13
  hgvsc: ENST00000541812.1:c.453G>C
  hgvsp: ENST00000541812.1:c.453G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360945
  ensembl transcript: ENST00000371878
  gene symbol: KLHL13
  hgvsc: ENST00000371878.1:c.348G>C
  hgvsp: ENST00000371878.1:c.348G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000419803
  ensembl transcript: ENST00000469946
  gene symbol: KLHL13
  hgvsc: ENST00000469946.1:c.348G>C
  hgvsp: ENST00000469946.1:c.348G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000443191
  ensembl transcript: ENST00000539496
  gene symbol: KLHL13
  hgvsc: ENST00000539496.1:c.510G>C
  hgvsp: ENST00000539496.1:c.510G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000440707
  ensembl transcript: ENST00000545703
  gene symbol: KLHL13
  hgvsc: ENST00000545703.1:c.375G>C
  hgvsp: ENST00000545703.1:c.375G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000262820
  ensembl transcript: ENST00000262820
  gene symbol: KLHL13
  hgvsc: ENST00000262820.3:c.501G>C
  hgvsp: ENST00000262820.3:c.501G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360949
  ensembl transcript: ENST00000371882
  gene symbol: KLHL13
  hgvsc: ENST00000371882.1:c.348G>C
  hgvsp: ENST00000371882.1:c.348G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000441029
  ensembl transcript: ENST00000540167
  gene symbol: KLHL13
  hgvsc: ENST00000540167.1:c.453G>C
  hgvsp: ENST00000540167.1:c.453G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2436
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11749
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11875
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31068
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Thr170Thr
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

X-117053554-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117053554
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117053554
    reference: chr 0
allele count: 3
allele frequency: 3.421649919591227e-5
allele num: 87677
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360949
  ensembl transcript: ENST00000371882
  gene symbol: KLHL13
  hgvsc: ENST00000371882.1:c.347C>T
  hgvsp: ENSP00000360949.1:p.Thr116Met
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000441029
  ensembl transcript: ENST00000540167
  gene symbol: KLHL13
  hgvsc: ENST00000540167.1:c.452C>T
  hgvsp: ENSP00000441029.1:p.Thr151Met
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000412640
  ensembl transcript: ENST00000447671
  gene symbol: KLHL13
  hgvsc: ENST00000447671.2:c.347C>T
  hgvsp: ENSP00000412640.2:p.Thr116Met
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000262820
  ensembl transcript: ENST00000262820
  gene symbol: KLHL13
  hgvsc: ENST00000262820.3:c.500C>T
  hgvsp: ENSP00000262820.3:p.Thr167Met
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360945
  ensembl transcript: ENST00000371878
  gene symbol: KLHL13
  hgvsc: ENST00000371878.1:c.347C>T
  hgvsp: ENSP00000360945.1:p.Thr116Met
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000443191
  ensembl transcript: ENST00000539496
  gene symbol: KLHL13
  hgvsc: ENST00000539496.1:c.509C>T
  hgvsp: ENSP00000443191.1:p.Thr170Met
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360943
  ensembl transcript: ENST00000371876
  gene symbol: KLHL13
  hgvsc: ENST00000371876.1:c.347C>T
  hgvsp: ENSP00000360943.1:p.Thr116Met
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000419803
  ensembl transcript: ENST00000469946
  gene symbol: KLHL13
  hgvsc: ENST00000469946.1:c.347C>T
  hgvsp: ENSP00000419803.1:p.Thr116Met
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000444450
  ensembl transcript: ENST00000541812
  gene symbol: KLHL13
  hgvsc: ENST00000541812.1:c.452C>T
  hgvsp: ENSP00000444450.1:p.Thr151Met
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000440707
  ensembl transcript: ENST00000545703
  gene symbol: KLHL13
  hgvsc: ENST00000545703.1:c.374C>T
  hgvsp: ENSP00000440707.1:p.Thr125Met
  variant of: http://identifiers.org/hgnc/22931
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11749
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2438
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1005
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31071
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11872
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41962
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Thr170Met
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum

X-117053570-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117053570
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117053570
    reference: chr 0
allele count: 1
allele frequency: 1.140680073459797e-5
allele num: 87667
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000412640
  ensembl transcript: ENST00000447671
  gene symbol: KLHL13
  hgvsc: ENST00000447671.2:c.331G>A
  hgvsp: ENSP00000412640.2:p.Asp111Asn
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000444450
  ensembl transcript: ENST00000541812
  gene symbol: KLHL13
  hgvsc: ENST00000541812.1:c.436G>A
  hgvsp: ENSP00000444450.1:p.Asp146Asn
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360945
  ensembl transcript: ENST00000371878
  gene symbol: KLHL13
  hgvsc: ENST00000371878.1:c.331G>A
  hgvsp: ENSP00000360945.1:p.Asp111Asn
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000440707
  ensembl transcript: ENST00000545703
  gene symbol: KLHL13
  hgvsc: ENST00000545703.1:c.358G>A
  hgvsp: ENSP00000440707.1:p.Asp120Asn
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000262820
  ensembl transcript: ENST00000262820
  gene symbol: KLHL13
  hgvsc: ENST00000262820.3:c.484G>A
  hgvsp: ENSP00000262820.3:p.Asp162Asn
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000419803
  ensembl transcript: ENST00000469946
  gene symbol: KLHL13
  hgvsc: ENST00000469946.1:c.331G>A
  hgvsp: ENSP00000419803.1:p.Asp111Asn
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360949
  ensembl transcript: ENST00000371882
  gene symbol: KLHL13
  hgvsc: ENST00000371882.1:c.331G>A
  hgvsp: ENSP00000360949.1:p.Asp111Asn
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360943
  ensembl transcript: ENST00000371876
  gene symbol: KLHL13
  hgvsc: ENST00000371876.1:c.331G>A
  hgvsp: ENSP00000360943.1:p.Asp111Asn
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000443191
  ensembl transcript: ENST00000539496
  gene symbol: KLHL13
  hgvsc: ENST00000539496.1:c.493G>A
  hgvsp: ENSP00000443191.1:p.Asp165Asn
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000441029
  ensembl transcript: ENST00000540167
  gene symbol: KLHL13
  hgvsc: ENST00000540167.1:c.436G>A
  hgvsp: ENSP00000441029.1:p.Asp146Asn
  variant of: http://identifiers.org/hgnc/22931
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11875
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11725
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2427
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31064
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Asp165Asn
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

X-117053574-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117053574
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117053574
    reference: chr 0
allele count: 2
allele frequency: 2.281256059586408e-5
allele num: 87671
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000262820
  ensembl transcript: ENST00000262820
  gene symbol: KLHL13
  hgvsc: ENST00000262820.3:c.480T>C
  hgvsp: ENST00000262820.3:c.480T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360945
  ensembl transcript: ENST00000371878
  gene symbol: KLHL13
  hgvsc: ENST00000371878.1:c.327T>C
  hgvsp: ENST00000371878.1:c.327T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000441029
  ensembl transcript: ENST00000540167
  gene symbol: KLHL13
  hgvsc: ENST00000540167.1:c.432T>C
  hgvsp: ENST00000540167.1:c.432T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000440707
  ensembl transcript: ENST00000545703
  gene symbol: KLHL13
  hgvsc: ENST00000545703.1:c.354T>C
  hgvsp: ENST00000545703.1:c.354T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360943
  ensembl transcript: ENST00000371876
  gene symbol: KLHL13
  hgvsc: ENST00000371876.1:c.327T>C
  hgvsp: ENST00000371876.1:c.327T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000444450
  ensembl transcript: ENST00000541812
  gene symbol: KLHL13
  hgvsc: ENST00000541812.1:c.432T>C
  hgvsp: ENST00000541812.1:c.432T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000443191
  ensembl transcript: ENST00000539496
  gene symbol: KLHL13
  hgvsc: ENST00000539496.1:c.489T>C
  hgvsp: ENST00000539496.1:c.489T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000419803
  ensembl transcript: ENST00000469946
  gene symbol: KLHL13
  hgvsc: ENST00000469946.1:c.327T>C
  hgvsp: ENST00000469946.1:c.327T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000412640
  ensembl transcript: ENST00000447671
  gene symbol: KLHL13
  hgvsc: ENST00000447671.2:c.327T>C
  hgvsp: ENST00000447671.2:c.327T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360949
  ensembl transcript: ENST00000371882
  gene symbol: KLHL13
  hgvsc: ENST00000371882.1:c.327T>C
  hgvsp: ENST00000371882.1:c.327T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11710
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2424
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11876
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31066
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Asn163Asn
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
reference allele: A
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: DP

X-117053580-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117053580
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117053580
    reference: chr 0
allele count: 1
allele frequency: 1.140680073459797e-5
allele num: 87667
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000440707
  ensembl transcript: ENST00000545703
  gene symbol: KLHL13
  hgvsc: ENST00000545703.1:c.348T>C
  hgvsp: ENST00000545703.1:c.348T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360949
  ensembl transcript: ENST00000371882
  gene symbol: KLHL13
  hgvsc: ENST00000371882.1:c.321T>C
  hgvsp: ENST00000371882.1:c.321T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360945
  ensembl transcript: ENST00000371878
  gene symbol: KLHL13
  hgvsc: ENST00000371878.1:c.321T>C
  hgvsp: ENST00000371878.1:c.321T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000443191
  ensembl transcript: ENST00000539496
  gene symbol: KLHL13
  hgvsc: ENST00000539496.1:c.483T>C
  hgvsp: ENST00000539496.1:c.483T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360943
  ensembl transcript: ENST00000371876
  gene symbol: KLHL13
  hgvsc: ENST00000371876.1:c.321T>C
  hgvsp: ENST00000371876.1:c.321T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000441029
  ensembl transcript: ENST00000540167
  gene symbol: KLHL13
  hgvsc: ENST00000540167.1:c.426T>C
  hgvsp: ENST00000540167.1:c.426T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000262820
  ensembl transcript: ENST00000262820
  gene symbol: KLHL13
  hgvsc: ENST00000262820.3:c.474T>C
  hgvsp: ENST00000262820.3:c.474T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000419803
  ensembl transcript: ENST00000469946
  gene symbol: KLHL13
  hgvsc: ENST00000469946.1:c.321T>C
  hgvsp: ENST00000469946.1:c.321T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000412640
  ensembl transcript: ENST00000447671
  gene symbol: KLHL13
  hgvsc: ENST00000447671.2:c.321T>C
  hgvsp: ENST00000447671.2:c.321T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000444450
  ensembl transcript: ENST00000541812
  gene symbol: KLHL13
  hgvsc: ENST00000541812.1:c.426T>C
  hgvsp: ENST00000541812.1:c.426T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31050
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2424
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11893
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11700
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ser161Ser
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum

X-117053599-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117053599
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117053599
    reference: chr 0
allele count: 2
allele frequency: 2.282922597509331e-5
allele num: 87607
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000419803
  ensembl transcript: ENST00000469946
  gene symbol: KLHL13
  hgvsc: ENST00000469946.1:c.302T>C
  hgvsp: ENSP00000419803.1:p.Ile101Thr
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000440707
  ensembl transcript: ENST00000545703
  gene symbol: KLHL13
  hgvsc: ENST00000545703.1:c.329T>C
  hgvsp: ENSP00000440707.1:p.Ile110Thr
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360949
  ensembl transcript: ENST00000371882
  gene symbol: KLHL13
  hgvsc: ENST00000371882.1:c.302T>C
  hgvsp: ENSP00000360949.1:p.Ile101Thr
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000262820
  ensembl transcript: ENST00000262820
  gene symbol: KLHL13
  hgvsc: ENST00000262820.3:c.455T>C
  hgvsp: ENSP00000262820.3:p.Ile152Thr
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000443191
  ensembl transcript: ENST00000539496
  gene symbol: KLHL13
  hgvsc: ENST00000539496.1:c.464T>C
  hgvsp: ENSP00000443191.1:p.Ile155Thr
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360945
  ensembl transcript: ENST00000371878
  gene symbol: KLHL13
  hgvsc: ENST00000371878.1:c.302T>C
  hgvsp: ENSP00000360945.1:p.Ile101Thr
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000412640
  ensembl transcript: ENST00000447671
  gene symbol: KLHL13
  hgvsc: ENST00000447671.2:c.302T>C
  hgvsp: ENSP00000412640.2:p.Ile101Thr
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000441029
  ensembl transcript: ENST00000540167
  gene symbol: KLHL13
  hgvsc: ENST00000540167.1:c.407T>C
  hgvsp: ENSP00000441029.1:p.Ile136Thr
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360943
  ensembl transcript: ENST00000371876
  gene symbol: KLHL13
  hgvsc: ENST00000371876.1:c.302T>C
  hgvsp: ENSP00000360943.1:p.Ile101Thr
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000444450
  ensembl transcript: ENST00000541812
  gene symbol: KLHL13
  hgvsc: ENST00000541812.1:c.407T>C
  hgvsp: ENSP00000444450.1:p.Ile136Thr
  variant of: http://identifiers.org/hgnc/22931
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11611
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30961
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11973
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2418
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ile155Thr
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
reference allele: A
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ

X-117053624-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117053624
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117053624
    reference: chr 0
allele count: 1
allele frequency: 1.144060040270913e-5
allele num: 87408
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000441029
  ensembl transcript: ENST00000540167
  gene symbol: KLHL13
  hgvsc: ENST00000540167.1:c.382G>A
  hgvsp: ENSP00000441029.1:p.Gly128Ser
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360949
  ensembl transcript: ENST00000371882
  gene symbol: KLHL13
  hgvsc: ENST00000371882.1:c.277G>A
  hgvsp: ENSP00000360949.1:p.Gly93Ser
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000440707
  ensembl transcript: ENST00000545703
  gene symbol: KLHL13
  hgvsc: ENST00000545703.1:c.304G>A
  hgvsp: ENSP00000440707.1:p.Gly102Ser
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000443191
  ensembl transcript: ENST00000539496
  gene symbol: KLHL13
  hgvsc: ENST00000539496.1:c.439G>A
  hgvsp: ENSP00000443191.1:p.Gly147Ser
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360943
  ensembl transcript: ENST00000371876
  gene symbol: KLHL13
  hgvsc: ENST00000371876.1:c.277G>A
  hgvsp: ENSP00000360943.1:p.Gly93Ser
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000419803
  ensembl transcript: ENST00000469946
  gene symbol: KLHL13
  hgvsc: ENST00000469946.1:c.277G>A
  hgvsp: ENSP00000419803.1:p.Gly93Ser
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000262820
  ensembl transcript: ENST00000262820
  gene symbol: KLHL13
  hgvsc: ENST00000262820.3:c.430G>A
  hgvsp: ENSP00000262820.3:p.Gly144Ser
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360945
  ensembl transcript: ENST00000371878
  gene symbol: KLHL13
  hgvsc: ENST00000371878.1:c.277G>A
  hgvsp: ENSP00000360945.1:p.Gly93Ser
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000444450
  ensembl transcript: ENST00000541812
  gene symbol: KLHL13
  hgvsc: ENST00000541812.1:c.382G>A
  hgvsp: ENSP00000444450.1:p.Gly128Ser
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000412640
  ensembl transcript: ENST00000447671
  gene symbol: KLHL13
  hgvsc: ENST00000447671.2:c.277G>A
  hgvsp: ENSP00000412640.2:p.Gly93Ser
  variant of: http://identifiers.org/hgnc/22931
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2387
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30753
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11539
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12002
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41663
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Gly147Ser
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

X-117053628-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117053628
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117053628
    reference: chr 0
allele count: 1
allele frequency: 1.144623132833515e-5
allele num: 87365
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360949
  ensembl transcript: ENST00000371882
  gene symbol: KLHL13
  hgvsc: ENST00000371882.1:c.273A>G
  hgvsp: ENST00000371882.1:c.273A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000262820
  ensembl transcript: ENST00000262820
  gene symbol: KLHL13
  hgvsc: ENST00000262820.3:c.426A>G
  hgvsp: ENST00000262820.3:c.426A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360943
  ensembl transcript: ENST00000371876
  gene symbol: KLHL13
  hgvsc: ENST00000371876.1:c.273A>G
  hgvsp: ENST00000371876.1:c.273A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000440707
  ensembl transcript: ENST00000545703
  gene symbol: KLHL13
  hgvsc: ENST00000545703.1:c.300A>G
  hgvsp: ENST00000545703.1:c.300A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000443191
  ensembl transcript: ENST00000539496
  gene symbol: KLHL13
  hgvsc: ENST00000539496.1:c.435A>G
  hgvsp: ENST00000539496.1:c.435A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000441029
  ensembl transcript: ENST00000540167
  gene symbol: KLHL13
  hgvsc: ENST00000540167.1:c.378A>G
  hgvsp: ENST00000540167.1:c.378A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360945
  ensembl transcript: ENST00000371878
  gene symbol: KLHL13
  hgvsc: ENST00000371878.1:c.273A>G
  hgvsp: ENST00000371878.1:c.273A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000412640
  ensembl transcript: ENST00000447671
  gene symbol: KLHL13
  hgvsc: ENST00000447671.2:c.273A>G
  hgvsp: ENST00000447671.2:c.273A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000444450
  ensembl transcript: ENST00000541812
  gene symbol: KLHL13
  hgvsc: ENST00000541812.1:c.378A>G
  hgvsp: ENST00000541812.1:c.378A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000419803
  ensembl transcript: ENST00000469946
  gene symbol: KLHL13
  hgvsc: ENST00000469946.1:c.273A>G
  hgvsp: ENST00000469946.1:c.273A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12022
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30725
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2373
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11486
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Lys145Lys
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

X-117053631-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117053631
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117053631
    reference: chr 0
allele count: 5
allele frequency: 5.725868327931931e-5
allele num: 87323
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360945
  ensembl transcript: ENST00000371878
  gene symbol: KLHL13
  hgvsc: ENST00000371878.1:c.270C>G
  hgvsp: ENSP00000360945.1:p.Ser90Arg
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000440707
  ensembl transcript: ENST00000545703
  gene symbol: KLHL13
  hgvsc: ENST00000545703.1:c.297C>G
  hgvsp: ENSP00000440707.1:p.Ser99Arg
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000262820
  ensembl transcript: ENST00000262820
  gene symbol: KLHL13
  hgvsc: ENST00000262820.3:c.423C>G
  hgvsp: ENSP00000262820.3:p.Ser141Arg
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360943
  ensembl transcript: ENST00000371876
  gene symbol: KLHL13
  hgvsc: ENST00000371876.1:c.270C>G
  hgvsp: ENSP00000360943.1:p.Ser90Arg
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000443191
  ensembl transcript: ENST00000539496
  gene symbol: KLHL13
  hgvsc: ENST00000539496.1:c.432C>G
  hgvsp: ENSP00000443191.1:p.Ser144Arg
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000419803
  ensembl transcript: ENST00000469946
  gene symbol: KLHL13
  hgvsc: ENST00000469946.1:c.270C>G
  hgvsp: ENSP00000419803.1:p.Ser90Arg
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000441029
  ensembl transcript: ENST00000540167
  gene symbol: KLHL13
  hgvsc: ENST00000540167.1:c.375C>G
  hgvsp: ENSP00000441029.1:p.Ser125Arg
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000412640
  ensembl transcript: ENST00000447671
  gene symbol: KLHL13
  hgvsc: ENST00000447671.2:c.270C>G
  hgvsp: ENSP00000412640.2:p.Ser90Arg
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000444450
  ensembl transcript: ENST00000541812
  gene symbol: KLHL13
  hgvsc: ENST00000541812.1:c.375C>G
  hgvsp: ENSP00000444450.1:p.Ser125Arg
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360949
  ensembl transcript: ENST00000371882
  gene symbol: KLHL13
  hgvsc: ENST00000371882.1:c.270C>G
  hgvsp: ENSP00000360949.1:p.Ser90Arg
  variant of: http://identifiers.org/hgnc/22931
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30689
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11467
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2372
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12013
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ser144Arg
num of homozygotes: 0
population: African
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ

X-117053666-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117053666
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117053666
    reference: chr 0
allele count: 1
allele frequency: 1.18070724363894e-5
allele num: 84695
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000443191
  ensembl transcript: ENST00000539496
  gene symbol: KLHL13
  hgvsc: ENST00000539496.1:c.397C>A
  hgvsp: ENSP00000443191.1:p.Gln133Lys
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360943
  ensembl transcript: ENST00000371876
  gene symbol: KLHL13
  hgvsc: ENST00000371876.1:c.235C>A
  hgvsp: ENSP00000360943.1:p.Gln79Lys
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000441029
  ensembl transcript: ENST00000540167
  gene symbol: KLHL13
  hgvsc: ENST00000540167.1:c.340C>A
  hgvsp: ENSP00000441029.1:p.Gln114Lys
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000262820
  ensembl transcript: ENST00000262820
  gene symbol: KLHL13
  hgvsc: ENST00000262820.3:c.388C>A
  hgvsp: ENSP00000262820.3:p.Gln130Lys
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000412640
  ensembl transcript: ENST00000447671
  gene symbol: KLHL13
  hgvsc: ENST00000447671.2:c.235C>A
  hgvsp: ENSP00000412640.2:p.Gln79Lys
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360949
  ensembl transcript: ENST00000371882
  gene symbol: KLHL13
  hgvsc: ENST00000371882.1:c.235C>A
  hgvsp: ENSP00000360949.1:p.Gln79Lys
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000440707
  ensembl transcript: ENST00000545703
  gene symbol: KLHL13
  hgvsc: ENST00000545703.1:c.262C>A
  hgvsp: ENSP00000440707.1:p.Gln88Lys
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360945
  ensembl transcript: ENST00000371878
  gene symbol: KLHL13
  hgvsc: ENST00000371878.1:c.235C>A
  hgvsp: ENSP00000360945.1:p.Gln79Lys
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000444450
  ensembl transcript: ENST00000541812
  gene symbol: KLHL13
  hgvsc: ENST00000541812.1:c.340C>A
  hgvsp: ENSP00000444450.1:p.Gln114Lys
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000419803
  ensembl transcript: ENST00000469946
  gene symbol: KLHL13
  hgvsc: ENST00000469946.1:c.235C>A
  hgvsp: ENSP00000419803.1:p.Gln79Lys
  variant of: http://identifiers.org/hgnc/22931
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2691
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10427
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2244
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 940
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3363
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10310
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27568
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5203
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Gln133Lys
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

X-117053697-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117053697
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117053697
    reference: chr 0
allele count: 26
allele frequency: 3.363257703153701e-4
allele num: 77306
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360945
  ensembl transcript: ENST00000371878
  gene symbol: KLHL13
  hgvsc: ENST00000371878.1:c.221-17A>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000443191
  ensembl transcript: ENST00000539496
  gene symbol: KLHL13
  hgvsc: ENST00000539496.1:c.383-17A>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000444450
  ensembl transcript: ENST00000541812
  gene symbol: KLHL13
  hgvsc: ENST00000541812.1:c.326-17A>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360949
  ensembl transcript: ENST00000371882
  gene symbol: KLHL13
  hgvsc: ENST00000371882.1:c.221-17A>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360943
  ensembl transcript: ENST00000371876
  gene symbol: KLHL13
  hgvsc: ENST00000371876.1:c.221-17A>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000262820
  ensembl transcript: ENST00000262820
  gene symbol: KLHL13
  hgvsc: ENST00000262820.3:c.374-17A>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000412640
  ensembl transcript: ENST00000447671
  gene symbol: KLHL13
  hgvsc: ENST00000447671.2:c.221-17A>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000440707
  ensembl transcript: ENST00000545703
  gene symbol: KLHL13
  hgvsc: ENST00000545703.1:c.248-17A>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000419803
  ensembl transcript: ENST00000469946
  gene symbol: KLHL13
  hgvsc: ENST00000469946.1:c.221-17A>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000441029
  ensembl transcript: ENST00000540167
  gene symbol: KLHL13
  hgvsc: ENST00000540167.1:c.326-17A>G
  variant of: http://identifiers.org/hgnc/22931
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3209
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1752
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6662
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8091
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1165
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15346
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15315
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5902
  bin: 3.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 2.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1142
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 480
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16542
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Other
reference allele: T
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: QD

X-117053698-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117053698
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117053698
    reference: chr 0
allele count: 1
allele frequency: 1.294163323411415e-5
allele num: 77270
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360949
  ensembl transcript: ENST00000371882
  gene symbol: KLHL13
  hgvsc: ENST00000371882.1:c.221-18A>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000444450
  ensembl transcript: ENST00000541812
  gene symbol: KLHL13
  hgvsc: ENST00000541812.1:c.326-18A>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360945
  ensembl transcript: ENST00000371878
  gene symbol: KLHL13
  hgvsc: ENST00000371878.1:c.221-18A>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000262820
  ensembl transcript: ENST00000262820
  gene symbol: KLHL13
  hgvsc: ENST00000262820.3:c.374-18A>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000443191
  ensembl transcript: ENST00000539496
  gene symbol: KLHL13
  hgvsc: ENST00000539496.1:c.383-18A>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000419803
  ensembl transcript: ENST00000469946
  gene symbol: KLHL13
  hgvsc: ENST00000469946.1:c.221-18A>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000441029
  ensembl transcript: ENST00000540167
  gene symbol: KLHL13
  hgvsc: ENST00000540167.1:c.326-18A>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360943
  ensembl transcript: ENST00000371876
  gene symbol: KLHL13
  hgvsc: ENST00000371876.1:c.221-18A>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000412640
  ensembl transcript: ENST00000447671
  gene symbol: KLHL13
  hgvsc: ENST00000447671.2:c.221-18A>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000440707
  ensembl transcript: ENST00000545703
  gene symbol: KLHL13
  hgvsc: ENST00000545703.1:c.248-18A>T
  variant of: http://identifiers.org/hgnc/22931
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6711
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1170
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5855
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15341
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3189
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8124
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15312
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1751
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4311
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1317
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 265
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1465
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQ

X-117053711-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117053711
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117053711
    reference: chr 0
allele count: 1
allele frequency: 1.342408011491013e-5
allele num: 74493
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360945
  ensembl transcript: ENST00000371878
  gene symbol: KLHL13
  hgvsc: ENST00000371878.1:c.221-31C>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000444450
  ensembl transcript: ENST00000541812
  gene symbol: KLHL13
  hgvsc: ENST00000541812.1:c.326-31C>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000443191
  ensembl transcript: ENST00000539496
  gene symbol: KLHL13
  hgvsc: ENST00000539496.1:c.383-31C>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000440707
  ensembl transcript: ENST00000545703
  gene symbol: KLHL13
  hgvsc: ENST00000545703.1:c.248-31C>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360943
  ensembl transcript: ENST00000371876
  gene symbol: KLHL13
  hgvsc: ENST00000371876.1:c.221-31C>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000441029
  ensembl transcript: ENST00000540167
  gene symbol: KLHL13
  hgvsc: ENST00000540167.1:c.326-31C>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360949
  ensembl transcript: ENST00000371882
  gene symbol: KLHL13
  hgvsc: ENST00000371882.1:c.221-31C>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000262820
  ensembl transcript: ENST00000262820
  gene symbol: KLHL13
  hgvsc: ENST00000262820.3:c.374-31C>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000412640
  ensembl transcript: ENST00000447671
  gene symbol: KLHL13
  hgvsc: ENST00000447671.2:c.221-31C>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000419803
  ensembl transcript: ENST00000469946
  gene symbol: KLHL13
  hgvsc: ENST00000469946.1:c.221-31C>T
  variant of: http://identifiers.org/hgnc/22931
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6705
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4182
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2324
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17528
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9329
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10262
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5500
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1593
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3243
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 181
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4312
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16706
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: East Asian
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum

X-117053713-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117053713
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117053713
    reference: chr 0
allele count: 2
allele frequency: 2.723942088991188e-5
allele num: 73423
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360945
  ensembl transcript: ENST00000371878
  gene symbol: KLHL13
  hgvsc: ENST00000371878.1:c.221-33A>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000262820
  ensembl transcript: ENST00000262820
  gene symbol: KLHL13
  hgvsc: ENST00000262820.3:c.374-33A>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360943
  ensembl transcript: ENST00000371876
  gene symbol: KLHL13
  hgvsc: ENST00000371876.1:c.221-33A>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360949
  ensembl transcript: ENST00000371882
  gene symbol: KLHL13
  hgvsc: ENST00000371882.1:c.221-33A>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000419803
  ensembl transcript: ENST00000469946
  gene symbol: KLHL13
  hgvsc: ENST00000469946.1:c.221-33A>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000441029
  ensembl transcript: ENST00000540167
  gene symbol: KLHL13
  hgvsc: ENST00000540167.1:c.326-33A>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000412640
  ensembl transcript: ENST00000447671
  gene symbol: KLHL13
  hgvsc: ENST00000447671.2:c.221-33A>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000444450
  ensembl transcript: ENST00000541812
  gene symbol: KLHL13
  hgvsc: ENST00000541812.1:c.326-33A>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000440707
  ensembl transcript: ENST00000545703
  gene symbol: KLHL13
  hgvsc: ENST00000545703.1:c.248-33A>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000443191
  ensembl transcript: ENST00000539496
  gene symbol: KLHL13
  hgvsc: ENST00000539496.1:c.383-33A>G
  variant of: http://identifiers.org/hgnc/22931
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8976
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8590
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3749
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1550
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9886
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2638
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4862
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17150
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 199
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2840
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1314
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3094
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQ

X-117053714-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117053714
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117053714
    reference: chr 0
allele count: 1
allele frequency: 1.367259601580552e-5
allele num: 73139
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000412640
  ensembl transcript: ENST00000447671
  gene symbol: KLHL13
  hgvsc: ENST00000447671.2:c.221-34C>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000262820
  ensembl transcript: ENST00000262820
  gene symbol: KLHL13
  hgvsc: ENST00000262820.3:c.374-34C>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360943
  ensembl transcript: ENST00000371876
  gene symbol: KLHL13
  hgvsc: ENST00000371876.1:c.221-34C>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360949
  ensembl transcript: ENST00000371882
  gene symbol: KLHL13
  hgvsc: ENST00000371882.1:c.221-34C>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000444450
  ensembl transcript: ENST00000541812
  gene symbol: KLHL13
  hgvsc: ENST00000541812.1:c.326-34C>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000443191
  ensembl transcript: ENST00000539496
  gene symbol: KLHL13
  hgvsc: ENST00000539496.1:c.383-34C>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000440707
  ensembl transcript: ENST00000545703
  gene symbol: KLHL13
  hgvsc: ENST00000545703.1:c.248-34C>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000419803
  ensembl transcript: ENST00000469946
  gene symbol: KLHL13
  hgvsc: ENST00000469946.1:c.221-34C>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000441029
  ensembl transcript: ENST00000540167
  gene symbol: KLHL13
  hgvsc: ENST00000540167.1:c.326-34C>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360945
  ensembl transcript: ENST00000371878
  gene symbol: KLHL13
  hgvsc: ENST00000371878.1:c.221-34C>T
  variant of: http://identifiers.org/hgnc/22931
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17125
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4942
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8955
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3719
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8542
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2643
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1542
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9936
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1314
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4403
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 532
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1351
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff

X-117054169-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117054169
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117054169
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 87068
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000440707
  ensembl transcript: ENST00000545703
  gene symbol: KLHL13
  hgvsc: ENST00000545703.1:c.247+32T>A
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000441029
  ensembl transcript: ENST00000540167
  gene symbol: KLHL13
  hgvsc: ENST00000540167.1:c.325+32T>A
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000419803
  ensembl transcript: ENST00000469946
  gene symbol: KLHL13
  hgvsc: ENST00000469946.1:c.220+32T>A
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360945
  ensembl transcript: ENST00000371878
  gene symbol: KLHL13
  hgvsc: ENST00000371878.1:c.220+32T>A
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360943
  ensembl transcript: ENST00000371876
  gene symbol: KLHL13
  hgvsc: ENST00000371876.1:c.220+32T>A
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000262820
  ensembl transcript: ENST00000262820
  gene symbol: KLHL13
  hgvsc: ENST00000262820.3:c.373+32T>A
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000443191
  ensembl transcript: ENST00000539496
  gene symbol: KLHL13
  hgvsc: ENST00000539496.1:c.382+32T>A
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000444450
  ensembl transcript: ENST00000541812
  gene symbol: KLHL13
  hgvsc: ENST00000541812.1:c.325+32T>A
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000412640
  ensembl transcript: ENST00000447671
  gene symbol: KLHL13
  hgvsc: ENST00000447671.2:c.220+32T>A
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360949
  ensembl transcript: ENST00000371882
  gene symbol: KLHL13
  hgvsc: ENST00000371882.1:c.220+32T>A
  variant of: http://identifiers.org/hgnc/22931
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2039
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5291
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1612
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2993
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16733
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1160
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4014
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9294
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11496
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1499
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2204
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: African
population: Latino
reference allele: A
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum

X-117054170-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117054170
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117054170
    reference: chr 0
allele count: 1
allele frequency: 1.14790793778339e-5
allele num: 87115
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360943
  ensembl transcript: ENST00000371876
  gene symbol: KLHL13
  hgvsc: ENST00000371876.1:c.220+31A>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000441029
  ensembl transcript: ENST00000540167
  gene symbol: KLHL13
  hgvsc: ENST00000540167.1:c.325+31A>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360949
  ensembl transcript: ENST00000371882
  gene symbol: KLHL13
  hgvsc: ENST00000371882.1:c.220+31A>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000443191
  ensembl transcript: ENST00000539496
  gene symbol: KLHL13
  hgvsc: ENST00000539496.1:c.382+31A>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000412640
  ensembl transcript: ENST00000447671
  gene symbol: KLHL13
  hgvsc: ENST00000447671.2:c.220+31A>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000419803
  ensembl transcript: ENST00000469946
  gene symbol: KLHL13
  hgvsc: ENST00000469946.1:c.220+31A>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360945
  ensembl transcript: ENST00000371878
  gene symbol: KLHL13
  hgvsc: ENST00000371878.1:c.220+31A>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000262820
  ensembl transcript: ENST00000262820
  gene symbol: KLHL13
  hgvsc: ENST00000262820.3:c.373+31A>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000444450
  ensembl transcript: ENST00000541812
  gene symbol: KLHL13
  hgvsc: ENST00000541812.1:c.325+31A>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000440707
  ensembl transcript: ENST00000545703
  gene symbol: KLHL13
  hgvsc: ENST00000545703.1:c.247+31A>G
  variant of: http://identifiers.org/hgnc/22931
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2993
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16758
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1053
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1612
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11658
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4017
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9295
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1499
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5292
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2038
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2808
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 378
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ReadPosRankSum

X-117054185-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117054185
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117054185
    reference: chr 0
allele count: 1
allele frequency: 1.144295686005264e-5
allele num: 87390
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000412640
  ensembl transcript: ENST00000447671
  gene symbol: KLHL13
  hgvsc: ENST00000447671.2:c.220+16A>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000441029
  ensembl transcript: ENST00000540167
  gene symbol: KLHL13
  hgvsc: ENST00000540167.1:c.325+16A>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360943
  ensembl transcript: ENST00000371876
  gene symbol: KLHL13
  hgvsc: ENST00000371876.1:c.220+16A>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000443191
  ensembl transcript: ENST00000539496
  gene symbol: KLHL13
  hgvsc: ENST00000539496.1:c.382+16A>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000419803
  ensembl transcript: ENST00000469946
  gene symbol: KLHL13
  hgvsc: ENST00000469946.1:c.220+16A>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000262820
  ensembl transcript: ENST00000262820
  gene symbol: KLHL13
  hgvsc: ENST00000262820.3:c.373+16A>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360945
  ensembl transcript: ENST00000371878
  gene symbol: KLHL13
  hgvsc: ENST00000371878.1:c.220+16A>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360949
  ensembl transcript: ENST00000371882
  gene symbol: KLHL13
  hgvsc: ENST00000371882.1:c.220+16A>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000440707
  ensembl transcript: ENST00000545703
  gene symbol: KLHL13
  hgvsc: ENST00000545703.1:c.247+16A>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000444450
  ensembl transcript: ENST00000541812
  gene symbol: KLHL13
  hgvsc: ENST00000541812.1:c.325+16A>T
  variant of: http://identifiers.org/hgnc/22931
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1612
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5295
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2993
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17054
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12506
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9374
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1499
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2038
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4019
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1297
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum

X-117054190-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117054190
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117054190
    reference: chr 0
allele count: 1
allele frequency: 1.143079226821211e-5
allele num: 87483
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000443191
  ensembl transcript: ENST00000539496
  gene symbol: KLHL13
  hgvsc: ENST00000539496.1:c.382+11T>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000412640
  ensembl transcript: ENST00000447671
  gene symbol: KLHL13
  hgvsc: ENST00000447671.2:c.220+11T>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000440707
  ensembl transcript: ENST00000545703
  gene symbol: KLHL13
  hgvsc: ENST00000545703.1:c.247+11T>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360943
  ensembl transcript: ENST00000371876
  gene symbol: KLHL13
  hgvsc: ENST00000371876.1:c.220+11T>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000441029
  ensembl transcript: ENST00000540167
  gene symbol: KLHL13
  hgvsc: ENST00000540167.1:c.325+11T>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000262820
  ensembl transcript: ENST00000262820
  gene symbol: KLHL13
  hgvsc: ENST00000262820.3:c.373+11T>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000444450
  ensembl transcript: ENST00000541812
  gene symbol: KLHL13
  hgvsc: ENST00000541812.1:c.325+11T>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000419803
  ensembl transcript: ENST00000469946
  gene symbol: KLHL13
  hgvsc: ENST00000469946.1:c.220+11T>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360949
  ensembl transcript: ENST00000371882
  gene symbol: KLHL13
  hgvsc: ENST00000371882.1:c.220+11T>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360945
  ensembl transcript: ENST00000371878
  gene symbol: KLHL13
  hgvsc: ENST00000371878.1:c.220+11T>G
  variant of: http://identifiers.org/hgnc/22931
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17128
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4021
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9417
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1499
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5301
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2994
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2039
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12603
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1612
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3541
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2399
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13437
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ

X-117054192-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117054192
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117054192
    reference: chr 0
allele count: 1
allele frequency: 1.142778780883597e-5
allele num: 87506
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360945
  ensembl transcript: ENST00000371878
  gene symbol: KLHL13
  hgvsc: ENST00000371878.1:c.220+9C>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000262820
  ensembl transcript: ENST00000262820
  gene symbol: KLHL13
  hgvsc: ENST00000262820.3:c.373+9C>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000441029
  ensembl transcript: ENST00000540167
  gene symbol: KLHL13
  hgvsc: ENST00000540167.1:c.325+9C>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000412640
  ensembl transcript: ENST00000447671
  gene symbol: KLHL13
  hgvsc: ENST00000447671.2:c.220+9C>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000419803
  ensembl transcript: ENST00000469946
  gene symbol: KLHL13
  hgvsc: ENST00000469946.1:c.220+9C>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000444450
  ensembl transcript: ENST00000541812
  gene symbol: KLHL13
  hgvsc: ENST00000541812.1:c.325+9C>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360949
  ensembl transcript: ENST00000371882
  gene symbol: KLHL13
  hgvsc: ENST00000371882.1:c.220+9C>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000440707
  ensembl transcript: ENST00000545703
  gene symbol: KLHL13
  hgvsc: ENST00000545703.1:c.247+9C>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000443191
  ensembl transcript: ENST00000539496
  gene symbol: KLHL13
  hgvsc: ENST00000539496.1:c.382+9C>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360943
  ensembl transcript: ENST00000371876
  gene symbol: KLHL13
  hgvsc: ENST00000371876.1:c.220+9C>G
  variant of: http://identifiers.org/hgnc/22931
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2038
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5304
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12613
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17152
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9430
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1499
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4022
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2995
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1613
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1299
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: African
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff

X-117054233-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117054233
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117054233
    reference: chr 0
allele count: 1
allele frequency: 1.140367882678952e-5
allele num: 87691
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360949
  ensembl transcript: ENST00000371882
  gene symbol: KLHL13
  hgvsc: ENST00000371882.1:c.188C>G
  hgvsp: ENSP00000360949.1:p.Ser63Cys
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000440707
  ensembl transcript: ENST00000545703
  gene symbol: KLHL13
  hgvsc: ENST00000545703.1:c.215C>G
  hgvsp: ENSP00000440707.1:p.Ser72Cys
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000262820
  ensembl transcript: ENST00000262820
  gene symbol: KLHL13
  hgvsc: ENST00000262820.3:c.341C>G
  hgvsp: ENSP00000262820.3:p.Ser114Cys
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000419803
  ensembl transcript: ENST00000469946
  gene symbol: KLHL13
  hgvsc: ENST00000469946.1:c.188C>G
  hgvsp: ENSP00000419803.1:p.Ser63Cys
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000443191
  ensembl transcript: ENST00000539496
  gene symbol: KLHL13
  hgvsc: ENST00000539496.1:c.350C>G
  hgvsp: ENSP00000443191.1:p.Ser117Cys
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360943
  ensembl transcript: ENST00000371876
  gene symbol: KLHL13
  hgvsc: ENST00000371876.1:c.188C>G
  hgvsp: ENSP00000360943.1:p.Ser63Cys
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000444450
  ensembl transcript: ENST00000541812
  gene symbol: KLHL13
  hgvsc: ENST00000541812.1:c.293C>G
  hgvsp: ENSP00000444450.1:p.Ser98Cys
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000412640
  ensembl transcript: ENST00000447671
  gene symbol: KLHL13
  hgvsc: ENST00000447671.2:c.188C>G
  hgvsp: ENSP00000412640.2:p.Ser63Cys
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000441029
  ensembl transcript: ENST00000540167
  gene symbol: KLHL13
  hgvsc: ENST00000540167.1:c.293C>G
  hgvsp: ENSP00000441029.1:p.Ser98Cys
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360945
  ensembl transcript: ENST00000371878
  gene symbol: KLHL13
  hgvsc: ENST00000371878.1:c.188C>G
  hgvsp: ENSP00000360945.1:p.Ser63Cys
  variant of: http://identifiers.org/hgnc/22931
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2038
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4028
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17399
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1613
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9504
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2994
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1499
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12575
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5319
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1305
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Ser117Cys
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum

X-117054259-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117054259
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117054259
    reference: chr 0
allele count: 1
allele frequency: 1.140159850411028e-5
allele num: 87707
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360949
  ensembl transcript: ENST00000371882
  gene symbol: KLHL13
  hgvsc: ENST00000371882.1:c.162C>T
  hgvsp: ENST00000371882.1:c.162C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000419803
  ensembl transcript: ENST00000469946
  gene symbol: KLHL13
  hgvsc: ENST00000469946.1:c.162C>T
  hgvsp: ENST00000469946.1:c.162C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000444450
  ensembl transcript: ENST00000541812
  gene symbol: KLHL13
  hgvsc: ENST00000541812.1:c.267C>T
  hgvsp: ENST00000541812.1:c.267C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000440707
  ensembl transcript: ENST00000545703
  gene symbol: KLHL13
  hgvsc: ENST00000545703.1:c.189C>T
  hgvsp: ENST00000545703.1:c.189C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000443191
  ensembl transcript: ENST00000539496
  gene symbol: KLHL13
  hgvsc: ENST00000539496.1:c.324C>T
  hgvsp: ENST00000539496.1:c.324C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360943
  ensembl transcript: ENST00000371876
  gene symbol: KLHL13
  hgvsc: ENST00000371876.1:c.162C>T
  hgvsp: ENST00000371876.1:c.162C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000412640
  ensembl transcript: ENST00000447671
  gene symbol: KLHL13
  hgvsc: ENST00000447671.2:c.162C>T
  hgvsp: ENST00000447671.2:c.162C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000441029
  ensembl transcript: ENST00000540167
  gene symbol: KLHL13
  hgvsc: ENST00000540167.1:c.267C>T
  hgvsp: ENST00000540167.1:c.267C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000262820
  ensembl transcript: ENST00000262820
  gene symbol: KLHL13
  hgvsc: ENST00000262820.3:c.315C>T
  hgvsp: ENST00000262820.3:c.315C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360945
  ensembl transcript: ENST00000371878
  gene symbol: KLHL13
  hgvsc: ENST00000371878.1:c.162C>T
  hgvsp: ENST00000371878.1:c.162C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4033
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5331
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2995
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1499
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17504
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9532
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2038
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1613
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12387
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27318
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Phe108Phe
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: DP

X-117054277-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117054277
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117054277
    reference: chr 0
allele count: 19
allele frequency: 2.166353115557836e-4
allele num: 87705
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000441029
  ensembl transcript: ENST00000540167
  gene symbol: KLHL13
  hgvsc: ENST00000540167.1:c.249T>C
  hgvsp: ENST00000540167.1:c.249T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000444450
  ensembl transcript: ENST00000541812
  gene symbol: KLHL13
  hgvsc: ENST00000541812.1:c.249T>C
  hgvsp: ENST00000541812.1:c.249T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000419803
  ensembl transcript: ENST00000469946
  gene symbol: KLHL13
  hgvsc: ENST00000469946.1:c.144T>C
  hgvsp: ENST00000469946.1:c.144T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360943
  ensembl transcript: ENST00000371876
  gene symbol: KLHL13
  hgvsc: ENST00000371876.1:c.144T>C
  hgvsp: ENST00000371876.1:c.144T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000440707
  ensembl transcript: ENST00000545703
  gene symbol: KLHL13
  hgvsc: ENST00000545703.1:c.171T>C
  hgvsp: ENST00000545703.1:c.171T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360945
  ensembl transcript: ENST00000371878
  gene symbol: KLHL13
  hgvsc: ENST00000371878.1:c.144T>C
  hgvsp: ENST00000371878.1:c.144T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000262820
  ensembl transcript: ENST00000262820
  gene symbol: KLHL13
  hgvsc: ENST00000262820.3:c.297T>C
  hgvsp: ENST00000262820.3:c.297T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000412640
  ensembl transcript: ENST00000447671
  gene symbol: KLHL13
  hgvsc: ENST00000447671.2:c.144T>C
  hgvsp: ENST00000447671.2:c.144T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360949
  ensembl transcript: ENST00000371882
  gene symbol: KLHL13
  hgvsc: ENST00000371882.1:c.144T>C
  hgvsp: ENST00000371882.1:c.144T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000443191
  ensembl transcript: ENST00000539496
  gene symbol: KLHL13
  hgvsc: ENST00000539496.1:c.306T>C
  hgvsp: ENST00000539496.1:c.306T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9583
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4046
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5348
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2993
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1498
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12217
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17589
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1622
  bin: 9.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2037
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Gly102Gly
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: Other
population: European (Finnish)
reference allele: A
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS

X-117054322-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117054322
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117054322
    reference: chr 0
allele count: 1
allele frequency: 1.141291942478886e-5
allele num: 87620
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360943
  ensembl transcript: ENST00000371876
  gene symbol: KLHL13
  hgvsc: ENST00000371876.1:c.99G>A
  hgvsp: ENST00000371876.1:c.99G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000412640
  ensembl transcript: ENST00000447671
  gene symbol: KLHL13
  hgvsc: ENST00000447671.2:c.99G>A
  hgvsp: ENST00000447671.2:c.99G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000441029
  ensembl transcript: ENST00000540167
  gene symbol: KLHL13
  hgvsc: ENST00000540167.1:c.204G>A
  hgvsp: ENST00000540167.1:c.204G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000262820
  ensembl transcript: ENST00000262820
  gene symbol: KLHL13
  hgvsc: ENST00000262820.3:c.252G>A
  hgvsp: ENST00000262820.3:c.252G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360945
  ensembl transcript: ENST00000371878
  gene symbol: KLHL13
  hgvsc: ENST00000371878.1:c.99G>A
  hgvsp: ENST00000371878.1:c.99G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000393807
  ensembl transcript: ENST00000453826
  gene symbol: KLHL13
  hgvsc: ENST00000453826.1:c.99G>A
  hgvsp: ENST00000453826.1:c.99G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000443191
  ensembl transcript: ENST00000539496
  gene symbol: KLHL13
  hgvsc: ENST00000539496.1:c.261G>A
  hgvsp: ENST00000539496.1:c.261G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360949
  ensembl transcript: ENST00000371882
  gene symbol: KLHL13
  hgvsc: ENST00000371882.1:c.99G>A
  hgvsp: ENST00000371882.1:c.99G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000440707
  ensembl transcript: ENST00000545703
  gene symbol: KLHL13
  hgvsc: ENST00000545703.1:c.126G>A
  hgvsp: ENST00000545703.1:c.126G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000419803
  ensembl transcript: ENST00000469946
  gene symbol: KLHL13
  hgvsc: ENST00000469946.1:c.99G>A
  hgvsp: ENST00000469946.1:c.99G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000444450
  ensembl transcript: ENST00000541812
  gene symbol: KLHL13
  hgvsc: ENST00000541812.1:c.204G>A
  hgvsp: ENST00000541812.1:c.204G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1618
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17501
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2034
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5366
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2996
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4054
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11893
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9627
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln87Gln
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
reference allele: C
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

X-117054325-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117054325
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117054325
    reference: chr 0
allele count: 1
allele frequency: 1.14148735802751e-5
allele num: 87605
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000262820
  ensembl transcript: ENST00000262820
  gene symbol: KLHL13
  hgvsc: ENST00000262820.3:c.249C>T
  hgvsp: ENST00000262820.3:c.249C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360949
  ensembl transcript: ENST00000371882
  gene symbol: KLHL13
  hgvsc: ENST00000371882.1:c.96C>T
  hgvsp: ENST00000371882.1:c.96C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360943
  ensembl transcript: ENST00000371876
  gene symbol: KLHL13
  hgvsc: ENST00000371876.1:c.96C>T
  hgvsp: ENST00000371876.1:c.96C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360945
  ensembl transcript: ENST00000371878
  gene symbol: KLHL13
  hgvsc: ENST00000371878.1:c.96C>T
  hgvsp: ENST00000371878.1:c.96C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000443191
  ensembl transcript: ENST00000539496
  gene symbol: KLHL13
  hgvsc: ENST00000539496.1:c.258C>T
  hgvsp: ENST00000539496.1:c.258C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000419803
  ensembl transcript: ENST00000469946
  gene symbol: KLHL13
  hgvsc: ENST00000469946.1:c.96C>T
  hgvsp: ENST00000469946.1:c.96C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000440707
  ensembl transcript: ENST00000545703
  gene symbol: KLHL13
  hgvsc: ENST00000545703.1:c.123C>T
  hgvsp: ENST00000545703.1:c.123C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000444450
  ensembl transcript: ENST00000541812
  gene symbol: KLHL13
  hgvsc: ENST00000541812.1:c.201C>T
  hgvsp: ENST00000541812.1:c.201C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000412640
  ensembl transcript: ENST00000447671
  gene symbol: KLHL13
  hgvsc: ENST00000447671.2:c.96C>T
  hgvsp: ENST00000447671.2:c.96C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000393807
  ensembl transcript: ENST00000453826
  gene symbol: KLHL13
  hgvsc: ENST00000453826.1:c.96C>T
  hgvsp: ENST00000453826.1:c.96C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000441029
  ensembl transcript: ENST00000540167
  gene symbol: KLHL13
  hgvsc: ENST00000540167.1:c.201C>T
  hgvsp: ENST00000540167.1:c.201C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1618
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2994
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11862
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2034
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9601
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5368
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17493
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4051
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp86Asp
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ

X-117054340-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117054340
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117054340
    reference: chr 0
allele count: 27
allele frequency: 3.08906813111378e-4
allele num: 87405
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000440707
  ensembl transcript: ENST00000545703
  gene symbol: KLHL13
  hgvsc: ENST00000545703.1:c.115-7G>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360945
  ensembl transcript: ENST00000371878
  gene symbol: KLHL13
  hgvsc: ENST00000371878.1:c.88-7G>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000262820
  ensembl transcript: ENST00000262820
  gene symbol: KLHL13
  hgvsc: ENST00000262820.3:c.241-7G>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360943
  ensembl transcript: ENST00000371876
  gene symbol: KLHL13
  hgvsc: ENST00000371876.1:c.88-7G>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000393807
  ensembl transcript: ENST00000453826
  gene symbol: KLHL13
  hgvsc: ENST00000453826.1:c.88-7G>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000441029
  ensembl transcript: ENST00000540167
  gene symbol: KLHL13
  hgvsc: ENST00000540167.1:c.193-7G>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000444450
  ensembl transcript: ENST00000541812
  gene symbol: KLHL13
  hgvsc: ENST00000541812.1:c.193-7G>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000443191
  ensembl transcript: ENST00000539496
  gene symbol: KLHL13
  hgvsc: ENST00000539496.1:c.250-7G>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000412640
  ensembl transcript: ENST00000447671
  gene symbol: KLHL13
  hgvsc: ENST00000447671.2:c.88-7G>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000419803
  ensembl transcript: ENST00000469946
  gene symbol: KLHL13
  hgvsc: ENST00000469946.1:c.88-7G>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360949
  ensembl transcript: ENST00000371882
  gene symbol: KLHL13
  hgvsc: ENST00000371882.1:c.88-7G>T
  variant of: http://identifiers.org/hgnc/22931
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2028
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2993
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1493
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11424
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 965
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4047
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 9455
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1620
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5340
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 17118
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: c.250-7G>T
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: MQRankSum

X-117054343-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117054343
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117054343
    reference: chr 0
allele count: 1
allele frequency: 1.144898333028027e-5
allele num: 87344
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000419803
  ensembl transcript: ENST00000469946
  gene symbol: KLHL13
  hgvsc: ENST00000469946.1:c.88-10C>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000441029
  ensembl transcript: ENST00000540167
  gene symbol: KLHL13
  hgvsc: ENST00000540167.1:c.193-10C>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360945
  ensembl transcript: ENST00000371878
  gene symbol: KLHL13
  hgvsc: ENST00000371878.1:c.88-10C>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360949
  ensembl transcript: ENST00000371882
  gene symbol: KLHL13
  hgvsc: ENST00000371882.1:c.88-10C>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360943
  ensembl transcript: ENST00000371876
  gene symbol: KLHL13
  hgvsc: ENST00000371876.1:c.88-10C>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000412640
  ensembl transcript: ENST00000447671
  gene symbol: KLHL13
  hgvsc: ENST00000447671.2:c.88-10C>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000262820
  ensembl transcript: ENST00000262820
  gene symbol: KLHL13
  hgvsc: ENST00000262820.3:c.241-10C>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000444450
  ensembl transcript: ENST00000541812
  gene symbol: KLHL13
  hgvsc: ENST00000541812.1:c.193-10C>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000393807
  ensembl transcript: ENST00000453826
  gene symbol: KLHL13
  hgvsc: ENST00000453826.1:c.88-10C>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000440707
  ensembl transcript: ENST00000545703
  gene symbol: KLHL13
  hgvsc: ENST00000545703.1:c.115-10C>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000443191
  ensembl transcript: ENST00000539496
  gene symbol: KLHL13
  hgvsc: ENST00000539496.1:c.250-10C>G
  variant of: http://identifiers.org/hgnc/22931
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2028
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1207
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1619
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5333
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11254
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16942
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9426
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4047
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1492
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2996
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 13418
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: Other
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum

X-117054351-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117054351
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117054351
    reference: chr 0
allele count: 2
allele frequency: 2.29344647669285e-5
allele num: 87205
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000443191
  ensembl transcript: ENST00000539496
  gene symbol: KLHL13
  hgvsc: ENST00000539496.1:c.250-18C>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000262820
  ensembl transcript: ENST00000262820
  gene symbol: KLHL13
  hgvsc: ENST00000262820.3:c.241-18C>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000412640
  ensembl transcript: ENST00000447671
  gene symbol: KLHL13
  hgvsc: ENST00000447671.2:c.88-18C>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360943
  ensembl transcript: ENST00000371876
  gene symbol: KLHL13
  hgvsc: ENST00000371876.1:c.88-18C>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360949
  ensembl transcript: ENST00000371882
  gene symbol: KLHL13
  hgvsc: ENST00000371882.1:c.88-18C>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000393807
  ensembl transcript: ENST00000453826
  gene symbol: KLHL13
  hgvsc: ENST00000453826.1:c.88-18C>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000419803
  ensembl transcript: ENST00000469946
  gene symbol: KLHL13
  hgvsc: ENST00000469946.1:c.88-18C>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000441029
  ensembl transcript: ENST00000540167
  gene symbol: KLHL13
  hgvsc: ENST00000540167.1:c.193-18C>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000444450
  ensembl transcript: ENST00000541812
  gene symbol: KLHL13
  hgvsc: ENST00000541812.1:c.193-18C>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000440707
  ensembl transcript: ENST00000545703
  gene symbol: KLHL13
  hgvsc: ENST00000545703.1:c.115-18C>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360945
  ensembl transcript: ENST00000371878
  gene symbol: KLHL13
  hgvsc: ENST00000371878.1:c.88-18C>T
  variant of: http://identifiers.org/hgnc/22931
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9238
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16216
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10514
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5320
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1619
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2997
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 893
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2265
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2027
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4043
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1491
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2290
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: Other
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

X-117054352-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117054352
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117054352
    reference: chr 0
allele count: 1
allele frequency: 1.146775839726609e-5
allele num: 87201
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000393807
  ensembl transcript: ENST00000453826
  gene symbol: KLHL13
  hgvsc: ENST00000453826.1:c.88-19A>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000419803
  ensembl transcript: ENST00000469946
  gene symbol: KLHL13
  hgvsc: ENST00000469946.1:c.88-19A>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360943
  ensembl transcript: ENST00000371876
  gene symbol: KLHL13
  hgvsc: ENST00000371876.1:c.88-19A>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000443191
  ensembl transcript: ENST00000539496
  gene symbol: KLHL13
  hgvsc: ENST00000539496.1:c.250-19A>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360945
  ensembl transcript: ENST00000371878
  gene symbol: KLHL13
  hgvsc: ENST00000371878.1:c.88-19A>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000444450
  ensembl transcript: ENST00000541812
  gene symbol: KLHL13
  hgvsc: ENST00000541812.1:c.193-19A>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000412640
  ensembl transcript: ENST00000447671
  gene symbol: KLHL13
  hgvsc: ENST00000447671.2:c.88-19A>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000440707
  ensembl transcript: ENST00000545703
  gene symbol: KLHL13
  hgvsc: ENST00000545703.1:c.115-19A>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000262820
  ensembl transcript: ENST00000262820
  gene symbol: KLHL13
  hgvsc: ENST00000262820.3:c.241-19A>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360949
  ensembl transcript: ENST00000371882
  gene symbol: KLHL13
  hgvsc: ENST00000371882.1:c.88-19A>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000441029
  ensembl transcript: ENST00000540167
  gene symbol: KLHL13
  hgvsc: ENST00000540167.1:c.193-19A>T
  variant of: http://identifiers.org/hgnc/22931
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1619
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10395
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 998
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2447
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16092
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4045
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5319
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2992
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9189
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1491
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2028
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 589
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: QD

X-117054352-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117054352
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117054352
    reference: chr 0
allele count: 2
allele frequency: 2.293551679453217e-5
allele num: 87201
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000262820
  ensembl transcript: ENST00000262820
  gene symbol: KLHL13
  hgvsc: ENST00000262820.3:c.241-19A>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000440707
  ensembl transcript: ENST00000545703
  gene symbol: KLHL13
  hgvsc: ENST00000545703.1:c.115-19A>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000412640
  ensembl transcript: ENST00000447671
  gene symbol: KLHL13
  hgvsc: ENST00000447671.2:c.88-19A>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360945
  ensembl transcript: ENST00000371878
  gene symbol: KLHL13
  hgvsc: ENST00000371878.1:c.88-19A>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000443191
  ensembl transcript: ENST00000539496
  gene symbol: KLHL13
  hgvsc: ENST00000539496.1:c.250-19A>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360943
  ensembl transcript: ENST00000371876
  gene symbol: KLHL13
  hgvsc: ENST00000371876.1:c.88-19A>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000393807
  ensembl transcript: ENST00000453826
  gene symbol: KLHL13
  hgvsc: ENST00000453826.1:c.88-19A>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360949
  ensembl transcript: ENST00000371882
  gene symbol: KLHL13
  hgvsc: ENST00000371882.1:c.88-19A>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000444450
  ensembl transcript: ENST00000541812
  gene symbol: KLHL13
  hgvsc: ENST00000541812.1:c.193-19A>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000419803
  ensembl transcript: ENST00000469946
  gene symbol: KLHL13
  hgvsc: ENST00000469946.1:c.88-19A>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000441029
  ensembl transcript: ENST00000540167
  gene symbol: KLHL13
  hgvsc: ENST00000540167.1:c.193-19A>G
  variant of: http://identifiers.org/hgnc/22931
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1619
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4045
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 998
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2028
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10395
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2447
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2992
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1491
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5319
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16092
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9189
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  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: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS

X-117054353-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117054353
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117054353
    reference: chr 0
allele count: 300
allele frequency: 3.440879947698625e-3
allele num: 87187
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000393807
  ensembl transcript: ENST00000453826
  gene symbol: KLHL13
  hgvsc: ENST00000453826.1:c.88-20A>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000262820
  ensembl transcript: ENST00000262820
  gene symbol: KLHL13
  hgvsc: ENST00000262820.3:c.241-20A>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000441029
  ensembl transcript: ENST00000540167
  gene symbol: KLHL13
  hgvsc: ENST00000540167.1:c.193-20A>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000443191
  ensembl transcript: ENST00000539496
  gene symbol: KLHL13
  hgvsc: ENST00000539496.1:c.250-20A>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000440707
  ensembl transcript: ENST00000545703
  gene symbol: KLHL13
  hgvsc: ENST00000545703.1:c.115-20A>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000419803
  ensembl transcript: ENST00000469946
  gene symbol: KLHL13
  hgvsc: ENST00000469946.1:c.88-20A>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000444450
  ensembl transcript: ENST00000541812
  gene symbol: KLHL13
  hgvsc: ENST00000541812.1:c.193-20A>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360943
  ensembl transcript: ENST00000371876
  gene symbol: KLHL13
  hgvsc: ENST00000371876.1:c.88-20A>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000412640
  ensembl transcript: ENST00000447671
  gene symbol: KLHL13
  hgvsc: ENST00000447671.2:c.88-20A>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360949
  ensembl transcript: ENST00000371882
  gene symbol: KLHL13
  hgvsc: ENST00000371882.1:c.88-20A>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360945
  ensembl transcript: ENST00000371878
  gene symbol: KLHL13
  hgvsc: ENST00000371878.1:c.88-20A>G
  variant of: http://identifiers.org/hgnc/22931
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4035
  bin: 4.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 1483
  bin: 5.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 6.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 2639
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2989
  bin: 4.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 7.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 15916
  bin: 2.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5310
  bin: 3.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 9139
  bin: 3.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 8.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 8.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 1668
  bin: 9.75e1
  variant carriers: 91
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 1.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 7.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 2023
  bin: 5.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 6.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 10232
  bin: 2.25e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 524
  bin: 3.75e1
  variant carriers: 1
num of homozygotes: 7
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: East Asian
reference allele: T
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum

X-117054354-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117054354
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117054354
    reference: chr 0
allele count: 40
allele frequency: 4.589050525446285e-4
allele num: 87164
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000412640
  ensembl transcript: ENST00000447671
  gene symbol: KLHL13
  hgvsc: ENST00000447671.2:c.88-21C>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000440707
  ensembl transcript: ENST00000545703
  gene symbol: KLHL13
  hgvsc: ENST00000545703.1:c.115-21C>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000444450
  ensembl transcript: ENST00000541812
  gene symbol: KLHL13
  hgvsc: ENST00000541812.1:c.193-21C>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360943
  ensembl transcript: ENST00000371876
  gene symbol: KLHL13
  hgvsc: ENST00000371876.1:c.88-21C>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000419803
  ensembl transcript: ENST00000469946
  gene symbol: KLHL13
  hgvsc: ENST00000469946.1:c.88-21C>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000262820
  ensembl transcript: ENST00000262820
  gene symbol: KLHL13
  hgvsc: ENST00000262820.3:c.241-21C>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000441029
  ensembl transcript: ENST00000540167
  gene symbol: KLHL13
  hgvsc: ENST00000540167.1:c.193-21C>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000443191
  ensembl transcript: ENST00000539496
  gene symbol: KLHL13
  hgvsc: ENST00000539496.1:c.250-21C>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360949
  ensembl transcript: ENST00000371882
  gene symbol: KLHL13
  hgvsc: ENST00000371882.1:c.88-21C>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360945
  ensembl transcript: ENST00000371878
  gene symbol: KLHL13
  hgvsc: ENST00000371878.1:c.88-21C>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000393807
  ensembl transcript: ENST00000453826
  gene symbol: KLHL13
  hgvsc: ENST00000453826.1:c.88-21C>G
  variant of: http://identifiers.org/hgnc/22931
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1481
  bin: 5.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 15812
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1239
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4049
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2020
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2992
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10156
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2786
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9134
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 5323
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1619
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 2268
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: Other
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: FS
site quality: ReadPosRankSum

X-117054366-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117054366
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117054366
    reference: chr 0
allele count: 1
allele frequency: 1.149398864393922e-5
allele num: 87002
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000444450
  ensembl transcript: ENST00000541812
  gene symbol: KLHL13
  hgvsc: ENST00000541812.1:c.193-33T>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000262820
  ensembl transcript: ENST00000262820
  gene symbol: KLHL13
  hgvsc: ENST00000262820.3:c.241-33T>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000443191
  ensembl transcript: ENST00000539496
  gene symbol: KLHL13
  hgvsc: ENST00000539496.1:c.250-33T>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360943
  ensembl transcript: ENST00000371876
  gene symbol: KLHL13
  hgvsc: ENST00000371876.1:c.88-33T>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000412640
  ensembl transcript: ENST00000447671
  gene symbol: KLHL13
  hgvsc: ENST00000447671.2:c.88-33T>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360945
  ensembl transcript: ENST00000371878
  gene symbol: KLHL13
  hgvsc: ENST00000371878.1:c.88-33T>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000419803
  ensembl transcript: ENST00000469946
  gene symbol: KLHL13
  hgvsc: ENST00000469946.1:c.88-33T>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000441029
  ensembl transcript: ENST00000540167
  gene symbol: KLHL13
  hgvsc: ENST00000540167.1:c.193-33T>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000440707
  ensembl transcript: ENST00000545703
  gene symbol: KLHL13
  hgvsc: ENST00000545703.1:c.115-33T>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360949
  ensembl transcript: ENST00000371882
  gene symbol: KLHL13
  hgvsc: ENST00000371882.1:c.88-33T>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000393807
  ensembl transcript: ENST00000453826
  gene symbol: KLHL13
  hgvsc: ENST00000453826.1:c.88-33T>G
  variant of: http://identifiers.org/hgnc/22931
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13000
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8282
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5260
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1616
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4887
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4638
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2017
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8308
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4026
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1477
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2986
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19012
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS

X-117054376-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117054376
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117054376
    reference: chr 0
allele count: 2
allele frequency: 2.306991337247529e-5
allele num: 86693
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000393807
  ensembl transcript: ENST00000453826
  gene symbol: KLHL13
  hgvsc: ENST00000453826.1:c.88-43C>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000262820
  ensembl transcript: ENST00000262820
  gene symbol: KLHL13
  hgvsc: ENST00000262820.3:c.241-43C>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360949
  ensembl transcript: ENST00000371882
  gene symbol: KLHL13
  hgvsc: ENST00000371882.1:c.88-43C>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000444450
  ensembl transcript: ENST00000541812
  gene symbol: KLHL13
  hgvsc: ENST00000541812.1:c.193-43C>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000419803
  ensembl transcript: ENST00000469946
  gene symbol: KLHL13
  hgvsc: ENST00000469946.1:c.88-43C>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360945
  ensembl transcript: ENST00000371878
  gene symbol: KLHL13
  hgvsc: ENST00000371878.1:c.88-43C>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360943
  ensembl transcript: ENST00000371876
  gene symbol: KLHL13
  hgvsc: ENST00000371876.1:c.88-43C>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000440707
  ensembl transcript: ENST00000545703
  gene symbol: KLHL13
  hgvsc: ENST00000545703.1:c.115-43C>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000441029
  ensembl transcript: ENST00000540167
  gene symbol: KLHL13
  hgvsc: ENST00000540167.1:c.193-43C>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000443191
  ensembl transcript: ENST00000539496
  gene symbol: KLHL13
  hgvsc: ENST00000539496.1:c.250-43C>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000412640
  ensembl transcript: ENST00000447671
  gene symbol: KLHL13
  hgvsc: ENST00000447671.2:c.88-43C>T
  variant of: http://identifiers.org/hgnc/22931
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5148
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7130
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4741
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9732
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2985
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9107
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8302
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1478
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1615
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2018
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4013
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 555
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: G
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

X-117054379-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117054379
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117054379
    reference: chr 0
allele count: 1
allele frequency: 1.155001155001155e-5
allele num: 86580
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360949
  ensembl transcript: ENST00000371882
  gene symbol: KLHL13
  hgvsc: ENST00000371882.1:c.88-46C>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000444450
  ensembl transcript: ENST00000541812
  gene symbol: KLHL13
  hgvsc: ENST00000541812.1:c.193-46C>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000412640
  ensembl transcript: ENST00000447671
  gene symbol: KLHL13
  hgvsc: ENST00000447671.2:c.88-46C>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000441029
  ensembl transcript: ENST00000540167
  gene symbol: KLHL13
  hgvsc: ENST00000540167.1:c.193-46C>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000262820
  ensembl transcript: ENST00000262820
  gene symbol: KLHL13
  hgvsc: ENST00000262820.3:c.241-46C>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000440707
  ensembl transcript: ENST00000545703
  gene symbol: KLHL13
  hgvsc: ENST00000545703.1:c.115-46C>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000443191
  ensembl transcript: ENST00000539496
  gene symbol: KLHL13
  hgvsc: ENST00000539496.1:c.250-46C>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360945
  ensembl transcript: ENST00000371878
  gene symbol: KLHL13
  hgvsc: ENST00000371878.1:c.88-46C>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000419803
  ensembl transcript: ENST00000469946
  gene symbol: KLHL13
  hgvsc: ENST00000469946.1:c.88-46C>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000393807
  ensembl transcript: ENST00000453826
  gene symbol: KLHL13
  hgvsc: ENST00000453826.1:c.88-46C>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360943
  ensembl transcript: ENST00000371876
  gene symbol: KLHL13
  hgvsc: ENST00000371876.1:c.88-46C>T
  variant of: http://identifiers.org/hgnc/22931
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6887
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1615
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4005
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2985
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10345
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4731
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5121
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8754
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2018
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8241
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1478
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 161
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: Latino
reference allele: G
site quality: MQ
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff

X-117054385-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117054385
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117054385
    reference: chr 0
allele count: 1
allele frequency: 1.161318793622037e-5
allele num: 86109
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360949
  ensembl transcript: ENST00000371882
  gene symbol: KLHL13
  hgvsc: ENST00000371882.1:c.88-52T>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000262820
  ensembl transcript: ENST00000262820
  gene symbol: KLHL13
  hgvsc: ENST00000262820.3:c.241-52T>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000441029
  ensembl transcript: ENST00000540167
  gene symbol: KLHL13
  hgvsc: ENST00000540167.1:c.193-52T>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000444450
  ensembl transcript: ENST00000541812
  gene symbol: KLHL13
  hgvsc: ENST00000541812.1:c.193-52T>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000393807
  ensembl transcript: ENST00000453826
  gene symbol: KLHL13
  hgvsc: ENST00000453826.1:c.88-52T>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000440707
  ensembl transcript: ENST00000545703
  gene symbol: KLHL13
  hgvsc: ENST00000545703.1:c.115-52T>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000412640
  ensembl transcript: ENST00000447671
  gene symbol: KLHL13
  hgvsc: ENST00000447671.2:c.88-52T>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360945
  ensembl transcript: ENST00000371878
  gene symbol: KLHL13
  hgvsc: ENST00000371878.1:c.88-52T>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000419803
  ensembl transcript: ENST00000469946
  gene symbol: KLHL13
  hgvsc: ENST00000469946.1:c.88-52T>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000443191
  ensembl transcript: ENST00000539496
  gene symbol: KLHL13
  hgvsc: ENST00000539496.1:c.250-52T>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360943
  ensembl transcript: ENST00000371876
  gene symbol: KLHL13
  hgvsc: ENST00000371876.1:c.88-52T>G
  variant of: http://identifiers.org/hgnc/22931
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2981
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5059
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8209
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2017
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8161
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4698
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4003
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11489
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1615
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1478
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6342
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2179
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
reference allele: A
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: VQSLOD

X-117079346-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117079346
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117079346
    reference: chr 0
allele count: 6
allele frequency: 7.055337362714894e-5
allele num: 85042
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360949
  ensembl transcript: ENST00000371882
  gene symbol: KLHL13
  hgvsc: ENST00000371882.1:c.87+51C>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000419803
  ensembl transcript: ENST00000469946
  gene symbol: KLHL13
  hgvsc: ENST00000469946.1:c.87+51C>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000444450
  ensembl transcript: ENST00000541812
  gene symbol: KLHL13
  hgvsc: ENST00000541812.1:c.192+51C>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360943
  ensembl transcript: ENST00000371876
  gene symbol: KLHL13
  hgvsc: ENST00000371876.1:c.87+51C>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000441029
  ensembl transcript: ENST00000540167
  gene symbol: KLHL13
  hgvsc: ENST00000540167.1:c.192+51C>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000440707
  ensembl transcript: ENST00000545703
  gene symbol: KLHL13
  hgvsc: ENST00000545703.1:c.114+51C>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360945
  ensembl transcript: ENST00000371878
  gene symbol: KLHL13
  hgvsc: ENST00000371878.1:c.87+51C>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000443191
  ensembl transcript: ENST00000539496
  gene symbol: KLHL13
  hgvsc: ENST00000539496.1:c.249+51C>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000262820
  ensembl transcript: ENST00000262820
  gene symbol: KLHL13
  hgvsc: ENST00000262820.3:c.240+51C>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000393807
  ensembl transcript: ENST00000453826
  gene symbol: KLHL13
  hgvsc: ENST00000453826.1:c.87+51C>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000412640
  ensembl transcript: ENST00000447671
  gene symbol: KLHL13
  hgvsc: ENST00000447671.2:c.87+51C>G
  variant of: http://identifiers.org/hgnc/22931
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3040
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26323
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2454
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1992
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9655
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12030
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2060
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 632
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: African
population: Other
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: QD

X-117079350-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117079350
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117079350
    reference: chr 0
allele count: 1
allele frequency: 1.175917215428034e-5
allele num: 85040
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360949
  ensembl transcript: ENST00000371882
  gene symbol: KLHL13
  hgvsc: ENST00000371882.1:c.87+47C>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000441029
  ensembl transcript: ENST00000540167
  gene symbol: KLHL13
  hgvsc: ENST00000540167.1:c.192+47C>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000412640
  ensembl transcript: ENST00000447671
  gene symbol: KLHL13
  hgvsc: ENST00000447671.2:c.87+47C>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360943
  ensembl transcript: ENST00000371876
  gene symbol: KLHL13
  hgvsc: ENST00000371876.1:c.87+47C>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000393807
  ensembl transcript: ENST00000453826
  gene symbol: KLHL13
  hgvsc: ENST00000453826.1:c.87+47C>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000444450
  ensembl transcript: ENST00000541812
  gene symbol: KLHL13
  hgvsc: ENST00000541812.1:c.192+47C>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360945
  ensembl transcript: ENST00000371878
  gene symbol: KLHL13
  hgvsc: ENST00000371878.1:c.87+47C>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000262820
  ensembl transcript: ENST00000262820
  gene symbol: KLHL13
  hgvsc: ENST00000262820.3:c.240+47C>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000443191
  ensembl transcript: ENST00000539496
  gene symbol: KLHL13
  hgvsc: ENST00000539496.1:c.249+47C>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000419803
  ensembl transcript: ENST00000469946
  gene symbol: KLHL13
  hgvsc: ENST00000469946.1:c.87+47C>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000440707
  ensembl transcript: ENST00000545703
  gene symbol: KLHL13
  hgvsc: ENST00000545703.1:c.114+47C>T
  variant of: http://identifiers.org/hgnc/22931
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2452
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2715
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1962
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2069
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12425
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9571
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26378
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1859
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: G
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ

X-117079364-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117079364
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117079364
    reference: chr 0
allele count: 17
allele frequency: 1.996406468356957e-4
allele num: 85153
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000393807
  ensembl transcript: ENST00000453826
  gene symbol: KLHL13
  hgvsc: ENST00000453826.1:c.87+33G>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000412640
  ensembl transcript: ENST00000447671
  gene symbol: KLHL13
  hgvsc: ENST00000447671.2:c.87+33G>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000444450
  ensembl transcript: ENST00000541812
  gene symbol: KLHL13
  hgvsc: ENST00000541812.1:c.192+33G>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000262820
  ensembl transcript: ENST00000262820
  gene symbol: KLHL13
  hgvsc: ENST00000262820.3:c.240+33G>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000440707
  ensembl transcript: ENST00000545703
  gene symbol: KLHL13
  hgvsc: ENST00000545703.1:c.114+33G>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000441029
  ensembl transcript: ENST00000540167
  gene symbol: KLHL13
  hgvsc: ENST00000540167.1:c.192+33G>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360945
  ensembl transcript: ENST00000371878
  gene symbol: KLHL13
  hgvsc: ENST00000371878.1:c.87+33G>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360943
  ensembl transcript: ENST00000371876
  gene symbol: KLHL13
  hgvsc: ENST00000371876.1:c.87+33G>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000419803
  ensembl transcript: ENST00000469946
  gene symbol: KLHL13
  hgvsc: ENST00000469946.1:c.87+33G>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360949
  ensembl transcript: ENST00000371882
  gene symbol: KLHL13
  hgvsc: ENST00000371882.1:c.87+33G>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000443191
  ensembl transcript: ENST00000539496
  gene symbol: KLHL13
  hgvsc: ENST00000539496.1:c.249+33G>T
  variant of: http://identifiers.org/hgnc/22931
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2210
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2086
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9545
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1938
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26792
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14100
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: African
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum

X-117079364-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117079364
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117079364
    reference: chr 0
allele count: 18
allele frequency: 2.11384214296619e-4
allele num: 85153
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000419803
  ensembl transcript: ENST00000469946
  gene symbol: KLHL13
  hgvsc: ENST00000469946.1:c.87+33G>A
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360943
  ensembl transcript: ENST00000371876
  gene symbol: KLHL13
  hgvsc: ENST00000371876.1:c.87+33G>A
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000393807
  ensembl transcript: ENST00000453826
  gene symbol: KLHL13
  hgvsc: ENST00000453826.1:c.87+33G>A
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000262820
  ensembl transcript: ENST00000262820
  gene symbol: KLHL13
  hgvsc: ENST00000262820.3:c.240+33G>A
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360945
  ensembl transcript: ENST00000371878
  gene symbol: KLHL13
  hgvsc: ENST00000371878.1:c.87+33G>A
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000443191
  ensembl transcript: ENST00000539496
  gene symbol: KLHL13
  hgvsc: ENST00000539496.1:c.249+33G>A
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000412640
  ensembl transcript: ENST00000447671
  gene symbol: KLHL13
  hgvsc: ENST00000447671.2:c.87+33G>A
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360949
  ensembl transcript: ENST00000371882
  gene symbol: KLHL13
  hgvsc: ENST00000371882.1:c.87+33G>A
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000441029
  ensembl transcript: ENST00000540167
  gene symbol: KLHL13
  hgvsc: ENST00000540167.1:c.192+33G>A
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000440707
  ensembl transcript: ENST00000545703
  gene symbol: KLHL13
  hgvsc: ENST00000545703.1:c.114+33G>A
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000444450
  ensembl transcript: ENST00000541812
  gene symbol: KLHL13
  hgvsc: ENST00000541812.1:c.192+33G>A
  variant of: http://identifiers.org/hgnc/22931
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26792
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 14100
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2086
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2210
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9545
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1938
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP

X-117079365-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117079365
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117079365
    reference: chr 0
allele count: 14
allele frequency: 1.641843555764044e-4
allele num: 85270
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360949
  ensembl transcript: ENST00000371882
  gene symbol: KLHL13
  hgvsc: ENST00000371882.1:c.87+32C>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000262820
  ensembl transcript: ENST00000262820
  gene symbol: KLHL13
  hgvsc: ENST00000262820.3:c.240+32C>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360943
  ensembl transcript: ENST00000371876
  gene symbol: KLHL13
  hgvsc: ENST00000371876.1:c.87+32C>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000441029
  ensembl transcript: ENST00000540167
  gene symbol: KLHL13
  hgvsc: ENST00000540167.1:c.192+32C>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360945
  ensembl transcript: ENST00000371878
  gene symbol: KLHL13
  hgvsc: ENST00000371878.1:c.87+32C>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000444450
  ensembl transcript: ENST00000541812
  gene symbol: KLHL13
  hgvsc: ENST00000541812.1:c.192+32C>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000440707
  ensembl transcript: ENST00000545703
  gene symbol: KLHL13
  hgvsc: ENST00000545703.1:c.114+32C>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000443191
  ensembl transcript: ENST00000539496
  gene symbol: KLHL13
  hgvsc: ENST00000539496.1:c.249+32C>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000412640
  ensembl transcript: ENST00000447671
  gene symbol: KLHL13
  hgvsc: ENST00000447671.2:c.87+32C>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000419803
  ensembl transcript: ENST00000469946
  gene symbol: KLHL13
  hgvsc: ENST00000469946.1:c.87+32C>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000393807
  ensembl transcript: ENST00000453826
  gene symbol: KLHL13
  hgvsc: ENST00000453826.1:c.87+32C>T
  variant of: http://identifiers.org/hgnc/22931
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2108
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14334
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9559
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1935
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2092
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 26830
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 5.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 317
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

X-117079380-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117079380
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117079380
    reference: chr 0
allele count: 208
allele frequency: 2.424214169998019e-3
allele num: 85801
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360943
  ensembl transcript: ENST00000371876
  gene symbol: KLHL13
  hgvsc: ENST00000371876.1:c.87+17C>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000443191
  ensembl transcript: ENST00000539496
  gene symbol: KLHL13
  hgvsc: ENST00000539496.1:c.249+17C>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000262820
  ensembl transcript: ENST00000262820
  gene symbol: KLHL13
  hgvsc: ENST00000262820.3:c.240+17C>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000419803
  ensembl transcript: ENST00000469946
  gene symbol: KLHL13
  hgvsc: ENST00000469946.1:c.87+17C>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000412640
  ensembl transcript: ENST00000447671
  gene symbol: KLHL13
  hgvsc: ENST00000447671.2:c.87+17C>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000393807
  ensembl transcript: ENST00000453826
  gene symbol: KLHL13
  hgvsc: ENST00000453826.1:c.87+17C>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000441029
  ensembl transcript: ENST00000540167
  gene symbol: KLHL13
  hgvsc: ENST00000540167.1:c.192+17C>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360949
  ensembl transcript: ENST00000371882
  gene symbol: KLHL13
  hgvsc: ENST00000371882.1:c.87+17C>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000444450
  ensembl transcript: ENST00000541812
  gene symbol: KLHL13
  hgvsc: ENST00000541812.1:c.192+17C>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000440707
  ensembl transcript: ENST00000545703
  gene symbol: KLHL13
  hgvsc: ENST00000545703.1:c.114+17C>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360945
  ensembl transcript: ENST00000371878
  gene symbol: KLHL13
  hgvsc: ENST00000371878.1:c.87+17C>T
  variant of: http://identifiers.org/hgnc/22931
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 6.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 5.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 27243
  bin: 2.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 4.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 9564
  bin: 3.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 6.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1927
  bin: 3.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 1347
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 4.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 15556
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 9.75e1
  variant carriers: 52
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 5.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 1750
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 1.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD

X-117079381-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117079381
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117079381
    reference: chr 0
allele count: 1
allele frequency: 1.164944490395033e-5
allele num: 85841
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000443191
  ensembl transcript: ENST00000539496
  gene symbol: KLHL13
  hgvsc: ENST00000539496.1:c.249+16T>C
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000441029
  ensembl transcript: ENST00000540167
  gene symbol: KLHL13
  hgvsc: ENST00000540167.1:c.192+16T>C
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360943
  ensembl transcript: ENST00000371876
  gene symbol: KLHL13
  hgvsc: ENST00000371876.1:c.87+16T>C
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000419803
  ensembl transcript: ENST00000469946
  gene symbol: KLHL13
  hgvsc: ENST00000469946.1:c.87+16T>C
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000444450
  ensembl transcript: ENST00000541812
  gene symbol: KLHL13
  hgvsc: ENST00000541812.1:c.192+16T>C
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000262820
  ensembl transcript: ENST00000262820
  gene symbol: KLHL13
  hgvsc: ENST00000262820.3:c.240+16T>C
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360945
  ensembl transcript: ENST00000371878
  gene symbol: KLHL13
  hgvsc: ENST00000371878.1:c.87+16T>C
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000393807
  ensembl transcript: ENST00000453826
  gene symbol: KLHL13
  hgvsc: ENST00000453826.1:c.87+16T>C
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000440707
  ensembl transcript: ENST00000545703
  gene symbol: KLHL13
  hgvsc: ENST00000545703.1:c.114+16T>C
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360949
  ensembl transcript: ENST00000371882
  gene symbol: KLHL13
  hgvsc: ENST00000371882.1:c.87+16T>C
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000412640
  ensembl transcript: ENST00000447671
  gene symbol: KLHL13
  hgvsc: ENST00000447671.2:c.87+16T>C
  variant of: http://identifiers.org/hgnc/22931
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1724
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1915
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1307
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15611
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9615
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27382
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 306
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: A
site quality: FS
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum

X-117079387-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117079387
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117079387
    reference: chr 0
allele count: 3
allele frequency: 3.484118227745195e-5
allele num: 86105
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000419803
  ensembl transcript: ENST00000469946
  gene symbol: KLHL13
  hgvsc: ENST00000469946.1:c.87+10G>A
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360949
  ensembl transcript: ENST00000371882
  gene symbol: KLHL13
  hgvsc: ENST00000371882.1:c.87+10G>A
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000393807
  ensembl transcript: ENST00000453826
  gene symbol: KLHL13
  hgvsc: ENST00000453826.1:c.87+10G>A
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000262820
  ensembl transcript: ENST00000262820
  gene symbol: KLHL13
  hgvsc: ENST00000262820.3:c.240+10G>A
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000441029
  ensembl transcript: ENST00000540167
  gene symbol: KLHL13
  hgvsc: ENST00000540167.1:c.192+10G>A
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000440707
  ensembl transcript: ENST00000545703
  gene symbol: KLHL13
  hgvsc: ENST00000545703.1:c.114+10G>A
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000444450
  ensembl transcript: ENST00000541812
  gene symbol: KLHL13
  hgvsc: ENST00000541812.1:c.192+10G>A
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000443191
  ensembl transcript: ENST00000539496
  gene symbol: KLHL13
  hgvsc: ENST00000539496.1:c.249+10G>A
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360943
  ensembl transcript: ENST00000371876
  gene symbol: KLHL13
  hgvsc: ENST00000371876.1:c.87+10G>A
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000412640
  ensembl transcript: ENST00000447671
  gene symbol: KLHL13
  hgvsc: ENST00000447671.2:c.87+10G>A
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360945
  ensembl transcript: ENST00000371878
  gene symbol: KLHL13
  hgvsc: ENST00000371878.1:c.87+10G>A
  variant of: http://identifiers.org/hgnc/22931
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9636
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27512
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1459
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1917
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16029
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1026
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD

X-117079393-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117079393
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117079393
    reference: chr 0
allele count: 1
allele frequency: 1.157193112386595e-5
allele num: 86416
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000393807
  ensembl transcript: ENST00000453826
  gene symbol: KLHL13
  hgvsc: ENST00000453826.1:c.87+4A>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000262820
  ensembl transcript: ENST00000262820
  gene symbol: KLHL13
  hgvsc: ENST00000262820.3:c.240+4A>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000441029
  ensembl transcript: ENST00000540167
  gene symbol: KLHL13
  hgvsc: ENST00000540167.1:c.192+4A>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000444450
  ensembl transcript: ENST00000541812
  gene symbol: KLHL13
  hgvsc: ENST00000541812.1:c.192+4A>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000419803
  ensembl transcript: ENST00000469946
  gene symbol: KLHL13
  hgvsc: ENST00000469946.1:c.87+4A>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360943
  ensembl transcript: ENST00000371876
  gene symbol: KLHL13
  hgvsc: ENST00000371876.1:c.87+4A>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360949
  ensembl transcript: ENST00000371882
  gene symbol: KLHL13
  hgvsc: ENST00000371882.1:c.87+4A>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000443191
  ensembl transcript: ENST00000539496
  gene symbol: KLHL13
  hgvsc: ENST00000539496.1:c.249+4A>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360945
  ensembl transcript: ENST00000371878
  gene symbol: KLHL13
  hgvsc: ENST00000371878.1:c.87+4A>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000412640
  ensembl transcript: ENST00000447671
  gene symbol: KLHL13
  hgvsc: ENST00000447671.2:c.87+4A>G
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000440707
  ensembl transcript: ENST00000545703
  gene symbol: KLHL13
  hgvsc: ENST00000545703.1:c.114+4A>G
  variant of: http://identifiers.org/hgnc/22931
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1212
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27611
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9625
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1912
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16555
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: c.249+4A>G
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD

X-117079416-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117079416
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117079416
    reference: chr 0
allele count: 2
allele frequency: 2.291685764048034e-5
allele num: 87272
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000440707
  ensembl transcript: ENST00000545703
  gene symbol: KLHL13
  hgvsc: ENST00000545703.1:c.95A>T
  hgvsp: ENSP00000440707.1:p.His32Leu
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000443191
  ensembl transcript: ENST00000539496
  gene symbol: KLHL13
  hgvsc: ENST00000539496.1:c.230A>T
  hgvsp: ENSP00000443191.1:p.His77Leu
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000419803
  ensembl transcript: ENST00000469946
  gene symbol: KLHL13
  hgvsc: ENST00000469946.1:c.68A>T
  hgvsp: ENSP00000419803.1:p.His23Leu
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360943
  ensembl transcript: ENST00000371876
  gene symbol: KLHL13
  hgvsc: ENST00000371876.1:c.68A>T
  hgvsp: ENSP00000360943.1:p.His23Leu
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000262820
  ensembl transcript: ENST00000262820
  gene symbol: KLHL13
  hgvsc: ENST00000262820.3:c.221A>T
  hgvsp: ENSP00000262820.3:p.His74Leu
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000441029
  ensembl transcript: ENST00000540167
  gene symbol: KLHL13
  hgvsc: ENST00000540167.1:c.173A>T
  hgvsp: ENSP00000441029.1:p.His58Leu
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000393807
  ensembl transcript: ENST00000453826
  gene symbol: KLHL13
  hgvsc: ENST00000453826.1:c.68A>T
  hgvsp: ENSP00000393807.1:p.His23Leu
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000444450
  ensembl transcript: ENST00000541812
  gene symbol: KLHL13
  hgvsc: ENST00000541812.1:c.173A>T
  hgvsp: ENSP00000444450.1:p.His58Leu
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360945
  ensembl transcript: ENST00000371878
  gene symbol: KLHL13
  hgvsc: ENST00000371878.1:c.68A>T
  hgvsp: ENSP00000360945.1:p.His23Leu
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360949
  ensembl transcript: ENST00000371882
  gene symbol: KLHL13
  hgvsc: ENST00000371882.1:c.68A>T
  hgvsp: ENSP00000360949.1:p.His23Leu
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000412640
  ensembl transcript: ENST00000447671
  gene symbol: KLHL13
  hgvsc: ENST00000447671.2:c.68A>T
  hgvsp: ENSP00000412640.2:p.His23Leu
  variant of: http://identifiers.org/hgnc/22931
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28211
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1914
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9687
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17436
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His77Leu
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
reference allele: T
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum

X-117079417-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117079417
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117079417
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 87283
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000443191
  ensembl transcript: ENST00000539496
  gene symbol: KLHL13
  hgvsc: ENST00000539496.1:c.229C>A
  hgvsp: ENSP00000443191.1:p.His77Asn
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000412640
  ensembl transcript: ENST00000447671
  gene symbol: KLHL13
  hgvsc: ENST00000447671.2:c.67C>A
  hgvsp: ENSP00000412640.2:p.His23Asn
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360945
  ensembl transcript: ENST00000371878
  gene symbol: KLHL13
  hgvsc: ENST00000371878.1:c.67C>A
  hgvsp: ENSP00000360945.1:p.His23Asn
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000393807
  ensembl transcript: ENST00000453826
  gene symbol: KLHL13
  hgvsc: ENST00000453826.1:c.67C>A
  hgvsp: ENSP00000393807.1:p.His23Asn
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360949
  ensembl transcript: ENST00000371882
  gene symbol: KLHL13
  hgvsc: ENST00000371882.1:c.67C>A
  hgvsp: ENSP00000360949.1:p.His23Asn
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000262820
  ensembl transcript: ENST00000262820
  gene symbol: KLHL13
  hgvsc: ENST00000262820.3:c.220C>A
  hgvsp: ENSP00000262820.3:p.His74Asn
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000419803
  ensembl transcript: ENST00000469946
  gene symbol: KLHL13
  hgvsc: ENST00000469946.1:c.67C>A
  hgvsp: ENSP00000419803.1:p.His23Asn
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360943
  ensembl transcript: ENST00000371876
  gene symbol: KLHL13
  hgvsc: ENST00000371876.1:c.67C>A
  hgvsp: ENSP00000360943.1:p.His23Asn
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000444450
  ensembl transcript: ENST00000541812
  gene symbol: KLHL13
  hgvsc: ENST00000541812.1:c.172C>A
  hgvsp: ENSP00000444450.1:p.His58Asn
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000441029
  ensembl transcript: ENST00000540167
  gene symbol: KLHL13
  hgvsc: ENST00000540167.1:c.172C>A
  hgvsp: ENSP00000441029.1:p.His58Asn
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000440707
  ensembl transcript: ENST00000545703
  gene symbol: KLHL13
  hgvsc: ENST00000545703.1:c.94C>A
  hgvsp: ENSP00000440707.1:p.His32Asn
  variant of: http://identifiers.org/hgnc/22931
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1920
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9693
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17427
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His77Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: African
population: Latino
reference allele: G
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff

X-117079427-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117079427
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117079427
    reference: chr 0
allele count: 1
allele frequency: 1.14432187485696e-5
allele num: 87388
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000419803
  ensembl transcript: ENST00000469946
  gene symbol: KLHL13
  hgvsc: ENST00000469946.1:c.57C>T
  hgvsp: ENST00000469946.1:c.57C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000393807
  ensembl transcript: ENST00000453826
  gene symbol: KLHL13
  hgvsc: ENST00000453826.1:c.57C>T
  hgvsp: ENST00000453826.1:c.57C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000444450
  ensembl transcript: ENST00000541812
  gene symbol: KLHL13
  hgvsc: ENST00000541812.1:c.162C>T
  hgvsp: ENST00000541812.1:c.162C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360949
  ensembl transcript: ENST00000371882
  gene symbol: KLHL13
  hgvsc: ENST00000371882.1:c.57C>T
  hgvsp: ENST00000371882.1:c.57C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360945
  ensembl transcript: ENST00000371878
  gene symbol: KLHL13
  hgvsc: ENST00000371878.1:c.57C>T
  hgvsp: ENST00000371878.1:c.57C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000262820
  ensembl transcript: ENST00000262820
  gene symbol: KLHL13
  hgvsc: ENST00000262820.3:c.210C>T
  hgvsp: ENST00000262820.3:c.210C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000412640
  ensembl transcript: ENST00000447671
  gene symbol: KLHL13
  hgvsc: ENST00000447671.2:c.57C>T
  hgvsp: ENST00000447671.2:c.57C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000440707
  ensembl transcript: ENST00000545703
  gene symbol: KLHL13
  hgvsc: ENST00000545703.1:c.84C>T
  hgvsp: ENST00000545703.1:c.84C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000443191
  ensembl transcript: ENST00000539496
  gene symbol: KLHL13
  hgvsc: ENST00000539496.1:c.219C>T
  hgvsp: ENST00000539496.1:c.219C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000441029
  ensembl transcript: ENST00000540167
  gene symbol: KLHL13
  hgvsc: ENST00000540167.1:c.162C>T
  hgvsp: ENST00000540167.1:c.162C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360943
  ensembl transcript: ENST00000371876
  gene symbol: KLHL13
  hgvsc: ENST00000371876.1:c.57C>T
  hgvsp: ENST00000371876.1:c.57C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17472
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9683
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28298
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1922
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr73Thr
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: South Asian
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

X-117079438-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117079438
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117079438
    reference: chr 0
allele count: 1
allele frequency: 1.144544528504881e-5
allele num: 87371
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360949
  ensembl transcript: ENST00000371882
  gene symbol: KLHL13
  hgvsc: ENST00000371882.1:c.46C>T
  hgvsp: ENSP00000360949.1:p.Arg16Cys
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000444450
  ensembl transcript: ENST00000541812
  gene symbol: KLHL13
  hgvsc: ENST00000541812.1:c.151C>T
  hgvsp: ENSP00000444450.1:p.Arg51Cys
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000393807
  ensembl transcript: ENST00000453826
  gene symbol: KLHL13
  hgvsc: ENST00000453826.1:c.46C>T
  hgvsp: ENSP00000393807.1:p.Arg16Cys
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360945
  ensembl transcript: ENST00000371878
  gene symbol: KLHL13
  hgvsc: ENST00000371878.1:c.46C>T
  hgvsp: ENSP00000360945.1:p.Arg16Cys
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000440707
  ensembl transcript: ENST00000545703
  gene symbol: KLHL13
  hgvsc: ENST00000545703.1:c.73C>T
  hgvsp: ENSP00000440707.1:p.Arg25Cys
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360943
  ensembl transcript: ENST00000371876
  gene symbol: KLHL13
  hgvsc: ENST00000371876.1:c.46C>T
  hgvsp: ENSP00000360943.1:p.Arg16Cys
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000441029
  ensembl transcript: ENST00000540167
  gene symbol: KLHL13
  hgvsc: ENST00000540167.1:c.151C>T
  hgvsp: ENSP00000441029.1:p.Arg51Cys
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000262820
  ensembl transcript: ENST00000262820
  gene symbol: KLHL13
  hgvsc: ENST00000262820.3:c.199C>T
  hgvsp: ENSP00000262820.3:p.Arg67Cys
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000419803
  ensembl transcript: ENST00000469946
  gene symbol: KLHL13
  hgvsc: ENST00000469946.1:c.46C>T
  hgvsp: ENSP00000419803.1:p.Arg16Cys
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000443191
  ensembl transcript: ENST00000539496
  gene symbol: KLHL13
  hgvsc: ENST00000539496.1:c.208C>T
  hgvsp: ENSP00000443191.1:p.Arg70Cys
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000412640
  ensembl transcript: ENST00000447671
  gene symbol: KLHL13
  hgvsc: ENST00000447671.2:c.46C>T
  hgvsp: ENSP00000412640.2:p.Arg16Cys
  variant of: http://identifiers.org/hgnc/22931
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9659
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1908
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17345
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28305
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg70Cys
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD

X-117079445-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117079445
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117079445
    reference: chr 0
allele count: 1
allele frequency: 1.144976985962582e-5
allele num: 87338
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360945
  ensembl transcript: ENST00000371878
  gene symbol: KLHL13
  hgvsc: ENST00000371878.1:c.39A>G
  hgvsp: ENST00000371878.1:c.39A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000444450
  ensembl transcript: ENST00000541812
  gene symbol: KLHL13
  hgvsc: ENST00000541812.1:c.144A>G
  hgvsp: ENST00000541812.1:c.144A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000412640
  ensembl transcript: ENST00000447671
  gene symbol: KLHL13
  hgvsc: ENST00000447671.2:c.39A>G
  hgvsp: ENST00000447671.2:c.39A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000440707
  ensembl transcript: ENST00000545703
  gene symbol: KLHL13
  hgvsc: ENST00000545703.1:c.66A>G
  hgvsp: ENST00000545703.1:c.66A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000443191
  ensembl transcript: ENST00000539496
  gene symbol: KLHL13
  hgvsc: ENST00000539496.1:c.201A>G
  hgvsp: ENST00000539496.1:c.201A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000393807
  ensembl transcript: ENST00000453826
  gene symbol: KLHL13
  hgvsc: ENST00000453826.1:c.39A>G
  hgvsp: ENST00000453826.1:c.39A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000262820
  ensembl transcript: ENST00000262820
  gene symbol: KLHL13
  hgvsc: ENST00000262820.3:c.192A>G
  hgvsp: ENST00000262820.3:c.192A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000419803
  ensembl transcript: ENST00000469946
  gene symbol: KLHL13
  hgvsc: ENST00000469946.1:c.39A>G
  hgvsp: ENST00000469946.1:c.39A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360943
  ensembl transcript: ENST00000371876
  gene symbol: KLHL13
  hgvsc: ENST00000371876.1:c.39A>G
  hgvsp: ENST00000371876.1:c.39A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360949
  ensembl transcript: ENST00000371882
  gene symbol: KLHL13
  hgvsc: ENST00000371882.1:c.39A>G
  hgvsp: ENST00000371882.1:c.39A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000441029
  ensembl transcript: ENST00000540167
  gene symbol: KLHL13
  hgvsc: ENST00000540167.1:c.144A>G
  hgvsp: ENST00000540167.1:c.144A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9613
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1902
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28255
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17285
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly67Gly
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ

X-117079451-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117079451
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117079451
    reference: chr 0
allele count: 1
allele frequency: 1.14558035100582e-5
allele num: 87292
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360943
  ensembl transcript: ENST00000371876
  gene symbol: KLHL13
  hgvsc: ENST00000371876.1:c.33G>A
  hgvsp: ENST00000371876.1:c.33G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000262820
  ensembl transcript: ENST00000262820
  gene symbol: KLHL13
  hgvsc: ENST00000262820.3:c.186G>A
  hgvsp: ENST00000262820.3:c.186G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000443191
  ensembl transcript: ENST00000539496
  gene symbol: KLHL13
  hgvsc: ENST00000539496.1:c.195G>A
  hgvsp: ENST00000539496.1:c.195G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000444450
  ensembl transcript: ENST00000541812
  gene symbol: KLHL13
  hgvsc: ENST00000541812.1:c.138G>A
  hgvsp: ENST00000541812.1:c.138G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360949
  ensembl transcript: ENST00000371882
  gene symbol: KLHL13
  hgvsc: ENST00000371882.1:c.33G>A
  hgvsp: ENST00000371882.1:c.33G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000419803
  ensembl transcript: ENST00000469946
  gene symbol: KLHL13
  hgvsc: ENST00000469946.1:c.33G>A
  hgvsp: ENST00000469946.1:c.33G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000393807
  ensembl transcript: ENST00000453826
  gene symbol: KLHL13
  hgvsc: ENST00000453826.1:c.33G>A
  hgvsp: ENST00000453826.1:c.33G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000440707
  ensembl transcript: ENST00000545703
  gene symbol: KLHL13
  hgvsc: ENST00000545703.1:c.60G>A
  hgvsp: ENST00000545703.1:c.60G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000412640
  ensembl transcript: ENST00000447671
  gene symbol: KLHL13
  hgvsc: ENST00000447671.2:c.33G>A
  hgvsp: ENST00000447671.2:c.33G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360945
  ensembl transcript: ENST00000371878
  gene symbol: KLHL13
  hgvsc: ENST00000371878.1:c.33G>A
  hgvsp: ENST00000371878.1:c.33G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000441029
  ensembl transcript: ENST00000540167
  gene symbol: KLHL13
  hgvsc: ENST00000540167.1:c.138G>A
  hgvsp: ENST00000540167.1:c.138G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1904
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17228
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 742
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9610
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28200
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Lys65Lys
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ReadPosRankSum

X-117079458-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117079458
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117079458
    reference: chr 0
allele count: 34
allele frequency: 3.897116134060795e-4
allele num: 87244
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000419803
  ensembl transcript: ENST00000469946
  gene symbol: KLHL13
  hgvsc: ENST00000469946.1:c.26C>A
  hgvsp: ENSP00000419803.1:p.Ser9Tyr
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000441029
  ensembl transcript: ENST00000540167
  gene symbol: KLHL13
  hgvsc: ENST00000540167.1:c.131C>A
  hgvsp: ENSP00000441029.1:p.Ser44Tyr
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000262820
  ensembl transcript: ENST00000262820
  gene symbol: KLHL13
  hgvsc: ENST00000262820.3:c.179C>A
  hgvsp: ENSP00000262820.3:p.Ser60Tyr
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360943
  ensembl transcript: ENST00000371876
  gene symbol: KLHL13
  hgvsc: ENST00000371876.1:c.26C>A
  hgvsp: ENSP00000360943.1:p.Ser9Tyr
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000443191
  ensembl transcript: ENST00000539496
  gene symbol: KLHL13
  hgvsc: ENST00000539496.1:c.188C>A
  hgvsp: ENSP00000443191.1:p.Ser63Tyr
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360945
  ensembl transcript: ENST00000371878
  gene symbol: KLHL13
  hgvsc: ENST00000371878.1:c.26C>A
  hgvsp: ENSP00000360945.1:p.Ser9Tyr
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000440707
  ensembl transcript: ENST00000545703
  gene symbol: KLHL13
  hgvsc: ENST00000545703.1:c.53C>A
  hgvsp: ENSP00000440707.1:p.Ser18Tyr
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000393807
  ensembl transcript: ENST00000453826
  gene symbol: KLHL13
  hgvsc: ENST00000453826.1:c.26C>A
  hgvsp: ENSP00000393807.1:p.Ser9Tyr
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000444450
  ensembl transcript: ENST00000541812
  gene symbol: KLHL13
  hgvsc: ENST00000541812.1:c.131C>A
  hgvsp: ENSP00000444450.1:p.Ser44Tyr
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000412640
  ensembl transcript: ENST00000447671
  gene symbol: KLHL13
  hgvsc: ENST00000447671.2:c.26C>A
  hgvsp: ENSP00000412640.2:p.Ser9Tyr
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360949
  ensembl transcript: ENST00000371882
  gene symbol: KLHL13
  hgvsc: ENST00000371882.1:c.26C>A
  hgvsp: ENSP00000360949.1:p.Ser9Tyr
  variant of: http://identifiers.org/hgnc/22931
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 9573
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1895
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 17223
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28125
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 4.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
hgvs: p.Ser63Tyr
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: Other
population: Latino
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ

X-117079478-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117079478
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117079478
    reference: chr 0
allele count: 1
allele frequency: 1.150337624092671e-5
allele num: 86931
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000412640
  ensembl transcript: ENST00000447671
  gene symbol: KLHL13
  hgvsc: ENST00000447671.2:c.6C>A
  hgvsp: ENST00000447671.2:c.6C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000419803
  ensembl transcript: ENST00000469946
  gene symbol: KLHL13
  hgvsc: ENST00000469946.1:c.6C>A
  hgvsp: ENST00000469946.1:c.6C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000443191
  ensembl transcript: ENST00000539496
  gene symbol: KLHL13
  hgvsc: ENST00000539496.1:c.168C>A
  hgvsp: ENST00000539496.1:c.168C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360943
  ensembl transcript: ENST00000371876
  gene symbol: KLHL13
  hgvsc: ENST00000371876.1:c.6C>A
  hgvsp: ENST00000371876.1:c.6C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000262820
  ensembl transcript: ENST00000262820
  gene symbol: KLHL13
  hgvsc: ENST00000262820.3:c.159C>A
  hgvsp: ENST00000262820.3:c.159C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360949
  ensembl transcript: ENST00000371882
  gene symbol: KLHL13
  hgvsc: ENST00000371882.1:c.6C>A
  hgvsp: ENST00000371882.1:c.6C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000440707
  ensembl transcript: ENST00000545703
  gene symbol: KLHL13
  hgvsc: ENST00000545703.1:c.33C>A
  hgvsp: ENST00000545703.1:c.33C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360945
  ensembl transcript: ENST00000371878
  gene symbol: KLHL13
  hgvsc: ENST00000371878.1:c.6C>A
  hgvsp: ENST00000371878.1:c.6C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000444450
  ensembl transcript: ENST00000541812
  gene symbol: KLHL13
  hgvsc: ENST00000541812.1:c.111C>A
  hgvsp: ENST00000541812.1:c.111C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000441029
  ensembl transcript: ENST00000540167
  gene symbol: KLHL13
  hgvsc: ENST00000540167.1:c.111C>A
  hgvsp: ENST00000540167.1:c.111C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000393807
  ensembl transcript: ENST00000453826
  gene symbol: KLHL13
  hgvsc: ENST00000453826.1:c.6C>A
  hgvsp: ENST00000453826.1:c.6C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16906
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9455
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27849
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1866
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly56Gly
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP

X-117079480-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117079480
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117079480
    reference: chr 0
allele count: 3
allele frequency: 3.45240287239919e-5
allele num: 86896
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360943
  ensembl transcript: ENST00000371876
  gene symbol: KLHL13
  hgvsc: ENST00000371876.1:c.4G>A
  hgvsp: ENSP00000360943.1:p.Gly2Ser
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000444450
  ensembl transcript: ENST00000541812
  gene symbol: KLHL13
  hgvsc: ENST00000541812.1:c.109G>A
  hgvsp: ENSP00000444450.1:p.Gly37Ser
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000440707
  ensembl transcript: ENST00000545703
  gene symbol: KLHL13
  hgvsc: ENST00000545703.1:c.31G>A
  hgvsp: ENSP00000440707.1:p.Gly11Ser
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000262820
  ensembl transcript: ENST00000262820
  gene symbol: KLHL13
  hgvsc: ENST00000262820.3:c.157G>A
  hgvsp: ENSP00000262820.3:p.Gly53Ser
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000443191
  ensembl transcript: ENST00000539496
  gene symbol: KLHL13
  hgvsc: ENST00000539496.1:c.166G>A
  hgvsp: ENSP00000443191.1:p.Gly56Ser
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360949
  ensembl transcript: ENST00000371882
  gene symbol: KLHL13
  hgvsc: ENST00000371882.1:c.4G>A
  hgvsp: ENSP00000360949.1:p.Gly2Ser
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360945
  ensembl transcript: ENST00000371878
  gene symbol: KLHL13
  hgvsc: ENST00000371878.1:c.4G>A
  hgvsp: ENSP00000360945.1:p.Gly2Ser
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000419803
  ensembl transcript: ENST00000469946
  gene symbol: KLHL13
  hgvsc: ENST00000469946.1:c.4G>A
  hgvsp: ENSP00000419803.1:p.Gly2Ser
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000393807
  ensembl transcript: ENST00000453826
  gene symbol: KLHL13
  hgvsc: ENST00000453826.1:c.4G>A
  hgvsp: ENSP00000393807.1:p.Gly2Ser
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000412640
  ensembl transcript: ENST00000447671
  gene symbol: KLHL13
  hgvsc: ENST00000447671.2:c.4G>A
  hgvsp: ENSP00000412640.2:p.Gly2Ser
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000441029
  ensembl transcript: ENST00000540167
  gene symbol: KLHL13
  hgvsc: ENST00000540167.1:c.109G>A
  hgvsp: ENSP00000441029.1:p.Gly37Ser
  variant of: http://identifiers.org/hgnc/22931
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9442
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16891
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27796
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1865
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Gly56Ser
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

X-117079484-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117079484
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117079484
    reference: chr 0
allele count: 1
allele frequency: 1.151582850628188e-5
allele num: 86837
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000443191
  ensembl transcript: ENST00000539496
  gene symbol: KLHL13
  hgvsc: ENST00000539496.1:c.162A>T
  hgvsp: ENSP00000443191.1:p.Glu54Asp
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360949
  ensembl transcript: ENST00000371882
  gene symbol: KLHL13
  hgvsc: ENST00000371882.1:c.-1A>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360945
  ensembl transcript: ENST00000371878
  gene symbol: KLHL13
  hgvsc: ENST00000371878.1:c.-1A>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000393807
  ensembl transcript: ENST00000453826
  gene symbol: KLHL13
  hgvsc: ENST00000453826.1:c.-1A>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000441029
  ensembl transcript: ENST00000540167
  gene symbol: KLHL13
  hgvsc: ENST00000540167.1:c.105A>T
  hgvsp: ENSP00000441029.1:p.Glu35Asp
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000440707
  ensembl transcript: ENST00000545703
  gene symbol: KLHL13
  hgvsc: ENST00000545703.1:c.27A>T
  hgvsp: ENSP00000440707.1:p.Glu9Asp
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000262820
  ensembl transcript: ENST00000262820
  gene symbol: KLHL13
  hgvsc: ENST00000262820.3:c.153A>T
  hgvsp: ENSP00000262820.3:p.Glu51Asp
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000412640
  ensembl transcript: ENST00000447671
  gene symbol: KLHL13
  hgvsc: ENST00000447671.2:c.-1A>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000444450
  ensembl transcript: ENST00000541812
  gene symbol: KLHL13
  hgvsc: ENST00000541812.1:c.105A>T
  hgvsp: ENSP00000444450.1:p.Glu35Asp
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000419803
  ensembl transcript: ENST00000469946
  gene symbol: KLHL13
  hgvsc: ENST00000469946.1:c.-1A>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360943
  ensembl transcript: ENST00000371876
  gene symbol: KLHL13
  hgvsc: ENST00000371876.1:c.-1A>T
  variant of: http://identifiers.org/hgnc/22931
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9376
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16963
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27653
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1856
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu54Asp
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: MQ

X-117079486-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117079486
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117079486
    reference: chr 0
allele count: 1
allele frequency: 1.152206475400392e-5
allele num: 86790
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000443191
  ensembl transcript: ENST00000539496
  gene symbol: KLHL13
  hgvsc: ENST00000539496.1:c.160G>A
  hgvsp: ENSP00000443191.1:p.Glu54Lys
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000262820
  ensembl transcript: ENST00000262820
  gene symbol: KLHL13
  hgvsc: ENST00000262820.3:c.151G>A
  hgvsp: ENSP00000262820.3:p.Glu51Lys
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360943
  ensembl transcript: ENST00000371876
  gene symbol: KLHL13
  hgvsc: ENST00000371876.1:c.-3G>A
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000444450
  ensembl transcript: ENST00000541812
  gene symbol: KLHL13
  hgvsc: ENST00000541812.1:c.103G>A
  hgvsp: ENSP00000444450.1:p.Glu35Lys
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000440707
  ensembl transcript: ENST00000545703
  gene symbol: KLHL13
  hgvsc: ENST00000545703.1:c.25G>A
  hgvsp: ENSP00000440707.1:p.Glu9Lys
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000393807
  ensembl transcript: ENST00000453826
  gene symbol: KLHL13
  hgvsc: ENST00000453826.1:c.-3G>A
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360949
  ensembl transcript: ENST00000371882
  gene symbol: KLHL13
  hgvsc: ENST00000371882.1:c.-3G>A
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000441029
  ensembl transcript: ENST00000540167
  gene symbol: KLHL13
  hgvsc: ENST00000540167.1:c.103G>A
  hgvsp: ENSP00000441029.1:p.Glu35Lys
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000419803
  ensembl transcript: ENST00000469946
  gene symbol: KLHL13
  hgvsc: ENST00000469946.1:c.-3G>A
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000412640
  ensembl transcript: ENST00000447671
  gene symbol: KLHL13
  hgvsc: ENST00000447671.2:c.-3G>A
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360945
  ensembl transcript: ENST00000371878
  gene symbol: KLHL13
  hgvsc: ENST00000371878.1:c.-3G>A
  variant of: http://identifiers.org/hgnc/22931
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16998
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1862
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27518
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9383
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu54Lys
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ

X-117079487-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117079487
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117079487
    reference: chr 0
allele count: 1
allele frequency: 1.152923814794318e-5
allele num: 86736
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000412640
  ensembl transcript: ENST00000447671
  gene symbol: KLHL13
  hgvsc: ENST00000447671.2:c.-4C>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000440707
  ensembl transcript: ENST00000545703
  gene symbol: KLHL13
  hgvsc: ENST00000545703.1:c.24C>T
  hgvsp: ENST00000545703.1:c.24C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000262820
  ensembl transcript: ENST00000262820
  gene symbol: KLHL13
  hgvsc: ENST00000262820.3:c.150C>T
  hgvsp: ENST00000262820.3:c.150C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000441029
  ensembl transcript: ENST00000540167
  gene symbol: KLHL13
  hgvsc: ENST00000540167.1:c.102C>T
  hgvsp: ENST00000540167.1:c.102C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000393807
  ensembl transcript: ENST00000453826
  gene symbol: KLHL13
  hgvsc: ENST00000453826.1:c.-4C>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360945
  ensembl transcript: ENST00000371878
  gene symbol: KLHL13
  hgvsc: ENST00000371878.1:c.-4C>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000443191
  ensembl transcript: ENST00000539496
  gene symbol: KLHL13
  hgvsc: ENST00000539496.1:c.159C>T
  hgvsp: ENST00000539496.1:c.159C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000419803
  ensembl transcript: ENST00000469946
  gene symbol: KLHL13
  hgvsc: ENST00000469946.1:c.-4C>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360949
  ensembl transcript: ENST00000371882
  gene symbol: KLHL13
  hgvsc: ENST00000371882.1:c.-4C>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000444450
  ensembl transcript: ENST00000541812
  gene symbol: KLHL13
  hgvsc: ENST00000541812.1:c.102C>T
  hgvsp: ENST00000541812.1:c.102C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360943
  ensembl transcript: ENST00000371876
  gene symbol: KLHL13
  hgvsc: ENST00000371876.1:c.-4C>T
  variant of: http://identifiers.org/hgnc/22931
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17011
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9356
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 841
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27478
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1859
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser53Ser
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQ

X-117079487-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117079487
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117079487
    reference: chr 0
allele count: 1
allele frequency: 1.152923814794318e-5
allele num: 86736
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000393807
  ensembl transcript: ENST00000453826
  gene symbol: KLHL13
  hgvsc: ENST00000453826.1:c.-4C>A
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000419803
  ensembl transcript: ENST00000469946
  gene symbol: KLHL13
  hgvsc: ENST00000469946.1:c.-4C>A
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000262820
  ensembl transcript: ENST00000262820
  gene symbol: KLHL13
  hgvsc: ENST00000262820.3:c.150C>A
  hgvsp: ENSP00000262820.3:p.Ser50Arg
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360943
  ensembl transcript: ENST00000371876
  gene symbol: KLHL13
  hgvsc: ENST00000371876.1:c.-4C>A
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000441029
  ensembl transcript: ENST00000540167
  gene symbol: KLHL13
  hgvsc: ENST00000540167.1:c.102C>A
  hgvsp: ENSP00000441029.1:p.Ser34Arg
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000444450
  ensembl transcript: ENST00000541812
  gene symbol: KLHL13
  hgvsc: ENST00000541812.1:c.102C>A
  hgvsp: ENSP00000444450.1:p.Ser34Arg
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360945
  ensembl transcript: ENST00000371878
  gene symbol: KLHL13
  hgvsc: ENST00000371878.1:c.-4C>A
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000412640
  ensembl transcript: ENST00000447671
  gene symbol: KLHL13
  hgvsc: ENST00000447671.2:c.-4C>A
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000443191
  ensembl transcript: ENST00000539496
  gene symbol: KLHL13
  hgvsc: ENST00000539496.1:c.159C>A
  hgvsp: ENSP00000443191.1:p.Ser53Arg
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000440707
  ensembl transcript: ENST00000545703
  gene symbol: KLHL13
  hgvsc: ENST00000545703.1:c.24C>A
  hgvsp: ENSP00000440707.1:p.Ser8Arg
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360949
  ensembl transcript: ENST00000371882
  gene symbol: KLHL13
  hgvsc: ENST00000371882.1:c.-4C>A
  variant of: http://identifiers.org/hgnc/22931
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9356
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1859
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17011
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 841
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27478
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser53Arg
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

X-117079506-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24117079506
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24117079506
    reference: chr 0
allele count: 4
allele frequency: 4.647866048500482e-5
allele num: 86061
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000419803
  ensembl transcript: ENST00000469946
  gene symbol: KLHL13
  hgvsc: ENST00000469946.1:c.-23A>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000444450
  ensembl transcript: ENST00000541812
  gene symbol: KLHL13
  hgvsc: ENST00000541812.1:c.83A>T
  hgvsp: ENSP00000444450.1:p.Lys28Ile
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000443191
  ensembl transcript: ENST00000539496
  gene symbol: KLHL13
  hgvsc: ENST00000539496.1:c.140A>T
  hgvsp: ENSP00000443191.1:p.Lys47Ile
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000440707
  ensembl transcript: ENST00000545703
  gene symbol: KLHL13
  hgvsc: ENST00000545703.1:c.5A>T
  hgvsp: ENSP00000440707.1:p.Lys2Ile
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000262820
  ensembl transcript: ENST00000262820
  gene symbol: KLHL13
  hgvsc: ENST00000262820.3:c.131A>T
  hgvsp: ENSP00000262820.3:p.Lys44Ile
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000412640
  ensembl transcript: ENST00000447671
  gene symbol: KLHL13
  hgvsc: ENST00000447671.2:c.-23A>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360949
  ensembl transcript: ENST00000371882
  gene symbol: KLHL13
  hgvsc: ENST00000371882.1:c.-23A>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000393807
  ensembl transcript: ENST00000453826
  gene symbol: KLHL13
  hgvsc: ENST00000453826.1:c.-23A>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000441029
  ensembl transcript: ENST00000540167
  gene symbol: KLHL13
  hgvsc: ENST00000540167.1:c.83A>T
  hgvsp: ENSP00000441029.1:p.Lys28Ile
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360943
  ensembl transcript: ENST00000371876
  gene symbol: KLHL13
  hgvsc: ENST00000371876.1:c.-23A>T
  variant of: http://identifiers.org/hgnc/22931
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000003096
  ensembl protein: ENSP00000360945
  ensembl transcript: ENST00000371878
  gene symbol: KLHL13
  hgvsc: ENST00000371878.1:c.-23A>T
  variant of: http://identifiers.org/hgnc/22931
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16754
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Lys47Ile
num of homozygotes: 0
reference allele: T

GenotypeQuality
all individuals: 21
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 9
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1883
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 329
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9025
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 122
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 557
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7809
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 36263
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1350
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9318
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6635
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.255335174491589e-4
allele num: 7966
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47775
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 631
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.0618e1

QD
type: SiteQuality
SIO_000300: 1.103e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.93e-1

DP
type: SiteQuality
SIO_000300: 2.022449e6

VQSLOD
type: SiteQuality
SIO_000300: 6.04e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 2.7e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.53e-1

MQ
type: SiteQuality
SIO_000300: 5.94e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.067e0

GenotypeQuality
all individuals: 32
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2090
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36419
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 26
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 27
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9025
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 17
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7818
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 557
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1359
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 328
bin: 2.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7972
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.506931886678722e-4
allele num: 6636
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 631
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9319
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47791
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10120
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.366e0

MQRankSum
type: SiteQuality
SIO_000300: -5.44e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -2.287e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.47e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.39e0

QD
type: SiteQuality
SIO_000300: 2.243e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.1e0

DP
type: SiteQuality
SIO_000300: 2.024439e6

GenotypeQuality
all individuals: 18
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 86
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1361
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9025
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 326
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 748
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 557
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7827
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1886
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7984
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 631
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 1.255361439481117e-4
allele num: 47795
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6636
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9318
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10121
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.4e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.84e-1

QD
type: SiteQuality
SIO_000300: 1.577e1

DP
type: SiteQuality
SIO_000300: 2.025056e6

FS
type: SiteQuality
SIO_000300: 5.620000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.94e-2

MQ
type: SiteQuality
SIO_000300: 5.94e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.839e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.96e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.75e-1

GenotypeQuality
all individuals: 10
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 54
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 748
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9023
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 36555
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 558
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1369
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 336
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1891
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6636
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9319
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8008
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10123
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 631
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 6.274050527020244e-5
allele num: 47816
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.57e-2

QD
type: SiteQuality
SIO_000300: 1.7e1

VQSLOD
type: SiteQuality
SIO_000300: -1.319e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.74e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.54e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.02e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.47e-1

FS
type: SiteQuality
SIO_000300: 5.71e-1

MQ
type: SiteQuality
SIO_000300: 5.955e1

DP
type: SiteQuality
SIO_000300: 2.026074e6

GenotypeQuality
all individuals: 30
bin: 4.25e1
variant carriers: 15

GenotypeQuality
all individuals: 19
bin: 2.75e1
variant carriers: 9

GenotypeQuality
all individuals: 48
bin: 4.75e1
variant carriers: 31

GenotypeQuality
all individuals: 92
bin: 2.25e1
variant carriers: 7

GenotypeQuality
all individuals: 18
bin: 2.5e0
variant carriers: 7

GenotypeQuality
all individuals: 387
bin: 8.75e1
variant carriers: 31

GenotypeQuality
all individuals: 50
bin: 5.25e1
variant carriers: 37

GenotypeQuality
all individuals: 15
bin: 1.75e1
variant carriers: 13

GenotypeQuality
all individuals: 41
bin: 3.75e1
variant carriers: 28

GenotypeQuality
all individuals: 7508
bin: 6.75e1
variant carriers: 42

GenotypeQuality
all individuals: 39
bin: 3.25e1
variant carriers: 22

GenotypeQuality
all individuals: 23
bin: 5.75e1
variant carriers: 17

GenotypeQuality
all individuals: 1782
bin: 7.75e1
variant carriers: 33

GenotypeQuality
all individuals: 35942
bin: 6.25e1
variant carriers: 35

GenotypeQuality
all individuals: 15
bin: 7.5e0
variant carriers: 7

GenotypeQuality
all individuals: 11357
bin: 9.75e1
variant carriers: 8998

GenotypeQuality
all individuals: 1721
bin: 7.25e1
variant carriers: 30

GenotypeQuality
all individuals: 529
bin: 9.25e1
variant carriers: 46

GenotypeQuality
all individuals: 1082
bin: 8.25e1
variant carriers: 48

African
type: Population
allele count: 5966
allele frequency: 7.070395828395354e-1
allele num: 8438
num of homozygotes: 1622

Latino
type: Population
allele count: 532
allele frequency: 5.711831651277646e-2
allele num: 9314
num of homozygotes: 20

European (Finnish)
type: Population
allele count: 272
allele frequency: 6.005740781629499e-2
allele num: 4529
num of homozygotes: 7

Other
type: Population
allele count: 61
allele frequency: 9.636650868878358e-2
allele num: 633
num of homozygotes: 1

East Asian
type: Population
allele count: 1
allele frequency: 1.506704836522525e-4
allele num: 6637
num of homozygotes: 0

South Asian
type: Population
allele count: 660
allele frequency: 6.519806381507458e-2
allele num: 10123
num of homozygotes: 12

European (Non-Finnish)
type: Population
allele count: 3683
allele frequency: 7.693111083260225e-2
allele num: 47874
num of homozygotes: 95

ClippingRankSum
type: SiteQuality
SIO_000300: -3.58e-1

FS
type: SiteQuality
SIO_000300: 5.27e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.567e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.669e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.52e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.64e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.115e0

MQ
type: SiteQuality
SIO_000300: 5.963e1

DP
type: SiteQuality
SIO_000300: 2.543211e6

QD
type: SiteQuality
SIO_000300: 2.029e1

GenotypeQuality
all individuals: 2037
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 455
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1299
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41777
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8884
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 47
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 630
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2188
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3063
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 13
bin: 5.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6638
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 633
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9322
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.176150007308262e-5
allele num: 47891
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8450
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.94e-1

DP
type: SiteQuality
SIO_000300: 1.764608e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 1.58e-1

QD
type: SiteQuality
SIO_000300: 1.49e1

VQSLOD
type: SiteQuality
SIO_000300: 1.19e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.1e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.5e0

FS
type: SiteQuality
SIO_000300: 5.478e0

MQ
type: SiteQuality
SIO_000300: 5.969e1

GenotypeQuality
all individuals: 455
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1299
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3061
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 18
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2185
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2037
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41933
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8890
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 630
bin: 9.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8464
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9321
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.086332436210386e-5
allele num: 47931
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6638
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 633
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.765896e6

QD
type: SiteQuality
SIO_000300: 1.113e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.3e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.38e0

MQ
type: SiteQuality
SIO_000300: 5.969e1

FS
type: SiteQuality
SIO_000300: 4.533e0

MQRankSum
type: SiteQuality
SIO_000300: 8.090000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.78e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.647e0

GenotypeQuality
all individuals: 19
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 8894
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2186
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 84
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1300
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2038
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41951
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 455
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 630
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3060
bin: 9.75e1
variant carriers: 2

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6638
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 633
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 2.14569252226156e-4
allele num: 9321
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47933
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8464
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 8.79e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.123e0

DP
type: SiteQuality
SIO_000300: 1.765923e6

BaseQRankSum
type: SiteQuality
SIO_000300: 6.24e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.63e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.629999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.72e-1

QD
type: SiteQuality
SIO_000300: 1.28e1

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

GenotypeQuality
all individuals: 16
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3058
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 41961
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 19
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1297
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2037
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 630
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2187
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8892
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.181195369714151e-4
allele num: 8466
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9321
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6638
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 633
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47935
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 1.52e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.34e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.23e-2

QD
type: SiteQuality
SIO_000300: 2.381e1

DP
type: SiteQuality
SIO_000300: 1.765847e6

MQ
type: SiteQuality
SIO_000300: 5.976e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.67e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.02e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.2e0

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

GenotypeQuality
all individuals: 3058
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 25
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 455
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8890
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 5.25e1
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: 41959
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2186
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1298
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 630
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 4.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47937
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8464
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 633
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9321
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6638
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.975503753457131e-4
allele num: 10124
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.765769e6

VQSLOD
type: SiteQuality
SIO_000300: 1.22e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.3e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 3.439e1

GenotypeQuality
all individuals: 19
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 12
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41967
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3055
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 26
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2183
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 455
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8882
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 629
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1295
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2031
bin: 7.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 633
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6638
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9316
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.085592725452574e-5
allele num: 47948
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -3.932e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.31e0

MQRankSum
type: SiteQuality
SIO_000300: -5.16e-1

DP
type: SiteQuality
SIO_000300: 1.766174e6

ClippingRankSum
type: SiteQuality
SIO_000300: -4.73e-1

FS
type: SiteQuality
SIO_000300: 8.080000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-3

MQ
type: SiteQuality
SIO_000300: 5.983e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.5e0

QD
type: SiteQuality
SIO_000300: 1.5e-1

GenotypeQuality
all individuals: 2031
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2183
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 455
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3055
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 14
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 629
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1295
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 4.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 16
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8882
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 3
allele frequency: 4.519433564326605e-4
allele num: 6638
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8484
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47952
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9316
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.901e0

QD
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VQSLOD
type: SiteQuality
SIO_000300: -1.331e0

InbreedingCoeff
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SIO_000300: 8.83e-2

MQ
type: SiteQuality
SIO_000300: 5.978e1

DP
type: SiteQuality
SIO_000300: 1.766109e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.91e-1

FS
type: SiteQuality
SIO_000300: 3.459e0

MQRankSum
type: SiteQuality
SIO_000300: 4.09e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.57e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8481
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4529
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 10119
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6638
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 2.085375263278627e-5
allele num: 47953
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 633
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.068e0

ClippingRankSum
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SIO_000300: 7.7e-2

InbreedingCoeff
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SIO_000300: -3.0e-4

MQRankSum
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SIO_000300: 8.4e-1

DP
type: SiteQuality
SIO_000300: 1.765188e6

MQ
type: SiteQuality
SIO_000300: 5.954e1

VQSLOD
type: SiteQuality
SIO_000300: 8.58e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.095e0

QD
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SIO_000300: 1.377e1

ReadPosRankSum
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SIO_000300: -6.8e-2

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9313
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 633
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10119
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6637
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 4.170402652376087e-5
allele num: 47957
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8482
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.971e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.01e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 9.61e-1

QD
type: SiteQuality
SIO_000300: 3.082e1

DP
type: SiteQuality
SIO_000300: 1.764762e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9313
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 633
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6637
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.8833761612967e-5
allele num: 10118
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8480
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4529
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47957
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.02e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.620000000000001e-1

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 2.106e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
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SIO_000300: 1.16e0

DP
type: SiteQuality
SIO_000300: 1.764147e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.79e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.257e0

GenotypeQuality
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variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4529
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.179245283018868e-4
allele num: 8480
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6633
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 47919
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 10104
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9309
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.579778830963665e-3
allele num: 633
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.67e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 3.369e1

DP
type: SiteQuality
SIO_000300: 1.761113e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.719999999999999e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8433
num of homozygotes: 0

Other
type: Population
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num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 9.941346058256288e-5
allele num: 10059
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 47829
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9300
num of homozygotes: 0

European (Finnish)
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num of homozygotes: 0

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 10043
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
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African
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allele count: 1
allele frequency: 1.186521120075937e-4
allele num: 8428
num of homozygotes: 0

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

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

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

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

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

African
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allele count: 5
allele frequency: 5.937537109606935e-4
allele num: 8421
num of homozygotes: 0

Other
type: Population
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num of homozygotes: 0

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

European (Finnish)
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num of homozygotes: 0

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

South Asian
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QD
type: SiteQuality
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VQSLOD
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FS
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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DP
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ClippingRankSum
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ReadPosRankSum
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MQ
type: SiteQuality
SIO_000300: 5.976e1

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6549
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9119
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4498
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9193
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.148320013749248e-5
allele num: 46548
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.653382e6

ClippingRankSum
type: SiteQuality
SIO_000300: -4.49e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.122e0

QD
type: SiteQuality
SIO_000300: 1.241e1

FS
type: SiteQuality
SIO_000300: 1.424e0

MQ
type: SiteQuality
SIO_000300: 5.892e1

VQSLOD
type: SiteQuality
SIO_000300: 1.12e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.58e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e0

GenotypeQuality
all individuals: 485
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 7.75e1
variant carriers: 1

GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 22

GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1005
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 4329
bin: 6.75e1
variant carriers: 1

Latino
type: Population
allele count: 4
allele frequency: 4.578754578754579e-4
allele num: 8736
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7357
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 42623
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6132
num of homozygotes: 0

African
type: Population
allele count: 22
allele frequency: 2.906208718626156e-3
allele num: 7570
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4329
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 559
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.56e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.0e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.7e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.5e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.37e0

DP
type: SiteQuality
SIO_000300: 1.302672e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.12e-2

QD
type: SiteQuality
SIO_000300: 1.916e1

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
all individuals: 1136
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7350
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7563
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 559
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6127
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8738
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4329
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.347197446249178e-5
allele num: 42604
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.28e0

FS
type: SiteQuality
SIO_000300: 4.058e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.07e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.717e0

VQSLOD
type: SiteQuality
SIO_000300: 2.13e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.24e-1

DP
type: SiteQuality
SIO_000300: 1.301397e6

QD
type: SiteQuality
SIO_000300: 1.413e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.8e-3

MQ
type: SiteQuality
SIO_000300: 5.957e1

GenotypeQuality
all individuals: 993
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2624
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 536
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variant carriers: 0

GenotypeQuality
all individuals: 2947
bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6577
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 41191
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 542
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.35795763172189e-4
allele num: 7364
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5957
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4274
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.68e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.5e-3

DP
type: SiteQuality
SIO_000300: 1.175344e6

QD
type: SiteQuality
SIO_000300: 1.471e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.72e-1

FS
type: SiteQuality
SIO_000300: 5.696e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.0e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.1e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.12e-1

GenotypeQuality
all individuals: 1153
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 757
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variant carriers: 0

GenotypeQuality
all individuals: 1302
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variant carriers: 0

GenotypeQuality
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variant carriers: 2

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 534
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6311
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8519
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7304
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 3.394433129667345e-4
allele num: 5892
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 531
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4249
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 40617
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.6e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.95e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.31e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.42e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.107e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.7e-3

DP
type: SiteQuality
SIO_000300: 1.1387e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.63e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 1475
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 638
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 356
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GenotypeQuality
all individuals: 958
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7277
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4237
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 40473
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 528
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6262
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.704158145875937e-4
allele num: 5868
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.697e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 3.47e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.54e-1

QD
type: SiteQuality
SIO_000300: 1.685e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.87e-1

DP
type: SiteQuality
SIO_000300: 1.137632e6

MQRankSum
type: SiteQuality
SIO_000300: 3.09e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.6e-3

GenotypeQuality
all individuals: 13429
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 18
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 78
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variant carriers: 0

GenotypeQuality
all individuals: 1288
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9750
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47772
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6634
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 626
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4528
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8455
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9303
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 2.186513e6

QD
type: SiteQuality
SIO_000300: 9.01e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 4.19e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.902e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.478e0

FS
type: SiteQuality
SIO_000300: 1.814e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.89e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.84e-1

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 135
bin: 4.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 1.074922068150059e-4
allele num: 9303
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4529
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9760
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47792
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6634
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8471
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 626
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.49e-1

MQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.188173e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

FS
type: SiteQuality
SIO_000300: 3.155e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.63e0

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.947e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.4e-2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 27158
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2837
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9309
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.009795011612643e-4
allele num: 9903
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6635
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8507
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47878
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

DP
type: SiteQuality
SIO_000300: 2.20232e6

MQRankSum
type: SiteQuality
SIO_000300: 1.57e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.09e-1

MQ
type: SiteQuality
SIO_000300: 5.918e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.793e0

QD
type: SiteQuality
SIO_000300: 1.107e1

FS
type: SiteQuality
SIO_000300: 3.333e0

VQSLOD
type: SiteQuality
SIO_000300: -6.646e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.65e0

GenotypeQuality
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variant carriers: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8510
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 9959
num of homozygotes: 0

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

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 629
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9310
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 2.087246921310791e-5
allele num: 47910
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.205861e6

ReadPosRankSum
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SIO_000300: -1.699e0

VQSLOD
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SIO_000300: -1.763e0

BaseQRankSum
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SIO_000300: -1.13e-1

InbreedingCoeff
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SIO_000300: 4.17e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.96e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 4.15e-1

MQ
type: SiteQuality
SIO_000300: 5.966e1

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

Latino
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allele frequency: 0.0e0
allele num: 9310
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 9974
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 2.087072671870435e-5
allele num: 47914
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6635
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 630
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8513
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.923e1

VQSLOD
type: SiteQuality
SIO_000300: 2.95e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.4e-1

DP
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ReadPosRankSum
type: SiteQuality
SIO_000300: 3.6e-1

QD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
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SIO_000300: 2.67e0

MQRankSum
type: SiteQuality
SIO_000300: 1.31e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.7e-3

GenotypeQuality
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variant carriers: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6638
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 47967
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9318
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 9.908838684106223e-5
allele num: 10092
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8514
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 632
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.44e-2

DP
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SIO_000300: 2.213232e6

ClippingRankSum
type: SiteQuality
SIO_000300: -6.28e-1

FS
type: SiteQuality
SIO_000300: 5.77e-1

BaseQRankSum
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SIO_000300: -9.79e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.435e0

QD
type: SiteQuality
SIO_000300: 1.374e1

MQ
type: SiteQuality
SIO_000300: 5.834e1

MQRankSum
type: SiteQuality
SIO_000300: 1.8e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.28e-1

GenotypeQuality
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variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6638
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 632
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8513
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9318
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 10103
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 2.084505867884018e-5
allele num: 47973
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.2e0

MQ
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SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.860000000000001e-1

VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ReadPosRankSum
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BaseQRankSum
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SIO_000300: 3.5e0

FS
type: SiteQuality
SIO_000300: 9.64e-1

QD
type: SiteQuality
SIO_000300: 1.06e1

DP
type: SiteQuality
SIO_000300: 2.214506e6

GenotypeQuality
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variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10105
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47973
num of homozygotes: 0

Latino
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allele frequency: 1.073537305421363e-4
allele num: 9315
num of homozygotes: 0

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

African
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allele count: 18
allele frequency: 2.114661654135338e-3
allele num: 8512
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 632
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

QD
type: SiteQuality
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MQ
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VQSLOD
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ClippingRankSum
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DP
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MQRankSum
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ReadPosRankSum
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InbreedingCoeff
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BaseQRankSum
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FS
type: SiteQuality
SIO_000300: 5.24e-1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

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

African
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allele count: 1
allele frequency: 1.175088131609871e-4
allele num: 8510
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4528
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 47927
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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Other
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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QD
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FS
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ReadPosRankSum
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MQ
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InbreedingCoeff
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VQSLOD
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MQRankSum
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BaseQRankSum
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ClippingRankSum
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DP
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GenotypeDepth
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variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 631
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 2.086942003881712e-5
allele num: 47917
num of homozygotes: 0

African
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num of homozygotes: 0

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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MQRankSum
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QD
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VQSLOD
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FS
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ClippingRankSum
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InbreedingCoeff
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ReadPosRankSum
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DP
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BaseQRankSum
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MQ
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GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 1

GenotypeQuality
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bin: 7.75e1
variant carriers: 2

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 47792
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 629
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9288
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8504
num of homozygotes: 0

East Asian
type: Population
allele count: 27
allele frequency: 4.080398972343962e-3
allele num: 6617
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4525
num of homozygotes: 0

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

BaseQRankSum
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SIO_000300: -3.856e0

InbreedingCoeff
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SIO_000300: 2.265e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.2e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.55e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.512e0

VQSLOD
type: SiteQuality
SIO_000300: 6.64e0

QD
type: SiteQuality
SIO_000300: 1.566e1

DP
type: SiteQuality
SIO_000300: 2.199692e6

MQRankSum
type: SiteQuality
SIO_000300: 5.35e-1

GenotypeQuality
all individuals: 277
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6615
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10037
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.093933873568273e-5
allele num: 47757
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4524
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9281
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8501
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 629
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.194113e6

BaseQRankSum
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SIO_000300: 2.53e0

MQ
type: SiteQuality
SIO_000300: 5.83e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

QD
type: SiteQuality
SIO_000300: 1.29e1

VQSLOD
type: SiteQuality
SIO_000300: -2.257e0

MQRankSum
type: SiteQuality
SIO_000300: 1.63e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.758e0

FS
type: SiteQuality
SIO_000300: 1.206e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.74e0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10027
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.097799408420567e-5
allele num: 47669
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9268
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.515610791148833e-4
allele num: 6598
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8491
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4524
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.07e1

BaseQRankSum
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SIO_000300: -4.384e0

DP
type: SiteQuality
SIO_000300: 2.173474e6

VQSLOD
type: SiteQuality
SIO_000300: 2.33e0

MQRankSum
type: SiteQuality
SIO_000300: 6.21e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.46e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.4e-1

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6597
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9270
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47664
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.97307270370001e-5
allele num: 10027
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4524
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 4.01e0

MQRankSum
type: SiteQuality
SIO_000300: 1.35e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.41e0

FS
type: SiteQuality
SIO_000300: 1.1665e1

VQSLOD
type: SiteQuality
SIO_000300: -1.424e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.198e0

DP
type: SiteQuality
SIO_000300: 2.169655e6

QD
type: SiteQuality
SIO_000300: 1.57e1

GenotypeQuality
all individuals: 24123
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 167
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variant carriers: 0

GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
all individuals: 455
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GenotypeQuality
all individuals: 1294
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variant carriers: 0

GenotypeQuality
all individuals: 1972
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GenotypeQuality
all individuals: 133
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2807
bin: 8.25e1
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GenotypeQuality
all individuals: 3448
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4524
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10027
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6597
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.078748651564186e-4
allele num: 9270
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8491
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: 1
allele frequency: 2.098019469620678e-5
allele num: 47664
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.41e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.57e1

ClippingRankSum
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SIO_000300: -1.198e0

BaseQRankSum
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SIO_000300: 4.01e0

VQSLOD
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SIO_000300: -1.424e0

DP
type: SiteQuality
SIO_000300: 2.169655e6

FS
type: SiteQuality
SIO_000300: 1.1665e1

GenotypeQuality
all individuals: 2804
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variant carriers: 5

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 258

GenotypeQuality
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bin: 5.25e1
variant carriers: 3

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

South Asian
type: Population
allele count: 2
allele frequency: 1.995609658750748e-4
allele num: 10022
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.196919461115541e-5
allele num: 47654
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4524
num of homozygotes: 0

Latino
type: Population
allele count: 20
allele frequency: 2.157497303128371e-3
allele num: 9270
num of homozygotes: 0

African
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allele count: 276
allele frequency: 3.251266344681352e-2
allele num: 8489
num of homozygotes: 7

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6600
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InbreedingCoeff
type: SiteQuality
SIO_000300: 3.743e-1

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
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ReadPosRankSum
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MQ
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MQRankSum
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QD
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DP
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BaseQRankSum
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SIO_000300: -3.206e0

ClippingRankSum
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SIO_000300: 5.5e-2

GenotypeQuality
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variant carriers: 1

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4524
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.983028850953379e-5
allele num: 10017
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 38
allele frequency: 7.975988077996768e-4
allele num: 47643
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9270
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.17827265229174e-4
allele num: 8487
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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Other
type: Population
allele count: 0
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num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.933e1

MQRankSum
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BaseQRankSum
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InbreedingCoeff
type: SiteQuality
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ClippingRankSum
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VQSLOD
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MQ
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DP
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FS
type: SiteQuality
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.103270585760858e-5
allele num: 47545
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6581
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4520
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 4.17e0

ReadPosRankSum
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InbreedingCoeff
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VQSLOD
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MQ
type: SiteQuality
SIO_000300: 5.98e1

DP
type: SiteQuality
SIO_000300: 2.097584e6

MQRankSum
type: SiteQuality
SIO_000300: 5.79e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.5e-1

QD
type: SiteQuality
SIO_000300: 1.767e1

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 3308
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3632
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4620
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13339
bin: 9.75e1
variant carriers: 2

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6552
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9239
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8468
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4514
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47367
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 625
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 2.01450443190975e-4
allele num: 9928
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -8.38e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.58e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.051e0

QD
type: SiteQuality
SIO_000300: 1.764e1

DP
type: SiteQuality
SIO_000300: 2.046232e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -9.21e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.79e-1

GenotypeQuality
all individuals: 1889
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1812
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2715
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4501
bin: 6.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4515
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8464
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47274
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6548
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 624
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.008369466572552e-4
allele num: 9917
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9238
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.957e1

QD
type: SiteQuality
SIO_000300: 3.018e1

DP
type: SiteQuality
SIO_000300: 2.037018e6

VQSLOD
type: SiteQuality
SIO_000300: 1.53e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.7e-3

GenotypeQuality
all individuals: 3949
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13332
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1469
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2710
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6511
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9200
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 622
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.129199846697611e-5
allele num: 46966
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9847
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4509
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8454
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.5e0

QD
type: SiteQuality
SIO_000300: 1.573e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.38e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 5.919e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.56e0

DP
type: SiteQuality
SIO_000300: 2.026813e6

MQRankSum
type: SiteQuality
SIO_000300: -3.5e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -7.259e-1

GenotypeQuality
all individuals: 397
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1122
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 615
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variant carriers: 0

GenotypeQuality
all individuals: 1108
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variant carriers: 0

GenotypeQuality
all individuals: 7813
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 756
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1640
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variant carriers: 0

GenotypeQuality
all individuals: 2035
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variant carriers: 0

GenotypeQuality
all individuals: 1186
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1913
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variant carriers: 0

GenotypeQuality
all individuals: 1152
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2290
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 1049
bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 1.056412423410099e-4
allele num: 47330
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4515
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8302
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9211
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.180080245456691e-4
allele num: 8474
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 604
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.624392e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.69e-1

FS
type: SiteQuality
SIO_000300: 7.19e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.89e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.75e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.45e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.39e0

MQ
type: SiteQuality
SIO_000300: 5.945e1

QD
type: SiteQuality
SIO_000300: 1.46e1

GenotypeQuality
all individuals: 7709
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 432
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1802
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 759
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1171
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1909
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variant carriers: 0

GenotypeQuality
all individuals: 1054
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 961
bin: 5.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 605
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.179662616491683e-4
allele num: 8477
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8298
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9211
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47331
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6605
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4513
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.291e1

DP
type: SiteQuality
SIO_000300: 1.624186e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.42e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.722e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.24e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.94e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.37e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.42e-1

FS
type: SiteQuality
SIO_000300: 8.547000000000001e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 947
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 419
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 89
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 960
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variant carriers: 0

GenotypeQuality
all individuals: 139
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 14

GenotypeQuality
all individuals: 1804
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 311
bin: 4.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9209
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47360
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 609
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6609
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8371
num of homozygotes: 0

African
type: Population
allele count: 17
allele frequency: 2.00424428200896e-3
allele num: 8482
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4513
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.47e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.5e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.39e-1

DP
type: SiteQuality
SIO_000300: 1.639694e6

MQ
type: SiteQuality
SIO_000300: 5.974e1

QD
type: SiteQuality
SIO_000300: 1.639e1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.99e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.55e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.7e-1

GenotypeQuality
all individuals: 7681
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 311
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2250
bin: 9.75e1
variant carriers: 15

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 1

GenotypeQuality
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bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 39304
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 960
bin: 3.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9209
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 609
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4513
num of homozygotes: 0

East Asian
type: Population
allele count: 8
allele frequency: 1.210470570434256e-3
allele num: 6609
num of homozygotes: 0

South Asian
type: Population
allele count: 5
allele frequency: 5.97300203082069e-4
allele num: 8371
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 1.055743243243243e-4
allele num: 47360
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.39e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.5e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -6.99e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.47e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.639e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.55e-1

MQ
type: SiteQuality
SIO_000300: 5.974e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.7e-1

DP
type: SiteQuality
SIO_000300: 1.639694e6

GenotypeQuality
all individuals: 1803
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
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variant carriers: 0

GenotypeQuality
all individuals: 650
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variant carriers: 0

GenotypeQuality
all individuals: 272
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 200
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GenotypeQuality
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GenotypeQuality
all individuals: 659
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GenotypeQuality
all individuals: 161
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GenotypeQuality
all individuals: 943
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GenotypeQuality
all individuals: 7700
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GenotypeQuality
all individuals: 90
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GenotypeQuality
all individuals: 417
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GenotypeQuality
all individuals: 39660
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GenotypeQuality
all individuals: 2224
bin: 9.75e1
variant carriers: 12

GenotypeQuality
all individuals: 357
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 932
bin: 3.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 609
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 2.171316903702095e-4
allele num: 9211
num of homozygotes: 0

African
type: Population
allele count: 8
allele frequency: 9.427292010370022e-4
allele num: 8486
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 8.44095551616443e-5
allele num: 47388
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8452
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4514
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.84e0

MQ
type: SiteQuality
SIO_000300: 5.954e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.06e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.19e0

FS
type: SiteQuality
SIO_000300: 5.96e-1

QD
type: SiteQuality
SIO_000300: 1.778e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.5e-2

MQRankSum
type: SiteQuality
SIO_000300: 4.93e-1

DP
type: SiteQuality
SIO_000300: 1.64104e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.9e-1

GenotypeQuality
all individuals: 46
bin: 1.75e1
variant carriers: 3

GenotypeQuality
all individuals: 134
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 2.5e0
variant carriers: 1

GenotypeQuality
all individuals: 7789
bin: 6.75e1
variant carriers: 5

GenotypeQuality
all individuals: 41313
bin: 6.25e1
variant carriers: 3

GenotypeQuality
all individuals: 2260
bin: 9.75e1
variant carriers: 172

GenotypeQuality
all individuals: 310
bin: 3.75e1
variant carriers: 4

GenotypeQuality
all individuals: 453
bin: 2.75e1
variant carriers: 2

GenotypeQuality
all individuals: 563
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1938
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 164
bin: 5.25e1
variant carriers: 3

GenotypeQuality
all individuals: 357
bin: 8.75e1
variant carriers: 6

GenotypeQuality
all individuals: 1813
bin: 7.75e1
variant carriers: 4

GenotypeQuality
all individuals: 112
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 931
bin: 8.25e1
variant carriers: 2

GenotypeQuality
all individuals: 1806
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 164
bin: 4.75e1
variant carriers: 2

GenotypeQuality
all individuals: 408
bin: 9.25e1
variant carriers: 5

African
type: Population
allele count: 3
allele frequency: 3.528996588636631e-4
allele num: 8501
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 189
allele frequency: 3.979031137497631e-3
allele num: 47499
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 3.26797385620915e-3
allele num: 612
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 3.254149040026033e-4
allele num: 9219
num of homozygotes: 0

South Asian
type: Population
allele count: 9
allele frequency: 1.018445173701482e-3
allele num: 8837
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6617
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 2
allele frequency: 4.428697962798937e-4
allele num: 4516
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.868e-1

MQ
type: SiteQuality
SIO_000300: 5.974e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.385e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.07e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.33e-1

QD
type: SiteQuality
SIO_000300: 1.731e1

MQRankSum
type: SiteQuality
SIO_000300: 3.66e-1

FS
type: SiteQuality
SIO_000300: 5.51e-1

DP
type: SiteQuality
SIO_000300: 1.664167e6

VQSLOD
type: SiteQuality
SIO_000300: 3.026e1

GenotypeQuality
all individuals: 19
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 169
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variant carriers: 0

GenotypeQuality
all individuals: 86
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variant carriers: 0

GenotypeQuality
all individuals: 7821
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variant carriers: 0

GenotypeQuality
all individuals: 1898
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variant carriers: 0

GenotypeQuality
all individuals: 41437
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variant carriers: 0

GenotypeQuality
all individuals: 156
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variant carriers: 0

GenotypeQuality
all individuals: 440
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variant carriers: 0

GenotypeQuality
all individuals: 148
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variant carriers: 0

GenotypeQuality
all individuals: 30
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variant carriers: 0

GenotypeQuality
all individuals: 406
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variant carriers: 0

GenotypeQuality
all individuals: 178
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 932
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2096
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 352
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variant carriers: 0

GenotypeQuality
all individuals: 545
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1817
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1821
bin: 7.75e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4518
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9219
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.176193836744295e-4
allele num: 8502
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47517
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8853
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 614
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.619e0

QD
type: SiteQuality
SIO_000300: 1.636e1

MQ
type: SiteQuality
SIO_000300: 5.98e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.4e-3

VQSLOD
type: SiteQuality
SIO_000300: 6.67e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.156e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.84e-1

DP
type: SiteQuality
SIO_000300: 1.656706e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.55e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.16e0

GenotypeQuality
all individuals: 41889
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 266
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1631
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 353
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 31
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 924
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variant carriers: 0

GenotypeQuality
all individuals: 349
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GenotypeQuality
all individuals: 1822
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 404
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 190
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 178
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 411
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1818
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2093
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 7851
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 203
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47569
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9220
num of homozygotes: 0

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

South Asian
type: Population
allele count: 3
allele frequency: 3.311623799536373e-4
allele num: 9059
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4518
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 615
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.65e-2

MQRankSum
type: SiteQuality
SIO_000300: 5.1e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.47e-1

MQ
type: SiteQuality
SIO_000300: 5.949e1

VQSLOD
type: SiteQuality
SIO_000300: 1.54e-1

DP
type: SiteQuality
SIO_000300: 1.66493e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.816e0

FS
type: SiteQuality
SIO_000300: 1.98e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.88e-1

QD
type: SiteQuality
SIO_000300: 1.586e1

GenotypeDepth
all individuals: 69
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1356
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 13
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variant carriers: 0

GenotypeQuality
all individuals: 1826
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variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
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variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 406
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variant carriers: 0

GenotypeQuality
all individuals: 229
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
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variant carriers: 0

GenotypeQuality
all individuals: 42679
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 307
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7874
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 354
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 161
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1827
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 929
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2090
bin: 9.75e1
variant carriers: 1

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.099032346088453e-5
allele num: 47641
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9222
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 621
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6620
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4518
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.113e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.75e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.97e-1

MQ
type: SiteQuality
SIO_000300: 5.905e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.53e0

DP
type: SiteQuality
SIO_000300: 1.671694e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.16e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

FS
type: SiteQuality
SIO_000300: 2.146e0

QD
type: SiteQuality
SIO_000300: 1.324e1

GenotypeDepth
all individuals: 197
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7943
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 92
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variant carriers: 0

GenotypeQuality
all individuals: 504
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variant carriers: 0

GenotypeQuality
all individuals: 104
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variant carriers: 0

GenotypeQuality
all individuals: 1821
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variant carriers: 0

GenotypeQuality
all individuals: 26
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variant carriers: 0

GenotypeQuality
all individuals: 100
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variant carriers: 0

GenotypeQuality
all individuals: 1819
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 406
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variant carriers: 0

GenotypeQuality
all individuals: 11
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GenotypeQuality
all individuals: 84
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
all individuals: 12
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GenotypeQuality
all individuals: 347
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51
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GenotypeQuality
all individuals: 44118
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 932
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2089
bin: 9.75e1
variant carriers: 2

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4520
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9925
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 2.166612501354133e-4
allele num: 9231
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6623
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47834
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8511
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.29e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.16e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.47e-2

QD
type: SiteQuality
SIO_000300: 2.098e1

VQSLOD
type: SiteQuality
SIO_000300: -1.194e0

MQ
type: SiteQuality
SIO_000300: 5.961e1

DP
type: SiteQuality
SIO_000300: 1.69361e6

FS
type: SiteQuality
SIO_000300: 8.710000000000001e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.53e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.28e-1

GenotypeDepth
all individuals: 28217
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
all individuals: 86
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variant carriers: 0

GenotypeQuality
all individuals: 16
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GenotypeQuality
all individuals: 488
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variant carriers: 0

GenotypeQuality
all individuals: 131
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GenotypeQuality
all individuals: 10
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GenotypeQuality
all individuals: 7932
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variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 2.75e1
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GenotypeQuality
all individuals: 97
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variant carriers: 0

GenotypeQuality
all individuals: 26
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GenotypeQuality
all individuals: 102
bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1815
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44166
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 929
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47839
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4518
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6623
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8511
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 8.5e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.437e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.86e0

FS
type: SiteQuality
SIO_000300: 1.328e0

MQRankSum
type: SiteQuality
SIO_000300: -6.76e-1

DP
type: SiteQuality
SIO_000300: 1.694376e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.31e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -4.296e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

GenotypeDepth
all individuals: 346
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 401
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
all individuals: 32
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GenotypeQuality
all individuals: 88
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GenotypeQuality
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GenotypeQuality
all individuals: 49
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GenotypeQuality
all individuals: 81
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variant carriers: 0

GenotypeQuality
all individuals: 7
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GenotypeQuality
all individuals: 8
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GenotypeQuality
all individuals: 7953
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2080
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GenotypeQuality
all individuals: 1803
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 4.75e1
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GenotypeQuality
all individuals: 11
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1802
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44409
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 922
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.510345869204048e-4
allele num: 6621
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47866
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9233
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10015
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4517
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.44e-1

FS
type: SiteQuality
SIO_000300: 1.323e0

VQSLOD
type: SiteQuality
SIO_000300: 2.14e0

DP
type: SiteQuality
SIO_000300: 1.696057e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.442e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.36e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.428e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.6e-2

GenotypeDepth
all individuals: 50
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 908
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 2075
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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GenotypeQuality
all individuals: 44240
bin: 6.25e1
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GenotypeQuality
all individuals: 42
bin: 7.5e0
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 630
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9223
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4518
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.089995193011056e-5
allele num: 47847
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10027
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8508
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.39e-2

DP
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SIO_000300: 1.694375e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.407e0

MQRankSum
type: SiteQuality
SIO_000300: 5.12e-1

BaseQRankSum
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SIO_000300: 8.5e0

QD
type: SiteQuality
SIO_000300: 1.82e1

FS
type: SiteQuality
SIO_000300: 5.772e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.31e0

VQSLOD
type: SiteQuality
SIO_000300: -9.747e-1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 2.213858755811379e-4
allele num: 4517
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 10031
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6616
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8507
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 630
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47824
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9213
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 9.16e-1

FS
type: SiteQuality
SIO_000300: 1.568e0

QD
type: SiteQuality
SIO_000300: 2.018e1

DP
type: SiteQuality
SIO_000300: 1.69203e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.8e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.37e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.16e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.26e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.965e0

MQ
type: SiteQuality
SIO_000300: 5.963e1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 339
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variant carriers: 0

GenotypeQuality
all individuals: 7806
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.175917215428034e-4
allele num: 8504
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47796
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4516
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6616
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9203
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10027
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 630
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.794e0

MQRankSum
type: SiteQuality
SIO_000300: 7.000000000000001e-2

ClippingRankSum
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SIO_000300: -3.369e0

FS
type: SiteQuality
SIO_000300: 1.3016e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.26e0

MQ
type: SiteQuality
SIO_000300: 5.979e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 1.690807e6

QD
type: SiteQuality
SIO_000300: 1.388e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.33e0

GenotypeDepth
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variant carriers: 1

GenotypeQuality
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variant carriers: 23

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 3

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47775
num of homozygotes: 0

South Asian
type: Population
allele count: 34
allele frequency: 3.392874962578585e-3
allele num: 10021
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4514
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 629
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9194
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6611
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.504e-1

FS
type: SiteQuality
SIO_000300: 5.21e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.3e-2

VQSLOD
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SIO_000300: 2.622e1

QD
type: SiteQuality
SIO_000300: 2.218e1

DP
type: SiteQuality
SIO_000300: 1.689382e6

BaseQRankSum
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SIO_000300: -2.511e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.4e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.52e-1

MQ
type: SiteQuality
SIO_000300: 5.979e1

GenotypeDepth
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 385
bin: 9.25e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8486
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9178
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4512
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9916
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6599
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 2.100310846005209e-5
allele num: 47612
num of homozygotes: 0

ClippingRankSum
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SIO_000300: 4.88e-1

FS
type: SiteQuality
SIO_000300: 2.187e0

VQSLOD
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MQRankSum
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QD
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MQ
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ReadPosRankSum
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InbreedingCoeff
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BaseQRankSum
type: SiteQuality
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DP
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SIO_000300: 1.677427e6

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8484
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9910
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4511
num of homozygotes: 0

European (Non-Finnish)
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allele count: 3
allele frequency: 6.304507723021961e-5
allele num: 47585
num of homozygotes: 0

East Asian
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allele count: 0
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allele num: 6601
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.487e0

InbreedingCoeff
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SIO_000300: 4.48e-2

ClippingRankSum
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MQ
type: SiteQuality
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MQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 2.5e0

ReadPosRankSum
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VQSLOD
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DP
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QD
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9889
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6599
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9176
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.102828304068973e-5
allele num: 47555
num of homozygotes: 0

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

Other
type: Population
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allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4509
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ReadPosRankSum
type: SiteQuality
SIO_000300: 3.05e-1

FS
type: SiteQuality
SIO_000300: 8.95e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

VQSLOD
type: SiteQuality
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BaseQRankSum
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MQRankSum
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SIO_000300: -5.97e-1

QD
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SIO_000300: 1.321e1

ClippingRankSum
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SIO_000300: -8.61e-1

DP
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SIO_000300: 1.672694e6

MQ
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SIO_000300: 5.955e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 317
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43095
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 199
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1640
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 1632
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 854
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.179245283018868e-4
allele num: 8480
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9870
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9175
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6595
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4508
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: 47534
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 9.24e-1

DP
type: SiteQuality
SIO_000300: 1.671346e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.03e-2

QD
type: SiteQuality
SIO_000300: 1.485e1

FS
type: SiteQuality
SIO_000300: 3.189e0

VQSLOD
type: SiteQuality
SIO_000300: 9.9e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.26e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.397e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.89e-1

MQ
type: SiteQuality
SIO_000300: 5.949e1

GenotypeQuality
all individuals: 1626
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 252
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2055
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1623
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 392
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1420
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 377
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 221
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 845
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43054
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 313
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7404
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 285
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 205
bin: 2.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8477
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6595
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9167
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4510
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47501
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 627
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.014301653311695e-4
allele num: 9859
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.9e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.35e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.6e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.09e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.530000000000001e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.21e-1

DP
type: SiteQuality
SIO_000300: 1.670316e6

VQSLOD
type: SiteQuality
SIO_000300: -1.217e0

FS
type: SiteQuality
SIO_000300: 3.538e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 2055
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 285
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 221
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 377
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1623
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7404
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1626
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 252
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 43054
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 392
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1420
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 845
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 205
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 313
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9859
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6595
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4510
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.179662616491683e-4
allele num: 8477
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47501
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 627
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9167
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.6e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.217e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.670316e6

FS
type: SiteQuality
SIO_000300: 3.538e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.530000000000001e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -6.35e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.09e0

QD
type: SiteQuality
SIO_000300: 1.9e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.21e-1