X-94318170-GCTTTTGCATTA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24094318170
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24094318159
    reference: chr 0
allele count: 2
allele frequency: 2.888253473124802e-5
allele num: 69246
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000221187
  ensembl transcript: ENST00000408260
  gene symbol: MIR548M
  hgvsc: ENST00000408260.1:n.45_55delTAATGCAAAAG
  variant of: http://identifiers.org/hgnc/35331
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3270
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
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  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6303
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 3.25e1
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genotype quality: GenotypeQuality
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  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 589
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 7.5e0
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genotype quality: GenotypeQuality
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  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.5e0
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genotype quality: GenotypeQuality
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  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 252
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 357
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 7.25e1
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genotype quality: GenotypeQuality
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  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 188
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 5395
  num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 6622
  num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 1
  allele frequency: 1.239771881973717e-4
  allele num: 8066
  num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: GCTTTTGCATTA
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: ReadPosRankSum

X-94318171-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24094318171
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24094318171
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 68262
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000221187
  ensembl transcript: ENST00000408260
  gene symbol: MIR548M
  hgvsc: ENST00000408260.1:n.55G>A
  variant of: http://identifiers.org/hgnc/35331
canonical: true
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 3288
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5283
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2510
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1187
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 1
genotype depth: GenotypeDepth
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  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 1
genotype depth: GenotypeDepth
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  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
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  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1799
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 3.75e1
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genotype quality: GenotypeQuality
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  bin: 5.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 287
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genotype quality: GenotypeQuality
  all individuals: 133
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genotype quality: GenotypeQuality
  all individuals: 801
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genotype quality: GenotypeQuality
  all individuals: 337
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 584
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 36411
  num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 6554
  num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 7976
  num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD

X-94318176-G-GT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24094318176
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24094318177
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 64828
alternate allele: GT
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000221187
  ensembl transcript: ENST00000408260
  gene symbol: MIR548M
  hgvsc: ENST00000408260.1:n.49_50insA
  variant of: http://identifiers.org/hgnc/35331
canonical: true
consequence: non coding transcript exon
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 3256
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10988
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1783
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 9.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 3622
  num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 7758
  num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 34233
  num of homozygotes: 0
population: Other
population: Latino
population: African
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

X-94318185-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24094318185
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24094318185
    reference: chr 0
allele count: 24
allele frequency: 4.156132026460707e-4
allele num: 57746
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000221187
  ensembl transcript: ENST00000408260
  gene symbol: MIR548M
  hgvsc: ENST00000408260.1:n.41A>G
  variant of: http://identifiers.org/hgnc/35331
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8051
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 3.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 2528
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 611
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  variant carriers: 0
num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 6556
  num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 440
  num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 3326
  num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum

X-94318191-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24094318191
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24094318191
    reference: chr 0
allele count: 1
allele frequency: 2.034505208333333e-5
allele num: 49152
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: mature_miRNA_variant
  ensembl gene: ENSG00000221187
  ensembl transcript: ENST00000408260
  gene symbol: MIR548M
  hgvsc: ENST00000408260.1:n.35G>C
  variant of: http://identifiers.org/hgnc/35331
canonical: true
consequence: mature miRNA
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4376
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.25e1
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genotype depth: GenotypeDepth
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  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: European (Finnish)
  type: Population
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  allele num: 2926
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population: Latino
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population: East Asian
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  allele frequency: 0.0e0
  allele num: 3602
  num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
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X-94318212-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24094318212
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24094318212
    reference: chr 0
allele count: 1
allele frequency: 2.9888218064439e-5
allele num: 33458
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000221187
  ensembl transcript: ENST00000408260
  gene symbol: MIR548M
  hgvsc: ENST00000408260.1:n.14G>A
  variant of: http://identifiers.org/hgnc/35331
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
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  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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population: East Asian
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population: European (Non-Finnish)
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population: South Asian
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population: Latino
population: African
population: Other
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
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site quality: ReadPosRankSum
site quality: FS
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site quality: DP
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X-94318218-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24094318218
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24094318218
    reference: chr 0
allele count: 1
allele frequency: 3.267119707266074e-5
allele num: 30608
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000221187
  ensembl transcript: ENST00000408260
  gene symbol: MIR548M
  hgvsc: ENST00000408260.1:n.8G>T
  variant of: http://identifiers.org/hgnc/35331
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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population: European (Finnish)
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population: African
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
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site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
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X-94318218-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24094318218
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24094318218
    reference: chr 0
allele count: 1
allele frequency: 3.267119707266074e-5
allele num: 30608
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000221187
  ensembl transcript: ENST00000408260
  gene symbol: MIR548M
  hgvsc: ENST00000408260.1:n.8G>C
  variant of: http://identifiers.org/hgnc/35331
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9567
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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num of homozygotes: 0
population: African
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population: Other
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population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
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X-94318238-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24094318238
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24094318238
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 21384
alternate allele: T
canonical: true
consequence: upstream gene
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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  bin: 2.75e1
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genotype quality: GenotypeQuality
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  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 271
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1007
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 9776
  num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 212
  num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 5403
  num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 1290
  num of homozygotes: 0
population: East Asian
population: African
population: Latino
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: VQSLOD

X-94318242-C-CA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24094318242
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24094318243
    reference: chr 0
allele count: 3
allele frequency: 1.571338780641106e-4
allele num: 19092
alternate allele: CA
canonical: true
consequence: upstream gene
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5112
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3006
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
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  bin: 2.5e0
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.25e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 9
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
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  bin: 6.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 564
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 138
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genotype quality: GenotypeQuality
  all individuals: 25686
  bin: 7.5e0
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 12317
  bin: 2.25e1
  variant carriers: 1
num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 5196
  num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 898
  num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 996
  num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 1163
  num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: QD

X-94318242-CA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24094318242
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24094318241
    reference: chr 0
allele count: 2
allele frequency: 1.047559187094071e-4
allele num: 19092
alternate allele: C
canonical: true
consequence: upstream gene
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 25916
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
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  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12561
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 170
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 69
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genotype quality: GenotypeQuality
  all individuals: 145
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genotype quality: GenotypeQuality
  all individuals: 149
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 361
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  variant carriers: 0
num of homozygotes: 0
population: African
  type: Population
  allele count: 1
  allele frequency: 5.025125628140704e-4
  allele num: 1990
  num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 193
  num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 1
  allele frequency: 1.155268022181146e-4
  allele num: 8656
  num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 996
  num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: CA
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD

X-94318253-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24094318253
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24094318253
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 16816
alternate allele: T
canonical: true
consequence: upstream gene
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9717
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 34
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
  all individuals: 29
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1864
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 268
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genotype quality: GenotypeQuality
  all individuals: 2992
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genotype quality: GenotypeQuality
  all individuals: 570
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 141
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  variant carriers: 0
num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 1707
  num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 655
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population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 710
  num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 962
  num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: QD

X-95940007-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24095940007
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24095940007
    reference: chr 0
allele count: 1
allele frequency: 1.710278775440397e-4
allele num: 5847
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362140
  ensembl transcript: ENST00000373049
  gene symbol: DIAPH2
  hgvsc: ENST00000373049.4:c.-51C>T
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000348082
  ensembl transcript: ENST00000355827
  gene symbol: DIAPH2
  hgvsc: ENST00000355827.4:c.-51C>T
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362145
  ensembl transcript: ENST00000373054
  gene symbol: DIAPH2
  hgvsc: ENST00000373054.4:c.-51C>T
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362152
  ensembl transcript: ENST00000373061
  gene symbol: DIAPH2
  hgvsc: ENST00000373061.3:c.-51C>T
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000321348
  ensembl transcript: ENST00000324765
  gene symbol: DIAPH2
  hgvsc: ENST00000324765.8:c.-51C>T
  variant of: http://identifiers.org/hgnc/2877
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1691
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: DP

X-95940009-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24095940009
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24095940009
    reference: chr 0
allele count: 1
allele frequency: 1.707067258449983e-4
allele num: 5858
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362140
  ensembl transcript: ENST00000373049
  gene symbol: DIAPH2
  hgvsc: ENST00000373049.4:c.-49G>T
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362145
  ensembl transcript: ENST00000373054
  gene symbol: DIAPH2
  hgvsc: ENST00000373054.4:c.-49G>T
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000321348
  ensembl transcript: ENST00000324765
  gene symbol: DIAPH2
  hgvsc: ENST00000324765.8:c.-49G>T
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000348082
  ensembl transcript: ENST00000355827
  gene symbol: DIAPH2
  hgvsc: ENST00000355827.4:c.-49G>T
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362152
  ensembl transcript: ENST00000373061
  gene symbol: DIAPH2
  hgvsc: ENST00000373061.3:c.-49G>T
  variant of: http://identifiers.org/hgnc/2877
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2934
  bin: 7.5e0
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 4.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1687
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: South Asian
population: European (Finnish)
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

X-95940101-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24095940101
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24095940101
    reference: chr 0
allele count: 1
allele frequency: 1.081548777849881e-4
allele num: 9246
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000348082
  ensembl transcript: ENST00000355827
  gene symbol: DIAPH2
  hgvsc: ENST00000355827.4:c.44G>A
  hgvsp: ENSP00000348082.4:p.Ser15Asn
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000321348
  ensembl transcript: ENST00000324765
  gene symbol: DIAPH2
  hgvsc: ENST00000324765.8:c.44G>A
  hgvsp: ENSP00000321348.8:p.Ser15Asn
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362140
  ensembl transcript: ENST00000373049
  gene symbol: DIAPH2
  hgvsc: ENST00000373049.4:c.44G>A
  hgvsp: ENSP00000362140.4:p.Ser15Asn
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362152
  ensembl transcript: ENST00000373061
  gene symbol: DIAPH2
  hgvsc: ENST00000373061.3:c.44G>A
  hgvsp: ENSP00000362152.3:p.Ser15Asn
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362145
  ensembl transcript: ENST00000373054
  gene symbol: DIAPH2
  hgvsc: ENST00000373054.4:c.44G>A
  hgvsp: ENSP00000362145.4:p.Ser15Asn
  variant of: http://identifiers.org/hgnc/2877
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 110
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ser15Asn
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
population: African
reference allele: G
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum

X-95940110-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24095940110
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24095940110
    reference: chr 0
allele count: 1
allele frequency: 9.434852344560808e-5
allele num: 10599
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362145
  ensembl transcript: ENST00000373054
  gene symbol: DIAPH2
  hgvsc: ENST00000373054.4:c.53C>A
  hgvsp: ENSP00000362145.4:p.Pro18His
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362152
  ensembl transcript: ENST00000373061
  gene symbol: DIAPH2
  hgvsc: ENST00000373061.3:c.53C>A
  hgvsp: ENSP00000362152.3:p.Pro18His
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000321348
  ensembl transcript: ENST00000324765
  gene symbol: DIAPH2
  hgvsc: ENST00000324765.8:c.53C>A
  hgvsp: ENSP00000321348.8:p.Pro18His
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362140
  ensembl transcript: ENST00000373049
  gene symbol: DIAPH2
  hgvsc: ENST00000373049.4:c.53C>A
  hgvsp: ENSP00000362140.4:p.Pro18His
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000348082
  ensembl transcript: ENST00000355827
  gene symbol: DIAPH2
  hgvsc: ENST00000355827.4:c.53C>A
  hgvsp: ENSP00000348082.4:p.Pro18His
  variant of: http://identifiers.org/hgnc/2877
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 1
hgvs: p.Pro18His
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ReadPosRankSum

X-95940130-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24095940130
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24095940130
    reference: chr 0
allele count: 1
allele frequency: 5.670220004536176e-5
allele num: 17636
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000321348
  ensembl transcript: ENST00000324765
  gene symbol: DIAPH2
  hgvsc: ENST00000324765.8:c.73A>C
  hgvsp: ENSP00000321348.8:p.Lys25Gln
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362145
  ensembl transcript: ENST00000373054
  gene symbol: DIAPH2
  hgvsc: ENST00000373054.4:c.73A>C
  hgvsp: ENSP00000362145.4:p.Lys25Gln
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000348082
  ensembl transcript: ENST00000355827
  gene symbol: DIAPH2
  hgvsc: ENST00000355827.4:c.73A>C
  hgvsp: ENSP00000348082.4:p.Lys25Gln
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362140
  ensembl transcript: ENST00000373049
  gene symbol: DIAPH2
  hgvsc: ENST00000373049.4:c.73A>C
  hgvsp: ENSP00000362140.4:p.Lys25Gln
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362152
  ensembl transcript: ENST00000373061
  gene symbol: DIAPH2
  hgvsc: ENST00000373061.3:c.73A>C
  hgvsp: ENSP00000362152.3:p.Lys25Gln
  variant of: http://identifiers.org/hgnc/2877
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1243
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 842
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  variant carriers: 0
hgvs: p.Lys25Gln
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: A
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: QD

X-95940138-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24095940138
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24095940138
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 19732
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000348082
  ensembl transcript: ENST00000355827
  gene symbol: DIAPH2
  hgvsc: ENST00000355827.4:c.81C>T
  hgvsp: ENST00000355827.4:c.81C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362152
  ensembl transcript: ENST00000373061
  gene symbol: DIAPH2
  hgvsc: ENST00000373061.3:c.81C>T
  hgvsp: ENST00000373061.3:c.81C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000321348
  ensembl transcript: ENST00000324765
  gene symbol: DIAPH2
  hgvsc: ENST00000324765.8:c.81C>T
  hgvsp: ENST00000324765.8:c.81C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362140
  ensembl transcript: ENST00000373049
  gene symbol: DIAPH2
  hgvsc: ENST00000373049.4:c.81C>T
  hgvsp: ENST00000373049.4:c.81C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362145
  ensembl transcript: ENST00000373054
  gene symbol: DIAPH2
  hgvsc: ENST00000373054.4:c.81C>T
  hgvsp: ENST00000373054.4:c.81C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2877
canonical: true
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 1
genotype depth: GenotypeDepth
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  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16898
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1343
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3189
  bin: 1.25e1
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genotype depth: GenotypeDepth
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  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.25e1
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genotype quality: GenotypeQuality
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  bin: 7.5e0
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genotype quality: GenotypeQuality
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  bin: 2.5e0
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genotype quality: GenotypeQuality
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  bin: 3.25e1
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genotype quality: GenotypeQuality
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  bin: 6.25e1
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genotype quality: GenotypeQuality
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  bin: 1.25e1
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genotype quality: GenotypeQuality
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  bin: 2.75e1
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genotype quality: GenotypeQuality
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  bin: 1.75e1
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genotype quality: GenotypeQuality
  all individuals: 590
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 548
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Ser27Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: Latino
population: South Asian
population: European (Finnish)
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD

X-95940141-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24095940141
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24095940141
    reference: chr 0
allele count: 2
allele frequency: 9.338376056403791e-5
allele num: 21417
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000348082
  ensembl transcript: ENST00000355827
  gene symbol: DIAPH2
  hgvsc: ENST00000355827.4:c.84G>A
  hgvsp: ENST00000355827.4:c.84G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362140
  ensembl transcript: ENST00000373049
  gene symbol: DIAPH2
  hgvsc: ENST00000373049.4:c.84G>A
  hgvsp: ENST00000373049.4:c.84G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362145
  ensembl transcript: ENST00000373054
  gene symbol: DIAPH2
  hgvsc: ENST00000373054.4:c.84G>A
  hgvsp: ENST00000373054.4:c.84G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362152
  ensembl transcript: ENST00000373061
  gene symbol: DIAPH2
  hgvsc: ENST00000373061.3:c.84G>A
  hgvsp: ENST00000373061.3:c.84G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000321348
  ensembl transcript: ENST00000324765
  gene symbol: DIAPH2
  hgvsc: ENST00000324765.8:c.84G>A
  hgvsp: ENST00000324765.8:c.84G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2877
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1486
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 119
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3240
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  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 400
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 124
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genotype quality: GenotypeQuality
  all individuals: 93
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ala28Ala
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ

X-95940146-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24095940146
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24095940146
    reference: chr 0
allele count: 1
allele frequency: 4.396763981709462e-5
allele num: 22744
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000348082
  ensembl transcript: ENST00000355827
  gene symbol: DIAPH2
  hgvsc: ENST00000355827.4:c.89A>G
  hgvsp: ENSP00000348082.4:p.Asn30Ser
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362152
  ensembl transcript: ENST00000373061
  gene symbol: DIAPH2
  hgvsc: ENST00000373061.3:c.89A>G
  hgvsp: ENSP00000362152.3:p.Asn30Ser
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362145
  ensembl transcript: ENST00000373054
  gene symbol: DIAPH2
  hgvsc: ENST00000373054.4:c.89A>G
  hgvsp: ENSP00000362145.4:p.Asn30Ser
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000321348
  ensembl transcript: ENST00000324765
  gene symbol: DIAPH2
  hgvsc: ENST00000324765.8:c.89A>G
  hgvsp: ENSP00000321348.8:p.Asn30Ser
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362140
  ensembl transcript: ENST00000373049
  gene symbol: DIAPH2
  hgvsc: ENST00000373049.4:c.89A>G
  hgvsp: ENSP00000362140.4:p.Asn30Ser
  variant of: http://identifiers.org/hgnc/2877
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3383
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  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 402
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 284
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  variant carriers: 0
hgvs: p.Asn30Ser
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: Other
reference allele: A
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum

X-95940147-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24095940147
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24095940147
    reference: chr 0
allele count: 1
allele frequency: 4.323015735777279e-5
allele num: 23132
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000321348
  ensembl transcript: ENST00000324765
  gene symbol: DIAPH2
  hgvsc: ENST00000324765.8:c.90C>G
  hgvsp: ENSP00000321348.8:p.Asn30Lys
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362145
  ensembl transcript: ENST00000373054
  gene symbol: DIAPH2
  hgvsc: ENST00000373054.4:c.90C>G
  hgvsp: ENSP00000362145.4:p.Asn30Lys
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000348082
  ensembl transcript: ENST00000355827
  gene symbol: DIAPH2
  hgvsc: ENST00000355827.4:c.90C>G
  hgvsp: ENSP00000348082.4:p.Asn30Lys
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362152
  ensembl transcript: ENST00000373061
  gene symbol: DIAPH2
  hgvsc: ENST00000373061.3:c.90C>G
  hgvsp: ENSP00000362152.3:p.Asn30Lys
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362140
  ensembl transcript: ENST00000373049
  gene symbol: DIAPH2
  hgvsc: ENST00000373049.4:c.90C>G
  hgvsp: ENSP00000362140.4:p.Asn30Lys
  variant of: http://identifiers.org/hgnc/2877
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28896
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 196
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1073
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Asn30Lys
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: C
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ

X-95940148-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24095940148
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24095940148
    reference: chr 0
allele count: 1
allele frequency: 4.289452236949342e-5
allele num: 23313
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362152
  ensembl transcript: ENST00000373061
  gene symbol: DIAPH2
  hgvsc: ENST00000373061.3:c.91C>T
  hgvsp: ENSP00000362152.3:p.Arg31Trp
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362145
  ensembl transcript: ENST00000373054
  gene symbol: DIAPH2
  hgvsc: ENST00000373054.4:c.91C>T
  hgvsp: ENSP00000362145.4:p.Arg31Trp
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000348082
  ensembl transcript: ENST00000355827
  gene symbol: DIAPH2
  hgvsc: ENST00000355827.4:c.91C>T
  hgvsp: ENSP00000348082.4:p.Arg31Trp
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000321348
  ensembl transcript: ENST00000324765
  gene symbol: DIAPH2
  hgvsc: ENST00000324765.8:c.91C>T
  hgvsp: ENSP00000321348.8:p.Arg31Trp
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362140
  ensembl transcript: ENST00000373049
  gene symbol: DIAPH2
  hgvsc: ENST00000373049.4:c.91C>T
  hgvsp: ENSP00000362140.4:p.Arg31Trp
  variant of: http://identifiers.org/hgnc/2877
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 924
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Arg31Trp
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
reference allele: C
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS

X-95940172-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24095940172
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24095940172
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 33077
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000321348
  ensembl transcript: ENST00000324765
  gene symbol: DIAPH2
  hgvsc: ENST00000324765.8:c.115A>G
  hgvsp: ENSP00000321348.8:p.Lys39Glu
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362140
  ensembl transcript: ENST00000373049
  gene symbol: DIAPH2
  hgvsc: ENST00000373049.4:c.115A>G
  hgvsp: ENSP00000362140.4:p.Lys39Glu
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362145
  ensembl transcript: ENST00000373054
  gene symbol: DIAPH2
  hgvsc: ENST00000373054.4:c.115A>G
  hgvsp: ENSP00000362145.4:p.Lys39Glu
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362152
  ensembl transcript: ENST00000373061
  gene symbol: DIAPH2
  hgvsc: ENST00000373061.3:c.115A>G
  hgvsp: ENSP00000362152.3:p.Lys39Glu
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000348082
  ensembl transcript: ENST00000355827
  gene symbol: DIAPH2
  hgvsc: ENST00000355827.4:c.115A>G
  hgvsp: ENSP00000348082.4:p.Lys39Glu
  variant of: http://identifiers.org/hgnc/2877
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 3935
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
hgvs: p.Lys39Glu
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: QD

X-95940180-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24095940180
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24095940180
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 33758
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362145
  ensembl transcript: ENST00000373054
  gene symbol: DIAPH2
  hgvsc: ENST00000373054.4:c.123A>G
  hgvsp: ENST00000373054.4:c.123A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000321348
  ensembl transcript: ENST00000324765
  gene symbol: DIAPH2
  hgvsc: ENST00000324765.8:c.123A>G
  hgvsp: ENST00000324765.8:c.123A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000348082
  ensembl transcript: ENST00000355827
  gene symbol: DIAPH2
  hgvsc: ENST00000355827.4:c.123A>G
  hgvsp: ENST00000355827.4:c.123A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362140
  ensembl transcript: ENST00000373049
  gene symbol: DIAPH2
  hgvsc: ENST00000373049.4:c.123A>G
  hgvsp: ENST00000373049.4:c.123A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362152
  ensembl transcript: ENST00000373061
  gene symbol: DIAPH2
  hgvsc: ENST00000373061.3:c.123A>G
  hgvsp: ENST00000373061.3:c.123A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2877
canonical: true
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 4805
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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hgvs: p.Lys41Lys
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: FS

X-95940226-AGGGAGAGCCCC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24095940226
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24095940215
    reference: chr 0
allele count: 27
allele frequency: 8.129102185825255e-4
allele num: 33214
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000321348
  ensembl transcript: ENST00000324765
  gene symbol: DIAPH2
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362145
  ensembl transcript: ENST00000373054
  gene symbol: DIAPH2
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362140
  ensembl transcript: ENST00000373049
  gene symbol: DIAPH2
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362152
  ensembl transcript: ENST00000373061
  gene symbol: DIAPH2
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000348082
  ensembl transcript: ENST00000355827
  gene symbol: DIAPH2
  variant of: http://identifiers.org/hgnc/2877
canonical: true
consequence: intron
filter: VQSRTrancheINDEL96.00to97.00
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2888
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 146
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 325
  bin: 9.75e1
  variant carriers: 30
genotype quality: GenotypeQuality
  all individuals: 20911
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 540
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 348
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3680
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Other
reference allele: AGGGAGAGCCCC
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

X-95940232-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24095940232
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24095940232
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 31665
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362145
  ensembl transcript: ENST00000373054
  gene symbol: DIAPH2
  hgvsc: ENST00000373054.4:c.132+43A>C
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000321348
  ensembl transcript: ENST00000324765
  gene symbol: DIAPH2
  hgvsc: ENST00000324765.8:c.132+43A>C
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362152
  ensembl transcript: ENST00000373061
  gene symbol: DIAPH2
  hgvsc: ENST00000373061.3:c.132+43A>C
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362140
  ensembl transcript: ENST00000373049
  gene symbol: DIAPH2
  hgvsc: ENST00000373049.4:c.132+43A>C
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000348082
  ensembl transcript: ENST00000355827
  gene symbol: DIAPH2
  hgvsc: ENST00000355827.4:c.132+43A>C
  variant of: http://identifiers.org/hgnc/2877
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13520
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8945
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2423
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1124
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4617
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22381
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3891
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 687
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 744
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1980
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2449
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4413
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14012
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1756
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16885
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3053
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 242
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
population: Other
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD

X-95940237-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24095940237
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24095940237
    reference: chr 0
allele count: 4
allele frequency: 1.341696575319491e-4
allele num: 29813
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362145
  ensembl transcript: ENST00000373054
  gene symbol: DIAPH2
  hgvsc: ENST00000373054.4:c.132+48C>G
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000348082
  ensembl transcript: ENST00000355827
  gene symbol: DIAPH2
  hgvsc: ENST00000355827.4:c.132+48C>G
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000321348
  ensembl transcript: ENST00000324765
  gene symbol: DIAPH2
  hgvsc: ENST00000324765.8:c.132+48C>G
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362140
  ensembl transcript: ENST00000373049
  gene symbol: DIAPH2
  hgvsc: ENST00000373049.4:c.132+48C>G
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362152
  ensembl transcript: ENST00000373061
  gene symbol: DIAPH2
  hgvsc: ENST00000373061.3:c.132+48C>G
  variant of: http://identifiers.org/hgnc/2877
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2535
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22744
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4543
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8504
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13539
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 965
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13267
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1554
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 768
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3009
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2372
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6463
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3043
  bin: 3.25e1
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genotype quality: GenotypeQuality
  all individuals: 147
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 299
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 392
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5155
  bin: 1.25e1
  variant carriers: 1
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS

X-95940238-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24095940238
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24095940238
    reference: chr 0
allele count: 3
allele frequency: 9.943652635067949e-5
allele num: 30170
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362145
  ensembl transcript: ENST00000373054
  gene symbol: DIAPH2
  hgvsc: ENST00000373054.4:c.132+49G>A
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000348082
  ensembl transcript: ENST00000355827
  gene symbol: DIAPH2
  hgvsc: ENST00000355827.4:c.132+49G>A
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362152
  ensembl transcript: ENST00000373061
  gene symbol: DIAPH2
  hgvsc: ENST00000373061.3:c.132+49G>A
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000321348
  ensembl transcript: ENST00000324765
  gene symbol: DIAPH2
  hgvsc: ENST00000324765.8:c.132+49G>A
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362140
  ensembl transcript: ENST00000373049
  gene symbol: DIAPH2
  hgvsc: ENST00000373049.4:c.132+49G>A
  variant of: http://identifiers.org/hgnc/2877
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13597
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22684
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 981
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4535
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 2.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 53
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
population: Latino
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: QD

X-95940240-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24095940240
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24095940240
    reference: chr 0
allele count: 5
allele frequency: 1.693308046599838e-4
allele num: 29528
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362145
  ensembl transcript: ENST00000373054
  gene symbol: DIAPH2
  hgvsc: ENST00000373054.4:c.132+51G>A
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000321348
  ensembl transcript: ENST00000324765
  gene symbol: DIAPH2
  hgvsc: ENST00000324765.8:c.132+51G>A
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000348082
  ensembl transcript: ENST00000355827
  gene symbol: DIAPH2
  hgvsc: ENST00000355827.4:c.132+51G>A
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362140
  ensembl transcript: ENST00000373049
  gene symbol: DIAPH2
  hgvsc: ENST00000373049.4:c.132+51G>A
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362152
  ensembl transcript: ENST00000373061
  gene symbol: DIAPH2
  hgvsc: ENST00000373061.3:c.132+51G>A
  variant of: http://identifiers.org/hgnc/2877
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13611
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4480
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22703
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1338
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5241
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2380
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum

X-95990713-TATC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24095990713
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24095990710
    reference: chr 0
allele count: 1
allele frequency: 1.145121211080193e-5
allele num: 87327
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000348082
  ensembl transcript: ENST00000355827
  gene symbol: DIAPH2
  hgvsc: ENST00000355827.4:c.133-43_133-41delATC
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362145
  ensembl transcript: ENST00000373054
  gene symbol: DIAPH2
  hgvsc: ENST00000373054.4:c.133-2871_133-2869delATC
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000321348
  ensembl transcript: ENST00000324765
  gene symbol: DIAPH2
  hgvsc: ENST00000324765.8:c.133-43_133-41delATC
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362140
  ensembl transcript: ENST00000373049
  gene symbol: DIAPH2
  hgvsc: ENST00000373049.4:c.133-43_133-41delATC
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362152
  ensembl transcript: ENST00000373061
  gene symbol: DIAPH2
  hgvsc: ENST00000373061.3:c.133-43_133-41delATC
  variant of: http://identifiers.org/hgnc/2877
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3631
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2007
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1837
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3545
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3396
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2299
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3914
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4091
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2524
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2797
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2142
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14073
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3018
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4172
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3996
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1926
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 213
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 868
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1190
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 245
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1299
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47818
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: Latino
reference allele: TATC
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ

X-95990719-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24095990719
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24095990719
    reference: chr 0
allele count: 2
allele frequency: 2.290399789283219e-5
allele num: 87321
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362152
  ensembl transcript: ENST00000373061
  gene symbol: DIAPH2
  hgvsc: ENST00000373061.3:c.133-38A>T
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362140
  ensembl transcript: ENST00000373049
  gene symbol: DIAPH2
  hgvsc: ENST00000373049.4:c.133-38A>T
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362145
  ensembl transcript: ENST00000373054
  gene symbol: DIAPH2
  hgvsc: ENST00000373054.4:c.133-2866A>T
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000348082
  ensembl transcript: ENST00000355827
  gene symbol: DIAPH2
  hgvsc: ENST00000355827.4:c.133-38A>T
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000321348
  ensembl transcript: ENST00000324765
  gene symbol: DIAPH2
  hgvsc: ENST00000324765.8:c.133-38A>T
  variant of: http://identifiers.org/hgnc/2877
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2145
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2525
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4180
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3000
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3547
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2298
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14073
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3431
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3999
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3940
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3017
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1925
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1837
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3642
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4102
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2007
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 853
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1309
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4540
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1583
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 354
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1272
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47823
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 864
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: Other
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP

X-95990723-G-GT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24095990723
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24095990724
    reference: chr 0
allele count: 5
allele frequency: 5.736313156807856e-5
allele num: 87164
alternate allele: GT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362152
  ensembl transcript: ENST00000373061
  gene symbol: DIAPH2
  hgvsc: ENST00000373061.3:c.133-26dupT
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000348082
  ensembl transcript: ENST00000355827
  gene symbol: DIAPH2
  hgvsc: ENST00000355827.4:c.133-26dupT
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362140
  ensembl transcript: ENST00000373049
  gene symbol: DIAPH2
  hgvsc: ENST00000373049.4:c.133-26dupT
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362145
  ensembl transcript: ENST00000373054
  gene symbol: DIAPH2
  hgvsc: ENST00000373054.4:c.133-2854dupT
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000321348
  ensembl transcript: ENST00000324765
  gene symbol: DIAPH2
  hgvsc: ENST00000324765.8:c.133-26dupT
  variant of: http://identifiers.org/hgnc/2877
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2155
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14078
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2533
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2834
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1839
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2013
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3514
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3957
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3024
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3648
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4182
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4015
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2311
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1926
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3566
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4217
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 791
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 209
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 57
  bin: 7.5e0
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 184
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1128
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 213
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 823
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 229
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4288
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1451
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1167
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

X-95990723-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24095990723
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24095990723
    reference: chr 0
allele count: 1
allele frequency: 1.147262631361571e-5
allele num: 87164
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362140
  ensembl transcript: ENST00000373049
  gene symbol: DIAPH2
  hgvsc: ENST00000373049.4:c.133-34G>T
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000348082
  ensembl transcript: ENST00000355827
  gene symbol: DIAPH2
  hgvsc: ENST00000355827.4:c.133-34G>T
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362145
  ensembl transcript: ENST00000373054
  gene symbol: DIAPH2
  hgvsc: ENST00000373054.4:c.133-2862G>T
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000321348
  ensembl transcript: ENST00000324765
  gene symbol: DIAPH2
  hgvsc: ENST00000324765.8:c.133-34G>T
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362152
  ensembl transcript: ENST00000373061
  gene symbol: DIAPH2
  hgvsc: ENST00000373061.3:c.133-34G>T
  variant of: http://identifiers.org/hgnc/2877
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3648
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1839
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1926
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2013
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2311
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2533
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3514
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3566
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4182
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2834
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3024
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14078
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4217
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2155
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3957
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4015
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1128
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 823
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1451
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4288
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 184
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 209
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 213
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 176
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 405
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1266
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 226
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: Latino
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

X-95990723-GT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24095990723
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24095990722
    reference: chr 0
allele count: 21
allele frequency: 2.4092515258593e-4
allele num: 87164
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362140
  ensembl transcript: ENST00000373049
  gene symbol: DIAPH2
  hgvsc: ENST00000373049.4:c.133-26delT
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000321348
  ensembl transcript: ENST00000324765
  gene symbol: DIAPH2
  hgvsc: ENST00000324765.8:c.133-26delT
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362145
  ensembl transcript: ENST00000373054
  gene symbol: DIAPH2
  hgvsc: ENST00000373054.4:c.133-2854delT
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000348082
  ensembl transcript: ENST00000355827
  gene symbol: DIAPH2
  hgvsc: ENST00000355827.4:c.133-26delT
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362152
  ensembl transcript: ENST00000373061
  gene symbol: DIAPH2
  hgvsc: ENST00000373061.3:c.133-26delT
  variant of: http://identifiers.org/hgnc/2877
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3514
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3566
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3648
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  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4015
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  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 314
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2533
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2013
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3024
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2311
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  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3957
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  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14078
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  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1926
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1839
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genotype quality: GenotypeQuality
  all individuals: 55
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1128
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genotype quality: GenotypeQuality
  all individuals: 184
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1167
  bin: 7.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 229
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 213
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: European (Finnish)
reference allele: GT
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff

X-95990728-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24095990728
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24095990728
    reference: chr 0
allele count: 1
allele frequency: 1.143719834389368e-5
allele num: 87434
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000348082
  ensembl transcript: ENST00000355827
  gene symbol: DIAPH2
  hgvsc: ENST00000355827.4:c.133-29T>C
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362145
  ensembl transcript: ENST00000373054
  gene symbol: DIAPH2
  hgvsc: ENST00000373054.4:c.133-2857T>C
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362152
  ensembl transcript: ENST00000373061
  gene symbol: DIAPH2
  hgvsc: ENST00000373061.3:c.133-29T>C
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362140
  ensembl transcript: ENST00000373049
  gene symbol: DIAPH2
  hgvsc: ENST00000373049.4:c.133-29T>C
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000321348
  ensembl transcript: ENST00000324765
  gene symbol: DIAPH2
  hgvsc: ENST00000324765.8:c.133-29T>C
  variant of: http://identifiers.org/hgnc/2877
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 4018
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4216
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3027
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1927
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3027
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2014
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3557
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3597
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
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  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2535
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14086
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1840
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3440
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 332
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 8.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 55
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genotype quality: GenotypeQuality
  all individuals: 5
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
reference allele: T
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ

X-95990728-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24095990728
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24095990728
    reference: chr 0
allele count: 1
allele frequency: 1.143719834389368e-5
allele num: 87434
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362140
  ensembl transcript: ENST00000373049
  gene symbol: DIAPH2
  hgvsc: ENST00000373049.4:c.133-29T>G
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000321348
  ensembl transcript: ENST00000324765
  gene symbol: DIAPH2
  hgvsc: ENST00000324765.8:c.133-29T>G
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362145
  ensembl transcript: ENST00000373054
  gene symbol: DIAPH2
  hgvsc: ENST00000373054.4:c.133-2857T>G
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362152
  ensembl transcript: ENST00000373061
  gene symbol: DIAPH2
  hgvsc: ENST00000373061.3:c.133-29T>G
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000348082
  ensembl transcript: ENST00000355827
  gene symbol: DIAPH2
  hgvsc: ENST00000355827.4:c.133-29T>G
  variant of: http://identifiers.org/hgnc/2877
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 4216
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14086
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3597
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3027
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3440
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2014
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.25e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 867
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: Other
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ

X-95990728-TTTTG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24095990728
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24095990724
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 87434
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000348082
  ensembl transcript: ENST00000355827
  gene symbol: DIAPH2
  hgvsc: ENST00000355827.4:c.133-21_133-18delGTTT
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362145
  ensembl transcript: ENST00000373054
  gene symbol: DIAPH2
  hgvsc: ENST00000373054.4:c.133-2849_133-2846delGTTT
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000321348
  ensembl transcript: ENST00000324765
  gene symbol: DIAPH2
  hgvsc: ENST00000324765.8:c.133-21_133-18delGTTT
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362152
  ensembl transcript: ENST00000373061
  gene symbol: DIAPH2
  hgvsc: ENST00000373061.3:c.133-21_133-18delGTTT
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362140
  ensembl transcript: ENST00000373049
  gene symbol: DIAPH2
  hgvsc: ENST00000373049.4:c.133-21_133-18delGTTT
  variant of: http://identifiers.org/hgnc/2877
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 2535
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3597
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1840
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3440
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14086
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
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  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4216
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2014
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 7.75e1
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genotype quality: GenotypeQuality
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  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 99
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 4916
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genotype quality: GenotypeQuality
  all individuals: 95
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
reference allele: TTTTG
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

X-95990732-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24095990732
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24095990732
    reference: chr 0
allele count: 2
allele frequency: 2.286498227963873e-5
allele num: 87470
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362152
  ensembl transcript: ENST00000373061
  gene symbol: DIAPH2
  hgvsc: ENST00000373061.3:c.133-25G>T
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000321348
  ensembl transcript: ENST00000324765
  gene symbol: DIAPH2
  hgvsc: ENST00000324765.8:c.133-25G>T
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362145
  ensembl transcript: ENST00000373054
  gene symbol: DIAPH2
  hgvsc: ENST00000373054.4:c.133-2853G>T
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362140
  ensembl transcript: ENST00000373049
  gene symbol: DIAPH2
  hgvsc: ENST00000373049.4:c.133-25G>T
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000348082
  ensembl transcript: ENST00000355827
  gene symbol: DIAPH2
  hgvsc: ENST00000355827.4:c.133-25G>T
  variant of: http://identifiers.org/hgnc/2877
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 4148
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1927
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 275
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2015
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1840
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1322
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num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: VQSLOD

X-95990736-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24095990736
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24095990736
    reference: chr 0
allele count: 2
allele frequency: 2.285897157486885e-5
allele num: 87493
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362140
  ensembl transcript: ENST00000373049
  gene symbol: DIAPH2
  hgvsc: ENST00000373049.4:c.133-21G>T
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000348082
  ensembl transcript: ENST00000355827
  gene symbol: DIAPH2
  hgvsc: ENST00000355827.4:c.133-21G>T
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000321348
  ensembl transcript: ENST00000324765
  gene symbol: DIAPH2
  hgvsc: ENST00000324765.8:c.133-21G>T
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362152
  ensembl transcript: ENST00000373061
  gene symbol: DIAPH2
  hgvsc: ENST00000373061.3:c.133-21G>T
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362145
  ensembl transcript: ENST00000373054
  gene symbol: DIAPH2
  hgvsc: ENST00000373054.4:c.133-2849G>T
  variant of: http://identifiers.org/hgnc/2877
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 14086
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
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genotype depth: GenotypeDepth
  all individuals: 3031
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 1927
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 3452
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2015
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  variant carriers: 1
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 1840
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 81
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  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: G
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: QD

X-95990740-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24095990740
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24095990740
    reference: chr 0
allele count: 3
allele frequency: 3.429629714311844e-5
allele num: 87473
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362145
  ensembl transcript: ENST00000373054
  gene symbol: DIAPH2
  hgvsc: ENST00000373054.4:c.133-2845C>T
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362152
  ensembl transcript: ENST00000373061
  gene symbol: DIAPH2
  hgvsc: ENST00000373061.3:c.133-17C>T
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362140
  ensembl transcript: ENST00000373049
  gene symbol: DIAPH2
  hgvsc: ENST00000373049.4:c.133-17C>T
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000348082
  ensembl transcript: ENST00000355827
  gene symbol: DIAPH2
  hgvsc: ENST00000355827.4:c.133-17C>T
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000321348
  ensembl transcript: ENST00000324765
  gene symbol: DIAPH2
  hgvsc: ENST00000324765.8:c.133-17C>T
  variant of: http://identifiers.org/hgnc/2877
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 14086
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1840
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: Other
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

X-95990752-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24095990752
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24095990752
    reference: chr 0
allele count: 2
allele frequency: 2.285662042010468e-5
allele num: 87502
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362145
  ensembl transcript: ENST00000373054
  gene symbol: DIAPH2
  hgvsc: ENST00000373054.4:c.133-2833A>T
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362140
  ensembl transcript: ENST00000373049
  gene symbol: DIAPH2
  hgvsc: ENST00000373049.4:c.133-5A>T
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000321348
  ensembl transcript: ENST00000324765
  gene symbol: DIAPH2
  hgvsc: ENST00000324765.8:c.133-5A>T
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
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  consequence: splice_region_variant
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  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362152
  ensembl transcript: ENST00000373061
  gene symbol: DIAPH2
  hgvsc: ENST00000373061.3:c.133-5A>T
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
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  gene symbol: DIAPH2
  hgvsc: ENST00000355827.4:c.133-5A>T
  variant of: http://identifiers.org/hgnc/2877
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 192
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
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genotype quality: GenotypeQuality
  all individuals: 79
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
hgvs: c.133-5A>T
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: A
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

X-95990753-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24095990753
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24095990753
    reference: chr 0
allele count: 1
allele frequency: 1.142831021005234e-5
allele num: 87502
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362152
  ensembl transcript: ENST00000373061
  gene symbol: DIAPH2
  hgvsc: ENST00000373061.3:c.133-4A>T
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000348082
  ensembl transcript: ENST00000355827
  gene symbol: DIAPH2
  hgvsc: ENST00000355827.4:c.133-4A>T
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362145
  ensembl transcript: ENST00000373054
  gene symbol: DIAPH2
  hgvsc: ENST00000373054.4:c.133-2832A>T
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000321348
  ensembl transcript: ENST00000324765
  gene symbol: DIAPH2
  hgvsc: ENST00000324765.8:c.133-4A>T
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362140
  ensembl transcript: ENST00000373049
  gene symbol: DIAPH2
  hgvsc: ENST00000373049.4:c.133-4A>T
  variant of: http://identifiers.org/hgnc/2877
canonical: true
consequence: splice region
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 3031
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2537
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genotype depth: GenotypeDepth
  all individuals: 133
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genotype depth: GenotypeDepth
  all individuals: 292
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genotype depth: GenotypeDepth
  all individuals: 21
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genotype depth: GenotypeDepth
  all individuals: 3559
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 4045
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 2014
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genotype depth: GenotypeDepth
  all individuals: 1927
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genotype depth: GenotypeDepth
  all individuals: 4150
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 5098
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1515
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genotype quality: GenotypeQuality
  all individuals: 50
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genotype quality: GenotypeQuality
  all individuals: 3
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genotype quality: GenotypeQuality
  all individuals: 4
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  variant carriers: 0
hgvs: c.133-4A>T
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD

X-95990759-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24095990759
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24095990759
    reference: chr 0
allele count: 2
allele frequency: 2.286236854138089e-5
allele num: 87480
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000348082
  ensembl transcript: ENST00000355827
  gene symbol: DIAPH2
  hgvsc: ENST00000355827.4:c.135C>T
  hgvsp: ENST00000355827.4:c.135C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362145
  ensembl transcript: ENST00000373054
  gene symbol: DIAPH2
  hgvsc: ENST00000373054.4:c.133-2826C>T
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362140
  ensembl transcript: ENST00000373049
  gene symbol: DIAPH2
  hgvsc: ENST00000373049.4:c.135C>T
  hgvsp: ENST00000373049.4:c.135C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000321348
  ensembl transcript: ENST00000324765
  gene symbol: DIAPH2
  hgvsc: ENST00000324765.8:c.135C>T
  hgvsp: ENST00000324765.8:c.135C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362152
  ensembl transcript: ENST00000373061
  gene symbol: DIAPH2
  hgvsc: ENST00000373061.3:c.135C>T
  hgvsp: ENST00000373061.3:c.135C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2877
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3067
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 2014
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genotype depth: GenotypeDepth
  all individuals: 1927
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1327
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
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  variant carriers: 0
hgvs: c.135C>T
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP

X-95990794-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24095990794
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24095990794
    reference: chr 0
allele count: 7
allele frequency: 8.018511306100941e-5
allele num: 87298
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000321348
  ensembl transcript: ENST00000324765
  gene symbol: DIAPH2
  hgvsc: ENST00000324765.8:c.165+5G>C
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362140
  ensembl transcript: ENST00000373049
  gene symbol: DIAPH2
  hgvsc: ENST00000373049.4:c.165+5G>C
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362152
  ensembl transcript: ENST00000373061
  gene symbol: DIAPH2
  hgvsc: ENST00000373061.3:c.165+5G>C
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000348082
  ensembl transcript: ENST00000355827
  gene symbol: DIAPH2
  hgvsc: ENST00000355827.4:c.165+5G>C
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362145
  ensembl transcript: ENST00000373054
  gene symbol: DIAPH2
  hgvsc: ENST00000373054.4:c.133-2791G>C
  variant of: http://identifiers.org/hgnc/2877
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14092
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 3550
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: c.165+5G>C
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: East Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum

X-95990795-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24095990795
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24095990795
    reference: chr 0
allele count: 1
allele frequency: 1.145514737047092e-5
allele num: 87297
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362140
  ensembl transcript: ENST00000373049
  gene symbol: DIAPH2
  hgvsc: ENST00000373049.4:c.165+6G>C
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362145
  ensembl transcript: ENST00000373054
  gene symbol: DIAPH2
  hgvsc: ENST00000373054.4:c.133-2790G>C
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000321348
  ensembl transcript: ENST00000324765
  gene symbol: DIAPH2
  hgvsc: ENST00000324765.8:c.165+6G>C
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000348082
  ensembl transcript: ENST00000355827
  gene symbol: DIAPH2
  hgvsc: ENST00000355827.4:c.165+6G>C
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362152
  ensembl transcript: ENST00000373061
  gene symbol: DIAPH2
  hgvsc: ENST00000373061.3:c.165+6G>C
  variant of: http://identifiers.org/hgnc/2877
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2014
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4150
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 222
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 238
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 1.75e1
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genotype quality: GenotypeQuality
  all individuals: 4383
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 39
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1180
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 5.75e1
  variant carriers: 0
hgvs: c.165+6G>C
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum

X-95990808-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24095990808
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24095990808
    reference: chr 0
allele count: 1
allele frequency: 1.147223146374201e-5
allele num: 87167
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362145
  ensembl transcript: ENST00000373054
  gene symbol: DIAPH2
  hgvsc: ENST00000373054.4:c.133-2777G>A
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362152
  ensembl transcript: ENST00000373061
  gene symbol: DIAPH2
  hgvsc: ENST00000373061.3:c.165+19G>A
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362140
  ensembl transcript: ENST00000373049
  gene symbol: DIAPH2
  hgvsc: ENST00000373049.4:c.165+19G>A
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000321348
  ensembl transcript: ENST00000324765
  gene symbol: DIAPH2
  hgvsc: ENST00000324765.8:c.165+19G>A
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000348082
  ensembl transcript: ENST00000355827
  gene symbol: DIAPH2
  hgvsc: ENST00000355827.4:c.165+19G>A
  variant of: http://identifiers.org/hgnc/2877
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2410
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4149
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genotype depth: GenotypeDepth
  all individuals: 3031
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genotype depth: GenotypeDepth
  all individuals: 4020
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genotype depth: GenotypeDepth
  all individuals: 437
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1927
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14091
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  variant carriers: 1
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 2014
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1175
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1324
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genotype quality: GenotypeQuality
  all individuals: 17
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genotype quality: GenotypeQuality
  all individuals: 875
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: Other
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

X-95990824-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24095990824
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24095990824
    reference: chr 0
allele count: 1
allele frequency: 1.149887885931122e-5
allele num: 86965
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000348082
  ensembl transcript: ENST00000355827
  gene symbol: DIAPH2
  hgvsc: ENST00000355827.4:c.165+35T>C
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362152
  ensembl transcript: ENST00000373061
  gene symbol: DIAPH2
  hgvsc: ENST00000373061.3:c.165+35T>C
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000321348
  ensembl transcript: ENST00000324765
  gene symbol: DIAPH2
  hgvsc: ENST00000324765.8:c.165+35T>C
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362145
  ensembl transcript: ENST00000373054
  gene symbol: DIAPH2
  hgvsc: ENST00000373054.4:c.133-2761T>C
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362140
  ensembl transcript: ENST00000373049
  gene symbol: DIAPH2
  hgvsc: ENST00000373049.4:c.165+35T>C
  variant of: http://identifiers.org/hgnc/2877
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1830
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1953
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1096
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4218
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3032
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2014
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2543
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1927
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 1842
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1431
  bin: 2.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1323
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 118
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  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum

X-95990835-TTTTAA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24095990835
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24095990830
    reference: chr 0
allele count: 4
allele frequency: 4.613344097802895e-5
allele num: 86705
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000321348
  ensembl transcript: ENST00000324765
  gene symbol: DIAPH2
  hgvsc: ENST00000324765.8:c.165+49_165+53delTAATT
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362145
  ensembl transcript: ENST00000373054
  gene symbol: DIAPH2
  hgvsc: ENST00000373054.4:c.133-2747_133-2743delTAATT
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362140
  ensembl transcript: ENST00000373049
  gene symbol: DIAPH2
  hgvsc: ENST00000373049.4:c.165+49_165+53delTAATT
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000348082
  ensembl transcript: ENST00000355827
  gene symbol: DIAPH2
  hgvsc: ENST00000355827.4:c.165+49_165+53delTAATT
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362152
  ensembl transcript: ENST00000373061
  gene symbol: DIAPH2
  hgvsc: ENST00000373061.3:c.165+49_165+53delTAATT
  variant of: http://identifiers.org/hgnc/2877
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 1770
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1254
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 1926
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2014
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
reference allele: TTTTAA
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

X-95990839-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24095990839
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24095990839
    reference: chr 0
allele count: 19402
allele frequency: 2.240234623067419e-1
allele num: 86607
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000348082
  ensembl transcript: ENST00000355827
  gene symbol: DIAPH2
  hgvsc: ENST00000355827.4:c.165+50A>T
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000321348
  ensembl transcript: ENST00000324765
  gene symbol: DIAPH2
  hgvsc: ENST00000324765.8:c.165+50A>T
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362152
  ensembl transcript: ENST00000373061
  gene symbol: DIAPH2
  hgvsc: ENST00000373061.3:c.165+50A>T
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362145
  ensembl transcript: ENST00000373054
  gene symbol: DIAPH2
  hgvsc: ENST00000373054.4:c.133-2746A>T
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362140
  ensembl transcript: ENST00000373049
  gene symbol: DIAPH2
  hgvsc: ENST00000373049.4:c.165+50A>T
  variant of: http://identifiers.org/hgnc/2877
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 7.5e0
  variant carriers: 202
genotype depth: GenotypeDepth
  all individuals: 1771
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genotype depth: GenotypeDepth
  all individuals: 1812
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  variant carriers: 239
genotype depth: GenotypeDepth
  all individuals: 1932
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  variant carriers: 598
genotype depth: GenotypeDepth
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  variant carriers: 609
genotype depth: GenotypeDepth
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  variant carriers: 391
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 607
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 554
genotype depth: GenotypeDepth
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  variant carriers: 419
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 49758
  bin: 9.75e1
  variant carriers: 16803
genotype quality: GenotypeQuality
  all individuals: 283
  bin: 1.75e1
  variant carriers: 54
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 7.5e0
  variant carriers: 13
genotype quality: GenotypeQuality
  all individuals: 309
  bin: 5.25e1
  variant carriers: 105
genotype quality: GenotypeQuality
  all individuals: 733
  bin: 3.25e1
  variant carriers: 136
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 1.25e1
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 572
  bin: 7.25e1
  variant carriers: 31
genotype quality: GenotypeQuality
  all individuals: 505
  bin: 2.75e1
  variant carriers: 78
genotype quality: GenotypeQuality
  all individuals: 288
  bin: 4.25e1
  variant carriers: 93
genotype quality: GenotypeQuality
  all individuals: 427
  bin: 4.75e1
  variant carriers: 137
num of homozygotes: 1581
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
reference allele: A
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff

X-95990840-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24095990840
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24095990840
    reference: chr 0
allele count: 1
allele frequency: 1.154321201417506e-5
allele num: 86631
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362152
  ensembl transcript: ENST00000373061
  gene symbol: DIAPH2
  hgvsc: ENST00000373061.3:c.165+51A>T
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362140
  ensembl transcript: ENST00000373049
  gene symbol: DIAPH2
  hgvsc: ENST00000373049.4:c.165+51A>T
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000348082
  ensembl transcript: ENST00000355827
  gene symbol: DIAPH2
  hgvsc: ENST00000355827.4:c.165+51A>T
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000321348
  ensembl transcript: ENST00000324765
  gene symbol: DIAPH2
  hgvsc: ENST00000324765.8:c.165+51A>T
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362145
  ensembl transcript: ENST00000373054
  gene symbol: DIAPH2
  hgvsc: ENST00000373054.4:c.133-2745A>T
  variant of: http://identifiers.org/hgnc/2877
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19319
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3107
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1228
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1953
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  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1695
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 2931
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1778
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1827
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 3433
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genotype depth: GenotypeDepth
  all individuals: 3512
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 2382
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 262
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1106
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genotype quality: GenotypeQuality
  all individuals: 801
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 717
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 1.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 593
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 314
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: QD

X-95993537-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24095993537
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24095993537
    reference: chr 0
allele count: 1
allele frequency: 2.108770375993758e-5
allele num: 47421
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000348082
  ensembl transcript: ENST00000355827
  gene symbol: DIAPH2
  hgvsc: ENST00000355827.4:c.166-48T>A
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362145
  ensembl transcript: ENST00000373054
  gene symbol: DIAPH2
  hgvsc: ENST00000373054.4:c.133-48T>A
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362152
  ensembl transcript: ENST00000373061
  gene symbol: DIAPH2
  hgvsc: ENST00000373061.3:c.166-48T>A
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000321348
  ensembl transcript: ENST00000324765
  gene symbol: DIAPH2
  hgvsc: ENST00000324765.8:c.166-48T>A
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362140
  ensembl transcript: ENST00000373049
  gene symbol: DIAPH2
  hgvsc: ENST00000373049.4:c.166-48T>A
  variant of: http://identifiers.org/hgnc/2877
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 940
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3700
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1834
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 1
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 494
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 421
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2302
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 7649
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genotype quality: GenotypeQuality
  all individuals: 612
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2004
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  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4332
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: Other
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: DP

X-95993541-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24095993541
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24095993541
    reference: chr 0
allele count: 1
allele frequency: 2.115551418477226e-5
allele num: 47269
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362145
  ensembl transcript: ENST00000373054
  gene symbol: DIAPH2
  hgvsc: ENST00000373054.4:c.133-44G>A
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000348082
  ensembl transcript: ENST00000355827
  gene symbol: DIAPH2
  hgvsc: ENST00000355827.4:c.166-44G>A
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362140
  ensembl transcript: ENST00000373049
  gene symbol: DIAPH2
  hgvsc: ENST00000373049.4:c.166-44G>A
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362152
  ensembl transcript: ENST00000373061
  gene symbol: DIAPH2
  hgvsc: ENST00000373061.3:c.166-44G>A
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000321348
  ensembl transcript: ENST00000324765
  gene symbol: DIAPH2
  hgvsc: ENST00000324765.8:c.166-44G>A
  variant of: http://identifiers.org/hgnc/2877
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4599
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 5632
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: Other
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: DP

X-95993544-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24095993544
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24095993544
    reference: chr 0
allele count: 1
allele frequency: 2.105529119467722e-5
allele num: 47494
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362140
  ensembl transcript: ENST00000373049
  gene symbol: DIAPH2
  hgvsc: ENST00000373049.4:c.166-41C>A
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000321348
  ensembl transcript: ENST00000324765
  gene symbol: DIAPH2
  hgvsc: ENST00000324765.8:c.166-41C>A
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000348082
  ensembl transcript: ENST00000355827
  gene symbol: DIAPH2
  hgvsc: ENST00000355827.4:c.166-41C>A
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362145
  ensembl transcript: ENST00000373054
  gene symbol: DIAPH2
  hgvsc: ENST00000373054.4:c.133-41C>A
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362152
  ensembl transcript: ENST00000373061
  gene symbol: DIAPH2
  hgvsc: ENST00000373061.3:c.166-41C>A
  variant of: http://identifiers.org/hgnc/2877
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1980
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21419
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ClippingRankSum

X-95993571-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24095993571
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24095993571
    reference: chr 0
allele count: 1
allele frequency: 1.826951183864367e-5
allele num: 54736
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362152
  ensembl transcript: ENST00000373061
  gene symbol: DIAPH2
  hgvsc: ENST00000373061.3:c.166-14A>C
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362140
  ensembl transcript: ENST00000373049
  gene symbol: DIAPH2
  hgvsc: ENST00000373049.4:c.166-14A>C
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362145
  ensembl transcript: ENST00000373054
  gene symbol: DIAPH2
  hgvsc: ENST00000373054.4:c.133-14A>C
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000348082
  ensembl transcript: ENST00000355827
  gene symbol: DIAPH2
  hgvsc: ENST00000355827.4:c.166-14A>C
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000321348
  ensembl transcript: ENST00000324765
  gene symbol: DIAPH2
  hgvsc: ENST00000324765.8:c.166-14A>C
  variant of: http://identifiers.org/hgnc/2877
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: DP

X-95993586-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24095993586
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24095993586
    reference: chr 0
allele count: 1
allele frequency: 1.495506004456608e-5
allele num: 66867
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362140
  ensembl transcript: ENST00000373049
  gene symbol: DIAPH2
  hgvsc: ENST00000373049.4:c.167G>A
  hgvsp: ENSP00000362140.4:p.Arg56His
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000321348
  ensembl transcript: ENST00000324765
  gene symbol: DIAPH2
  hgvsc: ENST00000324765.8:c.167G>A
  hgvsp: ENSP00000321348.8:p.Arg56His
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000147202
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  gene symbol: DIAPH2
  hgvsc: ENST00000355827.4:c.167G>A
  hgvsp: ENSP00000348082.4:p.Arg56His
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000147202
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  gene symbol: DIAPH2
  hgvsc: ENST00000373054.4:c.134G>A
  hgvsp: ENSP00000362145.4:p.Arg45His
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362152
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  gene symbol: DIAPH2
  hgvsc: ENST00000373061.3:c.167G>A
  hgvsp: ENSP00000362152.3:p.Arg56His
  variant of: http://identifiers.org/hgnc/2877
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: p.Arg56His
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ClippingRankSum

X-95993592-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24095993592
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24095993592
    reference: chr 0
allele count: 1
allele frequency: 1.409026221977991e-5
allele num: 70971
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000348082
  ensembl transcript: ENST00000355827
  gene symbol: DIAPH2
  hgvsc: ENST00000355827.4:c.173G>A
  hgvsp: ENSP00000348082.4:p.Arg58Gln
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362145
  ensembl transcript: ENST00000373054
  gene symbol: DIAPH2
  hgvsc: ENST00000373054.4:c.140G>A
  hgvsp: ENSP00000362145.4:p.Arg47Gln
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362140
  ensembl transcript: ENST00000373049
  gene symbol: DIAPH2
  hgvsc: ENST00000373049.4:c.173G>A
  hgvsp: ENSP00000362140.4:p.Arg58Gln
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000321348
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  gene symbol: DIAPH2
  hgvsc: ENST00000324765.8:c.173G>A
  hgvsp: ENSP00000321348.8:p.Arg58Gln
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362152
  ensembl transcript: ENST00000373061
  gene symbol: DIAPH2
  hgvsc: ENST00000373061.3:c.173G>A
  hgvsp: ENSP00000362152.3:p.Arg58Gln
  variant of: http://identifiers.org/hgnc/2877
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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hgvs: p.Arg58Gln
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
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site quality: DP
site quality: ReadPosRankSum
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site quality: InbreedingCoeff
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site quality: QD

X-95993605-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24095993605
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24095993605
    reference: chr 0
allele count: 1
allele frequency: 1.318252524453584e-5
allele num: 75858
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000348082
  ensembl transcript: ENST00000355827
  gene symbol: DIAPH2
  hgvsc: ENST00000355827.4:c.186T>C
  hgvsp: ENST00000355827.4:c.186T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362140
  ensembl transcript: ENST00000373049
  gene symbol: DIAPH2
  hgvsc: ENST00000373049.4:c.186T>C
  hgvsp: ENST00000373049.4:c.186T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362152
  ensembl transcript: ENST00000373061
  gene symbol: DIAPH2
  hgvsc: ENST00000373061.3:c.186T>C
  hgvsp: ENST00000373061.3:c.186T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
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  ensembl protein: ENSP00000362145
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  gene symbol: DIAPH2
  hgvsc: ENST00000373054.4:c.153T>C
  hgvsp: ENST00000373054.4:c.153T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000321348
  ensembl transcript: ENST00000324765
  gene symbol: DIAPH2
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  hgvsp: ENST00000324765.8:c.186T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2877
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
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  variant carriers: 1
genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 1.75e1
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genotype quality: GenotypeQuality
  all individuals: 643
  bin: 5.25e1
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genotype quality: GenotypeQuality
  all individuals: 3648
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 426
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1117
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genotype quality: GenotypeQuality
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  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 569
  bin: 3.75e1
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genotype quality: GenotypeQuality
  all individuals: 301
  bin: 7.5e0
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genotype quality: GenotypeQuality
  all individuals: 1372
  bin: 7.75e1
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genotype quality: GenotypeQuality
  all individuals: 10872
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 714
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Phe62Phe
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
reference allele: T
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: MQ

X-95993636-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24095993636
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24095993636
    reference: chr 0
allele count: 1
allele frequency: 1.194158178192283e-5
allele num: 83741
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000348082
  ensembl transcript: ENST00000355827
  gene symbol: DIAPH2
  hgvsc: ENST00000355827.4:c.217C>T
  hgvsp: ENSP00000348082.4:p.Leu73Phe
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362152
  ensembl transcript: ENST00000373061
  gene symbol: DIAPH2
  hgvsc: ENST00000373061.3:c.217C>T
  hgvsp: ENSP00000362152.3:p.Leu73Phe
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000321348
  ensembl transcript: ENST00000324765
  gene symbol: DIAPH2
  hgvsc: ENST00000324765.8:c.217C>T
  hgvsp: ENSP00000321348.8:p.Leu73Phe
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362145
  ensembl transcript: ENST00000373054
  gene symbol: DIAPH2
  hgvsc: ENST00000373054.4:c.184C>T
  hgvsp: ENSP00000362145.4:p.Leu62Phe
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362140
  ensembl transcript: ENST00000373049
  gene symbol: DIAPH2
  hgvsc: ENST00000373049.4:c.217C>T
  hgvsp: ENSP00000362140.4:p.Leu73Phe
  variant of: http://identifiers.org/hgnc/2877
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3754
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40767
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 23
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 721
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 20
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genotype depth: GenotypeDepth
  all individuals: 683
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 257
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genotype quality: GenotypeQuality
  all individuals: 1164
  bin: 7.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 2094
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 424
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Leu73Phe
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: DP

X-95993665-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24095993665
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24095993665
    reference: chr 0
allele count: 10
allele frequency: 1.151980831038972e-4
allele num: 86807
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000321348
  ensembl transcript: ENST00000324765
  gene symbol: DIAPH2
  hgvsc: ENST00000324765.8:c.246C>T
  hgvsp: ENST00000324765.8:c.246C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362152
  ensembl transcript: ENST00000373061
  gene symbol: DIAPH2
  hgvsc: ENST00000373061.3:c.246C>T
  hgvsp: ENST00000373061.3:c.246C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000348082
  ensembl transcript: ENST00000355827
  gene symbol: DIAPH2
  hgvsc: ENST00000355827.4:c.246C>T
  hgvsp: ENST00000355827.4:c.246C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362140
  ensembl transcript: ENST00000373049
  gene symbol: DIAPH2
  hgvsc: ENST00000373049.4:c.246C>T
  hgvsp: ENST00000373049.4:c.246C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362145
  ensembl transcript: ENST00000373054
  gene symbol: DIAPH2
  hgvsc: ENST00000373054.4:c.213C>T
  hgvsp: ENST00000373054.4:c.213C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2877
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
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genotype depth: GenotypeDepth
  all individuals: 700
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 39
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42665
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
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  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11117
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genotype depth: GenotypeDepth
  all individuals: 50
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 146
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1004
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 4321
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genotype quality: GenotypeQuality
  all individuals: 119
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 268
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Val82Val
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD

X-95993666-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24095993666
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24095993666
    reference: chr 0
allele count: 577
allele frequency: 6.63981588032221e-3
allele num: 86900
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000321348
  ensembl transcript: ENST00000324765
  gene symbol: DIAPH2
  hgvsc: ENST00000324765.8:c.247G>A
  hgvsp: ENSP00000321348.8:p.Ala83Thr
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362145
  ensembl transcript: ENST00000373054
  gene symbol: DIAPH2
  hgvsc: ENST00000373054.4:c.214G>A
  hgvsp: ENSP00000362145.4:p.Ala72Thr
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000348082
  ensembl transcript: ENST00000355827
  gene symbol: DIAPH2
  hgvsc: ENST00000355827.4:c.247G>A
  hgvsp: ENSP00000348082.4:p.Ala83Thr
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362140
  ensembl transcript: ENST00000373049
  gene symbol: DIAPH2
  hgvsc: ENST00000373049.4:c.247G>A
  hgvsp: ENSP00000362140.4:p.Ala83Thr
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362152
  ensembl transcript: ENST00000373061
  gene symbol: DIAPH2
  hgvsc: ENST00000373061.3:c.247G>A
  hgvsp: ENSP00000362152.3:p.Ala83Thr
  variant of: http://identifiers.org/hgnc/2877
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 6.75e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 42384
  bin: 2.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 3.75e1
  variant carriers: 48
genotype depth: GenotypeDepth
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  variant carriers: 93
genotype depth: GenotypeDepth
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  bin: 9.25e1
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genotype depth: GenotypeDepth
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  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 5.75e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 4.25e1
  variant carriers: 43
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 6.25e1
  variant carriers: 44
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 7.25e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 254
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  variant carriers: 40
genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 3.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 198
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genotype quality: GenotypeQuality
  all individuals: 1401
  bin: 7.75e1
  variant carriers: 8
hgvs: p.Ala83Thr
num of homozygotes: 1
population: Other
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: DP

X-95993667-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24095993667
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24095993667
    reference: chr 0
allele count: 1
allele frequency: 1.149993675034787e-5
allele num: 86957
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362140
  ensembl transcript: ENST00000373049
  gene symbol: DIAPH2
  hgvsc: ENST00000373049.4:c.248C>T
  hgvsp: ENSP00000362140.4:p.Ala83Val
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000348082
  ensembl transcript: ENST00000355827
  gene symbol: DIAPH2
  hgvsc: ENST00000355827.4:c.248C>T
  hgvsp: ENSP00000348082.4:p.Ala83Val
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000321348
  ensembl transcript: ENST00000324765
  gene symbol: DIAPH2
  hgvsc: ENST00000324765.8:c.248C>T
  hgvsp: ENSP00000321348.8:p.Ala83Val
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362152
  ensembl transcript: ENST00000373061
  gene symbol: DIAPH2
  hgvsc: ENST00000373061.3:c.248C>T
  hgvsp: ENSP00000362152.3:p.Ala83Val
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362145
  ensembl transcript: ENST00000373054
  gene symbol: DIAPH2
  hgvsc: ENST00000373054.4:c.215C>T
  hgvsp: ENSP00000362145.4:p.Ala72Val
  variant of: http://identifiers.org/hgnc/2877
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 42401
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 295
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 5.25e1
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genotype quality: GenotypeQuality
  all individuals: 1430
  bin: 7.75e1
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genotype quality: GenotypeQuality
  all individuals: 879
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ala83Val
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum

X-95993668-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24095993668
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24095993668
    reference: chr 0
allele count: 10
allele frequency: 1.14892345871918e-4
allele num: 87038
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000348082
  ensembl transcript: ENST00000355827
  gene symbol: DIAPH2
  hgvsc: ENST00000355827.4:c.249G>A
  hgvsp: ENST00000355827.4:c.249G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000321348
  ensembl transcript: ENST00000324765
  gene symbol: DIAPH2
  hgvsc: ENST00000324765.8:c.249G>A
  hgvsp: ENST00000324765.8:c.249G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362145
  ensembl transcript: ENST00000373054
  gene symbol: DIAPH2
  hgvsc: ENST00000373054.4:c.216G>A
  hgvsp: ENST00000373054.4:c.216G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362140
  ensembl transcript: ENST00000373049
  gene symbol: DIAPH2
  hgvsc: ENST00000373049.4:c.249G>A
  hgvsp: ENST00000373049.4:c.249G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362152
  ensembl transcript: ENST00000373061
  gene symbol: DIAPH2
  hgvsc: ENST00000373061.3:c.249G>A
  hgvsp: ENST00000373061.3:c.249G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2877
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 646
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 886
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  variant carriers: 0
hgvs: p.Ala83Ala
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: East Asian
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

X-95993670-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24095993670
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24095993670
    reference: chr 0
allele count: 1
allele frequency: 1.147539102394914e-5
allele num: 87143
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000321348
  ensembl transcript: ENST00000324765
  gene symbol: DIAPH2
  hgvsc: ENST00000324765.8:c.251T>C
  hgvsp: ENSP00000321348.8:p.Met84Thr
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362152
  ensembl transcript: ENST00000373061
  gene symbol: DIAPH2
  hgvsc: ENST00000373061.3:c.251T>C
  hgvsp: ENSP00000362152.3:p.Met84Thr
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000348082
  ensembl transcript: ENST00000355827
  gene symbol: DIAPH2
  hgvsc: ENST00000355827.4:c.251T>C
  hgvsp: ENSP00000348082.4:p.Met84Thr
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362140
  ensembl transcript: ENST00000373049
  gene symbol: DIAPH2
  hgvsc: ENST00000373049.4:c.251T>C
  hgvsp: ENSP00000362140.4:p.Met84Thr
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362145
  ensembl transcript: ENST00000373054
  gene symbol: DIAPH2
  hgvsc: ENST00000373054.4:c.218T>C
  hgvsp: ENSP00000362145.4:p.Met73Thr
  variant of: http://identifiers.org/hgnc/2877
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 218
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 72
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hgvs: p.Met84Thr
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum

X-95993681-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24095993681
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24095993681
    reference: chr 0
allele count: 3
allele frequency: 3.434065934065934e-5
allele num: 87360
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000348082
  ensembl transcript: ENST00000355827
  gene symbol: DIAPH2
  hgvsc: ENST00000355827.4:c.262C>T
  hgvsp: ENSP00000348082.4:p.Pro88Ser
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362152
  ensembl transcript: ENST00000373061
  gene symbol: DIAPH2
  hgvsc: ENST00000373061.3:c.262C>T
  hgvsp: ENSP00000362152.3:p.Pro88Ser
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362145
  ensembl transcript: ENST00000373054
  gene symbol: DIAPH2
  hgvsc: ENST00000373054.4:c.229C>T
  hgvsp: ENSP00000362145.4:p.Pro77Ser
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000321348
  ensembl transcript: ENST00000324765
  gene symbol: DIAPH2
  hgvsc: ENST00000324765.8:c.262C>T
  hgvsp: ENSP00000321348.8:p.Pro88Ser
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362140
  ensembl transcript: ENST00000373049
  gene symbol: DIAPH2
  hgvsc: ENST00000373049.4:c.262C>T
  hgvsp: ENSP00000362140.4:p.Pro88Ser
  variant of: http://identifiers.org/hgnc/2877
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: p.Pro88Ser
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum

X-95993697-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24095993697
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24095993697
    reference: chr 0
allele count: 1
allele frequency: 1.142974705969757e-5
allele num: 87491
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362145
  ensembl transcript: ENST00000373054
  gene symbol: DIAPH2
  hgvsc: ENST00000373054.4:c.245T>C
  hgvsp: ENSP00000362145.4:p.Leu82Ser
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000321348
  ensembl transcript: ENST00000324765
  gene symbol: DIAPH2
  hgvsc: ENST00000324765.8:c.278T>C
  hgvsp: ENSP00000321348.8:p.Leu93Ser
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000348082
  ensembl transcript: ENST00000355827
  gene symbol: DIAPH2
  hgvsc: ENST00000355827.4:c.278T>C
  hgvsp: ENSP00000348082.4:p.Leu93Ser
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362140
  ensembl transcript: ENST00000373049
  gene symbol: DIAPH2
  hgvsc: ENST00000373049.4:c.278T>C
  hgvsp: ENSP00000362140.4:p.Leu93Ser
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362152
  ensembl transcript: ENST00000373061
  gene symbol: DIAPH2
  hgvsc: ENST00000373061.3:c.278T>C
  hgvsp: ENSP00000362152.3:p.Leu93Ser
  variant of: http://identifiers.org/hgnc/2877
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 353
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 55
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Leu93Ser
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ

X-95993709-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24095993709
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24095993709
    reference: chr 0
allele count: 2
allele frequency: 2.286053928012162e-5
allele num: 87487
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362140
  ensembl transcript: ENST00000373049
  gene symbol: DIAPH2
  hgvsc: ENST00000373049.4:c.290G>C
  hgvsp: ENSP00000362140.4:p.Arg97Pro
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362145
  ensembl transcript: ENST00000373054
  gene symbol: DIAPH2
  hgvsc: ENST00000373054.4:c.257G>C
  hgvsp: ENSP00000362145.4:p.Arg86Pro
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362152
  ensembl transcript: ENST00000373061
  gene symbol: DIAPH2
  hgvsc: ENST00000373061.3:c.290G>C
  hgvsp: ENSP00000362152.3:p.Arg97Pro
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000348082
  ensembl transcript: ENST00000355827
  gene symbol: DIAPH2
  hgvsc: ENST00000355827.4:c.290G>C
  hgvsp: ENSP00000348082.4:p.Arg97Pro
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000321348
  ensembl transcript: ENST00000324765
  gene symbol: DIAPH2
  hgvsc: ENST00000324765.8:c.290G>C
  hgvsp: ENSP00000321348.8:p.Arg97Pro
  variant of: http://identifiers.org/hgnc/2877
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 416
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Arg97Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: FS
site quality: InbreedingCoeff

X-95993712-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24095993712
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24095993712
    reference: chr 0
allele count: 1
allele frequency: 1.143301397114307e-5
allele num: 87466
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362145
  ensembl transcript: ENST00000373054
  gene symbol: DIAPH2
  hgvsc: ENST00000373054.4:c.260C>T
  hgvsp: ENSP00000362145.4:p.Ser87Phe
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000348082
  ensembl transcript: ENST00000355827
  gene symbol: DIAPH2
  hgvsc: ENST00000355827.4:c.293C>T
  hgvsp: ENSP00000348082.4:p.Ser98Phe
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362140
  ensembl transcript: ENST00000373049
  gene symbol: DIAPH2
  hgvsc: ENST00000373049.4:c.293C>T
  hgvsp: ENSP00000362140.4:p.Ser98Phe
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362152
  ensembl transcript: ENST00000373061
  gene symbol: DIAPH2
  hgvsc: ENST00000373061.3:c.293C>T
  hgvsp: ENSP00000362152.3:p.Ser98Phe
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000321348
  ensembl transcript: ENST00000324765
  gene symbol: DIAPH2
  hgvsc: ENST00000324765.8:c.293C>T
  hgvsp: ENSP00000321348.8:p.Ser98Phe
  variant of: http://identifiers.org/hgnc/2877
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 84
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  variant carriers: 0
hgvs: p.Ser98Phe
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: European (Finnish)
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum

X-95993715-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24095993715
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24095993715
    reference: chr 0
allele count: 2
allele frequency: 2.287021154945683e-5
allele num: 87450
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000321348
  ensembl transcript: ENST00000324765
  gene symbol: DIAPH2
  hgvsc: ENST00000324765.8:c.296T>G
  hgvsp: ENSP00000321348.8:p.Leu99Trp
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362145
  ensembl transcript: ENST00000373054
  gene symbol: DIAPH2
  hgvsc: ENST00000373054.4:c.263T>G
  hgvsp: ENSP00000362145.4:p.Leu88Trp
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362140
  ensembl transcript: ENST00000373049
  gene symbol: DIAPH2
  hgvsc: ENST00000373049.4:c.296T>G
  hgvsp: ENSP00000362140.4:p.Leu99Trp
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000348082
  ensembl transcript: ENST00000355827
  gene symbol: DIAPH2
  hgvsc: ENST00000355827.4:c.296T>G
  hgvsp: ENSP00000348082.4:p.Leu99Trp
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362152
  ensembl transcript: ENST00000373061
  gene symbol: DIAPH2
  hgvsc: ENST00000373061.3:c.296T>G
  hgvsp: ENSP00000362152.3:p.Leu99Trp
  variant of: http://identifiers.org/hgnc/2877
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12130
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 69
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Leu99Trp
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: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff

X-95993767-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24095993767
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24095993767
    reference: chr 0
allele count: 22
allele frequency: 2.579525601791598e-4
allele num: 85287
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000321348
  ensembl transcript: ENST00000324765
  gene symbol: DIAPH2
  hgvsc: ENST00000324765.8:c.342+6T>C
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362140
  ensembl transcript: ENST00000373049
  gene symbol: DIAPH2
  hgvsc: ENST00000373049.4:c.342+6T>C
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362152
  ensembl transcript: ENST00000373061
  gene symbol: DIAPH2
  hgvsc: ENST00000373061.3:c.342+6T>C
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362145
  ensembl transcript: ENST00000373054
  gene symbol: DIAPH2
  hgvsc: ENST00000373054.4:c.309+6T>C
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000348082
  ensembl transcript: ENST00000355827
  gene symbol: DIAPH2
  hgvsc: ENST00000355827.4:c.342+6T>C
  variant of: http://identifiers.org/hgnc/2877
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
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  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 12
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  variant carriers: 0
hgvs: c.342+6T>C
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
reference allele: T
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: DP

X-95993774-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24095993774
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24095993774
    reference: chr 0
allele count: 1
allele frequency: 1.181921331316188e-5
allele num: 84608
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362152
  ensembl transcript: ENST00000373061
  gene symbol: DIAPH2
  hgvsc: ENST00000373061.3:c.342+13C>G
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000321348
  ensembl transcript: ENST00000324765
  gene symbol: DIAPH2
  hgvsc: ENST00000324765.8:c.342+13C>G
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362145
  ensembl transcript: ENST00000373054
  gene symbol: DIAPH2
  hgvsc: ENST00000373054.4:c.309+13C>G
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362140
  ensembl transcript: ENST00000373049
  gene symbol: DIAPH2
  hgvsc: ENST00000373049.4:c.342+13C>G
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000348082
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  gene symbol: DIAPH2
  hgvsc: ENST00000355827.4:c.342+13C>G
  variant of: http://identifiers.org/hgnc/2877
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 5563
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  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

X-95993787-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24095993787
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24095993787
    reference: chr 0
allele count: 1
allele frequency: 1.196959722305344e-5
allele num: 83545
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000348082
  ensembl transcript: ENST00000355827
  gene symbol: DIAPH2
  hgvsc: ENST00000355827.4:c.342+26T>G
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362145
  ensembl transcript: ENST00000373054
  gene symbol: DIAPH2
  hgvsc: ENST00000373054.4:c.309+26T>G
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000321348
  ensembl transcript: ENST00000324765
  gene symbol: DIAPH2
  hgvsc: ENST00000324765.8:c.342+26T>G
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362152
  ensembl transcript: ENST00000373061
  gene symbol: DIAPH2
  hgvsc: ENST00000373061.3:c.342+26T>G
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362140
  ensembl transcript: ENST00000373049
  gene symbol: DIAPH2
  hgvsc: ENST00000373049.4:c.342+26T>G
  variant of: http://identifiers.org/hgnc/2877
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQ

X-95993801-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24095993801
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24095993801
    reference: chr 0
allele count: 1
allele frequency: 1.218486882988705e-5
allele num: 82069
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000321348
  ensembl transcript: ENST00000324765
  gene symbol: DIAPH2
  hgvsc: ENST00000324765.8:c.342+40G>T
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362145
  ensembl transcript: ENST00000373054
  gene symbol: DIAPH2
  hgvsc: ENST00000373054.4:c.309+40G>T
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362152
  ensembl transcript: ENST00000373061
  gene symbol: DIAPH2
  hgvsc: ENST00000373061.3:c.342+40G>T
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362140
  ensembl transcript: ENST00000373049
  gene symbol: DIAPH2
  hgvsc: ENST00000373049.4:c.342+40G>T
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000348082
  ensembl transcript: ENST00000355827
  gene symbol: DIAPH2
  hgvsc: ENST00000355827.4:c.342+40G>T
  variant of: http://identifiers.org/hgnc/2877
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

X-96013104-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24096013104
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24096013104
    reference: chr 0
allele count: 1
allele frequency: 1.517174414370676e-5
allele num: 65912
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362140
  ensembl transcript: ENST00000373049
  gene symbol: DIAPH2
  hgvsc: ENST00000373049.4:c.343-49T>C
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000321348
  ensembl transcript: ENST00000324765
  gene symbol: DIAPH2
  hgvsc: ENST00000324765.8:c.343-49T>C
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362145
  ensembl transcript: ENST00000373054
  gene symbol: DIAPH2
  hgvsc: ENST00000373054.4:c.310-49T>C
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362152
  ensembl transcript: ENST00000373061
  gene symbol: DIAPH2
  hgvsc: ENST00000373061.3:c.343-49T>C
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000348082
  ensembl transcript: ENST00000355827
  gene symbol: DIAPH2
  hgvsc: ENST00000355827.4:c.343-49T>C
  variant of: http://identifiers.org/hgnc/2877
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4129
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2221
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: Other
reference allele: T
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD

X-96013109-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24096013109
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24096013109
    reference: chr 0
allele count: 1
allele frequency: 1.515495946048344e-5
allele num: 65985
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362152
  ensembl transcript: ENST00000373061
  gene symbol: DIAPH2
  hgvsc: ENST00000373061.3:c.343-44A>G
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000348082
  ensembl transcript: ENST00000355827
  gene symbol: DIAPH2
  hgvsc: ENST00000355827.4:c.343-44A>G
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362140
  ensembl transcript: ENST00000373049
  gene symbol: DIAPH2
  hgvsc: ENST00000373049.4:c.343-44A>G
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362145
  ensembl transcript: ENST00000373054
  gene symbol: DIAPH2
  hgvsc: ENST00000373054.4:c.310-44A>G
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000321348
  ensembl transcript: ENST00000324765
  gene symbol: DIAPH2
  hgvsc: ENST00000324765.8:c.343-44A>G
  variant of: http://identifiers.org/hgnc/2877
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15098
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

X-96013110-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24096013110
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24096013110
    reference: chr 0
allele count: 1
allele frequency: 1.515472979116782e-5
allele num: 65986
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000348082
  ensembl transcript: ENST00000355827
  gene symbol: DIAPH2
  hgvsc: ENST00000355827.4:c.343-43G>T
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000321348
  ensembl transcript: ENST00000324765
  gene symbol: DIAPH2
  hgvsc: ENST00000324765.8:c.343-43G>T
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362145
  ensembl transcript: ENST00000373054
  gene symbol: DIAPH2
  hgvsc: ENST00000373054.4:c.310-43G>T
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362140
  ensembl transcript: ENST00000373049
  gene symbol: DIAPH2
  hgvsc: ENST00000373049.4:c.343-43G>T
  variant of: http://identifiers.org/hgnc/2877
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147202
  ensembl protein: ENSP00000362152
  ensembl transcript: ENST00000373061
  gene symbol: DIAPH2
  hgvsc: ENST00000373061.3:c.343-43G>T
  variant of: http://identifiers.org/hgnc/2877
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 6249
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  variant carriers: 0
num of homozygotes: 0
reference allele: G

Latino
type: Population
allele count: 1
allele frequency: 1.27420998980632e-4
allele num: 7848
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 36998
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 492
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3825
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -4.243e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.37e-1

DP
type: SiteQuality
SIO_000300: 1.136776e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.5e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.77e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.64e-1

MQ
type: SiteQuality
SIO_000300: 3.846e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 6.74e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.35e-1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 484
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3767
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5310
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7760
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.85e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.200000000000001e-3

QD
type: SiteQuality
SIO_000300: 7.24e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.31e-1

MQ
type: SiteQuality
SIO_000300: 5.119e1

FS
type: SiteQuality
SIO_000300: 1.856e0

MQRankSum
type: SiteQuality
SIO_000300: -1.123e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.31e-1

DP
type: SiteQuality
SIO_000300: 1.120894e6

VQSLOD
type: SiteQuality
SIO_000300: -1.961e0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 468
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6293
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5014
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.22e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.04e0

DP
type: SiteQuality
SIO_000300: 1.044551e6

MQRankSum
type: SiteQuality
SIO_000300: -1.179e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.21e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.900000000000001e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.526e0

QD
type: SiteQuality
SIO_000300: 7.92e0

MQ
type: SiteQuality
SIO_000300: 4.917e1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5807
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4366
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 29849
num of homozygotes: 0

South Asian
type: Population
allele count: 24
allele frequency: 3.242366927857336e-3
allele num: 7402
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.952e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.18e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.9e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -3.4e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.17e-1

FS
type: SiteQuality
SIO_000300: 1.207e0

QD
type: SiteQuality
SIO_000300: 2.043e1

DP
type: SiteQuality
SIO_000300: 9.23064e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.09e-1

African
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allele count: 0
allele frequency: 0.0e0
allele num: 5056
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 4.040404040404041e-5
allele num: 24750
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6905
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 383
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -4.433e-1

DP
type: SiteQuality
SIO_000300: 8.1828e5

BaseQRankSum
type: SiteQuality
SIO_000300: -2.921e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.28e-2

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.77e-1

QD
type: SiteQuality
SIO_000300: 1.298e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.44e-1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3147
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 2.792516056967327e-4
allele num: 3581
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 282
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2140
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.36e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.73e-1

QD
type: SiteQuality
SIO_000300: 2.999e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.552e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.82e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.0e-1

DP
type: SiteQuality
SIO_000300: 5.85805e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -2.008e0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3294
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2703
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 274
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14514
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -1.84e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.21e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.286e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.41e0

DP
type: SiteQuality
SIO_000300: 5.55617e5

VQSLOD
type: SiteQuality
SIO_000300: -2.569e0

QD
type: SiteQuality
SIO_000300: 1.953e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.408e0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14514
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1910
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2703
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1932
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.21e-2

MQRankSum
type: SiteQuality
SIO_000300: -1.84e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.41e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 5.55617e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.408e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -2.569e0

QD
type: SiteQuality
SIO_000300: 1.953e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.286e0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1133
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2286
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1284
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.5e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.5e-1

DP
type: SiteQuality
SIO_000300: 4.48134e5

BaseQRankSum
type: SiteQuality
SIO_000300: 5.5e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.28e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 5.5e-1

QD
type: SiteQuality
SIO_000300: 8.640000000000001e0

VQSLOD
type: SiteQuality
SIO_000300: -1.621e0

African
type: Population
allele count: 2
allele frequency: 1.005025125628141e-3
allele num: 1990
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.155268022181146e-4
allele num: 8656
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 193
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 6.3832e1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.070000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.37e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.963e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.93e-2

DP
type: SiteQuality
SIO_000300: 4.40059e5

ClippingRankSum
type: SiteQuality
SIO_000300: -1.0e-1

QD
type: SiteQuality
SIO_000300: 6.73e0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1163
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5196
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.070000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.93e-2

DP
type: SiteQuality
SIO_000300: 4.40059e5

FS
type: SiteQuality
SIO_000300: 6.3832e1

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.37e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.0e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -2.963e0

QD
type: SiteQuality
SIO_000300: 6.73e0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7512
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5093
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 177
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.73e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.31e-1

DP
type: SiteQuality
SIO_000300: 3.87509e5

BaseQRankSum
type: SiteQuality
SIO_000300: -1.537e0

MQRankSum
type: SiteQuality
SIO_000300: -2.48e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.6e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.972e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.159e1

GenotypeQuality
all individuals: 74
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 280
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 9.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3422
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 334
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 214
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 275
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 6.596306068601583e-4
allele num: 1516
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 27
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -7.241e-1

QD
type: SiteQuality
SIO_000300: 1.305e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.15e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.596e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.7e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.1e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.799999999999999e-2

DP
type: SiteQuality
SIO_000300: 1.6768e5

GenotypeQuality
all individuals: 81
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 239
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 331
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 949
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 5.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3439
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 4.672897196261682e-3
allele num: 214
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1511
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 276
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 27
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.68321e5

ClippingRankSum
type: SiteQuality
SIO_000300: 5.97e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -9.249000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.245e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.78e-1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.54e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.78e-1

GenotypeQuality
all individuals: 1281
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 401
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 282
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1767
bin: 6.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 509
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5438
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 110
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 75
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 702
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 422
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 5.025125628140704e-4
allele num: 1990
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 8.43e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.453e0

DP
type: SiteQuality
SIO_000300: 3.16508e5

MQRankSum
type: SiteQuality
SIO_000300: 1.1e0

VQSLOD
type: SiteQuality
SIO_000300: -1.769e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.92e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -8.51e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.76e-1

GenotypeQuality
all individuals: 1865
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 285
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 18047
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6164
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 78
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 490
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 704
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 871
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2160
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 7.575757575757576e-3
allele num: 132
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -6.105e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.6e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.49e-1

QD
type: SiteQuality
SIO_000300: 9.65e0

DP
type: SiteQuality
SIO_000300: 3.46774e5

BaseQRankSum
type: SiteQuality
SIO_000300: -1.741e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.25e-2

FS
type: SiteQuality
SIO_000300: 1.901e0

MQ
type: SiteQuality
SIO_000300: 5.911e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.33e-1

GenotypeQuality
all individuals: 570
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 509
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 292
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 223
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4652
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 887
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2792
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1678
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 311
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 9.767532721234616e-5
allele num: 10238
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1615
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 115
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.56e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 4.52e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.901e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.02e-1

DP
type: SiteQuality
SIO_000300: 4.48232e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.1e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -2.28e-1

QD
type: SiteQuality
SIO_000300: 7.81e0

GenotypeQuality
all individuals: 326
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 207
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 294
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 322
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11440
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3007
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1896
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 125
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1912
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 991
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 361
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.097e1

MQRankSum
type: SiteQuality
SIO_000300: 5.5e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.370000000000001e-1

DP
type: SiteQuality
SIO_000300: 4.73942e5

ClippingRankSum
type: SiteQuality
SIO_000300: -5.5e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.370000000000001e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.26e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.23e0

GenotypeQuality
all individuals: 161
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 531
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 184
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 178
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 237
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 296
bin: 9.75e1
variant carriers: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 140
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 6.341154090044388e-4
allele num: 3154
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12355
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2073
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 421
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1089
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2185
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 4.94695e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.44e0

MQRankSum
type: SiteQuality
SIO_000300: 8.25e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.94e0

QD
type: SiteQuality
SIO_000300: 4.23e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.11e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.43e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.606e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 167
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 188
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14119
bin: 7.5e0
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GenotypeQuality
all individuals: 675
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variant carriers: 0

GenotypeQuality
all individuals: 553
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 296
bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1162
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2237
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 7.63708568810142e-5
allele num: 13094
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3268
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 445
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2390
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 148
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 5.06291e5

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.17e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.96e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.43e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.532e0

QD
type: SiteQuality
SIO_000300: 6.68e0

VQSLOD
type: SiteQuality
SIO_000300: -1.979e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.66e-1

GenotypeQuality
all individuals: 199
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6393
bin: 6.25e1
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GenotypeQuality
all individuals: 261
bin: 5.75e1
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GenotypeQuality
all individuals: 297
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variant carriers: 1

GenotypeQuality
all individuals: 62
bin: 9.25e1
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GenotypeQuality
all individuals: 392
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variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1172
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13306
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2437
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2291
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 3.028467595396729e-4
allele num: 3302
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 152
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 472
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.65e-1

QD
type: SiteQuality
SIO_000300: 7.84e0

VQSLOD
type: SiteQuality
SIO_000300: -5.048e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.65e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.83e-2

DP
type: SiteQuality
SIO_000300: 5.10981e5

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.65e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 13713
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 266
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 192
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1188
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 3.008423586040915e-4
allele num: 3324
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 153
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13406
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2470
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 468
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2304
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 2.991e1

DP
type: SiteQuality
SIO_000300: 5.15691e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.46e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.75e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.92e-2

MQ
type: SiteQuality
SIO_000300: 5.871e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.4e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.81e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.4e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28844
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1025
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4039
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4219
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 18888
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3279
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 796
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 202
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.91e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 6.18092e5

VQSLOD
type: SiteQuality
SIO_000300: 3.11e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.829e1

GenotypeQuality
all individuals: 421
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 299
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 181
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variant carriers: 0

GenotypeQuality
all individuals: 299
bin: 9.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4285
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3358
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1712
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4123
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 804
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 19269
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 207
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.91e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 3.82e0

QD
type: SiteQuality
SIO_000300: 1.33e1

DP
type: SiteQuality
SIO_000300: 6.132e5

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 2460
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variant carriers: 1

GenotypeQuality
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bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 64
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variant carriers: 2

GenotypeQuality
all individuals: 161
bin: 7.25e1
variant carriers: 1

Latino
type: Population
allele count: 2
allele frequency: 4.752851711026616e-4
allele num: 4208
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 18936
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3413
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 719
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1707
num of homozygotes: 0

African
type: Population
allele count: 24
allele frequency: 5.952380952380952e-3
allele num: 4032
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 5.025125628140704e-3
allele num: 199
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 4.35e0

MQ
type: SiteQuality
SIO_000300: 5.139e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.73e-1

DP
type: SiteQuality
SIO_000300: 5.1104e5

ClippingRankSum
type: SiteQuality
SIO_000300: 4.06e-1

FS
type: SiteQuality
SIO_000300: 3.139e0

VQSLOD
type: SiteQuality
SIO_000300: 7.64e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.431e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.98e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.51e-2

GenotypeQuality
all individuals: 295
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2345
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 45
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variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 18041
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4063
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3286
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3832
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1619
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 185
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 639
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.434e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.05e-2

DP
type: SiteQuality
SIO_000300: 4.90041e5

VQSLOD
type: SiteQuality
SIO_000300: 4.46e0

GenotypeQuality
all individuals: 13070
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1028
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 44
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variant carriers: 0

GenotypeQuality
all individuals: 2043
bin: 3.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3779
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 17045
num of homozygotes: 0

African
type: Population
allele count: 4
allele frequency: 1.104972375690608e-3
allele num: 3620
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 575
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3101
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1521
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.31e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.561e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.39e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.48e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.31e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.48e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.619e-1

DP
type: SiteQuality
SIO_000300: 4.84675e5

FS
type: SiteQuality
SIO_000300: 8.31e-1

GenotypeQuality
all individuals: 1655
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variant carriers: 0

GenotypeQuality
all individuals: 3051
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 150
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GenotypeQuality
all individuals: 102
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1545
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3664
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 17268
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 173
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3132
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 601
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 7.921837866385001e-4
allele num: 3787
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.94e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.379999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.658e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -7.199999999999999e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.24e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.93e-1

DP
type: SiteQuality
SIO_000300: 4.8592e5

QD
type: SiteQuality
SIO_000300: 7.64e0

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: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3103
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3731
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3607
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 2.973889252364242e-4
allele num: 16813
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1518
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 584
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.45e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 7.09e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.67e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.04e-1

MQRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.498e1

DP
type: SiteQuality
SIO_000300: 4.8561e5

BaseQRankSum
type: SiteQuality
SIO_000300: 2.48e-1

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6570
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10048
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4524
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European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.091044058298308e-5
allele num: 47823
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8419
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: -2.024e0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.46e-1

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 3.892e0

DP
type: SiteQuality
SIO_000300: 4.313334e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.15e-1

QD
type: SiteQuality
SIO_000300: 1.407e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.105e0

MQ
type: SiteQuality
SIO_000300: 5.39e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 93
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GenotypeQuality
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GenotypeQuality
all individuals: 54
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GenotypeQuality
all individuals: 1185
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 2
allele frequency: 2.372760707082691e-4
allele num: 8429
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47821
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6570
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10033
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9315
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.592e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.5e-3

MQ
type: SiteQuality
SIO_000300: 5.956e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.257e0

QD
type: SiteQuality
SIO_000300: 1.263e1

VQSLOD
type: SiteQuality
SIO_000300: 2.34e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.28e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.34e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.38e-1

DP
type: SiteQuality
SIO_000300: 4.316787e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 226
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GenotypeQuality
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bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 1266
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GenotypeQuality
all individuals: 405
bin: 2.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9302
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: 1
allele frequency: 1.185817621249852e-4
allele num: 8433
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.093670833071625e-5
allele num: 47763
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 4.568991775814804e-4
allele num: 6566
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9947
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4523
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.37e-1

MQ
type: SiteQuality
SIO_000300: 6.014e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.395e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.75e-1

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.402e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.96e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.22e-1

DP
type: SiteQuality
SIO_000300: 4.326009e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1167
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GenotypeQuality
all individuals: 47663
bin: 9.75e1
variant carriers: 1

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47763
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 1.005328239670252e-4
allele num: 9947
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4523
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9302
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.75e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.22e-1

QD
type: SiteQuality
SIO_000300: 1.402e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.014e1

VQSLOD
type: SiteQuality
SIO_000300: 3.56e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.395e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.96e-1

DP
type: SiteQuality
SIO_000300: 4.326009e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.37e-1

GenotypeQuality
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bin: 7.25e1
variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 17

GenotypeQuality
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bin: 5.75e1
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: 6566
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9302
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47763
num of homozygotes: 0

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

South Asian
type: Population
allele count: 21
allele frequency: 2.11118930330753e-3
allele num: 9947
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4523
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.75e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.96e-1

QD
type: SiteQuality
SIO_000300: 1.402e1

MQ
type: SiteQuality
SIO_000300: 6.014e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.22e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.56e0

DP
type: SiteQuality
SIO_000300: 4.326009e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.37e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.395e-1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8451
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 47868
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6607
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9315
num of homozygotes: 0

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

South Asian
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allele count: 1
allele frequency: 9.963136395337252e-5
allele num: 10037
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 4.325993e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.12e0

QD
type: SiteQuality
SIO_000300: 1.824e1

MQRankSum
type: SiteQuality
SIO_000300: -8.83e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.78e-2

FS
type: SiteQuality
SIO_000300: 1.0555e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.746e0

VQSLOD
type: SiteQuality
SIO_000300: -9.964e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.245e0

MQ
type: SiteQuality
SIO_000300: 5.803e1

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47868
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9315
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8451
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.513546238837597e-4
allele num: 6607
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.0555e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.245e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.78e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.746e0

DP
type: SiteQuality
SIO_000300: 4.325993e6

QD
type: SiteQuality
SIO_000300: 1.824e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.12e0

MQRankSum
type: SiteQuality
SIO_000300: -8.83e-1

VQSLOD
type: SiteQuality
SIO_000300: -9.964e-1

MQ
type: SiteQuality
SIO_000300: 5.803e1

GenotypeQuality
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bin: 8.25e1
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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bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47868
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8451
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9315
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6607
num of homozygotes: 0

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: -8.83e-1

FS
type: SiteQuality
SIO_000300: 1.0555e1

VQSLOD
type: SiteQuality
SIO_000300: -9.964e-1

MQ
type: SiteQuality
SIO_000300: 5.803e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.746e0

QD
type: SiteQuality
SIO_000300: 1.824e1

DP
type: SiteQuality
SIO_000300: 4.325993e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.12e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.78e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.245e0

GenotypeQuality
all individuals: 1570
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 29
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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6621
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10034
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9315
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8459
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4527
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: 2
allele frequency: 4.176760504552669e-5
allele num: 47884
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -1.909e0

FS
type: SiteQuality
SIO_000300: 1.077e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.116e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.19e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.362e0

QD
type: SiteQuality
SIO_000300: 6.67e0

DP
type: SiteQuality
SIO_000300: 4.326965e6

MQ
type: SiteQuality
SIO_000300: 5.308e1

VQSLOD
type: SiteQuality
SIO_000300: -2.715e0

GenotypeQuality
all individuals: 5050
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6626
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4528
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: 8473
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.176237210273544e-5
allele num: 47890
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10029
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.616e0

FS
type: SiteQuality
SIO_000300: 4.5148e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.321e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.45e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.592e0

MQ
type: SiteQuality
SIO_000300: 5.295e1

DP
type: SiteQuality
SIO_000300: 4.327699e6

MQRankSum
type: SiteQuality
SIO_000300: -2.704e0

QD
type: SiteQuality
SIO_000300: 2.79e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 821
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6631
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 6.267103971254883e-5
allele num: 47869
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8475
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9315
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10023
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.916e0

ReadPosRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 2.0065e1

MQ
type: SiteQuality
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DP
type: SiteQuality
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VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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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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variant carriers: 3

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: 6637
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 10000
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9318
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 2
allele frequency: 4.176586058555736e-5
allele num: 47886
num of homozygotes: 0

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

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

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

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

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

European (Finnish)
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allele frequency: 0.0e0
allele num: 4529
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African
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Latino
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allele frequency: 0.0e0
allele num: 9318
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 9997
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European (Non-Finnish)
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allele count: 1
allele frequency: 2.088162208440352e-5
allele num: 47889
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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MQ
type: SiteQuality
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FS
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 4.328158e6

ClippingRankSum
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VQSLOD
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 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 num: 631
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Latino
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African
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 2.088293029277868e-5
allele num: 47886
num of homozygotes: 0

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

South Asian
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allele count: 1
allele frequency: 1.003009027081244e-4
allele num: 9970
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.162e0

ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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MQ
type: SiteQuality
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FS
type: SiteQuality
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MQRankSum
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BaseQRankSum
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ClippingRankSum
type: SiteQuality
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QD
type: SiteQuality
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.462599247806101e-4
allele num: 47860
num of homozygotes: 0

South Asian
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Other
type: Population
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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East Asian
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
allele num: 9319
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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FS
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QD
type: SiteQuality
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DP
type: SiteQuality
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ClippingRankSum
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SIO_000300: -4.89e-1

MQ
type: SiteQuality
SIO_000300: 5.946e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.402e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.03e-1

GenotypeQuality
all individuals: 1325
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 786
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1356
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 875
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47879
bin: 9.75e1
variant carriers: 1

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: 9818
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: 47858
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6637
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: 1
allele frequency: 1.175502527330434e-4
allele num: 8507
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.49e-1

DP
type: SiteQuality
SIO_000300: 4.314682e6

FS
type: SiteQuality
SIO_000300: 3.317e0

QD
type: SiteQuality
SIO_000300: 1.333e1

VQSLOD
type: SiteQuality
SIO_000300: 1.37e0

MQRankSum
type: SiteQuality
SIO_000300: 4.8e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 6.53e0

MQ
type: SiteQuality
SIO_000300: 5.929e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.13e-1

GenotypeQuality
all individuals: 3710
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47878
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 50
bin: 5.25e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.506704836522525e-4
allele num: 6637
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: 47833
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: 8506
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9715
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 627
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.973e1

MQRankSum
type: SiteQuality
SIO_000300: -3.24e-1

DP
type: SiteQuality
SIO_000300: 4.304438e6

QD
type: SiteQuality
SIO_000300: 9.41e0

FS
type: SiteQuality
SIO_000300: 9.395e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.321e0

VQSLOD
type: SiteQuality
SIO_000300: -5.546e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.37e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 4.9e-1

GenotypeQuality
all individuals: 748
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 70
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 750
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47878
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8505
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.092750711535242e-5
allele num: 47784
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: 6637
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9565
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.4e-3

QD
type: SiteQuality
SIO_000300: 1.341e1

VQSLOD
type: SiteQuality
SIO_000300: 3.57e-1

MQ
type: SiteQuality
SIO_000300: 5.981e1

MQRankSum
type: SiteQuality
SIO_000300: 1.39e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.685e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.56e0

DP
type: SiteQuality
SIO_000300: 4.28941e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.983e0

GenotypeQuality
all individuals: 781
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1084
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 873
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 243
bin: 4.25e1
variant carriers: 0

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

African
type: Population
allele count: 4
allele frequency: 4.703668861712136e-4
allele num: 8504
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9315
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47719
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 624
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: 9379
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 4.283557e6

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.4e-3

MQRankSum
type: SiteQuality
SIO_000300: -7.919e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.8e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.7e0

MQ
type: SiteQuality
SIO_000300: 5.11e1

VQSLOD
type: SiteQuality
SIO_000300: 6.51e-1

QD
type: SiteQuality
SIO_000300: 1.067e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.56e-1

GenotypeQuality
all individuals: 935
bin: 8.25e1
variant carriers: 51

GenotypeQuality
all individuals: 882
bin: 7.75e1
variant carriers: 52

GenotypeQuality
all individuals: 708
bin: 8.75e1
variant carriers: 40

GenotypeQuality
all individuals: 827
bin: 6.75e1
variant carriers: 45

GenotypeQuality
all individuals: 1015
bin: 2.25e1
variant carriers: 81

African
type: Population
allele count: 1596
allele frequency: 1.877647058823529e-1
allele num: 8500
num of homozygotes: 103

South Asian
type: Population
allele count: 2276
allele frequency: 2.435266424138669e-1
allele num: 9346
num of homozygotes: 125

Latino
type: Population
allele count: 3310
allele frequency: 3.556845046206749e-1
allele num: 9306
num of homozygotes: 496

European (Non-Finnish)
type: Population
allele count: 9076
allele frequency: 1.903483567878191e-1
allele num: 47681
num of homozygotes: 552

East Asian
type: Population
allele count: 2224
allele frequency: 3.357994866374754e-1
allele num: 6623
num of homozygotes: 256

European (Finnish)
type: Population
allele count: 782
allele frequency: 1.727413297989839e-1
allele num: 4527
num of homozygotes: 37

Other
type: Population
allele count: 138
allele frequency: 2.211538461538461e-1
allele num: 624
num of homozygotes: 12

MQ
type: SiteQuality
SIO_000300: 5.969e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.948e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.46e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.006e1

QD
type: SiteQuality
SIO_000300: 2.05e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.02e-1

DP
type: SiteQuality
SIO_000300: 5.168736e6

MQRankSum
type: SiteQuality
SIO_000300: 9.8e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.572e-1

GenotypeQuality
all individuals: 1147
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49225
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1002
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 424
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 887
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8496
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: 9315
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9329
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 623
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.096304215667778e-5
allele num: 47703
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.914e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 2.91e-1

DP
type: SiteQuality
SIO_000300: 5.121961e6

QD
type: SiteQuality
SIO_000300: 2.634e1

GenotypeQuality
all individuals: 1331
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 477
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 230
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2598
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1157
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4095
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 24767
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.675322499581169e-4
allele num: 5969
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3109
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5613
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 389
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3479
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.67e-2

QD
type: SiteQuality
SIO_000300: 1.348e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.44e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.22e0

MQRankSum
type: SiteQuality
SIO_000300: -7.97e-1

VQSLOD
type: SiteQuality
SIO_000300: -8.169999999999999e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.199e0

MQ
type: SiteQuality
SIO_000300: 5.972e1

DP
type: SiteQuality
SIO_000300: 7.44978e5

GenotypeQuality
all individuals: 288
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 170
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 228
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1186
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 484
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.050222762251924e-5
allele num: 24690
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3465
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4079
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5603
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3099
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5945
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 388
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.763e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.65e-2

VQSLOD
type: SiteQuality
SIO_000300: -7.501e-1

QD
type: SiteQuality
SIO_000300: 2.208e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 7.55939e5

GenotypeQuality
all individuals: 434
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2009
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 211
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 642
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 492
bin: 7.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 387
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5954
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.784758165268606e-4
allele num: 5603
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4101
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3105
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 24861
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3483
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.916e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 7.65611e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.902e0

MQRankSum
type: SiteQuality
SIO_000300: -4.65e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.64e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.425e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.626e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.65e-1

GenotypeQuality
all individuals: 23052
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 282
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 239
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2810
bin: 2.75e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 420
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6657
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4423
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6421
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 2.167316861725184e-4
allele num: 4614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 28807
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3394
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.77e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.83e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.699999999999999e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.62e0

VQSLOD
type: SiteQuality
SIO_000300: -2.759e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.09e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.76e1

DP
type: SiteQuality
SIO_000300: 9.67129e5

GenotypeQuality
all individuals: 343
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 361
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 399
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 759
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 321
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 225
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1164
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28075
bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3837
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 498
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.795795124133303e-5
allele num: 35768
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6281
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5416
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7223
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7844
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.02e-1

MQ
type: SiteQuality
SIO_000300: 5.956e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.22e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.17e-1

QD
type: SiteQuality
SIO_000300: 8.369999999999999e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.2e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.974e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.160298e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.79e-1

GenotypeQuality
all individuals: 14670
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 410
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 793
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 463
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 330
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 669
bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7448
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.766472354707649e-4
allele num: 5661
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 38128
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7060
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 527
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3997
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.56e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.11e0

VQSLOD
type: SiteQuality
SIO_000300: 9.57e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.4e0

DP
type: SiteQuality
SIO_000300: 1.22379e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.25e0

FS
type: SiteQuality
SIO_000300: 1.288e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.361e1

GenotypeQuality
all individuals: 345
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 855
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2093
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 284
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 485
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 504
bin: 5.75e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4181
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8514
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.232437761893024e-4
allele num: 8114
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 40785
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7755
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5948
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 561
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.293763e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.68e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.64e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.91e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.6e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.43e-2

QD
type: SiteQuality
SIO_000300: 2.971e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.8e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 43922
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 523
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 298
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 347
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 400
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9032
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8333
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 45376
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.566416040100251e-4
allele num: 6384
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 610
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4428
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9578
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -9.27e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.697e0

QD
type: SiteQuality
SIO_000300: 1.23e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.17e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.25e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.39e0

FS
type: SiteQuality
SIO_000300: 1.0232e1

MQ
type: SiteQuality
SIO_000300: 5.974e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.9e-3

DP
type: SiteQuality
SIO_000300: 1.429186e6

GenotypeQuality
all individuals: 352
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1425
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47813
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 426
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 210
bin: 4.75e1
variant carriers: 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: 625
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.687977381103093e-4
allele num: 47394
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 2.00300450676014e-4
allele num: 9985
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9248
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4507
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.27e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.956e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.24e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.04e-1

DP
type: SiteQuality
SIO_000300: 1.492005e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.5e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.733e0

MQRankSum
type: SiteQuality
SIO_000300: -8.799999999999999e-2

QD
type: SiteQuality
SIO_000300: 1.815e1

GenotypeQuality
all individuals: 101
bin: 2.75e1
variant carriers: 2

GenotypeQuality
all individuals: 84
bin: 5.75e1
variant carriers: 4

GenotypeQuality
all individuals: 2551
bin: 9.75e1
variant carriers: 488

GenotypeQuality
all individuals: 865
bin: 8.25e1
variant carriers: 13

GenotypeQuality
all individuals: 891
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 435
bin: 9.25e1
variant carriers: 19

Other
type: Population
allele count: 5
allele frequency: 7.987220447284345e-3
allele num: 626
num of homozygotes: 0

Latino
type: Population
allele count: 24
allele frequency: 2.593473092716663e-3
allele num: 9254
num of homozygotes: 0

African
type: Population
allele count: 13
allele frequency: 1.534647621296187e-3
allele num: 8471
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6587
num of homozygotes: 0

South Asian
type: Population
allele count: 17
allele frequency: 1.7001700170017e-3
allele num: 9999
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 484
allele frequency: 1.019956588624534e-2
allele num: 47453
num of homozygotes: 1

European (Finnish)
type: Population
allele count: 34
allele frequency: 7.53880266075388e-3
allele num: 4510
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.31e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.252e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.563e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.33e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.169999999999999e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.905e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.13e0

DP
type: SiteQuality
SIO_000300: 1.519275e6

GenotypeQuality
all individuals: 843
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2172
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4365
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 441
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4510
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
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: 47493
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10008
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9252
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 1.12e0

VQSLOD
type: SiteQuality
SIO_000300: 8.94e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.5e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -3.53e-1

DP
type: SiteQuality
SIO_000300: 1.502431e6

FS
type: SiteQuality
SIO_000300: 2.5e0

MQ
type: SiteQuality
SIO_000300: 5.929e1

QD
type: SiteQuality
SIO_000300: 1.336e1

MQRankSum
type: SiteQuality
SIO_000300: 9.1e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.47e-1

GenotypeQuality
all individuals: 1202
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2180
bin: 9.75e1
variant carriers: 9

GenotypeQuality
all individuals: 4396
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1429
bin: 7.75e1
variant carriers: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47532
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.080030240846744e-4
allele num: 9259
num of homozygotes: 0

African
type: Population
allele count: 9
allele frequency: 1.060945420252269e-3
allele num: 8483
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6603
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10023
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.91e-2

FS
type: SiteQuality
SIO_000300: 5.600000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.556e1

MQRankSum
type: SiteQuality
SIO_000300: -1.33e-1

MQ
type: SiteQuality
SIO_000300: 5.967e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.55e0

VQSLOD
type: SiteQuality
SIO_000300: 2.73e0

DP
type: SiteQuality
SIO_000300: 1.504897e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.87e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.13e-1

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 56
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variant carriers: 0

GenotypeQuality
all individuals: 96
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variant carriers: 0

GenotypeQuality
all individuals: 90
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variant carriers: 0

GenotypeQuality
all individuals: 48477
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variant carriers: 0

GenotypeQuality
all individuals: 1448
bin: 7.75e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 1
allele frequency: 2.216312056737589e-4
allele num: 4512
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9271
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47601
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: 7.9e-2

FS
type: SiteQuality
SIO_000300: 5.041e0

QD
type: SiteQuality
SIO_000300: 1.626e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.2e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.2e0

MQ
type: SiteQuality
SIO_000300: 5.971e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.26e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.47e-1

DP
type: SiteQuality
SIO_000300: 1.505569e6

MQRankSum
type: SiteQuality
SIO_000300: 1.81e-1

GenotypeQuality
all individuals: 55
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 887
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variant carriers: 0

GenotypeQuality
all individuals: 4464
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variant carriers: 0

GenotypeQuality
all individuals: 2179
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variant carriers: 3

GenotypeQuality
all individuals: 48825
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variant carriers: 0

GenotypeQuality
all individuals: 355
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.509433962264151e-4
allele num: 6625
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47741
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.355435166647038e-4
allele num: 8491
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: 627
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.69e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.88e-2

DP
type: SiteQuality
SIO_000300: 1.51088e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.921e0

QD
type: SiteQuality
SIO_000300: 1.689e1

VQSLOD
type: SiteQuality
SIO_000300: -4.436e-1

FS
type: SiteQuality
SIO_000300: 1.918e0

MQRankSum
type: SiteQuality
SIO_000300: -1.017e0

MQ
type: SiteQuality
SIO_000300: 5.912e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.252e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2174
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GenotypeQuality
all individuals: 49
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variant carriers: 0

GenotypeQuality
all individuals: 55
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variant carriers: 0

GenotypeQuality
all individuals: 1215
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GenotypeQuality
all individuals: 440
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.1768859597505e-4
allele num: 8497
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9296
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4519
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47836
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -2.016e0

FS
type: SiteQuality
SIO_000300: 1.266e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.11e-2

QD
type: SiteQuality
SIO_000300: 2.073e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.36e0

MQRankSum
type: SiteQuality
SIO_000300: -1.075e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.84e0

DP
type: SiteQuality
SIO_000300: 1.514558e6

VQSLOD
type: SiteQuality
SIO_000300: -1.399e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 1210
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 69
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GenotypeQuality
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GenotypeQuality
all individuals: 353
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GenotypeQuality
all individuals: 49021
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 438
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47845
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9297
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8497
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4521
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6628
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.985900109224506e-4
allele num: 10071
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.03e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.34e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.93e-1

QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 1.22e0

VQSLOD
type: SiteQuality
SIO_000300: -1.742e0

DP
type: SiteQuality
SIO_000300: 1.515232e6

MQ
type: SiteQuality
SIO_000300: 5.937e1

FS
type: SiteQuality
SIO_000300: 3.462e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.81e-2

GenotypeQuality
all individuals: 48992
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 438
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 892
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GenotypeQuality
all individuals: 353
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.945300845350572e-5
allele num: 10055
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9299
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47838
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8490
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4522
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 2.805e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.28e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -3.28e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.305e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.21e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.65e-2

DP
type: SiteQuality
SIO_000300: 1.514696e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.66e-1

GenotypeQuality
all individuals: 425
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 3.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 4460
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 892
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10042
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 3.01568154402895e-4
allele num: 6632
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9301
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47835
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8490
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: 4522
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.19e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.0e-1

QD
type: SiteQuality
SIO_000300: 1.398e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.659999999999999e-1

DP
type: SiteQuality
SIO_000300: 1.514159e6

MQRankSum
type: SiteQuality
SIO_000300: 9.98e-1

FS
type: SiteQuality
SIO_000300: 7.351e0

MQ
type: SiteQuality
SIO_000300: 5.976e1

VQSLOD
type: SiteQuality
SIO_000300: 4.76e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

GenotypeQuality
all individuals: 279
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 439
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1367
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 622
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 870
bin: 8.25e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 1
allele frequency: 2.219755826859046e-4
allele num: 4505
num of homozygotes: 0

African
type: Population
allele count: 5
allele frequency: 6.031363088057901e-4
allele num: 8290
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 14
allele frequency: 2.968302766882222e-4
allele num: 47165
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6593
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 2.161461147735869e-4
allele num: 9253
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 612
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8869
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 2.086e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.8e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.93e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.47e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.91e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.115e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.49e0

FS
type: SiteQuality
SIO_000300: 1.42e0

DP
type: SiteQuality
SIO_000300: 1.446915e6

GenotypeQuality
all individuals: 863
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2179
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1124
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3969
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 439
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46906
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.21256214380987e-4
allele num: 8247
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9225
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 610
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4495
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6570
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8555
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 8.023e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.05e0

VQSLOD
type: SiteQuality
SIO_000300: 9.7e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.6e-3

DP
type: SiteQuality
SIO_000300: 1.419185e6

MQRankSum
type: SiteQuality
SIO_000300: 4.04e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.04e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.45e-1

QD
type: SiteQuality
SIO_000300: 1.175e1

GenotypeQuality
all individuals: 34785
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 239
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 347
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 323
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 855
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4484
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9184
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8127
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6539
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 603
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46539
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.239310943115628e-4
allele num: 8069
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.47e-1

DP
type: SiteQuality
SIO_000300: 1.349989e6

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.3e-3

QD
type: SiteQuality
SIO_000300: 3.154e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 439
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1064
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6713
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3300
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2735
bin: 2.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9136
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6484
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4466
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.176325926570763e-5
allele num: 45949
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 588
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7966
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.8e-1

DP
type: SiteQuality
SIO_000300: 1.278008e6

FS
type: SiteQuality
SIO_000300: 2.012e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.338e0

VQSLOD
type: SiteQuality
SIO_000300: -1.087e0

MQRankSum
type: SiteQuality
SIO_000300: -1.639e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 3.4e-1

QD
type: SiteQuality
SIO_000300: 1.697e1

GenotypeQuality
all individuals: 2482
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 955
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3581
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 446
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6618
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.75148580233326e-5
allele num: 36344
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7218
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4706
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3977
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5026
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8164
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 477
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.063302e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.7e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 4.45e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.02e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.26e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.33e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.9e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.132e1

GenotypeQuality
all individuals: 2065
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 928
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9418
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 577
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 247
bin: 5.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3985
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5032
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8168
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4719
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7232
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 477
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.749367645441549e-5
allele num: 36372
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.22e0

QD
type: SiteQuality
SIO_000300: 2.059e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -4.36e-1

DP
type: SiteQuality
SIO_000300: 1.080496e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.19e0

VQSLOD
type: SiteQuality
SIO_000300: -1.828e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.45e-1