X-70472494-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24070472494
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24070472494
    reference: chr 0
allele count: 1
allele frequency: 1.342930812204555e-5
allele num: 74464
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363094
  ensembl transcript: ENST00000373982
  gene symbol: ZMYM3
  hgvsc: ENST00000373982.1:c.612C>T
  hgvsp: ENST00000373982.1:c.612C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363110
  ensembl transcript: ENST00000373998
  gene symbol: ZMYM3
  hgvsc: ENST00000373998.1:c.612C>T
  hgvsp: ENST00000373998.1:c.612C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363090
  ensembl transcript: ENST00000373978
  gene symbol: ZMYM3
  hgvsc: ENST00000373978.1:c.612C>T
  hgvsp: ENST00000373978.1:c.612C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363096
  ensembl transcript: ENST00000373984
  gene symbol: ZMYM3
  hgvsc: ENST00000373984.3:c.612C>T
  hgvsp: ENST00000373984.3:c.612C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000322845
  ensembl transcript: ENST00000314425
  gene symbol: ZMYM3
  hgvsc: ENST00000314425.5:c.612C>T
  hgvsp: ENST00000314425.5:c.612C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000343909
  ensembl transcript: ENST00000353904
  gene symbol: ZMYM3
  hgvsc: ENST00000353904.2:c.612C>T
  hgvsp: ENST00000353904.2:c.612C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147130
  ensembl transcript: ENST00000489332
  gene symbol: ZMYM3
  hgvsc: ENST00000489332.1:n.730C>T
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363100
  ensembl transcript: ENST00000373988
  gene symbol: ZMYM3
  hgvsc: ENST00000373988.1:c.612C>T
  hgvsp: ENST00000373988.1:c.612C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363093
  ensembl transcript: ENST00000373981
  gene symbol: ZMYM3
  hgvsc: ENST00000373981.1:c.612C>T
  hgvsp: ENST00000373981.1:c.612C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31361
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6825
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1558
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3395
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3841
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3197
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9172
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 216
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 258
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7712
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Asn204Asn
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQ

X-70472501-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24070472501
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24070472501
    reference: chr 0
allele count: 1
allele frequency: 1.332764687066851e-5
allele num: 75032
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363100
  ensembl transcript: ENST00000373988
  gene symbol: ZMYM3
  hgvsc: ENST00000373988.1:c.605G>C
  hgvsp: ENSP00000363100.1:p.Gly202Ala
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000322845
  ensembl transcript: ENST00000314425
  gene symbol: ZMYM3
  hgvsc: ENST00000314425.5:c.605G>C
  hgvsp: ENSP00000322845.5:p.Gly202Ala
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000343909
  ensembl transcript: ENST00000353904
  gene symbol: ZMYM3
  hgvsc: ENST00000353904.2:c.605G>C
  hgvsp: ENSP00000343909.2:p.Gly202Ala
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363110
  ensembl transcript: ENST00000373998
  gene symbol: ZMYM3
  hgvsc: ENST00000373998.1:c.605G>C
  hgvsp: ENSP00000363110.1:p.Gly202Ala
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363094
  ensembl transcript: ENST00000373982
  gene symbol: ZMYM3
  hgvsc: ENST00000373982.1:c.605G>C
  hgvsp: ENSP00000363094.1:p.Gly202Ala
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363090
  ensembl transcript: ENST00000373978
  gene symbol: ZMYM3
  hgvsc: ENST00000373978.1:c.605G>C
  hgvsp: ENSP00000363090.1:p.Gly202Ala
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363093
  ensembl transcript: ENST00000373981
  gene symbol: ZMYM3
  hgvsc: ENST00000373981.1:c.605G>C
  hgvsp: ENSP00000363093.1:p.Gly202Ala
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147130
  ensembl transcript: ENST00000489332
  gene symbol: ZMYM3
  hgvsc: ENST00000489332.1:n.723G>C
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363096
  ensembl transcript: ENST00000373984
  gene symbol: ZMYM3
  hgvsc: ENST00000373984.3:c.605G>C
  hgvsp: ENSP00000363096.3:p.Gly202Ala
  variant of: http://identifiers.org/hgnc/13054
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9473
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3740
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1609
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6552
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3120
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31636
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3411
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35462
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 256
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 777
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 286
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Gly202Ala
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

X-70472508-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24070472508
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24070472508
    reference: chr 0
allele count: 1
allele frequency: 1.319713886029509e-5
allele num: 75774
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000343909
  ensembl transcript: ENST00000353904
  gene symbol: ZMYM3
  hgvsc: ENST00000353904.2:c.598G>A
  hgvsp: ENSP00000343909.2:p.Gly200Arg
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363093
  ensembl transcript: ENST00000373981
  gene symbol: ZMYM3
  hgvsc: ENST00000373981.1:c.598G>A
  hgvsp: ENSP00000363093.1:p.Gly200Arg
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363090
  ensembl transcript: ENST00000373978
  gene symbol: ZMYM3
  hgvsc: ENST00000373978.1:c.598G>A
  hgvsp: ENSP00000363090.1:p.Gly200Arg
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147130
  ensembl transcript: ENST00000489332
  gene symbol: ZMYM3
  hgvsc: ENST00000489332.1:n.716G>A
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363100
  ensembl transcript: ENST00000373988
  gene symbol: ZMYM3
  hgvsc: ENST00000373988.1:c.598G>A
  hgvsp: ENSP00000363100.1:p.Gly200Arg
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363096
  ensembl transcript: ENST00000373984
  gene symbol: ZMYM3
  hgvsc: ENST00000373984.3:c.598G>A
  hgvsp: ENSP00000363096.3:p.Gly200Arg
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000322845
  ensembl transcript: ENST00000314425
  gene symbol: ZMYM3
  hgvsc: ENST00000314425.5:c.598G>A
  hgvsp: ENSP00000322845.5:p.Gly200Arg
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363110
  ensembl transcript: ENST00000373998
  gene symbol: ZMYM3
  hgvsc: ENST00000373998.1:c.598G>A
  hgvsp: ENSP00000363110.1:p.Gly200Arg
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363094
  ensembl transcript: ENST00000373982
  gene symbol: ZMYM3
  hgvsc: ENST00000373982.1:c.598G>A
  hgvsp: ENSP00000363094.1:p.Gly200Arg
  variant of: http://identifiers.org/hgnc/13054
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3000
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6352
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3162
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10036
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32044
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3511
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1647
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 204
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 266
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Gly200Arg
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ

X-70472511-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24070472511
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24070472511
    reference: chr 0
allele count: 1
allele frequency: 1.3137324452502e-5
allele num: 76119
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363100
  ensembl transcript: ENST00000373988
  gene symbol: ZMYM3
  hgvsc: ENST00000373988.1:c.595C>G
  hgvsp: ENSP00000363100.1:p.Leu199Val
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363096
  ensembl transcript: ENST00000373984
  gene symbol: ZMYM3
  hgvsc: ENST00000373984.3:c.595C>G
  hgvsp: ENSP00000363096.3:p.Leu199Val
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147130
  ensembl transcript: ENST00000489332
  gene symbol: ZMYM3
  hgvsc: ENST00000489332.1:n.713C>G
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000343909
  ensembl transcript: ENST00000353904
  gene symbol: ZMYM3
  hgvsc: ENST00000353904.2:c.595C>G
  hgvsp: ENSP00000343909.2:p.Leu199Val
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363090
  ensembl transcript: ENST00000373978
  gene symbol: ZMYM3
  hgvsc: ENST00000373978.1:c.595C>G
  hgvsp: ENSP00000363090.1:p.Leu199Val
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000322845
  ensembl transcript: ENST00000314425
  gene symbol: ZMYM3
  hgvsc: ENST00000314425.5:c.595C>G
  hgvsp: ENSP00000322845.5:p.Leu199Val
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363094
  ensembl transcript: ENST00000373982
  gene symbol: ZMYM3
  hgvsc: ENST00000373982.1:c.595C>G
  hgvsp: ENSP00000363094.1:p.Leu199Val
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363110
  ensembl transcript: ENST00000373998
  gene symbol: ZMYM3
  hgvsc: ENST00000373998.1:c.595C>G
  hgvsp: ENSP00000363110.1:p.Leu199Val
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363093
  ensembl transcript: ENST00000373981
  gene symbol: ZMYM3
  hgvsc: ENST00000373981.1:c.595C>G
  hgvsp: ENSP00000363093.1:p.Leu199Val
  variant of: http://identifiers.org/hgnc/13054
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2920
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32369
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1640
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3056
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6234
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3386
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10199
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7085
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 194
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37341
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Leu199Val
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: African
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: QD

X-70472512-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24070472512
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24070472512
    reference: chr 0
allele count: 1
allele frequency: 1.312043244945353e-5
allele num: 76217
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000322845
  ensembl transcript: ENST00000314425
  gene symbol: ZMYM3
  hgvsc: ENST00000314425.5:c.594T>C
  hgvsp: ENST00000314425.5:c.594T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000343909
  ensembl transcript: ENST00000353904
  gene symbol: ZMYM3
  hgvsc: ENST00000353904.2:c.594T>C
  hgvsp: ENST00000353904.2:c.594T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363110
  ensembl transcript: ENST00000373998
  gene symbol: ZMYM3
  hgvsc: ENST00000373998.1:c.594T>C
  hgvsp: ENST00000373998.1:c.594T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363096
  ensembl transcript: ENST00000373984
  gene symbol: ZMYM3
  hgvsc: ENST00000373984.3:c.594T>C
  hgvsp: ENST00000373984.3:c.594T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363100
  ensembl transcript: ENST00000373988
  gene symbol: ZMYM3
  hgvsc: ENST00000373988.1:c.594T>C
  hgvsp: ENST00000373988.1:c.594T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147130
  ensembl transcript: ENST00000489332
  gene symbol: ZMYM3
  hgvsc: ENST00000489332.1:n.712T>C
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363090
  ensembl transcript: ENST00000373978
  gene symbol: ZMYM3
  hgvsc: ENST00000373978.1:c.594T>C
  hgvsp: ENST00000373978.1:c.594T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363094
  ensembl transcript: ENST00000373982
  gene symbol: ZMYM3
  hgvsc: ENST00000373982.1:c.594T>C
  hgvsp: ENST00000373982.1:c.594T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363093
  ensembl transcript: ENST00000373981
  gene symbol: ZMYM3
  hgvsc: ENST00000373981.1:c.594T>C
  hgvsp: ENST00000373981.1:c.594T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3065
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32438
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1629
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2892
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3343
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6210
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10242
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 256
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3525
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1345
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3178
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Thr198Thr
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

X-70472514-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24070472514
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24070472514
    reference: chr 0
allele count: 1
allele frequency: 1.308951922195898e-5
allele num: 76397
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363100
  ensembl transcript: ENST00000373988
  gene symbol: ZMYM3
  hgvsc: ENST00000373988.1:c.592A>G
  hgvsp: ENSP00000363100.1:p.Thr198Ala
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147130
  ensembl transcript: ENST00000489332
  gene symbol: ZMYM3
  hgvsc: ENST00000489332.1:n.710A>G
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363093
  ensembl transcript: ENST00000373981
  gene symbol: ZMYM3
  hgvsc: ENST00000373981.1:c.592A>G
  hgvsp: ENSP00000363093.1:p.Thr198Ala
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363096
  ensembl transcript: ENST00000373984
  gene symbol: ZMYM3
  hgvsc: ENST00000373984.3:c.592A>G
  hgvsp: ENSP00000363096.3:p.Thr198Ala
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363094
  ensembl transcript: ENST00000373982
  gene symbol: ZMYM3
  hgvsc: ENST00000373982.1:c.592A>G
  hgvsp: ENSP00000363094.1:p.Thr198Ala
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000343909
  ensembl transcript: ENST00000353904
  gene symbol: ZMYM3
  hgvsc: ENST00000353904.2:c.592A>G
  hgvsp: ENSP00000343909.2:p.Thr198Ala
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363090
  ensembl transcript: ENST00000373978
  gene symbol: ZMYM3
  hgvsc: ENST00000373978.1:c.592A>G
  hgvsp: ENSP00000363090.1:p.Thr198Ala
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000322845
  ensembl transcript: ENST00000314425
  gene symbol: ZMYM3
  hgvsc: ENST00000314425.5:c.592A>G
  hgvsp: ENSP00000322845.5:p.Thr198Ala
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363110
  ensembl transcript: ENST00000373998
  gene symbol: ZMYM3
  hgvsc: ENST00000373998.1:c.592A>G
  hgvsp: ENSP00000363110.1:p.Thr198Ala
  variant of: http://identifiers.org/hgnc/13054
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2874
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2994
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10325
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1639
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3269
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32581
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6173
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 193
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 196
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 597
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1098
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Thr198Ala
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ClippingRankSum

X-70472515-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24070472515
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24070472515
    reference: chr 0
allele count: 1
allele frequency: 1.306813726771386e-5
allele num: 76522
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363110
  ensembl transcript: ENST00000373998
  gene symbol: ZMYM3
  hgvsc: ENST00000373998.1:c.591G>C
  hgvsp: ENSP00000363110.1:p.Glu197Asp
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147130
  ensembl transcript: ENST00000489332
  gene symbol: ZMYM3
  hgvsc: ENST00000489332.1:n.709G>C
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363100
  ensembl transcript: ENST00000373988
  gene symbol: ZMYM3
  hgvsc: ENST00000373988.1:c.591G>C
  hgvsp: ENSP00000363100.1:p.Glu197Asp
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000343909
  ensembl transcript: ENST00000353904
  gene symbol: ZMYM3
  hgvsc: ENST00000353904.2:c.591G>C
  hgvsp: ENSP00000343909.2:p.Glu197Asp
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363094
  ensembl transcript: ENST00000373982
  gene symbol: ZMYM3
  hgvsc: ENST00000373982.1:c.591G>C
  hgvsp: ENSP00000363094.1:p.Glu197Asp
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000322845
  ensembl transcript: ENST00000314425
  gene symbol: ZMYM3
  hgvsc: ENST00000314425.5:c.591G>C
  hgvsp: ENSP00000322845.5:p.Glu197Asp
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363093
  ensembl transcript: ENST00000373981
  gene symbol: ZMYM3
  hgvsc: ENST00000373981.1:c.591G>C
  hgvsp: ENSP00000363093.1:p.Glu197Asp
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363090
  ensembl transcript: ENST00000373978
  gene symbol: ZMYM3
  hgvsc: ENST00000373978.1:c.591G>C
  hgvsp: ENSP00000363090.1:p.Glu197Asp
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363096
  ensembl transcript: ENST00000373984
  gene symbol: ZMYM3
  hgvsc: ENST00000373984.3:c.591G>C
  hgvsp: ENSP00000363096.3:p.Glu197Asp
  variant of: http://identifiers.org/hgnc/13054
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3216
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10368
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2906
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2840
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1665
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6115
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32768
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37812
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 946
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 266
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1062
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Glu197Asp
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ

X-70472530-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24070472530
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24070472530
    reference: chr 0
allele count: 4
allele frequency: 5.127876418178322e-5
allele num: 78005
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363090
  ensembl transcript: ENST00000373978
  gene symbol: ZMYM3
  hgvsc: ENST00000373978.1:c.576C>T
  hgvsp: ENST00000373978.1:c.576C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000343909
  ensembl transcript: ENST00000353904
  gene symbol: ZMYM3
  hgvsc: ENST00000353904.2:c.576C>T
  hgvsp: ENST00000353904.2:c.576C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147130
  ensembl transcript: ENST00000489332
  gene symbol: ZMYM3
  hgvsc: ENST00000489332.1:n.694C>T
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363096
  ensembl transcript: ENST00000373984
  gene symbol: ZMYM3
  hgvsc: ENST00000373984.3:c.576C>T
  hgvsp: ENST00000373984.3:c.576C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000322845
  ensembl transcript: ENST00000314425
  gene symbol: ZMYM3
  hgvsc: ENST00000314425.5:c.576C>T
  hgvsp: ENST00000314425.5:c.576C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363094
  ensembl transcript: ENST00000373982
  gene symbol: ZMYM3
  hgvsc: ENST00000373982.1:c.576C>T
  hgvsp: ENST00000373982.1:c.576C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363100
  ensembl transcript: ENST00000373988
  gene symbol: ZMYM3
  hgvsc: ENST00000373988.1:c.576C>T
  hgvsp: ENST00000373988.1:c.576C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363093
  ensembl transcript: ENST00000373981
  gene symbol: ZMYM3
  hgvsc: ENST00000373981.1:c.576C>T
  hgvsp: ENST00000373981.1:c.576C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363110
  ensembl transcript: ENST00000373998
  gene symbol: ZMYM3
  hgvsc: ENST00000373998.1:c.576C>T
  hgvsp: ENST00000373998.1:c.576C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33563
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1790
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2508
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2368
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2442
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5827
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11539
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 839
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 404
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38779
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1164
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ser192Ser
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: South Asian
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum

X-70472534-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24070472534
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24070472534
    reference: chr 0
allele count: 4
allele frequency: 5.097034800005097e-5
allele num: 78477
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363096
  ensembl transcript: ENST00000373984
  gene symbol: ZMYM3
  hgvsc: ENST00000373984.3:c.572C>T
  hgvsp: ENSP00000363096.3:p.Pro191Leu
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363110
  ensembl transcript: ENST00000373998
  gene symbol: ZMYM3
  hgvsc: ENST00000373998.1:c.572C>T
  hgvsp: ENSP00000363110.1:p.Pro191Leu
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363090
  ensembl transcript: ENST00000373978
  gene symbol: ZMYM3
  hgvsc: ENST00000373978.1:c.572C>T
  hgvsp: ENSP00000363090.1:p.Pro191Leu
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000322845
  ensembl transcript: ENST00000314425
  gene symbol: ZMYM3
  hgvsc: ENST00000314425.5:c.572C>T
  hgvsp: ENSP00000322845.5:p.Pro191Leu
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363100
  ensembl transcript: ENST00000373988
  gene symbol: ZMYM3
  hgvsc: ENST00000373988.1:c.572C>T
  hgvsp: ENSP00000363100.1:p.Pro191Leu
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000343909
  ensembl transcript: ENST00000353904
  gene symbol: ZMYM3
  hgvsc: ENST00000353904.2:c.572C>T
  hgvsp: ENSP00000343909.2:p.Pro191Leu
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363094
  ensembl transcript: ENST00000373982
  gene symbol: ZMYM3
  hgvsc: ENST00000373982.1:c.572C>T
  hgvsp: ENSP00000363094.1:p.Pro191Leu
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363093
  ensembl transcript: ENST00000373981
  gene symbol: ZMYM3
  hgvsc: ENST00000373981.1:c.572C>T
  hgvsp: ENSP00000363093.1:p.Pro191Leu
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147130
  ensembl transcript: ENST00000489332
  gene symbol: ZMYM3
  hgvsc: ENST00000489332.1:n.690C>T
  variant of: http://identifiers.org/hgnc/13054
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34183
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2076
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2368
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11743
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5779
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2140
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1782
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 452
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 254
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Pro191Leu
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: African
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD

X-70472534-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24070472534
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24070472534
    reference: chr 0
allele count: 1
allele frequency: 1.274258700001274e-5
allele num: 78477
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363093
  ensembl transcript: ENST00000373981
  gene symbol: ZMYM3
  hgvsc: ENST00000373981.1:c.572C>G
  hgvsp: ENSP00000363093.1:p.Pro191Arg
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363100
  ensembl transcript: ENST00000373988
  gene symbol: ZMYM3
  hgvsc: ENST00000373988.1:c.572C>G
  hgvsp: ENSP00000363100.1:p.Pro191Arg
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363090
  ensembl transcript: ENST00000373978
  gene symbol: ZMYM3
  hgvsc: ENST00000373978.1:c.572C>G
  hgvsp: ENSP00000363090.1:p.Pro191Arg
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000343909
  ensembl transcript: ENST00000353904
  gene symbol: ZMYM3
  hgvsc: ENST00000353904.2:c.572C>G
  hgvsp: ENSP00000343909.2:p.Pro191Arg
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147130
  ensembl transcript: ENST00000489332
  gene symbol: ZMYM3
  hgvsc: ENST00000489332.1:n.690C>G
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363094
  ensembl transcript: ENST00000373982
  gene symbol: ZMYM3
  hgvsc: ENST00000373982.1:c.572C>G
  hgvsp: ENSP00000363094.1:p.Pro191Arg
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363096
  ensembl transcript: ENST00000373984
  gene symbol: ZMYM3
  hgvsc: ENST00000373984.3:c.572C>G
  hgvsp: ENSP00000363096.3:p.Pro191Arg
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000322845
  ensembl transcript: ENST00000314425
  gene symbol: ZMYM3
  hgvsc: ENST00000314425.5:c.572C>G
  hgvsp: ENSP00000322845.5:p.Pro191Arg
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363110
  ensembl transcript: ENST00000373998
  gene symbol: ZMYM3
  hgvsc: ENST00000373998.1:c.572C>G
  hgvsp: ENSP00000363110.1:p.Pro191Arg
  variant of: http://identifiers.org/hgnc/13054
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1782
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2076
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5779
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11743
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2368
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2140
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34183
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 850
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 254
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 645
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6438
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Pro191Arg
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD

X-70472536-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24070472536
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24070472536
    reference: chr 0
allele count: 2
allele frequency: 2.545533225572427e-5
allele num: 78569
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363100
  ensembl transcript: ENST00000373988
  gene symbol: ZMYM3
  hgvsc: ENST00000373988.1:c.570G>A
  hgvsp: ENST00000373988.1:c.570G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000322845
  ensembl transcript: ENST00000314425
  gene symbol: ZMYM3
  hgvsc: ENST00000314425.5:c.570G>A
  hgvsp: ENST00000314425.5:c.570G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147130
  ensembl transcript: ENST00000489332
  gene symbol: ZMYM3
  hgvsc: ENST00000489332.1:n.688G>A
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363110
  ensembl transcript: ENST00000373998
  gene symbol: ZMYM3
  hgvsc: ENST00000373998.1:c.570G>A
  hgvsp: ENST00000373998.1:c.570G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000343909
  ensembl transcript: ENST00000353904
  gene symbol: ZMYM3
  hgvsc: ENST00000353904.2:c.570G>A
  hgvsp: ENST00000353904.2:c.570G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363094
  ensembl transcript: ENST00000373982
  gene symbol: ZMYM3
  hgvsc: ENST00000373982.1:c.570G>A
  hgvsp: ENST00000373982.1:c.570G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363096
  ensembl transcript: ENST00000373984
  gene symbol: ZMYM3
  hgvsc: ENST00000373984.3:c.570G>A
  hgvsp: ENST00000373984.3:c.570G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363090
  ensembl transcript: ENST00000373978
  gene symbol: ZMYM3
  hgvsc: ENST00000373978.1:c.570G>A
  hgvsp: ENST00000373978.1:c.570G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363093
  ensembl transcript: ENST00000373981
  gene symbol: ZMYM3
  hgvsc: ENST00000373981.1:c.570G>A
  hgvsp: ENST00000373981.1:c.570G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5674
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34241
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2356
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1860
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2127
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1965
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11847
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 326
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40827
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 716
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Pro190Pro
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: DP

X-70472537-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24070472537
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24070472537
    reference: chr 0
allele count: 1
allele frequency: 1.269470503852843e-5
allele num: 78773
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000343909
  ensembl transcript: ENST00000353904
  gene symbol: ZMYM3
  hgvsc: ENST00000353904.2:c.569C>T
  hgvsp: ENSP00000343909.2:p.Pro190Leu
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363093
  ensembl transcript: ENST00000373981
  gene symbol: ZMYM3
  hgvsc: ENST00000373981.1:c.569C>T
  hgvsp: ENSP00000363093.1:p.Pro190Leu
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363096
  ensembl transcript: ENST00000373984
  gene symbol: ZMYM3
  hgvsc: ENST00000373984.3:c.569C>T
  hgvsp: ENSP00000363096.3:p.Pro190Leu
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363094
  ensembl transcript: ENST00000373982
  gene symbol: ZMYM3
  hgvsc: ENST00000373982.1:c.569C>T
  hgvsp: ENSP00000363094.1:p.Pro190Leu
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363110
  ensembl transcript: ENST00000373998
  gene symbol: ZMYM3
  hgvsc: ENST00000373998.1:c.569C>T
  hgvsp: ENSP00000363110.1:p.Pro190Leu
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147130
  ensembl transcript: ENST00000489332
  gene symbol: ZMYM3
  hgvsc: ENST00000489332.1:n.687C>T
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000322845
  ensembl transcript: ENST00000314425
  gene symbol: ZMYM3
  hgvsc: ENST00000314425.5:c.569C>T
  hgvsp: ENSP00000322845.5:p.Pro190Leu
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363090
  ensembl transcript: ENST00000373978
  gene symbol: ZMYM3
  hgvsc: ENST00000373978.1:c.569C>T
  hgvsp: ENSP00000363090.1:p.Pro190Leu
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363100
  ensembl transcript: ENST00000373988
  gene symbol: ZMYM3
  hgvsc: ENST00000373988.1:c.569C>T
  hgvsp: ENSP00000363100.1:p.Pro190Leu
  variant of: http://identifiers.org/hgnc/13054
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34257
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2123
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11901
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5689
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2344
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1880
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1879
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 346
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 668
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1021
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 825
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Pro190Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum

X-70472560-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24070472560
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24070472560
    reference: chr 0
allele count: 17
allele frequency: 2.13003220107504e-4
allele num: 79811
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363100
  ensembl transcript: ENST00000373988
  gene symbol: ZMYM3
  hgvsc: ENST00000373988.1:c.546G>C
  hgvsp: ENST00000373988.1:c.546G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363096
  ensembl transcript: ENST00000373984
  gene symbol: ZMYM3
  hgvsc: ENST00000373984.3:c.546G>C
  hgvsp: ENST00000373984.3:c.546G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363094
  ensembl transcript: ENST00000373982
  gene symbol: ZMYM3
  hgvsc: ENST00000373982.1:c.546G>C
  hgvsp: ENST00000373982.1:c.546G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000322845
  ensembl transcript: ENST00000314425
  gene symbol: ZMYM3
  hgvsc: ENST00000314425.5:c.546G>C
  hgvsp: ENST00000314425.5:c.546G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363090
  ensembl transcript: ENST00000373978
  gene symbol: ZMYM3
  hgvsc: ENST00000373978.1:c.546G>C
  hgvsp: ENST00000373978.1:c.546G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000343909
  ensembl transcript: ENST00000353904
  gene symbol: ZMYM3
  hgvsc: ENST00000353904.2:c.546G>C
  hgvsp: ENST00000353904.2:c.546G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363110
  ensembl transcript: ENST00000373998
  gene symbol: ZMYM3
  hgvsc: ENST00000373998.1:c.546G>C
  hgvsp: ENST00000373998.1:c.546G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363093
  ensembl transcript: ENST00000373981
  gene symbol: ZMYM3
  hgvsc: ENST00000373981.1:c.546G>C
  hgvsp: ENST00000373981.1:c.546G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147130
  ensembl transcript: ENST00000489332
  gene symbol: ZMYM3
  hgvsc: ENST00000489332.1:n.664G>C
  variant of: http://identifiers.org/hgnc/13054
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 1711
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2001
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5251
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12626
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2215
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34871
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 620
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 870
  bin: 7.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 244
  bin: 1.25e1
  variant carriers: 1
hgvs: p.Gly182Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
population: Other
reference allele: C
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum

X-70472568-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24070472568
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24070472568
    reference: chr 0
allele count: 1
allele frequency: 1.230072820310962e-5
allele num: 81296
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363096
  ensembl transcript: ENST00000373984
  gene symbol: ZMYM3
  hgvsc: ENST00000373984.3:c.538C>T
  hgvsp: ENSP00000363096.3:p.Pro180Ser
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363100
  ensembl transcript: ENST00000373988
  gene symbol: ZMYM3
  hgvsc: ENST00000373988.1:c.538C>T
  hgvsp: ENSP00000363100.1:p.Pro180Ser
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363093
  ensembl transcript: ENST00000373981
  gene symbol: ZMYM3
  hgvsc: ENST00000373981.1:c.538C>T
  hgvsp: ENSP00000363093.1:p.Pro180Ser
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000343909
  ensembl transcript: ENST00000353904
  gene symbol: ZMYM3
  hgvsc: ENST00000353904.2:c.538C>T
  hgvsp: ENSP00000343909.2:p.Pro180Ser
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147130
  ensembl transcript: ENST00000489332
  gene symbol: ZMYM3
  hgvsc: ENST00000489332.1:n.656C>T
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363094
  ensembl transcript: ENST00000373982
  gene symbol: ZMYM3
  hgvsc: ENST00000373982.1:c.538C>T
  hgvsp: ENSP00000363094.1:p.Pro180Ser
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000322845
  ensembl transcript: ENST00000314425
  gene symbol: ZMYM3
  hgvsc: ENST00000314425.5:c.538C>T
  hgvsp: ENSP00000322845.5:p.Pro180Ser
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363090
  ensembl transcript: ENST00000373978
  gene symbol: ZMYM3
  hgvsc: ENST00000373978.1:c.538C>T
  hgvsp: ENSP00000363090.1:p.Pro180Ser
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363110
  ensembl transcript: ENST00000373998
  gene symbol: ZMYM3
  hgvsc: ENST00000373998.1:c.538C>T
  hgvsp: ENSP00000363110.1:p.Pro180Ser
  variant of: http://identifiers.org/hgnc/13054
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35302
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5155
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1609
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13216
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2274
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1945
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 919
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 634
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 678
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Pro180Ser
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: QD

X-70472585-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24070472585
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24070472585
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 82306
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147130
  ensembl transcript: ENST00000489332
  gene symbol: ZMYM3
  hgvsc: ENST00000489332.1:n.639G>A
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363094
  ensembl transcript: ENST00000373982
  gene symbol: ZMYM3
  hgvsc: ENST00000373982.1:c.521G>A
  hgvsp: ENSP00000363094.1:p.Gly174Glu
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363110
  ensembl transcript: ENST00000373998
  gene symbol: ZMYM3
  hgvsc: ENST00000373998.1:c.521G>A
  hgvsp: ENSP00000363110.1:p.Gly174Glu
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363090
  ensembl transcript: ENST00000373978
  gene symbol: ZMYM3
  hgvsc: ENST00000373978.1:c.521G>A
  hgvsp: ENSP00000363090.1:p.Gly174Glu
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363096
  ensembl transcript: ENST00000373984
  gene symbol: ZMYM3
  hgvsc: ENST00000373984.3:c.521G>A
  hgvsp: ENSP00000363096.3:p.Gly174Glu
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000343909
  ensembl transcript: ENST00000353904
  gene symbol: ZMYM3
  hgvsc: ENST00000353904.2:c.521G>A
  hgvsp: ENSP00000343909.2:p.Gly174Glu
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363100
  ensembl transcript: ENST00000373988
  gene symbol: ZMYM3
  hgvsc: ENST00000373988.1:c.521G>A
  hgvsp: ENSP00000363100.1:p.Gly174Glu
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000322845
  ensembl transcript: ENST00000314425
  gene symbol: ZMYM3
  hgvsc: ENST00000314425.5:c.521G>A
  hgvsp: ENSP00000322845.5:p.Gly174Glu
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363093
  ensembl transcript: ENST00000373981
  gene symbol: ZMYM3
  hgvsc: ENST00000373981.1:c.521G>A
  hgvsp: ENSP00000363093.1:p.Gly174Glu
  variant of: http://identifiers.org/hgnc/13054
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 2647
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4738
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1958
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1502
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35325
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13694
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 379
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 818
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 635
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Gly174Glu
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: QD

X-70472593-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24070472593
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24070472593
    reference: chr 0
allele count: 2
allele frequency: 2.412021515231916e-5
allele num: 82918
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363090
  ensembl transcript: ENST00000373978
  gene symbol: ZMYM3
  hgvsc: ENST00000373978.1:c.513C>A
  hgvsp: ENST00000373978.1:c.513C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363096
  ensembl transcript: ENST00000373984
  gene symbol: ZMYM3
  hgvsc: ENST00000373984.3:c.513C>A
  hgvsp: ENST00000373984.3:c.513C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363100
  ensembl transcript: ENST00000373988
  gene symbol: ZMYM3
  hgvsc: ENST00000373988.1:c.513C>A
  hgvsp: ENST00000373988.1:c.513C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363110
  ensembl transcript: ENST00000373998
  gene symbol: ZMYM3
  hgvsc: ENST00000373998.1:c.513C>A
  hgvsp: ENST00000373998.1:c.513C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363093
  ensembl transcript: ENST00000373981
  gene symbol: ZMYM3
  hgvsc: ENST00000373981.1:c.513C>A
  hgvsp: ENST00000373981.1:c.513C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000343909
  ensembl transcript: ENST00000353904
  gene symbol: ZMYM3
  hgvsc: ENST00000353904.2:c.513C>A
  hgvsp: ENST00000353904.2:c.513C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000322845
  ensembl transcript: ENST00000314425
  gene symbol: ZMYM3
  hgvsc: ENST00000314425.5:c.513C>A
  hgvsp: ENST00000314425.5:c.513C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363094
  ensembl transcript: ENST00000373982
  gene symbol: ZMYM3
  hgvsc: ENST00000373982.1:c.513C>A
  hgvsp: ENST00000373982.1:c.513C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147130
  ensembl transcript: ENST00000489332
  gene symbol: ZMYM3
  hgvsc: ENST00000489332.1:n.631C>A
  variant of: http://identifiers.org/hgnc/13054
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35462
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2894
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4394
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1393
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13868
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1954
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5660
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 634
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Gly171Gly
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: DP

X-70472607-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24070472607
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24070472607
    reference: chr 0
allele count: 1
allele frequency: 1.19618655725547e-5
allele num: 83599
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000322845
  ensembl transcript: ENST00000314425
  gene symbol: ZMYM3
  hgvsc: ENST00000314425.5:c.499A>G
  hgvsp: ENSP00000322845.5:p.Thr167Ala
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363110
  ensembl transcript: ENST00000373998
  gene symbol: ZMYM3
  hgvsc: ENST00000373998.1:c.499A>G
  hgvsp: ENSP00000363110.1:p.Thr167Ala
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363094
  ensembl transcript: ENST00000373982
  gene symbol: ZMYM3
  hgvsc: ENST00000373982.1:c.499A>G
  hgvsp: ENSP00000363094.1:p.Thr167Ala
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363096
  ensembl transcript: ENST00000373984
  gene symbol: ZMYM3
  hgvsc: ENST00000373984.3:c.499A>G
  hgvsp: ENSP00000363096.3:p.Thr167Ala
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363090
  ensembl transcript: ENST00000373978
  gene symbol: ZMYM3
  hgvsc: ENST00000373978.1:c.499A>G
  hgvsp: ENSP00000363090.1:p.Thr167Ala
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000343909
  ensembl transcript: ENST00000353904
  gene symbol: ZMYM3
  hgvsc: ENST00000353904.2:c.499A>G
  hgvsp: ENSP00000343909.2:p.Thr167Ala
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363100
  ensembl transcript: ENST00000373988
  gene symbol: ZMYM3
  hgvsc: ENST00000373988.1:c.499A>G
  hgvsp: ENSP00000363100.1:p.Thr167Ala
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147130
  ensembl transcript: ENST00000489332
  gene symbol: ZMYM3
  hgvsc: ENST00000489332.1:n.617A>G
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363093
  ensembl transcript: ENST00000373981
  gene symbol: ZMYM3
  hgvsc: ENST00000373981.1:c.499A>G
  hgvsp: ENSP00000363093.1:p.Thr167Ala
  variant of: http://identifiers.org/hgnc/13054
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35400
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13826
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3902
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1553
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3460
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1900
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 285
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 687
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Thr167Ala
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD

X-70472612-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24070472612
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24070472612
    reference: chr 0
allele count: 1
allele frequency: 1.194300796598631e-5
allele num: 83731
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363090
  ensembl transcript: ENST00000373978
  gene symbol: ZMYM3
  hgvsc: ENST00000373978.1:c.494T>A
  hgvsp: ENSP00000363090.1:p.Ile165Lys
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147130
  ensembl transcript: ENST00000489332
  gene symbol: ZMYM3
  hgvsc: ENST00000489332.1:n.612T>A
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000343909
  ensembl transcript: ENST00000353904
  gene symbol: ZMYM3
  hgvsc: ENST00000353904.2:c.494T>A
  hgvsp: ENSP00000343909.2:p.Ile165Lys
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363093
  ensembl transcript: ENST00000373981
  gene symbol: ZMYM3
  hgvsc: ENST00000373981.1:c.494T>A
  hgvsp: ENSP00000363093.1:p.Ile165Lys
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363094
  ensembl transcript: ENST00000373982
  gene symbol: ZMYM3
  hgvsc: ENST00000373982.1:c.494T>A
  hgvsp: ENSP00000363094.1:p.Ile165Lys
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363100
  ensembl transcript: ENST00000373988
  gene symbol: ZMYM3
  hgvsc: ENST00000373988.1:c.494T>A
  hgvsp: ENSP00000363100.1:p.Ile165Lys
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363110
  ensembl transcript: ENST00000373998
  gene symbol: ZMYM3
  hgvsc: ENST00000373998.1:c.494T>A
  hgvsp: ENSP00000363110.1:p.Ile165Lys
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363096
  ensembl transcript: ENST00000373984
  gene symbol: ZMYM3
  hgvsc: ENST00000373984.3:c.494T>A
  hgvsp: ENSP00000363096.3:p.Ile165Lys
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000322845
  ensembl transcript: ENST00000314425
  gene symbol: ZMYM3
  hgvsc: ENST00000314425.5:c.494T>A
  hgvsp: ENSP00000322845.5:p.Ile165Lys
  variant of: http://identifiers.org/hgnc/13054
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1679
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35239
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3816
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3769
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13654
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1886
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5761
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3884
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44266
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Ile165Lys
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum

X-70472621-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24070472621
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24070472621
    reference: chr 0
allele count: 1
allele frequency: 1.1953143676787e-5
allele num: 83660
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363096
  ensembl transcript: ENST00000373984
  gene symbol: ZMYM3
  hgvsc: ENST00000373984.3:c.485C>A
  hgvsp: ENSP00000363096.3:p.Thr162Asn
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000343909
  ensembl transcript: ENST00000353904
  gene symbol: ZMYM3
  hgvsc: ENST00000353904.2:c.485C>A
  hgvsp: ENSP00000343909.2:p.Thr162Asn
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000322845
  ensembl transcript: ENST00000314425
  gene symbol: ZMYM3
  hgvsc: ENST00000314425.5:c.485C>A
  hgvsp: ENSP00000322845.5:p.Thr162Asn
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363090
  ensembl transcript: ENST00000373978
  gene symbol: ZMYM3
  hgvsc: ENST00000373978.1:c.485C>A
  hgvsp: ENSP00000363090.1:p.Thr162Asn
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363100
  ensembl transcript: ENST00000373988
  gene symbol: ZMYM3
  hgvsc: ENST00000373988.1:c.485C>A
  hgvsp: ENSP00000363100.1:p.Thr162Asn
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147130
  ensembl transcript: ENST00000489332
  gene symbol: ZMYM3
  hgvsc: ENST00000489332.1:n.603C>A
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363094
  ensembl transcript: ENST00000373982
  gene symbol: ZMYM3
  hgvsc: ENST00000373982.1:c.485C>A
  hgvsp: ENSP00000363094.1:p.Thr162Asn
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363110
  ensembl transcript: ENST00000373998
  gene symbol: ZMYM3
  hgvsc: ENST00000373998.1:c.485C>A
  hgvsp: ENSP00000363110.1:p.Thr162Asn
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363093
  ensembl transcript: ENST00000373981
  gene symbol: ZMYM3
  hgvsc: ENST00000373981.1:c.485C>A
  hgvsp: ENSP00000363093.1:p.Thr162Asn
  variant of: http://identifiers.org/hgnc/13054
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2088
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34211
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1832
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13330
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3810
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4756
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1342
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 346
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Thr162Asn
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: African
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff

X-70472622-TCTC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24070472622
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24070472619
    reference: chr 0
allele count: 2
allele frequency: 2.393203302620558e-5
allele num: 83570
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363090
  ensembl transcript: ENST00000373978
  gene symbol: ZMYM3
  hgvsc: ENST00000373978.1:c.481_483delGAG
  hgvsp: ENSP00000363090.1:p.Glu161del
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363100
  ensembl transcript: ENST00000373988
  gene symbol: ZMYM3
  hgvsc: ENST00000373988.1:c.481_483delGAG
  hgvsp: ENSP00000363100.1:p.Glu161del
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363094
  ensembl transcript: ENST00000373982
  gene symbol: ZMYM3
  hgvsc: ENST00000373982.1:c.481_483delGAG
  hgvsp: ENSP00000363094.1:p.Glu161del
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363096
  ensembl transcript: ENST00000373984
  gene symbol: ZMYM3
  hgvsc: ENST00000373984.3:c.481_483delGAG
  hgvsp: ENSP00000363096.3:p.Glu161del
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000322845
  ensembl transcript: ENST00000314425
  gene symbol: ZMYM3
  hgvsc: ENST00000314425.5:c.481_483delGAG
  hgvsp: ENSP00000322845.5:p.Glu161del
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363093
  ensembl transcript: ENST00000373981
  gene symbol: ZMYM3
  hgvsc: ENST00000373981.1:c.481_483delGAG
  hgvsp: ENSP00000363093.1:p.Glu161del
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147130
  ensembl transcript: ENST00000489332
  gene symbol: ZMYM3
  hgvsc: ENST00000489332.1:n.599_601delGAG
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000343909
  ensembl transcript: ENST00000353904
  gene symbol: ZMYM3
  hgvsc: ENST00000353904.2:c.481_483delGAG
  hgvsp: ENSP00000343909.2:p.Glu161del
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363110
  ensembl transcript: ENST00000373998
  gene symbol: ZMYM3
  hgvsc: ENST00000373998.1:c.481_483delGAG
  hgvsp: ENSP00000363110.1:p.Glu161del
  variant of: http://identifiers.org/hgnc/13054
canonical: true
consequence: inframe deletion
filter: VQSRTrancheINDEL96.00to97.00
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3885
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2234
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33787
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5049
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1830
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13235
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 571
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3769
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 729
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42169
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Glu161del
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: Latino
reference allele: TCTC
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum

X-70472629-CTCT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24070472629
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24070472626
    reference: chr 0
allele count: 1
allele frequency: 1.200278464603788e-5
allele num: 83314
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000322845
  ensembl transcript: ENST00000314425
  gene symbol: ZMYM3
  hgvsc: ENST00000314425.5:c.474_476delAGA
  hgvsp: ENSP00000322845.5:p.Glu161del
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363094
  ensembl transcript: ENST00000373982
  gene symbol: ZMYM3
  hgvsc: ENST00000373982.1:c.474_476delAGA
  hgvsp: ENSP00000363094.1:p.Glu161del
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363093
  ensembl transcript: ENST00000373981
  gene symbol: ZMYM3
  hgvsc: ENST00000373981.1:c.474_476delAGA
  hgvsp: ENSP00000363093.1:p.Glu161del
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363110
  ensembl transcript: ENST00000373998
  gene symbol: ZMYM3
  hgvsc: ENST00000373998.1:c.474_476delAGA
  hgvsp: ENSP00000363110.1:p.Glu161del
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363096
  ensembl transcript: ENST00000373984
  gene symbol: ZMYM3
  hgvsc: ENST00000373984.3:c.474_476delAGA
  hgvsp: ENSP00000363096.3:p.Glu161del
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363100
  ensembl transcript: ENST00000373988
  gene symbol: ZMYM3
  hgvsc: ENST00000373988.1:c.474_476delAGA
  hgvsp: ENSP00000363100.1:p.Glu161del
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363090
  ensembl transcript: ENST00000373978
  gene symbol: ZMYM3
  hgvsc: ENST00000373978.1:c.474_476delAGA
  hgvsp: ENSP00000363090.1:p.Glu161del
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000343909
  ensembl transcript: ENST00000353904
  gene symbol: ZMYM3
  hgvsc: ENST00000353904.2:c.474_476delAGA
  hgvsp: ENSP00000343909.2:p.Glu161del
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147130
  ensembl transcript: ENST00000489332
  gene symbol: ZMYM3
  hgvsc: ENST00000489332.1:n.592_594delAGA
  variant of: http://identifiers.org/hgnc/13054
canonical: true
consequence: inframe deletion
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32715
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4078
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2586
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12854
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5931
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1830
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1092
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 803
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1748
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Glu161del
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: CTCT
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum

X-70472641-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24070472641
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24070472641
    reference: chr 0
allele count: 3
allele frequency: 3.62375735320763e-5
allele num: 82787
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000322845
  ensembl transcript: ENST00000314425
  gene symbol: ZMYM3
  hgvsc: ENST00000314425.5:c.465A>G
  hgvsp: ENST00000314425.5:c.465A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363096
  ensembl transcript: ENST00000373984
  gene symbol: ZMYM3
  hgvsc: ENST00000373984.3:c.465A>G
  hgvsp: ENST00000373984.3:c.465A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363093
  ensembl transcript: ENST00000373981
  gene symbol: ZMYM3
  hgvsc: ENST00000373981.1:c.465A>G
  hgvsp: ENST00000373981.1:c.465A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147130
  ensembl transcript: ENST00000489332
  gene symbol: ZMYM3
  hgvsc: ENST00000489332.1:n.583A>G
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363094
  ensembl transcript: ENST00000373982
  gene symbol: ZMYM3
  hgvsc: ENST00000373982.1:c.465A>G
  hgvsp: ENST00000373982.1:c.465A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363090
  ensembl transcript: ENST00000373978
  gene symbol: ZMYM3
  hgvsc: ENST00000373978.1:c.465A>G
  hgvsp: ENST00000373978.1:c.465A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000343909
  ensembl transcript: ENST00000353904
  gene symbol: ZMYM3
  hgvsc: ENST00000353904.2:c.465A>G
  hgvsp: ENST00000353904.2:c.465A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363110
  ensembl transcript: ENST00000373998
  gene symbol: ZMYM3
  hgvsc: ENST00000373998.1:c.465A>G
  hgvsp: ENST00000373998.1:c.465A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363100
  ensembl transcript: ENST00000373988
  gene symbol: ZMYM3
  hgvsc: ENST00000373988.1:c.465A>G
  hgvsp: ENST00000373988.1:c.465A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30405
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4458
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1752
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7841
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3383
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12073
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2266
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 232
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1502
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Pro155Pro
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum

X-70472644-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24070472644
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24070472644
    reference: chr 0
allele count: 1
allele frequency: 1.21256214380987e-5
allele num: 82470
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363100
  ensembl transcript: ENST00000373988
  gene symbol: ZMYM3
  hgvsc: ENST00000373988.1:c.462C>T
  hgvsp: ENST00000373988.1:c.462C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000343909
  ensembl transcript: ENST00000353904
  gene symbol: ZMYM3
  hgvsc: ENST00000353904.2:c.462C>T
  hgvsp: ENST00000353904.2:c.462C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363094
  ensembl transcript: ENST00000373982
  gene symbol: ZMYM3
  hgvsc: ENST00000373982.1:c.462C>T
  hgvsp: ENST00000373982.1:c.462C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363110
  ensembl transcript: ENST00000373998
  gene symbol: ZMYM3
  hgvsc: ENST00000373998.1:c.462C>T
  hgvsp: ENST00000373998.1:c.462C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363093
  ensembl transcript: ENST00000373981
  gene symbol: ZMYM3
  hgvsc: ENST00000373981.1:c.462C>T
  hgvsp: ENST00000373981.1:c.462C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363096
  ensembl transcript: ENST00000373984
  gene symbol: ZMYM3
  hgvsc: ENST00000373984.3:c.462C>T
  hgvsp: ENST00000373984.3:c.462C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000322845
  ensembl transcript: ENST00000314425
  gene symbol: ZMYM3
  hgvsc: ENST00000314425.5:c.462C>T
  hgvsp: ENST00000314425.5:c.462C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363090
  ensembl transcript: ENST00000373978
  gene symbol: ZMYM3
  hgvsc: ENST00000373978.1:c.462C>T
  hgvsp: ENST00000373978.1:c.462C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147130
  ensembl transcript: ENST00000489332
  gene symbol: ZMYM3
  hgvsc: ENST00000489332.1:n.580C>T
  variant of: http://identifiers.org/hgnc/13054
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1749
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29339
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3808
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8565
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4666
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11755
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 264
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 751
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ser154Ser
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: African
population: Latino
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum

X-70472661-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24070472661
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24070472661
    reference: chr 0
allele count: 3
allele frequency: 3.695172872504219e-5
allele num: 81187
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000322845
  ensembl transcript: ENST00000314425
  gene symbol: ZMYM3
  hgvsc: ENST00000314425.5:c.445C>T
  hgvsp: ENSP00000322845.5:p.Pro149Ser
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147130
  ensembl transcript: ENST00000489332
  gene symbol: ZMYM3
  hgvsc: ENST00000489332.1:n.563C>T
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363093
  ensembl transcript: ENST00000373981
  gene symbol: ZMYM3
  hgvsc: ENST00000373981.1:c.445C>T
  hgvsp: ENSP00000363093.1:p.Pro149Ser
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363094
  ensembl transcript: ENST00000373982
  gene symbol: ZMYM3
  hgvsc: ENST00000373982.1:c.445C>T
  hgvsp: ENSP00000363094.1:p.Pro149Ser
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363096
  ensembl transcript: ENST00000373984
  gene symbol: ZMYM3
  hgvsc: ENST00000373984.3:c.445C>T
  hgvsp: ENSP00000363096.3:p.Pro149Ser
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363090
  ensembl transcript: ENST00000373978
  gene symbol: ZMYM3
  hgvsc: ENST00000373978.1:c.445C>T
  hgvsp: ENSP00000363090.1:p.Pro149Ser
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363100
  ensembl transcript: ENST00000373988
  gene symbol: ZMYM3
  hgvsc: ENST00000373988.1:c.445C>T
  hgvsp: ENSP00000363100.1:p.Pro149Ser
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363110
  ensembl transcript: ENST00000373998
  gene symbol: ZMYM3
  hgvsc: ENST00000373998.1:c.445C>T
  hgvsp: ENSP00000363110.1:p.Pro149Ser
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000343909
  ensembl transcript: ENST00000353904
  gene symbol: ZMYM3
  hgvsc: ENST00000353904.2:c.445C>T
  hgvsp: ENSP00000343909.2:p.Pro149Ser
  variant of: http://identifiers.org/hgnc/13054
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10215
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6074
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25017
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5547
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1635
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11202
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 295
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1392
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Pro149Ser
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: African
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD

X-70472663-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24070472663
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24070472663
    reference: chr 0
allele count: 1
allele frequency: 1.231784979613959e-5
allele num: 81183
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000322845
  ensembl transcript: ENST00000314425
  gene symbol: ZMYM3
  hgvsc: ENST00000314425.5:c.443C>G
  hgvsp: ENSP00000322845.5:p.Ser148Cys
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363090
  ensembl transcript: ENST00000373978
  gene symbol: ZMYM3
  hgvsc: ENST00000373978.1:c.443C>G
  hgvsp: ENSP00000363090.1:p.Ser148Cys
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363100
  ensembl transcript: ENST00000373988
  gene symbol: ZMYM3
  hgvsc: ENST00000373988.1:c.443C>G
  hgvsp: ENSP00000363100.1:p.Ser148Cys
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363093
  ensembl transcript: ENST00000373981
  gene symbol: ZMYM3
  hgvsc: ENST00000373981.1:c.443C>G
  hgvsp: ENSP00000363093.1:p.Ser148Cys
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363094
  ensembl transcript: ENST00000373982
  gene symbol: ZMYM3
  hgvsc: ENST00000373982.1:c.443C>G
  hgvsp: ENSP00000363094.1:p.Ser148Cys
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147130
  ensembl transcript: ENST00000489332
  gene symbol: ZMYM3
  hgvsc: ENST00000489332.1:n.561C>G
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363110
  ensembl transcript: ENST00000373998
  gene symbol: ZMYM3
  hgvsc: ENST00000373998.1:c.443C>G
  hgvsp: ENSP00000363110.1:p.Ser148Cys
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363096
  ensembl transcript: ENST00000373984
  gene symbol: ZMYM3
  hgvsc: ENST00000373984.3:c.443C>G
  hgvsp: ENSP00000363096.3:p.Ser148Cys
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000343909
  ensembl transcript: ENST00000353904
  gene symbol: ZMYM3
  hgvsc: ENST00000353904.2:c.443C>G
  hgvsp: ENSP00000343909.2:p.Ser148Cys
  variant of: http://identifiers.org/hgnc/13054
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10229
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5587
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11220
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5961
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1603
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25097
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 954
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 305
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 207
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3976
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ser148Cys
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: DP

X-70472686-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24070472686
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24070472686
    reference: chr 0
allele count: 1
allele frequency: 1.253462690683012e-5
allele num: 79779
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363093
  ensembl transcript: ENST00000373981
  gene symbol: ZMYM3
  hgvsc: ENST00000373981.1:c.420A>C
  hgvsp: ENST00000373981.1:c.420A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000322845
  ensembl transcript: ENST00000314425
  gene symbol: ZMYM3
  hgvsc: ENST00000314425.5:c.420A>C
  hgvsp: ENST00000314425.5:c.420A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363110
  ensembl transcript: ENST00000373998
  gene symbol: ZMYM3
  hgvsc: ENST00000373998.1:c.420A>C
  hgvsp: ENST00000373998.1:c.420A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363094
  ensembl transcript: ENST00000373982
  gene symbol: ZMYM3
  hgvsc: ENST00000373982.1:c.420A>C
  hgvsp: ENST00000373982.1:c.420A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363100
  ensembl transcript: ENST00000373988
  gene symbol: ZMYM3
  hgvsc: ENST00000373988.1:c.420A>C
  hgvsp: ENST00000373988.1:c.420A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000343909
  ensembl transcript: ENST00000353904
  gene symbol: ZMYM3
  hgvsc: ENST00000353904.2:c.420A>C
  hgvsp: ENST00000353904.2:c.420A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363090
  ensembl transcript: ENST00000373978
  gene symbol: ZMYM3
  hgvsc: ENST00000373978.1:c.420A>C
  hgvsp: ENST00000373978.1:c.420A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147130
  ensembl transcript: ENST00000489332
  gene symbol: ZMYM3
  hgvsc: ENST00000489332.1:n.538A>C
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363096
  ensembl transcript: ENST00000373984
  gene symbol: ZMYM3
  hgvsc: ENST00000373984.3:c.420A>C
  hgvsp: ENST00000373984.3:c.420A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22544
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7184
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12732
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6631
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1499
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8898
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3177
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1091
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 568
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 576
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Leu140Leu
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: Other
population: European (Finnish)
reference allele: T
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP

X-70472702-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24070472702
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24070472702
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 79121
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363094
  ensembl transcript: ENST00000373982
  gene symbol: ZMYM3
  hgvsc: ENST00000373982.1:c.404G>A
  hgvsp: ENSP00000363094.1:p.Cys135Tyr
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363093
  ensembl transcript: ENST00000373981
  gene symbol: ZMYM3
  hgvsc: ENST00000373981.1:c.404G>A
  hgvsp: ENSP00000363093.1:p.Cys135Tyr
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363096
  ensembl transcript: ENST00000373984
  gene symbol: ZMYM3
  hgvsc: ENST00000373984.3:c.404G>A
  hgvsp: ENSP00000363096.3:p.Cys135Tyr
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363100
  ensembl transcript: ENST00000373988
  gene symbol: ZMYM3
  hgvsc: ENST00000373988.1:c.404G>A
  hgvsp: ENSP00000363100.1:p.Cys135Tyr
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000322845
  ensembl transcript: ENST00000314425
  gene symbol: ZMYM3
  hgvsc: ENST00000314425.5:c.404G>A
  hgvsp: ENSP00000322845.5:p.Cys135Tyr
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147130
  ensembl transcript: ENST00000489332
  gene symbol: ZMYM3
  hgvsc: ENST00000489332.1:n.522G>A
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363110
  ensembl transcript: ENST00000373998
  gene symbol: ZMYM3
  hgvsc: ENST00000373998.1:c.404G>A
  hgvsp: ENSP00000363110.1:p.Cys135Tyr
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000343909
  ensembl transcript: ENST00000353904
  gene symbol: ZMYM3
  hgvsc: ENST00000353904.2:c.404G>A
  hgvsp: ENSP00000343909.2:p.Cys135Tyr
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363090
  ensembl transcript: ENST00000373978
  gene symbol: ZMYM3
  hgvsc: ENST00000373978.1:c.404G>A
  hgvsp: ENSP00000363090.1:p.Cys135Tyr
  variant of: http://identifiers.org/hgnc/13054
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7068
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1519
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13341
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21049
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7806
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8616
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1453
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5012
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 664
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Cys135Tyr
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: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

X-70472712-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24070472712
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24070472712
    reference: chr 0
allele count: 1
allele frequency: 1.270615740387792e-5
allele num: 78702
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000322845
  ensembl transcript: ENST00000314425
  gene symbol: ZMYM3
  hgvsc: ENST00000314425.5:c.394G>A
  hgvsp: ENSP00000322845.5:p.Ala132Thr
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147130
  ensembl transcript: ENST00000489332
  gene symbol: ZMYM3
  hgvsc: ENST00000489332.1:n.512G>A
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000343909
  ensembl transcript: ENST00000353904
  gene symbol: ZMYM3
  hgvsc: ENST00000353904.2:c.394G>A
  hgvsp: ENSP00000343909.2:p.Ala132Thr
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363093
  ensembl transcript: ENST00000373981
  gene symbol: ZMYM3
  hgvsc: ENST00000373981.1:c.394G>A
  hgvsp: ENSP00000363093.1:p.Ala132Thr
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363110
  ensembl transcript: ENST00000373998
  gene symbol: ZMYM3
  hgvsc: ENST00000373998.1:c.394G>A
  hgvsp: ENSP00000363110.1:p.Ala132Thr
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363096
  ensembl transcript: ENST00000373984
  gene symbol: ZMYM3
  hgvsc: ENST00000373984.3:c.394G>A
  hgvsp: ENSP00000363096.3:p.Ala132Thr
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363090
  ensembl transcript: ENST00000373978
  gene symbol: ZMYM3
  hgvsc: ENST00000373978.1:c.394G>A
  hgvsp: ENSP00000363090.1:p.Ala132Thr
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363094
  ensembl transcript: ENST00000373982
  gene symbol: ZMYM3
  hgvsc: ENST00000373982.1:c.394G>A
  hgvsp: ENSP00000363094.1:p.Ala132Thr
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363100
  ensembl transcript: ENST00000373988
  gene symbol: ZMYM3
  hgvsc: ENST00000373988.1:c.394G>A
  hgvsp: ENSP00000363100.1:p.Ala132Thr
  variant of: http://identifiers.org/hgnc/13054
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20630
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8389
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13383
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7203
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1564
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8192
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 753
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 476
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4465
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ala132Thr
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ

X-70472720-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24070472720
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24070472720
    reference: chr 0
allele count: 1
allele frequency: 1.268761815344405e-5
allele num: 78817
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147130
  ensembl transcript: ENST00000489332
  gene symbol: ZMYM3
  hgvsc: ENST00000489332.1:n.504G>A
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000343909
  ensembl transcript: ENST00000353904
  gene symbol: ZMYM3
  hgvsc: ENST00000353904.2:c.386G>A
  hgvsp: ENSP00000343909.2:p.Gly129Glu
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363090
  ensembl transcript: ENST00000373978
  gene symbol: ZMYM3
  hgvsc: ENST00000373978.1:c.386G>A
  hgvsp: ENSP00000363090.1:p.Gly129Glu
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363096
  ensembl transcript: ENST00000373984
  gene symbol: ZMYM3
  hgvsc: ENST00000373984.3:c.386G>A
  hgvsp: ENSP00000363096.3:p.Gly129Glu
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363094
  ensembl transcript: ENST00000373982
  gene symbol: ZMYM3
  hgvsc: ENST00000373982.1:c.386G>A
  hgvsp: ENSP00000363094.1:p.Gly129Glu
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000322845
  ensembl transcript: ENST00000314425
  gene symbol: ZMYM3
  hgvsc: ENST00000314425.5:c.386G>A
  hgvsp: ENSP00000322845.5:p.Gly129Glu
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363100
  ensembl transcript: ENST00000373988
  gene symbol: ZMYM3
  hgvsc: ENST00000373988.1:c.386G>A
  hgvsp: ENSP00000363100.1:p.Gly129Glu
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363093
  ensembl transcript: ENST00000373981
  gene symbol: ZMYM3
  hgvsc: ENST00000373981.1:c.386G>A
  hgvsp: ENSP00000363093.1:p.Gly129Glu
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363110
  ensembl transcript: ENST00000373998
  gene symbol: ZMYM3
  hgvsc: ENST00000373998.1:c.386G>A
  hgvsp: ENSP00000363110.1:p.Gly129Glu
  variant of: http://identifiers.org/hgnc/13054
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8003
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8586
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7343
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1560
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13269
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20613
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 201
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3371
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24779
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1115
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Gly129Glu
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: QD

X-70472727-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24070472727
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24070472727
    reference: chr 0
allele count: 1
allele frequency: 1.271326502072262e-5
allele num: 78658
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147130
  ensembl transcript: ENST00000489332
  gene symbol: ZMYM3
  hgvsc: ENST00000489332.1:n.497G>A
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000343909
  ensembl transcript: ENST00000353904
  gene symbol: ZMYM3
  hgvsc: ENST00000353904.2:c.379G>A
  hgvsp: ENSP00000343909.2:p.Asp127Asn
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363100
  ensembl transcript: ENST00000373988
  gene symbol: ZMYM3
  hgvsc: ENST00000373988.1:c.379G>A
  hgvsp: ENSP00000363100.1:p.Asp127Asn
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363093
  ensembl transcript: ENST00000373981
  gene symbol: ZMYM3
  hgvsc: ENST00000373981.1:c.379G>A
  hgvsp: ENSP00000363093.1:p.Asp127Asn
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363090
  ensembl transcript: ENST00000373978
  gene symbol: ZMYM3
  hgvsc: ENST00000373978.1:c.379G>A
  hgvsp: ENSP00000363090.1:p.Asp127Asn
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363094
  ensembl transcript: ENST00000373982
  gene symbol: ZMYM3
  hgvsc: ENST00000373982.1:c.379G>A
  hgvsp: ENSP00000363094.1:p.Asp127Asn
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363110
  ensembl transcript: ENST00000373998
  gene symbol: ZMYM3
  hgvsc: ENST00000373998.1:c.379G>A
  hgvsp: ENSP00000363110.1:p.Asp127Asn
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000322845
  ensembl transcript: ENST00000314425
  gene symbol: ZMYM3
  hgvsc: ENST00000314425.5:c.379G>A
  hgvsp: ENSP00000322845.5:p.Asp127Asn
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363096
  ensembl transcript: ENST00000373984
  gene symbol: ZMYM3
  hgvsc: ENST00000373984.3:c.379G>A
  hgvsp: ENSP00000363096.3:p.Asp127Asn
  variant of: http://identifiers.org/hgnc/13054
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7952
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8697
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1623
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20689
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7405
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13036
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4340
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1662
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12029
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2654
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Asp127Asn
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ

X-70472736-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24070472736
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24070472736
    reference: chr 0
allele count: 2
allele frequency: 2.536847713031787e-5
allele num: 78838
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363096
  ensembl transcript: ENST00000373984
  gene symbol: ZMYM3
  hgvsc: ENST00000373984.3:c.370G>A
  hgvsp: ENSP00000363096.3:p.Val124Ile
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363094
  ensembl transcript: ENST00000373982
  gene symbol: ZMYM3
  hgvsc: ENST00000373982.1:c.370G>A
  hgvsp: ENSP00000363094.1:p.Val124Ile
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363090
  ensembl transcript: ENST00000373978
  gene symbol: ZMYM3
  hgvsc: ENST00000373978.1:c.370G>A
  hgvsp: ENSP00000363090.1:p.Val124Ile
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363100
  ensembl transcript: ENST00000373988
  gene symbol: ZMYM3
  hgvsc: ENST00000373988.1:c.370G>A
  hgvsp: ENSP00000363100.1:p.Val124Ile
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147130
  ensembl transcript: ENST00000489332
  gene symbol: ZMYM3
  hgvsc: ENST00000489332.1:n.488G>A
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000343909
  ensembl transcript: ENST00000353904
  gene symbol: ZMYM3
  hgvsc: ENST00000353904.2:c.370G>A
  hgvsp: ENSP00000343909.2:p.Val124Ile
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363110
  ensembl transcript: ENST00000373998
  gene symbol: ZMYM3
  hgvsc: ENST00000373998.1:c.370G>A
  hgvsp: ENSP00000363110.1:p.Val124Ile
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363093
  ensembl transcript: ENST00000373981
  gene symbol: ZMYM3
  hgvsc: ENST00000373981.1:c.370G>A
  hgvsp: ENSP00000363093.1:p.Val124Ile
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000322845
  ensembl transcript: ENST00000314425
  gene symbol: ZMYM3
  hgvsc: ENST00000314425.5:c.370G>A
  hgvsp: ENSP00000322845.5:p.Val124Ile
  variant of: http://identifiers.org/hgnc/13054
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21651
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7385
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12520
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1679
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7255
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9005
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 543
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 698
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 431
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Val124Ile
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ

X-70472739-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24070472739
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24070472739
    reference: chr 0
allele count: 4
allele frequency: 5.065599513702447e-5
allele num: 78964
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363094
  ensembl transcript: ENST00000373982
  gene symbol: ZMYM3
  hgvsc: ENST00000373982.1:c.367G>A
  hgvsp: ENSP00000363094.1:p.Val123Met
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363100
  ensembl transcript: ENST00000373988
  gene symbol: ZMYM3
  hgvsc: ENST00000373988.1:c.367G>A
  hgvsp: ENSP00000363100.1:p.Val123Met
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363110
  ensembl transcript: ENST00000373998
  gene symbol: ZMYM3
  hgvsc: ENST00000373998.1:c.367G>A
  hgvsp: ENSP00000363110.1:p.Val123Met
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363090
  ensembl transcript: ENST00000373978
  gene symbol: ZMYM3
  hgvsc: ENST00000373978.1:c.367G>A
  hgvsp: ENSP00000363090.1:p.Val123Met
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147130
  ensembl transcript: ENST00000489332
  gene symbol: ZMYM3
  hgvsc: ENST00000489332.1:n.485G>A
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363096
  ensembl transcript: ENST00000373984
  gene symbol: ZMYM3
  hgvsc: ENST00000373984.3:c.367G>A
  hgvsp: ENSP00000363096.3:p.Val123Met
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000343909
  ensembl transcript: ENST00000353904
  gene symbol: ZMYM3
  hgvsc: ENST00000353904.2:c.367G>A
  hgvsp: ENSP00000343909.2:p.Val123Met
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363093
  ensembl transcript: ENST00000373981
  gene symbol: ZMYM3
  hgvsc: ENST00000373981.1:c.367G>A
  hgvsp: ENSP00000363093.1:p.Val123Met
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000322845
  ensembl transcript: ENST00000314425
  gene symbol: ZMYM3
  hgvsc: ENST00000314425.5:c.367G>A
  hgvsp: ENSP00000322845.5:p.Val123Met
  variant of: http://identifiers.org/hgnc/13054
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9235
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21892
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12308
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7310
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7080
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 707
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 209
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 400
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Val123Met
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: African
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: QD

X-70472740-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24070472740
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24070472740
    reference: chr 0
allele count: 3
allele frequency: 3.800547278808148e-5
allele num: 78936
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147130
  ensembl transcript: ENST00000489332
  gene symbol: ZMYM3
  hgvsc: ENST00000489332.1:n.484G>C
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363110
  ensembl transcript: ENST00000373998
  gene symbol: ZMYM3
  hgvsc: ENST00000373998.1:c.366G>C
  hgvsp: ENSP00000363110.1:p.Glu122Asp
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363096
  ensembl transcript: ENST00000373984
  gene symbol: ZMYM3
  hgvsc: ENST00000373984.3:c.366G>C
  hgvsp: ENSP00000363096.3:p.Glu122Asp
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363093
  ensembl transcript: ENST00000373981
  gene symbol: ZMYM3
  hgvsc: ENST00000373981.1:c.366G>C
  hgvsp: ENSP00000363093.1:p.Glu122Asp
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000322845
  ensembl transcript: ENST00000314425
  gene symbol: ZMYM3
  hgvsc: ENST00000314425.5:c.366G>C
  hgvsp: ENSP00000322845.5:p.Glu122Asp
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363090
  ensembl transcript: ENST00000373978
  gene symbol: ZMYM3
  hgvsc: ENST00000373978.1:c.366G>C
  hgvsp: ENSP00000363090.1:p.Glu122Asp
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363100
  ensembl transcript: ENST00000373988
  gene symbol: ZMYM3
  hgvsc: ENST00000373988.1:c.366G>C
  hgvsp: ENSP00000363100.1:p.Glu122Asp
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363094
  ensembl transcript: ENST00000373982
  gene symbol: ZMYM3
  hgvsc: ENST00000373982.1:c.366G>C
  hgvsp: ENSP00000363094.1:p.Glu122Asp
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000343909
  ensembl transcript: ENST00000353904
  gene symbol: ZMYM3
  hgvsc: ENST00000353904.2:c.366G>C
  hgvsp: ENSP00000343909.2:p.Glu122Asp
  variant of: http://identifiers.org/hgnc/13054
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12207
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7303
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21970
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7035
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1699
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9305
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 548
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 407
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4028
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Glu122Asp
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum

X-70472744-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24070472744
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24070472744
    reference: chr 0
allele count: 2
allele frequency: 2.527262847972503e-5
allele num: 79137
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000322845
  ensembl transcript: ENST00000314425
  gene symbol: ZMYM3
  hgvsc: ENST00000314425.5:c.362C>T
  hgvsp: ENSP00000322845.5:p.Pro121Leu
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147130
  ensembl transcript: ENST00000489332
  gene symbol: ZMYM3
  hgvsc: ENST00000489332.1:n.480C>T
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363110
  ensembl transcript: ENST00000373998
  gene symbol: ZMYM3
  hgvsc: ENST00000373998.1:c.362C>T
  hgvsp: ENSP00000363110.1:p.Pro121Leu
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000343909
  ensembl transcript: ENST00000353904
  gene symbol: ZMYM3
  hgvsc: ENST00000353904.2:c.362C>T
  hgvsp: ENSP00000343909.2:p.Pro121Leu
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363096
  ensembl transcript: ENST00000373984
  gene symbol: ZMYM3
  hgvsc: ENST00000373984.3:c.362C>T
  hgvsp: ENSP00000363096.3:p.Pro121Leu
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363090
  ensembl transcript: ENST00000373978
  gene symbol: ZMYM3
  hgvsc: ENST00000373978.1:c.362C>T
  hgvsp: ENSP00000363090.1:p.Pro121Leu
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363093
  ensembl transcript: ENST00000373981
  gene symbol: ZMYM3
  hgvsc: ENST00000373981.1:c.362C>T
  hgvsp: ENSP00000363093.1:p.Pro121Leu
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363100
  ensembl transcript: ENST00000373988
  gene symbol: ZMYM3
  hgvsc: ENST00000373988.1:c.362C>T
  hgvsp: ENSP00000363100.1:p.Pro121Leu
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363094
  ensembl transcript: ENST00000373982
  gene symbol: ZMYM3
  hgvsc: ENST00000373982.1:c.362C>T
  hgvsp: ENSP00000363094.1:p.Pro121Leu
  variant of: http://identifiers.org/hgnc/13054
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11704
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6438
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22968
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1696
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7225
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9535
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1078
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11591
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 362
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Pro121Leu
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: QD

X-70472752-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24070472752
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24070472752
    reference: chr 0
allele count: 8
allele frequency: 1.009947987678635e-4
allele num: 79212
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000343909
  ensembl transcript: ENST00000353904
  gene symbol: ZMYM3
  hgvsc: ENST00000353904.2:c.354C>T
  hgvsp: ENST00000353904.2:c.354C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363094
  ensembl transcript: ENST00000373982
  gene symbol: ZMYM3
  hgvsc: ENST00000373982.1:c.354C>T
  hgvsp: ENST00000373982.1:c.354C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000322845
  ensembl transcript: ENST00000314425
  gene symbol: ZMYM3
  hgvsc: ENST00000314425.5:c.354C>T
  hgvsp: ENST00000314425.5:c.354C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363090
  ensembl transcript: ENST00000373978
  gene symbol: ZMYM3
  hgvsc: ENST00000373978.1:c.354C>T
  hgvsp: ENST00000373978.1:c.354C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363110
  ensembl transcript: ENST00000373998
  gene symbol: ZMYM3
  hgvsc: ENST00000373998.1:c.354C>T
  hgvsp: ENST00000373998.1:c.354C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363096
  ensembl transcript: ENST00000373984
  gene symbol: ZMYM3
  hgvsc: ENST00000373984.3:c.354C>T
  hgvsp: ENST00000373984.3:c.354C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147130
  ensembl transcript: ENST00000489332
  gene symbol: ZMYM3
  hgvsc: ENST00000489332.1:n.472C>T
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363100
  ensembl transcript: ENST00000373988
  gene symbol: ZMYM3
  hgvsc: ENST00000373988.1:c.354C>T
  hgvsp: ENST00000373988.1:c.354C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363093
  ensembl transcript: ENST00000373981
  gene symbol: ZMYM3
  hgvsc: ENST00000373981.1:c.354C>T
  hgvsp: ENST00000373981.1:c.354C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1868
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24332
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5668
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6993
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10696
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10072
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1041
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 736
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2995
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 583
  bin: 7.75e1
  variant carriers: 1
hgvs: p.Gly118Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: Other
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

X-70472753-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24070472753
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24070472753
    reference: chr 0
allele count: 1
allele frequency: 1.262100387464819e-5
allele num: 79233
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000343909
  ensembl transcript: ENST00000353904
  gene symbol: ZMYM3
  hgvsc: ENST00000353904.2:c.353G>T
  hgvsp: ENSP00000343909.2:p.Gly118Val
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363100
  ensembl transcript: ENST00000373988
  gene symbol: ZMYM3
  hgvsc: ENST00000373988.1:c.353G>T
  hgvsp: ENSP00000363100.1:p.Gly118Val
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147130
  ensembl transcript: ENST00000489332
  gene symbol: ZMYM3
  hgvsc: ENST00000489332.1:n.471G>T
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363090
  ensembl transcript: ENST00000373978
  gene symbol: ZMYM3
  hgvsc: ENST00000373978.1:c.353G>T
  hgvsp: ENSP00000363090.1:p.Gly118Val
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363094
  ensembl transcript: ENST00000373982
  gene symbol: ZMYM3
  hgvsc: ENST00000373982.1:c.353G>T
  hgvsp: ENSP00000363094.1:p.Gly118Val
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363096
  ensembl transcript: ENST00000373984
  gene symbol: ZMYM3
  hgvsc: ENST00000373984.3:c.353G>T
  hgvsp: ENSP00000363096.3:p.Gly118Val
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363110
  ensembl transcript: ENST00000373998
  gene symbol: ZMYM3
  hgvsc: ENST00000373998.1:c.353G>T
  hgvsp: ENSP00000363110.1:p.Gly118Val
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000322845
  ensembl transcript: ENST00000314425
  gene symbol: ZMYM3
  hgvsc: ENST00000314425.5:c.353G>T
  hgvsp: ENSP00000322845.5:p.Gly118Val
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363093
  ensembl transcript: ENST00000373981
  gene symbol: ZMYM3
  hgvsc: ENST00000373981.1:c.353G>T
  hgvsp: ENSP00000363093.1:p.Gly118Val
  variant of: http://identifiers.org/hgnc/13054
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6947
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5598
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24456
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10206
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1918
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10527
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 508
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 780
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29038
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Gly118Val
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
reference allele: C
site quality: MQ
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

X-70472758-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24070472758
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24070472758
    reference: chr 0
allele count: 1
allele frequency: 1.250390747108471e-5
allele num: 79975
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000322845
  ensembl transcript: ENST00000314425
  gene symbol: ZMYM3
  hgvsc: ENST00000314425.5:c.348A>T
  hgvsp: ENST00000314425.5:c.348A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363096
  ensembl transcript: ENST00000373984
  gene symbol: ZMYM3
  hgvsc: ENST00000373984.3:c.348A>T
  hgvsp: ENST00000373984.3:c.348A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363093
  ensembl transcript: ENST00000373981
  gene symbol: ZMYM3
  hgvsc: ENST00000373981.1:c.348A>T
  hgvsp: ENST00000373981.1:c.348A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363110
  ensembl transcript: ENST00000373998
  gene symbol: ZMYM3
  hgvsc: ENST00000373998.1:c.348A>T
  hgvsp: ENST00000373998.1:c.348A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363100
  ensembl transcript: ENST00000373988
  gene symbol: ZMYM3
  hgvsc: ENST00000373988.1:c.348A>T
  hgvsp: ENST00000373988.1:c.348A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363090
  ensembl transcript: ENST00000373978
  gene symbol: ZMYM3
  hgvsc: ENST00000373978.1:c.348A>T
  hgvsp: ENST00000373978.1:c.348A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363094
  ensembl transcript: ENST00000373982
  gene symbol: ZMYM3
  hgvsc: ENST00000373982.1:c.348A>T
  hgvsp: ENST00000373982.1:c.348A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000343909
  ensembl transcript: ENST00000353904
  gene symbol: ZMYM3
  hgvsc: ENST00000353904.2:c.348A>T
  hgvsp: ENST00000353904.2:c.348A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147130
  ensembl transcript: ENST00000489332
  gene symbol: ZMYM3
  hgvsc: ENST00000489332.1:n.466A>T
  variant of: http://identifiers.org/hgnc/13054
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 26178
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6702
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1920
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4651
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9510
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10762
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 795
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 244
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3350
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 630
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Pro116Pro
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ

X-70472767-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24070472767
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24070472767
    reference: chr 0
allele count: 13
allele frequency: 1.608890979072041e-4
allele num: 80801
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363096
  ensembl transcript: ENST00000373984
  gene symbol: ZMYM3
  hgvsc: ENST00000373984.3:c.339G>T
  hgvsp: ENSP00000363096.3:p.Glu113Asp
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363100
  ensembl transcript: ENST00000373988
  gene symbol: ZMYM3
  hgvsc: ENST00000373988.1:c.339G>T
  hgvsp: ENSP00000363100.1:p.Glu113Asp
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363094
  ensembl transcript: ENST00000373982
  gene symbol: ZMYM3
  hgvsc: ENST00000373982.1:c.339G>T
  hgvsp: ENSP00000363094.1:p.Glu113Asp
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363090
  ensembl transcript: ENST00000373978
  gene symbol: ZMYM3
  hgvsc: ENST00000373978.1:c.339G>T
  hgvsp: ENSP00000363090.1:p.Glu113Asp
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363110
  ensembl transcript: ENST00000373998
  gene symbol: ZMYM3
  hgvsc: ENST00000373998.1:c.339G>T
  hgvsp: ENSP00000363110.1:p.Glu113Asp
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000322845
  ensembl transcript: ENST00000314425
  gene symbol: ZMYM3
  hgvsc: ENST00000314425.5:c.339G>T
  hgvsp: ENSP00000322845.5:p.Glu113Asp
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363093
  ensembl transcript: ENST00000373981
  gene symbol: ZMYM3
  hgvsc: ENST00000373981.1:c.339G>T
  hgvsp: ENSP00000363093.1:p.Glu113Asp
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147130
  ensembl transcript: ENST00000489332
  gene symbol: ZMYM3
  hgvsc: ENST00000489332.1:n.457G>T
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000343909
  ensembl transcript: ENST00000353904
  gene symbol: ZMYM3
  hgvsc: ENST00000353904.2:c.339G>T
  hgvsp: ENSP00000343909.2:p.Glu113Asp
  variant of: http://identifiers.org/hgnc/13054
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7344
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2938
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11641
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29811
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6029
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2065
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 733
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 881
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 197
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1463
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Glu113Asp
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

X-70472772-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24070472772
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24070472772
    reference: chr 0
allele count: 1
allele frequency: 1.226722932358497e-5
allele num: 81518
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147130
  ensembl transcript: ENST00000489332
  gene symbol: ZMYM3
  hgvsc: ENST00000489332.1:n.452C>G
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000322845
  ensembl transcript: ENST00000314425
  gene symbol: ZMYM3
  hgvsc: ENST00000314425.5:c.334C>G
  hgvsp: ENSP00000322845.5:p.Leu112Val
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363090
  ensembl transcript: ENST00000373978
  gene symbol: ZMYM3
  hgvsc: ENST00000373978.1:c.334C>G
  hgvsp: ENSP00000363090.1:p.Leu112Val
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363100
  ensembl transcript: ENST00000373988
  gene symbol: ZMYM3
  hgvsc: ENST00000373988.1:c.334C>G
  hgvsp: ENSP00000363100.1:p.Leu112Val
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363110
  ensembl transcript: ENST00000373998
  gene symbol: ZMYM3
  hgvsc: ENST00000373998.1:c.334C>G
  hgvsp: ENSP00000363110.1:p.Leu112Val
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363094
  ensembl transcript: ENST00000373982
  gene symbol: ZMYM3
  hgvsc: ENST00000373982.1:c.334C>G
  hgvsp: ENSP00000363094.1:p.Leu112Val
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363093
  ensembl transcript: ENST00000373981
  gene symbol: ZMYM3
  hgvsc: ENST00000373981.1:c.334C>G
  hgvsp: ENSP00000363093.1:p.Leu112Val
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000343909
  ensembl transcript: ENST00000353904
  gene symbol: ZMYM3
  hgvsc: ENST00000353904.2:c.334C>G
  hgvsp: ENSP00000343909.2:p.Leu112Val
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363096
  ensembl transcript: ENST00000373984
  gene symbol: ZMYM3
  hgvsc: ENST00000373984.3:c.334C>G
  hgvsp: ENSP00000363096.3:p.Leu112Val
  variant of: http://identifiers.org/hgnc/13054
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32347
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2145
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12032
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5464
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5945
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1959
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 334
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 217
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Leu112Val
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

X-70472773-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24070472773
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24070472773
    reference: chr 0
allele count: 1
allele frequency: 1.224904763654626e-5
allele num: 81639
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000343909
  ensembl transcript: ENST00000353904
  gene symbol: ZMYM3
  hgvsc: ENST00000353904.2:c.333C>T
  hgvsp: ENST00000353904.2:c.333C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363090
  ensembl transcript: ENST00000373978
  gene symbol: ZMYM3
  hgvsc: ENST00000373978.1:c.333C>T
  hgvsp: ENST00000373978.1:c.333C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000322845
  ensembl transcript: ENST00000314425
  gene symbol: ZMYM3
  hgvsc: ENST00000314425.5:c.333C>T
  hgvsp: ENST00000314425.5:c.333C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363096
  ensembl transcript: ENST00000373984
  gene symbol: ZMYM3
  hgvsc: ENST00000373984.3:c.333C>T
  hgvsp: ENST00000373984.3:c.333C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363100
  ensembl transcript: ENST00000373988
  gene symbol: ZMYM3
  hgvsc: ENST00000373988.1:c.333C>T
  hgvsp: ENST00000373988.1:c.333C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363110
  ensembl transcript: ENST00000373998
  gene symbol: ZMYM3
  hgvsc: ENST00000373998.1:c.333C>T
  hgvsp: ENST00000373998.1:c.333C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363094
  ensembl transcript: ENST00000373982
  gene symbol: ZMYM3
  hgvsc: ENST00000373982.1:c.333C>T
  hgvsp: ENST00000373982.1:c.333C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147130
  ensembl transcript: ENST00000489332
  gene symbol: ZMYM3
  hgvsc: ENST00000489332.1:n.451C>T
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363093
  ensembl transcript: ENST00000373981
  gene symbol: ZMYM3
  hgvsc: ENST00000373981.1:c.333C>T
  hgvsp: ENST00000373981.1:c.333C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1852
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5738
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32660
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5378
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12127
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2143
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8039
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3848
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Thr111Thr
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: DP
site quality: FS

X-70472786-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24070472786
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24070472786
    reference: chr 0
allele count: 1
allele frequency: 1.210272795488103e-5
allele num: 82626
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363093
  ensembl transcript: ENST00000373981
  gene symbol: ZMYM3
  hgvsc: ENST00000373981.1:c.320C>T
  hgvsp: ENSP00000363093.1:p.Ala107Val
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363100
  ensembl transcript: ENST00000373988
  gene symbol: ZMYM3
  hgvsc: ENST00000373988.1:c.320C>T
  hgvsp: ENSP00000363100.1:p.Ala107Val
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000322845
  ensembl transcript: ENST00000314425
  gene symbol: ZMYM3
  hgvsc: ENST00000314425.5:c.320C>T
  hgvsp: ENSP00000322845.5:p.Ala107Val
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363090
  ensembl transcript: ENST00000373978
  gene symbol: ZMYM3
  hgvsc: ENST00000373978.1:c.320C>T
  hgvsp: ENSP00000363090.1:p.Ala107Val
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363096
  ensembl transcript: ENST00000373984
  gene symbol: ZMYM3
  hgvsc: ENST00000373984.3:c.320C>T
  hgvsp: ENSP00000363096.3:p.Ala107Val
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363094
  ensembl transcript: ENST00000373982
  gene symbol: ZMYM3
  hgvsc: ENST00000373982.1:c.320C>T
  hgvsp: ENSP00000363094.1:p.Ala107Val
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000343909
  ensembl transcript: ENST00000353904
  gene symbol: ZMYM3
  hgvsc: ENST00000353904.2:c.320C>T
  hgvsp: ENSP00000343909.2:p.Ala107Val
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147130
  ensembl transcript: ENST00000489332
  gene symbol: ZMYM3
  hgvsc: ENST00000489332.1:n.438C>T
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363110
  ensembl transcript: ENST00000373998
  gene symbol: ZMYM3
  hgvsc: ENST00000373998.1:c.320C>T
  hgvsp: ENSP00000363110.1:p.Ala107Val
  variant of: http://identifiers.org/hgnc/13054
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1175
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4399
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2325
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34792
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13021
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4191
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 352
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 775
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 992
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 646
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ala107Val
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: East Asian
population: Latino
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

X-70472804-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24070472804
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24070472804
    reference: chr 0
allele count: 1
allele frequency: 1.207627374497325e-5
allele num: 82807
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000343909
  ensembl transcript: ENST00000353904
  gene symbol: ZMYM3
  hgvsc: ENST00000353904.2:c.302G>A
  hgvsp: ENSP00000343909.2:p.Gly101Glu
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363093
  ensembl transcript: ENST00000373981
  gene symbol: ZMYM3
  hgvsc: ENST00000373981.1:c.302G>A
  hgvsp: ENSP00000363093.1:p.Gly101Glu
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363096
  ensembl transcript: ENST00000373984
  gene symbol: ZMYM3
  hgvsc: ENST00000373984.3:c.302G>A
  hgvsp: ENSP00000363096.3:p.Gly101Glu
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363090
  ensembl transcript: ENST00000373978
  gene symbol: ZMYM3
  hgvsc: ENST00000373978.1:c.302G>A
  hgvsp: ENSP00000363090.1:p.Gly101Glu
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147130
  ensembl transcript: ENST00000489332
  gene symbol: ZMYM3
  hgvsc: ENST00000489332.1:n.420G>A
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000322845
  ensembl transcript: ENST00000314425
  gene symbol: ZMYM3
  hgvsc: ENST00000314425.5:c.302G>A
  hgvsp: ENSP00000322845.5:p.Gly101Glu
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363094
  ensembl transcript: ENST00000373982
  gene symbol: ZMYM3
  hgvsc: ENST00000373982.1:c.302G>A
  hgvsp: ENSP00000363094.1:p.Gly101Glu
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363100
  ensembl transcript: ENST00000373988
  gene symbol: ZMYM3
  hgvsc: ENST00000373988.1:c.302G>A
  hgvsp: ENSP00000363100.1:p.Gly101Glu
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363110
  ensembl transcript: ENST00000373998
  gene symbol: ZMYM3
  hgvsc: ENST00000373998.1:c.302G>A
  hgvsp: ENSP00000363110.1:p.Gly101Glu
  variant of: http://identifiers.org/hgnc/13054
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4060
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2346
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13457
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4480
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33931
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1545
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42422
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1130
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 239
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 501
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Gly101Glu
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum

X-70472814-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24070472814
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24070472814
    reference: chr 0
allele count: 19
allele frequency: 2.305713314887627e-4
allele num: 82404
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363110
  ensembl transcript: ENST00000373998
  gene symbol: ZMYM3
  hgvsc: ENST00000373998.1:c.292G>A
  hgvsp: ENSP00000363110.1:p.Gly98Ser
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363094
  ensembl transcript: ENST00000373982
  gene symbol: ZMYM3
  hgvsc: ENST00000373982.1:c.292G>A
  hgvsp: ENSP00000363094.1:p.Gly98Ser
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363090
  ensembl transcript: ENST00000373978
  gene symbol: ZMYM3
  hgvsc: ENST00000373978.1:c.292G>A
  hgvsp: ENSP00000363090.1:p.Gly98Ser
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363096
  ensembl transcript: ENST00000373984
  gene symbol: ZMYM3
  hgvsc: ENST00000373984.3:c.292G>A
  hgvsp: ENSP00000363096.3:p.Gly98Ser
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363100
  ensembl transcript: ENST00000373988
  gene symbol: ZMYM3
  hgvsc: ENST00000373988.1:c.292G>A
  hgvsp: ENSP00000363100.1:p.Gly98Ser
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147130
  ensembl transcript: ENST00000489332
  gene symbol: ZMYM3
  hgvsc: ENST00000489332.1:n.410G>A
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000343909
  ensembl transcript: ENST00000353904
  gene symbol: ZMYM3
  hgvsc: ENST00000353904.2:c.292G>A
  hgvsp: ENSP00000343909.2:p.Gly98Ser
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363093
  ensembl transcript: ENST00000373981
  gene symbol: ZMYM3
  hgvsc: ENST00000373981.1:c.292G>A
  hgvsp: ENSP00000363093.1:p.Gly98Ser
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000322845
  ensembl transcript: ENST00000314425
  gene symbol: ZMYM3
  hgvsc: ENST00000314425.5:c.292G>A
  hgvsp: ENSP00000322845.5:p.Gly98Ser
  variant of: http://identifiers.org/hgnc/13054
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5309
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4166
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2340
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32206
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2026
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13621
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7513
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1131
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 629
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Gly98Ser
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD

X-70472815-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24070472815
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24070472815
    reference: chr 0
allele count: 1
allele frequency: 1.212841566506167e-5
allele num: 82451
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147130
  ensembl transcript: ENST00000489332
  gene symbol: ZMYM3
  hgvsc: ENST00000489332.1:n.409C>T
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363096
  ensembl transcript: ENST00000373984
  gene symbol: ZMYM3
  hgvsc: ENST00000373984.3:c.291C>T
  hgvsp: ENST00000373984.3:c.291C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363110
  ensembl transcript: ENST00000373998
  gene symbol: ZMYM3
  hgvsc: ENST00000373998.1:c.291C>T
  hgvsp: ENST00000373998.1:c.291C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363093
  ensembl transcript: ENST00000373981
  gene symbol: ZMYM3
  hgvsc: ENST00000373981.1:c.291C>T
  hgvsp: ENST00000373981.1:c.291C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363094
  ensembl transcript: ENST00000373982
  gene symbol: ZMYM3
  hgvsc: ENST00000373982.1:c.291C>T
  hgvsp: ENST00000373982.1:c.291C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000322845
  ensembl transcript: ENST00000314425
  gene symbol: ZMYM3
  hgvsc: ENST00000314425.5:c.291C>T
  hgvsp: ENST00000314425.5:c.291C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363090
  ensembl transcript: ENST00000373978
  gene symbol: ZMYM3
  hgvsc: ENST00000373978.1:c.291C>T
  hgvsp: ENST00000373978.1:c.291C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363100
  ensembl transcript: ENST00000373988
  gene symbol: ZMYM3
  hgvsc: ENST00000373988.1:c.291C>T
  hgvsp: ENST00000373988.1:c.291C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000343909
  ensembl transcript: ENST00000353904
  gene symbol: ZMYM3
  hgvsc: ENST00000353904.2:c.291C>T
  hgvsp: ENST00000353904.2:c.291C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1947
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13698
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4140
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32226
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5304
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2359
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 220
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 259
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7511
  bin: 2.25e1
  variant carriers: 0
hgvs: p.His97His
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD

X-70472827-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24070472827
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24070472827
    reference: chr 0
allele count: 1
allele frequency: 1.23751655178388e-5
allele num: 80807
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363100
  ensembl transcript: ENST00000373988
  gene symbol: ZMYM3
  hgvsc: ENST00000373988.1:c.279G>A
  hgvsp: ENST00000373988.1:c.279G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363093
  ensembl transcript: ENST00000373981
  gene symbol: ZMYM3
  hgvsc: ENST00000373981.1:c.279G>A
  hgvsp: ENST00000373981.1:c.279G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363096
  ensembl transcript: ENST00000373984
  gene symbol: ZMYM3
  hgvsc: ENST00000373984.3:c.279G>A
  hgvsp: ENST00000373984.3:c.279G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363094
  ensembl transcript: ENST00000373982
  gene symbol: ZMYM3
  hgvsc: ENST00000373982.1:c.279G>A
  hgvsp: ENST00000373982.1:c.279G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363090
  ensembl transcript: ENST00000373978
  gene symbol: ZMYM3
  hgvsc: ENST00000373978.1:c.279G>A
  hgvsp: ENST00000373978.1:c.279G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000343909
  ensembl transcript: ENST00000353904
  gene symbol: ZMYM3
  hgvsc: ENST00000353904.2:c.279G>A
  hgvsp: ENST00000353904.2:c.279G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363110
  ensembl transcript: ENST00000373998
  gene symbol: ZMYM3
  hgvsc: ENST00000373998.1:c.279G>A
  hgvsp: ENST00000373998.1:c.279G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147130
  ensembl transcript: ENST00000489332
  gene symbol: ZMYM3
  hgvsc: ENST00000489332.1:n.397G>A
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000322845
  ensembl transcript: ENST00000314425
  gene symbol: ZMYM3
  hgvsc: ENST00000314425.5:c.279G>A
  hgvsp: ENST00000314425.5:c.279G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13632
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7195
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3141
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2376
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4543
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28422
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 437
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 444
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1245
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 811
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Pro93Pro
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ

X-70472834-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24070472834
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24070472834
    reference: chr 0
allele count: 2
allele frequency: 2.473563787026158e-5
allele num: 80855
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363100
  ensembl transcript: ENST00000373988
  gene symbol: ZMYM3
  hgvsc: ENST00000373988.1:c.272C>T
  hgvsp: ENSP00000363100.1:p.Ser91Phe
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363110
  ensembl transcript: ENST00000373998
  gene symbol: ZMYM3
  hgvsc: ENST00000373998.1:c.272C>T
  hgvsp: ENSP00000363110.1:p.Ser91Phe
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363094
  ensembl transcript: ENST00000373982
  gene symbol: ZMYM3
  hgvsc: ENST00000373982.1:c.272C>T
  hgvsp: ENSP00000363094.1:p.Ser91Phe
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363090
  ensembl transcript: ENST00000373978
  gene symbol: ZMYM3
  hgvsc: ENST00000373978.1:c.272C>T
  hgvsp: ENSP00000363090.1:p.Ser91Phe
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147130
  ensembl transcript: ENST00000489332
  gene symbol: ZMYM3
  hgvsc: ENST00000489332.1:n.390C>T
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000343909
  ensembl transcript: ENST00000353904
  gene symbol: ZMYM3
  hgvsc: ENST00000353904.2:c.272C>T
  hgvsp: ENSP00000343909.2:p.Ser91Phe
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363096
  ensembl transcript: ENST00000373984
  gene symbol: ZMYM3
  hgvsc: ENST00000373984.3:c.272C>T
  hgvsp: ENSP00000363096.3:p.Ser91Phe
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363093
  ensembl transcript: ENST00000373981
  gene symbol: ZMYM3
  hgvsc: ENST00000373981.1:c.272C>T
  hgvsp: ENSP00000363093.1:p.Ser91Phe
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000322845
  ensembl transcript: ENST00000314425
  gene symbol: ZMYM3
  hgvsc: ENST00000314425.5:c.272C>T
  hgvsp: ENSP00000322845.5:p.Ser91Phe
  variant of: http://identifiers.org/hgnc/13054
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 842
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3563
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8016
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27090
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2320
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4778
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13348
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 292
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 370
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 245
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ser91Phe
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

X-70472836-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24070472836
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24070472836
    reference: chr 0
allele count: 3
allele frequency: 3.721437963629146e-5
allele num: 80614
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363093
  ensembl transcript: ENST00000373981
  gene symbol: ZMYM3
  hgvsc: ENST00000373981.1:c.270C>T
  hgvsp: ENST00000373981.1:c.270C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363090
  ensembl transcript: ENST00000373978
  gene symbol: ZMYM3
  hgvsc: ENST00000373978.1:c.270C>T
  hgvsp: ENST00000373978.1:c.270C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363096
  ensembl transcript: ENST00000373984
  gene symbol: ZMYM3
  hgvsc: ENST00000373984.3:c.270C>T
  hgvsp: ENST00000373984.3:c.270C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000343909
  ensembl transcript: ENST00000353904
  gene symbol: ZMYM3
  hgvsc: ENST00000353904.2:c.270C>T
  hgvsp: ENST00000353904.2:c.270C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363100
  ensembl transcript: ENST00000373988
  gene symbol: ZMYM3
  hgvsc: ENST00000373988.1:c.270C>T
  hgvsp: ENST00000373988.1:c.270C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363094
  ensembl transcript: ENST00000373982
  gene symbol: ZMYM3
  hgvsc: ENST00000373982.1:c.270C>T
  hgvsp: ENST00000373982.1:c.270C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363110
  ensembl transcript: ENST00000373998
  gene symbol: ZMYM3
  hgvsc: ENST00000373998.1:c.270C>T
  hgvsp: ENST00000373998.1:c.270C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000322845
  ensembl transcript: ENST00000314425
  gene symbol: ZMYM3
  hgvsc: ENST00000314425.5:c.270C>T
  hgvsp: ENST00000314425.5:c.270C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147130
  ensembl transcript: ENST00000489332
  gene symbol: ZMYM3
  hgvsc: ENST00000489332.1:n.388C>T
  variant of: http://identifiers.org/hgnc/13054
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4843
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8345
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4212
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2354
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13193
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26063
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1245
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 436
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 926
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 368
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Pro90Pro
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: Other
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ

X-70472846-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24070472846
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24070472846
    reference: chr 0
allele count: 3
allele frequency: 3.816988141890173e-5
allele num: 78596
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147130
  ensembl transcript: ENST00000489332
  gene symbol: ZMYM3
  hgvsc: ENST00000489332.1:n.378A>G
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363094
  ensembl transcript: ENST00000373982
  gene symbol: ZMYM3
  hgvsc: ENST00000373982.1:c.260A>G
  hgvsp: ENSP00000363094.1:p.Tyr87Cys
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363093
  ensembl transcript: ENST00000373981
  gene symbol: ZMYM3
  hgvsc: ENST00000373981.1:c.260A>G
  hgvsp: ENSP00000363093.1:p.Tyr87Cys
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000343909
  ensembl transcript: ENST00000353904
  gene symbol: ZMYM3
  hgvsc: ENST00000353904.2:c.260A>G
  hgvsp: ENSP00000343909.2:p.Tyr87Cys
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363090
  ensembl transcript: ENST00000373978
  gene symbol: ZMYM3
  hgvsc: ENST00000373978.1:c.260A>G
  hgvsp: ENSP00000363090.1:p.Tyr87Cys
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363110
  ensembl transcript: ENST00000373998
  gene symbol: ZMYM3
  hgvsc: ENST00000373998.1:c.260A>G
  hgvsp: ENSP00000363110.1:p.Tyr87Cys
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000322845
  ensembl transcript: ENST00000314425
  gene symbol: ZMYM3
  hgvsc: ENST00000314425.5:c.260A>G
  hgvsp: ENSP00000322845.5:p.Tyr87Cys
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363100
  ensembl transcript: ENST00000373988
  gene symbol: ZMYM3
  hgvsc: ENST00000373988.1:c.260A>G
  hgvsp: ENSP00000363100.1:p.Tyr87Cys
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363096
  ensembl transcript: ENST00000373984
  gene symbol: ZMYM3
  hgvsc: ENST00000373984.3:c.260A>G
  hgvsp: ENSP00000363096.3:p.Tyr87Cys
  variant of: http://identifiers.org/hgnc/13054
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8964
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5903
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1160
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2139
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11343
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7930
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22378
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1076
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28292
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 823
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Tyr87Cys
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
reference allele: T
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: BaseQRankSum

X-70472853-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24070472853
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24070472853
    reference: chr 0
allele count: 9
allele frequency: 1.385958698430787e-4
allele num: 64937
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363096
  ensembl transcript: ENST00000373984
  gene symbol: ZMYM3
  hgvsc: ENST00000373984.3:c.253C>G
  hgvsp: ENSP00000363096.3:p.Leu85Val
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000322845
  ensembl transcript: ENST00000314425
  gene symbol: ZMYM3
  hgvsc: ENST00000314425.5:c.253C>G
  hgvsp: ENSP00000322845.5:p.Leu85Val
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147130
  ensembl transcript: ENST00000489332
  gene symbol: ZMYM3
  hgvsc: ENST00000489332.1:n.371C>G
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000343909
  ensembl transcript: ENST00000353904
  gene symbol: ZMYM3
  hgvsc: ENST00000353904.2:c.253C>G
  hgvsp: ENSP00000343909.2:p.Leu85Val
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363100
  ensembl transcript: ENST00000373988
  gene symbol: ZMYM3
  hgvsc: ENST00000373988.1:c.253C>G
  hgvsp: ENSP00000363100.1:p.Leu85Val
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363093
  ensembl transcript: ENST00000373981
  gene symbol: ZMYM3
  hgvsc: ENST00000373981.1:c.253C>G
  hgvsp: ENSP00000363093.1:p.Leu85Val
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363110
  ensembl transcript: ENST00000373998
  gene symbol: ZMYM3
  hgvsc: ENST00000373998.1:c.253C>G
  hgvsp: ENSP00000363110.1:p.Leu85Val
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363094
  ensembl transcript: ENST00000373982
  gene symbol: ZMYM3
  hgvsc: ENST00000373982.1:c.253C>G
  hgvsp: ENSP00000363094.1:p.Leu85Val
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363090
  ensembl transcript: ENST00000373978
  gene symbol: ZMYM3
  hgvsc: ENST00000373978.1:c.253C>G
  hgvsp: ENSP00000363090.1:p.Leu85Val
  variant of: http://identifiers.org/hgnc/13054
canonical: true
consequence: missense
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2812
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 10246
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1155
  bin: 3.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 6504
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8809
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1178
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8898
  bin: 1.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19784
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7514
  bin: 2.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 2757
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6695
  bin: 2.5e0
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Leu85Val
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum

X-70472853-G-GC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24070472853
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24070472854
    reference: chr 0
allele count: 67
allele frequency: 1.031769253276252e-3
allele num: 64937
alternate allele: GC
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363096
  ensembl transcript: ENST00000373984
  gene symbol: ZMYM3
  hgvsc: ENST00000373984.3:c.252dupG
  hgvsp: ENSP00000363096.3:p.Leu85AlafsTer4
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363110
  ensembl transcript: ENST00000373998
  gene symbol: ZMYM3
  hgvsc: ENST00000373998.1:c.252dupG
  hgvsp: ENSP00000363110.1:p.Leu85AlafsTer4
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363100
  ensembl transcript: ENST00000373988
  gene symbol: ZMYM3
  hgvsc: ENST00000373988.1:c.252dupG
  hgvsp: ENSP00000363100.1:p.Leu85AlafsTer4
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363093
  ensembl transcript: ENST00000373981
  gene symbol: ZMYM3
  hgvsc: ENST00000373981.1:c.252dupG
  hgvsp: ENSP00000363093.1:p.Leu85AlafsTer4
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363090
  ensembl transcript: ENST00000373978
  gene symbol: ZMYM3
  hgvsc: ENST00000373978.1:c.252dupG
  hgvsp: ENSP00000363090.1:p.Leu85AlafsTer4
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000322845
  ensembl transcript: ENST00000314425
  gene symbol: ZMYM3
  hgvsc: ENST00000314425.5:c.252dupG
  hgvsp: ENSP00000322845.5:p.Leu85AlafsTer4
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363094
  ensembl transcript: ENST00000373982
  gene symbol: ZMYM3
  hgvsc: ENST00000373982.1:c.252dupG
  hgvsp: ENSP00000363094.1:p.Leu85AlafsTer4
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000343909
  ensembl transcript: ENST00000353904
  gene symbol: ZMYM3
  hgvsc: ENST00000353904.2:c.252dupG
  hgvsp: ENSP00000343909.2:p.Leu85AlafsTer4
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147130
  ensembl transcript: ENST00000489332
  gene symbol: ZMYM3
  hgvsc: ENST00000489332.1:n.370dupG
  variant of: http://identifiers.org/hgnc/13054
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 8898
  bin: 1.75e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1155
  bin: 3.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10246
  bin: 2.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6504
  bin: 7.5e0
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19784
  bin: 2.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1178
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2812
  bin: 3.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 8809
  bin: 1.25e1
  variant carriers: 25
genotype quality: GenotypeQuality
  all individuals: 2071
  bin: 4.25e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 9.75e1
  variant carriers: 20
genotype quality: GenotypeQuality
  all individuals: 6695
  bin: 2.5e0
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 2625
  bin: 7.5e0
  variant carriers: 6
hgvs: p.Leu85AlafsTer4
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD

X-70472853-G-GCC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24070472853
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24070472855
    reference: chr 0
allele count: 2
allele frequency: 3.079908218735082e-5
allele num: 64937
alternate allele: GCC
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363094
  ensembl transcript: ENST00000373982
  gene symbol: ZMYM3
  hgvsc: ENST00000373982.1:c.251_252dupGG
  hgvsp: ENSP00000363094.1:p.Leu85GlyfsTer29
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363090
  ensembl transcript: ENST00000373978
  gene symbol: ZMYM3
  hgvsc: ENST00000373978.1:c.251_252dupGG
  hgvsp: ENSP00000363090.1:p.Leu85GlyfsTer29
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363093
  ensembl transcript: ENST00000373981
  gene symbol: ZMYM3
  hgvsc: ENST00000373981.1:c.251_252dupGG
  hgvsp: ENSP00000363093.1:p.Leu85GlyfsTer29
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363100
  ensembl transcript: ENST00000373988
  gene symbol: ZMYM3
  hgvsc: ENST00000373988.1:c.251_252dupGG
  hgvsp: ENSP00000363100.1:p.Leu85GlyfsTer29
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363096
  ensembl transcript: ENST00000373984
  gene symbol: ZMYM3
  hgvsc: ENST00000373984.3:c.251_252dupGG
  hgvsp: ENSP00000363096.3:p.Leu85GlyfsTer29
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000343909
  ensembl transcript: ENST00000353904
  gene symbol: ZMYM3
  hgvsc: ENST00000353904.2:c.251_252dupGG
  hgvsp: ENSP00000343909.2:p.Leu85GlyfsTer29
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000322845
  ensembl transcript: ENST00000314425
  gene symbol: ZMYM3
  hgvsc: ENST00000314425.5:c.251_252dupGG
  hgvsp: ENSP00000322845.5:p.Leu85GlyfsTer29
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363110
  ensembl transcript: ENST00000373998
  gene symbol: ZMYM3
  hgvsc: ENST00000373998.1:c.251_252dupGG
  hgvsp: ENSP00000363110.1:p.Leu85GlyfsTer29
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147130
  ensembl transcript: ENST00000489332
  gene symbol: ZMYM3
  hgvsc: ENST00000489332.1:n.369_370dupGG
  variant of: http://identifiers.org/hgnc/13054
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 2812
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8809
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19784
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1155
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1178
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6504
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8898
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10246
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 340
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2757
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1553
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Leu85GlyfsTer29
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

X-70472854-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24070472854
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24070472854
    reference: chr 0
allele count: 1
allele frequency: 1.294716262930979e-5
allele num: 77237
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000343909
  ensembl transcript: ENST00000353904
  gene symbol: ZMYM3
  hgvsc: ENST00000353904.2:c.252G>T
  hgvsp: ENST00000353904.2:c.252G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363096
  ensembl transcript: ENST00000373984
  gene symbol: ZMYM3
  hgvsc: ENST00000373984.3:c.252G>T
  hgvsp: ENST00000373984.3:c.252G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363090
  ensembl transcript: ENST00000373978
  gene symbol: ZMYM3
  hgvsc: ENST00000373978.1:c.252G>T
  hgvsp: ENST00000373978.1:c.252G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363094
  ensembl transcript: ENST00000373982
  gene symbol: ZMYM3
  hgvsc: ENST00000373982.1:c.252G>T
  hgvsp: ENST00000373982.1:c.252G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147130
  ensembl transcript: ENST00000489332
  gene symbol: ZMYM3
  hgvsc: ENST00000489332.1:n.370G>T
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363110
  ensembl transcript: ENST00000373998
  gene symbol: ZMYM3
  hgvsc: ENST00000373998.1:c.252G>T
  hgvsp: ENST00000373998.1:c.252G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000322845
  ensembl transcript: ENST00000314425
  gene symbol: ZMYM3
  hgvsc: ENST00000314425.5:c.252G>T
  hgvsp: ENST00000314425.5:c.252G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363093
  ensembl transcript: ENST00000373981
  gene symbol: ZMYM3
  hgvsc: ENST00000373981.1:c.252G>T
  hgvsp: ENST00000373981.1:c.252G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363100
  ensembl transcript: ENST00000373988
  gene symbol: ZMYM3
  hgvsc: ENST00000373988.1:c.252G>T
  hgvsp: ENST00000373988.1:c.252G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20165
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1092
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4655
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16682
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6199
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3466
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7379
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 798
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2389
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 638
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1754
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Gly84Gly
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: African
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum

X-70472857-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24070472857
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24070472857
    reference: chr 0
allele count: 1
allele frequency: 1.270260657486916e-5
allele num: 78724
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363094
  ensembl transcript: ENST00000373982
  gene symbol: ZMYM3
  hgvsc: ENST00000373982.1:c.249G>A
  hgvsp: ENST00000373982.1:c.249G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147130
  ensembl transcript: ENST00000489332
  gene symbol: ZMYM3
  hgvsc: ENST00000489332.1:n.367G>A
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000343909
  ensembl transcript: ENST00000353904
  gene symbol: ZMYM3
  hgvsc: ENST00000353904.2:c.249G>A
  hgvsp: ENST00000353904.2:c.249G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363096
  ensembl transcript: ENST00000373984
  gene symbol: ZMYM3
  hgvsc: ENST00000373984.3:c.249G>A
  hgvsp: ENST00000373984.3:c.249G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363100
  ensembl transcript: ENST00000373988
  gene symbol: ZMYM3
  hgvsc: ENST00000373988.1:c.249G>A
  hgvsp: ENST00000373988.1:c.249G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000322845
  ensembl transcript: ENST00000314425
  gene symbol: ZMYM3
  hgvsc: ENST00000314425.5:c.249G>A
  hgvsp: ENST00000314425.5:c.249G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363093
  ensembl transcript: ENST00000373981
  gene symbol: ZMYM3
  hgvsc: ENST00000373981.1:c.249G>A
  hgvsp: ENST00000373981.1:c.249G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363110
  ensembl transcript: ENST00000373998
  gene symbol: ZMYM3
  hgvsc: ENST00000373998.1:c.249G>A
  hgvsp: ENST00000373998.1:c.249G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363090
  ensembl transcript: ENST00000373978
  gene symbol: ZMYM3
  hgvsc: ENST00000373978.1:c.249G>A
  hgvsp: ENST00000373978.1:c.249G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6366
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6899
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21705
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2833
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17834
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3300
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1857
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 403
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1744
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Gly83Gly
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: European (Finnish)
reference allele: C
site quality: FS
site quality: DP
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff

X-70472863-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24070472863
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24070472863
    reference: chr 0
allele count: 27
allele frequency: 3.442560244804284e-4
allele num: 78430
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363100
  ensembl transcript: ENST00000373988
  gene symbol: ZMYM3
  hgvsc: ENST00000373988.1:c.243G>A
  hgvsp: ENST00000373988.1:c.243G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363096
  ensembl transcript: ENST00000373984
  gene symbol: ZMYM3
  hgvsc: ENST00000373984.3:c.243G>A
  hgvsp: ENST00000373984.3:c.243G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000343909
  ensembl transcript: ENST00000353904
  gene symbol: ZMYM3
  hgvsc: ENST00000353904.2:c.243G>A
  hgvsp: ENST00000353904.2:c.243G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363094
  ensembl transcript: ENST00000373982
  gene symbol: ZMYM3
  hgvsc: ENST00000373982.1:c.243G>A
  hgvsp: ENST00000373982.1:c.243G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000322845
  ensembl transcript: ENST00000314425
  gene symbol: ZMYM3
  hgvsc: ENST00000314425.5:c.243G>A
  hgvsp: ENST00000314425.5:c.243G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363090
  ensembl transcript: ENST00000373978
  gene symbol: ZMYM3
  hgvsc: ENST00000373978.1:c.243G>A
  hgvsp: ENST00000373978.1:c.243G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147130
  ensembl transcript: ENST00000489332
  gene symbol: ZMYM3
  hgvsc: ENST00000489332.1:n.361G>A
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363110
  ensembl transcript: ENST00000373998
  gene symbol: ZMYM3
  hgvsc: ENST00000373998.1:c.243G>A
  hgvsp: ENST00000373998.1:c.243G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363093
  ensembl transcript: ENST00000373981
  gene symbol: ZMYM3
  hgvsc: ENST00000373981.1:c.243G>A
  hgvsp: ENST00000373981.1:c.243G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17537
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6642
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6470
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1964
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3226
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 23128
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 274
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 221
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Gly81Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: African
population: European (Finnish)
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff

X-70472889-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24070472889
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24070472889
    reference: chr 0
allele count: 1
allele frequency: 1.346148668658967e-5
allele num: 74286
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363100
  ensembl transcript: ENST00000373988
  gene symbol: ZMYM3
  hgvsc: ENST00000373988.1:c.217C>T
  hgvsp: ENST00000373988.1:c.217C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147130
  ensembl transcript: ENST00000489332
  gene symbol: ZMYM3
  hgvsc: ENST00000489332.1:n.335C>T
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363096
  ensembl transcript: ENST00000373984
  gene symbol: ZMYM3
  hgvsc: ENST00000373984.3:c.217C>T
  hgvsp: ENST00000373984.3:c.217C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363094
  ensembl transcript: ENST00000373982
  gene symbol: ZMYM3
  hgvsc: ENST00000373982.1:c.217C>T
  hgvsp: ENST00000373982.1:c.217C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363110
  ensembl transcript: ENST00000373998
  gene symbol: ZMYM3
  hgvsc: ENST00000373998.1:c.217C>T
  hgvsp: ENST00000373998.1:c.217C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000343909
  ensembl transcript: ENST00000353904
  gene symbol: ZMYM3
  hgvsc: ENST00000353904.2:c.217C>T
  hgvsp: ENST00000353904.2:c.217C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363093
  ensembl transcript: ENST00000373981
  gene symbol: ZMYM3
  hgvsc: ENST00000373981.1:c.217C>T
  hgvsp: ENST00000373981.1:c.217C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000322845
  ensembl transcript: ENST00000314425
  gene symbol: ZMYM3
  hgvsc: ENST00000314425.5:c.217C>T
  hgvsp: ENST00000314425.5:c.217C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363090
  ensembl transcript: ENST00000373978
  gene symbol: ZMYM3
  hgvsc: ENST00000373978.1:c.217C>T
  hgvsp: ENST00000373978.1:c.217C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18357
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10229
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2925
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1393
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2612
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10064
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14484
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2151
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 639
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 379
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 816
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Leu73Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: Other
reference allele: G
site quality: QD
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff

X-70472890-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24070472890
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24070472890
    reference: chr 0
allele count: 1
allele frequency: 1.345225123424405e-5
allele num: 74337
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363096
  ensembl transcript: ENST00000373984
  gene symbol: ZMYM3
  hgvsc: ENST00000373984.3:c.216C>A
  hgvsp: ENST00000373984.3:c.216C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000343909
  ensembl transcript: ENST00000353904
  gene symbol: ZMYM3
  hgvsc: ENST00000353904.2:c.216C>A
  hgvsp: ENST00000353904.2:c.216C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363090
  ensembl transcript: ENST00000373978
  gene symbol: ZMYM3
  hgvsc: ENST00000373978.1:c.216C>A
  hgvsp: ENST00000373978.1:c.216C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147130
  ensembl transcript: ENST00000489332
  gene symbol: ZMYM3
  hgvsc: ENST00000489332.1:n.334C>A
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363100
  ensembl transcript: ENST00000373988
  gene symbol: ZMYM3
  hgvsc: ENST00000373988.1:c.216C>A
  hgvsp: ENST00000373988.1:c.216C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363110
  ensembl transcript: ENST00000373998
  gene symbol: ZMYM3
  hgvsc: ENST00000373998.1:c.216C>A
  hgvsp: ENST00000373998.1:c.216C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000322845
  ensembl transcript: ENST00000314425
  gene symbol: ZMYM3
  hgvsc: ENST00000314425.5:c.216C>A
  hgvsp: ENST00000314425.5:c.216C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363094
  ensembl transcript: ENST00000373982
  gene symbol: ZMYM3
  hgvsc: ENST00000373982.1:c.216C>A
  hgvsp: ENST00000373982.1:c.216C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363093
  ensembl transcript: ENST00000373981
  gene symbol: ZMYM3
  hgvsc: ENST00000373981.1:c.216C>A
  hgvsp: ENST00000373981.1:c.216C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14475
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18423
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10093
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10218
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2893
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2575
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1094
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1497
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 448
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Val72Val
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff

X-70472898-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24070472898
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24070472898
    reference: chr 0
allele count: 4
allele frequency: 5.504107440177232e-5
allele num: 72673
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147130
  ensembl transcript: ENST00000489332
  gene symbol: ZMYM3
  hgvsc: ENST00000489332.1:n.326C>G
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363094
  ensembl transcript: ENST00000373982
  gene symbol: ZMYM3
  hgvsc: ENST00000373982.1:c.208C>G
  hgvsp: ENSP00000363094.1:p.Pro70Ala
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363090
  ensembl transcript: ENST00000373978
  gene symbol: ZMYM3
  hgvsc: ENST00000373978.1:c.208C>G
  hgvsp: ENSP00000363090.1:p.Pro70Ala
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000322845
  ensembl transcript: ENST00000314425
  gene symbol: ZMYM3
  hgvsc: ENST00000314425.5:c.208C>G
  hgvsp: ENSP00000322845.5:p.Pro70Ala
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000343909
  ensembl transcript: ENST00000353904
  gene symbol: ZMYM3
  hgvsc: ENST00000353904.2:c.208C>G
  hgvsp: ENSP00000343909.2:p.Pro70Ala
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363110
  ensembl transcript: ENST00000373998
  gene symbol: ZMYM3
  hgvsc: ENST00000373998.1:c.208C>G
  hgvsp: ENSP00000363110.1:p.Pro70Ala
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363093
  ensembl transcript: ENST00000373981
  gene symbol: ZMYM3
  hgvsc: ENST00000373981.1:c.208C>G
  hgvsp: ENSP00000363093.1:p.Pro70Ala
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363096
  ensembl transcript: ENST00000373984
  gene symbol: ZMYM3
  hgvsc: ENST00000373984.3:c.208C>G
  hgvsp: ENSP00000363096.3:p.Pro70Ala
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363100
  ensembl transcript: ENST00000373988
  gene symbol: ZMYM3
  hgvsc: ENST00000373988.1:c.208C>G
  hgvsp: ENSP00000363100.1:p.Pro70Ala
  variant of: http://identifiers.org/hgnc/13054
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1553
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2313
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16791
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3556
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11905
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12658
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11311
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26021
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 528
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1656
  bin: 7.5e0
  variant carriers: 1
hgvs: p.Pro70Ala
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: DP

X-70472910-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24070472910
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24070472910
    reference: chr 0
allele count: 1
allele frequency: 1.434020707259013e-5
allele num: 69734
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363090
  ensembl transcript: ENST00000373978
  gene symbol: ZMYM3
  hgvsc: ENST00000373978.1:c.196C>T
  hgvsp: ENST00000373978.1:c.196C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363093
  ensembl transcript: ENST00000373981
  gene symbol: ZMYM3
  hgvsc: ENST00000373981.1:c.196C>T
  hgvsp: ENST00000373981.1:c.196C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147130
  ensembl transcript: ENST00000489332
  gene symbol: ZMYM3
  hgvsc: ENST00000489332.1:n.314C>T
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363100
  ensembl transcript: ENST00000373988
  gene symbol: ZMYM3
  hgvsc: ENST00000373988.1:c.196C>T
  hgvsp: ENST00000373988.1:c.196C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363096
  ensembl transcript: ENST00000373984
  gene symbol: ZMYM3
  hgvsc: ENST00000373984.3:c.196C>T
  hgvsp: ENST00000373984.3:c.196C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000343909
  ensembl transcript: ENST00000353904
  gene symbol: ZMYM3
  hgvsc: ENST00000353904.2:c.196C>T
  hgvsp: ENST00000353904.2:c.196C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000322845
  ensembl transcript: ENST00000314425
  gene symbol: ZMYM3
  hgvsc: ENST00000314425.5:c.196C>T
  hgvsp: ENST00000314425.5:c.196C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363094
  ensembl transcript: ENST00000373982
  gene symbol: ZMYM3
  hgvsc: ENST00000373982.1:c.196C>T
  hgvsp: ENST00000373982.1:c.196C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363110
  ensembl transcript: ENST00000373998
  gene symbol: ZMYM3
  hgvsc: ENST00000373998.1:c.196C>T
  hgvsp: ENST00000373998.1:c.196C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4574
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14022
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1812
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9978
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14440
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1998
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13285
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1084
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 694
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1334
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Leu66Leu
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum

X-70472911-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24070472911
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24070472911
    reference: chr 0
allele count: 65
allele frequency: 9.3319742150374e-4
allele num: 69653
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363090
  ensembl transcript: ENST00000373978
  gene symbol: ZMYM3
  hgvsc: ENST00000373978.1:c.195C>G
  hgvsp: ENST00000373978.1:c.195C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363093
  ensembl transcript: ENST00000373981
  gene symbol: ZMYM3
  hgvsc: ENST00000373981.1:c.195C>G
  hgvsp: ENST00000373981.1:c.195C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363096
  ensembl transcript: ENST00000373984
  gene symbol: ZMYM3
  hgvsc: ENST00000373984.3:c.195C>G
  hgvsp: ENST00000373984.3:c.195C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363100
  ensembl transcript: ENST00000373988
  gene symbol: ZMYM3
  hgvsc: ENST00000373988.1:c.195C>G
  hgvsp: ENST00000373988.1:c.195C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363110
  ensembl transcript: ENST00000373998
  gene symbol: ZMYM3
  hgvsc: ENST00000373998.1:c.195C>G
  hgvsp: ENST00000373998.1:c.195C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147130
  ensembl transcript: ENST00000489332
  gene symbol: ZMYM3
  hgvsc: ENST00000489332.1:n.313C>G
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363094
  ensembl transcript: ENST00000373982
  gene symbol: ZMYM3
  hgvsc: ENST00000373982.1:c.195C>G
  hgvsp: ENST00000373982.1:c.195C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000322845
  ensembl transcript: ENST00000314425
  gene symbol: ZMYM3
  hgvsc: ENST00000314425.5:c.195C>G
  hgvsp: ENST00000314425.5:c.195C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000343909
  ensembl transcript: ENST00000353904
  gene symbol: ZMYM3
  hgvsc: ENST00000353904.2:c.195C>G
  hgvsp: ENST00000353904.2:c.195C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13353
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14074
  bin: 2.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1766
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 4.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 3.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 4522
  bin: 1.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 1996
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14426
  bin: 1.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9963
  bin: 2.75e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 3595
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 574
  bin: 5.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 753
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 275
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Gly65Gly
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: Latino
reference allele: G
site quality: MQ
site quality: DP
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

X-70472919-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24070472919
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24070472919
    reference: chr 0
allele count: 1
allele frequency: 1.463743083813929e-5
allele num: 68318
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363100
  ensembl transcript: ENST00000373988
  gene symbol: ZMYM3
  hgvsc: ENST00000373988.1:c.187C>T
  hgvsp: ENSP00000363100.1:p.Pro63Ser
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363094
  ensembl transcript: ENST00000373982
  gene symbol: ZMYM3
  hgvsc: ENST00000373982.1:c.187C>T
  hgvsp: ENSP00000363094.1:p.Pro63Ser
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000343909
  ensembl transcript: ENST00000353904
  gene symbol: ZMYM3
  hgvsc: ENST00000353904.2:c.187C>T
  hgvsp: ENSP00000343909.2:p.Pro63Ser
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363096
  ensembl transcript: ENST00000373984
  gene symbol: ZMYM3
  hgvsc: ENST00000373984.3:c.187C>T
  hgvsp: ENSP00000363096.3:p.Pro63Ser
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147130
  ensembl transcript: ENST00000489332
  gene symbol: ZMYM3
  hgvsc: ENST00000489332.1:n.305C>T
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363093
  ensembl transcript: ENST00000373981
  gene symbol: ZMYM3
  hgvsc: ENST00000373981.1:c.187C>T
  hgvsp: ENSP00000363093.1:p.Pro63Ser
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363090
  ensembl transcript: ENST00000373978
  gene symbol: ZMYM3
  hgvsc: ENST00000373978.1:c.187C>T
  hgvsp: ENSP00000363090.1:p.Pro63Ser
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000322845
  ensembl transcript: ENST00000314425
  gene symbol: ZMYM3
  hgvsc: ENST00000314425.5:c.187C>T
  hgvsp: ENSP00000322845.5:p.Pro63Ser
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363110
  ensembl transcript: ENST00000373998
  gene symbol: ZMYM3
  hgvsc: ENST00000373998.1:c.187C>T
  hgvsp: ENSP00000363110.1:p.Pro63Ser
  variant of: http://identifiers.org/hgnc/13054
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1549
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4611
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2230
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9045
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15017
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13389
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14282
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 647
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 388
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 614
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Pro63Ser
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQ

X-70472920-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24070472920
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24070472920
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 68174
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363100
  ensembl transcript: ENST00000373988
  gene symbol: ZMYM3
  hgvsc: ENST00000373988.1:c.186C>A
  hgvsp: ENST00000373988.1:c.186C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363093
  ensembl transcript: ENST00000373981
  gene symbol: ZMYM3
  hgvsc: ENST00000373981.1:c.186C>A
  hgvsp: ENST00000373981.1:c.186C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363090
  ensembl transcript: ENST00000373978
  gene symbol: ZMYM3
  hgvsc: ENST00000373978.1:c.186C>A
  hgvsp: ENST00000373978.1:c.186C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363096
  ensembl transcript: ENST00000373984
  gene symbol: ZMYM3
  hgvsc: ENST00000373984.3:c.186C>A
  hgvsp: ENST00000373984.3:c.186C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000343909
  ensembl transcript: ENST00000353904
  gene symbol: ZMYM3
  hgvsc: ENST00000353904.2:c.186C>A
  hgvsp: ENST00000353904.2:c.186C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000322845
  ensembl transcript: ENST00000314425
  gene symbol: ZMYM3
  hgvsc: ENST00000314425.5:c.186C>A
  hgvsp: ENST00000314425.5:c.186C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147130
  ensembl transcript: ENST00000489332
  gene symbol: ZMYM3
  hgvsc: ENST00000489332.1:n.304C>A
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363094
  ensembl transcript: ENST00000373982
  gene symbol: ZMYM3
  hgvsc: ENST00000373982.1:c.186C>A
  hgvsp: ENST00000373982.1:c.186C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363110
  ensembl transcript: ENST00000373998
  gene symbol: ZMYM3
  hgvsc: ENST00000373998.1:c.186C>A
  hgvsp: ENST00000373998.1:c.186C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 2251
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14401
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13204
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4651
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1531
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8895
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15193
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21757
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 816
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 626
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Thr62Thr
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

X-70472921-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24070472921
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24070472921
    reference: chr 0
allele count: 2
allele frequency: 2.947895939273344e-5
allele num: 67845
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000322845
  ensembl transcript: ENST00000314425
  gene symbol: ZMYM3
  hgvsc: ENST00000314425.5:c.185C>T
  hgvsp: ENSP00000322845.5:p.Thr62Ile
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363094
  ensembl transcript: ENST00000373982
  gene symbol: ZMYM3
  hgvsc: ENST00000373982.1:c.185C>T
  hgvsp: ENSP00000363094.1:p.Thr62Ile
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147130
  ensembl transcript: ENST00000489332
  gene symbol: ZMYM3
  hgvsc: ENST00000489332.1:n.303C>T
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000343909
  ensembl transcript: ENST00000353904
  gene symbol: ZMYM3
  hgvsc: ENST00000353904.2:c.185C>T
  hgvsp: ENSP00000343909.2:p.Thr62Ile
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363110
  ensembl transcript: ENST00000373998
  gene symbol: ZMYM3
  hgvsc: ENST00000373998.1:c.185C>T
  hgvsp: ENSP00000363110.1:p.Thr62Ile
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363100
  ensembl transcript: ENST00000373988
  gene symbol: ZMYM3
  hgvsc: ENST00000373988.1:c.185C>T
  hgvsp: ENSP00000363100.1:p.Thr62Ile
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363093
  ensembl transcript: ENST00000373981
  gene symbol: ZMYM3
  hgvsc: ENST00000373981.1:c.185C>T
  hgvsp: ENSP00000363093.1:p.Thr62Ile
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363096
  ensembl transcript: ENST00000373984
  gene symbol: ZMYM3
  hgvsc: ENST00000373984.3:c.185C>T
  hgvsp: ENSP00000363096.3:p.Thr62Ile
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363090
  ensembl transcript: ENST00000373978
  gene symbol: ZMYM3
  hgvsc: ENST00000373978.1:c.185C>T
  hgvsp: ENSP00000363090.1:p.Thr62Ile
  variant of: http://identifiers.org/hgnc/13054
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15377
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12846
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1491
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14576
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8632
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2333
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4863
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2215
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1198
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Thr62Ile
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

X-70472925-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24070472925
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24070472925
    reference: chr 0
allele count: 1
allele frequency: 1.495707319991624e-5
allele num: 66858
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363110
  ensembl transcript: ENST00000373998
  gene symbol: ZMYM3
  hgvsc: ENST00000373998.1:c.181G>C
  hgvsp: ENSP00000363110.1:p.Asp61His
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363100
  ensembl transcript: ENST00000373988
  gene symbol: ZMYM3
  hgvsc: ENST00000373988.1:c.181G>C
  hgvsp: ENSP00000363100.1:p.Asp61His
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363090
  ensembl transcript: ENST00000373978
  gene symbol: ZMYM3
  hgvsc: ENST00000373978.1:c.181G>C
  hgvsp: ENSP00000363090.1:p.Asp61His
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363094
  ensembl transcript: ENST00000373982
  gene symbol: ZMYM3
  hgvsc: ENST00000373982.1:c.181G>C
  hgvsp: ENSP00000363094.1:p.Asp61His
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363096
  ensembl transcript: ENST00000373984
  gene symbol: ZMYM3
  hgvsc: ENST00000373984.3:c.181G>C
  hgvsp: ENSP00000363096.3:p.Asp61His
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363093
  ensembl transcript: ENST00000373981
  gene symbol: ZMYM3
  hgvsc: ENST00000373981.1:c.181G>C
  hgvsp: ENSP00000363093.1:p.Asp61His
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000322845
  ensembl transcript: ENST00000314425
  gene symbol: ZMYM3
  hgvsc: ENST00000314425.5:c.181G>C
  hgvsp: ENSP00000322845.5:p.Asp61His
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000343909
  ensembl transcript: ENST00000353904
  gene symbol: ZMYM3
  hgvsc: ENST00000353904.2:c.181G>C
  hgvsp: ENSP00000343909.2:p.Asp61His
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147130
  ensembl transcript: ENST00000489332
  gene symbol: ZMYM3
  hgvsc: ENST00000489332.1:n.299G>C
  variant of: http://identifiers.org/hgnc/13054
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15700
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2543
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1416
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15040
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11960
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8151
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5306
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1647
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 772
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 498
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16102
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Asp61His
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
reference allele: C
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD

X-70472929-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24070472929
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24070472929
    reference: chr 0
allele count: 2
allele frequency: 3.010234798314269e-5
allele num: 66440
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363100
  ensembl transcript: ENST00000373988
  gene symbol: ZMYM3
  hgvsc: ENST00000373988.1:c.177G>C
  hgvsp: ENST00000373988.1:c.177G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000322845
  ensembl transcript: ENST00000314425
  gene symbol: ZMYM3
  hgvsc: ENST00000314425.5:c.177G>C
  hgvsp: ENST00000314425.5:c.177G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363090
  ensembl transcript: ENST00000373978
  gene symbol: ZMYM3
  hgvsc: ENST00000373978.1:c.177G>C
  hgvsp: ENST00000373978.1:c.177G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147130
  ensembl transcript: ENST00000489332
  gene symbol: ZMYM3
  hgvsc: ENST00000489332.1:n.295G>C
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363094
  ensembl transcript: ENST00000373982
  gene symbol: ZMYM3
  hgvsc: ENST00000373982.1:c.177G>C
  hgvsp: ENST00000373982.1:c.177G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000343909
  ensembl transcript: ENST00000353904
  gene symbol: ZMYM3
  hgvsc: ENST00000353904.2:c.177G>C
  hgvsp: ENST00000353904.2:c.177G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363096
  ensembl transcript: ENST00000373984
  gene symbol: ZMYM3
  hgvsc: ENST00000373984.3:c.177G>C
  hgvsp: ENST00000373984.3:c.177G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363110
  ensembl transcript: ENST00000373998
  gene symbol: ZMYM3
  hgvsc: ENST00000373998.1:c.177G>C
  hgvsp: ENST00000373998.1:c.177G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363093
  ensembl transcript: ENST00000373981
  gene symbol: ZMYM3
  hgvsc: ENST00000373981.1:c.177G>C
  hgvsp: ENST00000373981.1:c.177G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 7837
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2621
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5309
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15771
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11823
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15376
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1370
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1976
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2071
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22197
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Leu59Leu
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum

X-70472935-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24070472935
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24070472935
    reference: chr 0
allele count: 2
allele frequency: 3.055767761650114e-5
allele num: 65450
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147130
  ensembl transcript: ENST00000489332
  gene symbol: ZMYM3
  hgvsc: ENST00000489332.1:n.289G>A
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000343909
  ensembl transcript: ENST00000353904
  gene symbol: ZMYM3
  hgvsc: ENST00000353904.2:c.171G>A
  hgvsp: ENST00000353904.2:c.171G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363094
  ensembl transcript: ENST00000373982
  gene symbol: ZMYM3
  hgvsc: ENST00000373982.1:c.171G>A
  hgvsp: ENST00000373982.1:c.171G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363110
  ensembl transcript: ENST00000373998
  gene symbol: ZMYM3
  hgvsc: ENST00000373998.1:c.171G>A
  hgvsp: ENST00000373998.1:c.171G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363096
  ensembl transcript: ENST00000373984
  gene symbol: ZMYM3
  hgvsc: ENST00000373984.3:c.171G>A
  hgvsp: ENST00000373984.3:c.171G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363090
  ensembl transcript: ENST00000373978
  gene symbol: ZMYM3
  hgvsc: ENST00000373978.1:c.171G>A
  hgvsp: ENST00000373978.1:c.171G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000322845
  ensembl transcript: ENST00000314425
  gene symbol: ZMYM3
  hgvsc: ENST00000314425.5:c.171G>A
  hgvsp: ENST00000314425.5:c.171G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363100
  ensembl transcript: ENST00000373988
  gene symbol: ZMYM3
  hgvsc: ENST00000373988.1:c.171G>A
  hgvsp: ENST00000373988.1:c.171G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363093
  ensembl transcript: ENST00000373981
  gene symbol: ZMYM3
  hgvsc: ENST00000373981.1:c.171G>A
  hgvsp: ENST00000373981.1:c.171G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10899
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1264
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5909
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7152
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16031
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15926
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2908
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1529
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 974
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2323
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3291
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Leu57Leu
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

X-70472937-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24070472937
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24070472937
    reference: chr 0
allele count: 2
allele frequency: 3.085895912730864e-5
allele num: 64811
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363096
  ensembl transcript: ENST00000373984
  gene symbol: ZMYM3
  hgvsc: ENST00000373984.3:c.169C>T
  hgvsp: ENST00000373984.3:c.169C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363090
  ensembl transcript: ENST00000373978
  gene symbol: ZMYM3
  hgvsc: ENST00000373978.1:c.169C>T
  hgvsp: ENST00000373978.1:c.169C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000322845
  ensembl transcript: ENST00000314425
  gene symbol: ZMYM3
  hgvsc: ENST00000314425.5:c.169C>T
  hgvsp: ENST00000314425.5:c.169C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363110
  ensembl transcript: ENST00000373998
  gene symbol: ZMYM3
  hgvsc: ENST00000373998.1:c.169C>T
  hgvsp: ENST00000373998.1:c.169C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000343909
  ensembl transcript: ENST00000353904
  gene symbol: ZMYM3
  hgvsc: ENST00000353904.2:c.169C>T
  hgvsp: ENST00000353904.2:c.169C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363094
  ensembl transcript: ENST00000373982
  gene symbol: ZMYM3
  hgvsc: ENST00000373982.1:c.169C>T
  hgvsp: ENST00000373982.1:c.169C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147130
  ensembl transcript: ENST00000489332
  gene symbol: ZMYM3
  hgvsc: ENST00000489332.1:n.287C>T
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363100
  ensembl transcript: ENST00000373988
  gene symbol: ZMYM3
  hgvsc: ENST00000373988.1:c.169C>T
  hgvsp: ENST00000373988.1:c.169C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363093
  ensembl transcript: ENST00000373981
  gene symbol: ZMYM3
  hgvsc: ENST00000373981.1:c.169C>T
  hgvsp: ENST00000373981.1:c.169C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16300
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15981
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10629
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6225
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1177
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3071
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6698
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1716
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2162
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Leu57Leu
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum

X-70472939-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24070472939
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24070472939
    reference: chr 0
allele count: 2
allele frequency: 3.087992341778993e-5
allele num: 64767
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363093
  ensembl transcript: ENST00000373981
  gene symbol: ZMYM3
  hgvsc: ENST00000373981.1:c.167C>T
  hgvsp: ENSP00000363093.1:p.Ala56Val
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363090
  ensembl transcript: ENST00000373978
  gene symbol: ZMYM3
  hgvsc: ENST00000373978.1:c.167C>T
  hgvsp: ENSP00000363090.1:p.Ala56Val
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363094
  ensembl transcript: ENST00000373982
  gene symbol: ZMYM3
  hgvsc: ENST00000373982.1:c.167C>T
  hgvsp: ENSP00000363094.1:p.Ala56Val
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363100
  ensembl transcript: ENST00000373988
  gene symbol: ZMYM3
  hgvsc: ENST00000373988.1:c.167C>T
  hgvsp: ENSP00000363100.1:p.Ala56Val
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363110
  ensembl transcript: ENST00000373998
  gene symbol: ZMYM3
  hgvsc: ENST00000373998.1:c.167C>T
  hgvsp: ENSP00000363110.1:p.Ala56Val
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000322845
  ensembl transcript: ENST00000314425
  gene symbol: ZMYM3
  hgvsc: ENST00000314425.5:c.167C>T
  hgvsp: ENSP00000322845.5:p.Ala56Val
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363096
  ensembl transcript: ENST00000373984
  gene symbol: ZMYM3
  hgvsc: ENST00000373984.3:c.167C>T
  hgvsp: ENSP00000363096.3:p.Ala56Val
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000343909
  ensembl transcript: ENST00000353904
  gene symbol: ZMYM3
  hgvsc: ENST00000353904.2:c.167C>T
  hgvsp: ENSP00000343909.2:p.Ala56Val
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147130
  ensembl transcript: ENST00000489332
  gene symbol: ZMYM3
  hgvsc: ENST00000489332.1:n.285C>T
  variant of: http://identifiers.org/hgnc/13054
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6087
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16430
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6716
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1138
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15943
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10703
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3075
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1254
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4516
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 324
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ala56Val
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: QD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

X-70472940-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24070472940
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24070472940
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 64628
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363090
  ensembl transcript: ENST00000373978
  gene symbol: ZMYM3
  hgvsc: ENST00000373978.1:c.166G>A
  hgvsp: ENSP00000363090.1:p.Ala56Thr
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000322845
  ensembl transcript: ENST00000314425
  gene symbol: ZMYM3
  hgvsc: ENST00000314425.5:c.166G>A
  hgvsp: ENSP00000322845.5:p.Ala56Thr
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363093
  ensembl transcript: ENST00000373981
  gene symbol: ZMYM3
  hgvsc: ENST00000373981.1:c.166G>A
  hgvsp: ENSP00000363093.1:p.Ala56Thr
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147130
  ensembl transcript: ENST00000489332
  gene symbol: ZMYM3
  hgvsc: ENST00000489332.1:n.284G>A
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363110
  ensembl transcript: ENST00000373998
  gene symbol: ZMYM3
  hgvsc: ENST00000373998.1:c.166G>A
  hgvsp: ENSP00000363110.1:p.Ala56Thr
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363096
  ensembl transcript: ENST00000373984
  gene symbol: ZMYM3
  hgvsc: ENST00000373984.3:c.166G>A
  hgvsp: ENSP00000363096.3:p.Ala56Thr
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363094
  ensembl transcript: ENST00000373982
  gene symbol: ZMYM3
  hgvsc: ENST00000373982.1:c.166G>A
  hgvsp: ENSP00000363094.1:p.Ala56Thr
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363100
  ensembl transcript: ENST00000373988
  gene symbol: ZMYM3
  hgvsc: ENST00000373988.1:c.166G>A
  hgvsp: ENSP00000363100.1:p.Ala56Thr
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000343909
  ensembl transcript: ENST00000353904
  gene symbol: ZMYM3
  hgvsc: ENST00000353904.2:c.166G>A
  hgvsp: ENSP00000343909.2:p.Ala56Thr
  variant of: http://identifiers.org/hgnc/13054
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6638
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10704
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3088
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15922
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6117
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16490
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 405
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1277
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2432
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ala56Thr
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: MQRankSum

X-70472941-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24070472941
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24070472941
    reference: chr 0
allele count: 1
allele frequency: 1.549474728067185e-5
allele num: 64538
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000343909
  ensembl transcript: ENST00000353904
  gene symbol: ZMYM3
  hgvsc: ENST00000353904.2:c.165A>T
  hgvsp: ENST00000353904.2:c.165A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363094
  ensembl transcript: ENST00000373982
  gene symbol: ZMYM3
  hgvsc: ENST00000373982.1:c.165A>T
  hgvsp: ENST00000373982.1:c.165A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363093
  ensembl transcript: ENST00000373981
  gene symbol: ZMYM3
  hgvsc: ENST00000373981.1:c.165A>T
  hgvsp: ENST00000373981.1:c.165A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363110
  ensembl transcript: ENST00000373998
  gene symbol: ZMYM3
  hgvsc: ENST00000373998.1:c.165A>T
  hgvsp: ENST00000373998.1:c.165A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363096
  ensembl transcript: ENST00000373984
  gene symbol: ZMYM3
  hgvsc: ENST00000373984.3:c.165A>T
  hgvsp: ENST00000373984.3:c.165A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147130
  ensembl transcript: ENST00000489332
  gene symbol: ZMYM3
  hgvsc: ENST00000489332.1:n.283A>T
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363100
  ensembl transcript: ENST00000373988
  gene symbol: ZMYM3
  hgvsc: ENST00000373988.1:c.165A>T
  hgvsp: ENST00000373988.1:c.165A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000322845
  ensembl transcript: ENST00000314425
  gene symbol: ZMYM3
  hgvsc: ENST00000314425.5:c.165A>T
  hgvsp: ENST00000314425.5:c.165A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363090
  ensembl transcript: ENST00000373978
  gene symbol: ZMYM3
  hgvsc: ENST00000373978.1:c.165A>T
  hgvsp: ENST00000373978.1:c.165A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15935
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3135
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6140
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10638
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6519
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16615
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1101
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3487
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 433
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22437
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1025
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Gly55Gly
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: QD

X-70472944-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24070472944
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24070472944
    reference: chr 0
allele count: 1
allele frequency: 1.565312671206073e-5
allele num: 63885
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363094
  ensembl transcript: ENST00000373982
  gene symbol: ZMYM3
  hgvsc: ENST00000373982.1:c.162G>C
  hgvsp: ENST00000373982.1:c.162G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000343909
  ensembl transcript: ENST00000353904
  gene symbol: ZMYM3
  hgvsc: ENST00000353904.2:c.162G>C
  hgvsp: ENST00000353904.2:c.162G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147130
  ensembl transcript: ENST00000489332
  gene symbol: ZMYM3
  hgvsc: ENST00000489332.1:n.280G>C
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363090
  ensembl transcript: ENST00000373978
  gene symbol: ZMYM3
  hgvsc: ENST00000373978.1:c.162G>C
  hgvsp: ENST00000373978.1:c.162G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363093
  ensembl transcript: ENST00000373981
  gene symbol: ZMYM3
  hgvsc: ENST00000373981.1:c.162G>C
  hgvsp: ENST00000373981.1:c.162G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363096
  ensembl transcript: ENST00000373984
  gene symbol: ZMYM3
  hgvsc: ENST00000373984.3:c.162G>C
  hgvsp: ENST00000373984.3:c.162G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363110
  ensembl transcript: ENST00000373998
  gene symbol: ZMYM3
  hgvsc: ENST00000373998.1:c.162G>C
  hgvsp: ENST00000373998.1:c.162G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000363100
  ensembl transcript: ENST00000373988
  gene symbol: ZMYM3
  hgvsc: ENST00000373988.1:c.162G>C
  hgvsp: ENST00000373988.1:c.162G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147130
  ensembl protein: ENSP00000322845
  ensembl transcript: ENST00000314425
  gene symbol: ZMYM3
  hgvsc: ENST00000314425.5:c.162G>C
  hgvsp: ENST00000314425.5:c.162G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13054
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1106
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6255
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10457
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3219
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16812
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6295
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15939
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1016
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 407
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4488
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Ser54Ser
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: African
reference allele: C

GenotypeQuality
all individuals: 1457
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 247
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1283
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1129
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 502
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1265
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3320
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 666
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3617
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 755
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 598
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 215
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1064
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35256
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7927
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 42574
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3839
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.613163413453783e-4
allele num: 6199
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8755
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4677
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 493
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.581e1

FS
type: SiteQuality
SIO_000300: 3.077e0

MQRankSum
type: SiteQuality
SIO_000300: 8.96e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.0e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 8.96e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.26e0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.86e-1

DP
type: SiteQuality
SIO_000300: 1.156809e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6227
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3899
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 506
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7968
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8792
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4758
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.331980784478336e-5
allele num: 42882
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

DP
type: SiteQuality
SIO_000300: 1.169869e6

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 9.340000000000001e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 5.5e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.3e0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.370000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.3e0

GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8028
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.309895592719209e-5
allele num: 43292
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 511
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4886
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8857
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6261
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3939
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.04e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.26e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.882e0

DP
type: SiteQuality
SIO_000300: 1.189167e6

FS
type: SiteQuality
SIO_000300: 2.414e0

VQSLOD
type: SiteQuality
SIO_000300: -1.382e0

MQRankSum
type: SiteQuality
SIO_000300: -5.09e-1

QD
type: SiteQuality
SIO_000300: 1.275e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.6e-3

MQ
type: SiteQuality
SIO_000300: 5.855e1

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 3523
bin: 6.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3972
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 2.023472278429786e-4
allele num: 4942
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 43476
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8887
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 513
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8048
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.262e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -1.106e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.659999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.82e-1

DP
type: SiteQuality
SIO_000300: 1.196674e6

VQSLOD
type: SiteQuality
SIO_000300: -2.448e0

FS
type: SiteQuality
SIO_000300: 3.09e0

MQ
type: SiteQuality
SIO_000300: 5.87e1

QD
type: SiteQuality
SIO_000300: 2.861e1

GenotypeQuality
all individuals: 578
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 809
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8054
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 43531
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4956
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.12410071942446e-4
allele num: 8896
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3978
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6288
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 514
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.51e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.86e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.69e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.31e-1

QD
type: SiteQuality
SIO_000300: 1.466e1

FS
type: SiteQuality
SIO_000300: 4.341e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.6e-3

MQ
type: SiteQuality
SIO_000300: 5.896e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.199999999999999e-2

DP
type: SiteQuality
SIO_000300: 1.198444e6

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4989
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8072
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.122334455667789e-4
allele num: 8910
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 43624
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3987
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6300
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 515
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.4e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.24e-1

BaseQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.955e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.03e-1

DP
type: SiteQuality
SIO_000300: 1.202325e6

VQSLOD
type: SiteQuality
SIO_000300: 1.11e0

QD
type: SiteQuality
SIO_000300: 9.130000000000001e0

FS
type: SiteQuality
SIO_000300: 1.091e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.82e-1

GenotypeQuality
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variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3992
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 516
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5008
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8081
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6312
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.288591372010528e-5
allele num: 43695
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.0e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.81e-1

VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.205763e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.3e-3

QD
type: SiteQuality
SIO_000300: 1.086e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.6e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.8e-1

FS
type: SiteQuality
SIO_000300: 5.449e0

MQ
type: SiteQuality
SIO_000300: 5.925e1

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6409
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 3.330373001776199e-4
allele num: 9008
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.249061017025392e-5
allele num: 44463
num of homozygotes: 0

Other
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European (Finnish)
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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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South Asian
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DP
type: SiteQuality
SIO_000300: 1.244124e6

MQRankSum
type: SiteQuality
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FS
type: SiteQuality
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ReadPosRankSum
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InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.942e1

VQSLOD
type: SiteQuality
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ClippingRankSum
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QD
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4109
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5493
num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 532
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European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44681
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African
type: Population
allele count: 4
allele frequency: 4.882216526302942e-4
allele num: 8193
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.283e0

QD
type: SiteQuality
SIO_000300: 1.919e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.29e0

DP
type: SiteQuality
SIO_000300: 1.255541e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.479e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.3e-3

FS
type: SiteQuality
SIO_000300: 3.677e0

MQRankSum
type: SiteQuality
SIO_000300: -1.39e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 6.900000000000001e-2

GenotypeQuality
all individuals: 452
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3741
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40823
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 286
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 865
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6434
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5493
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9035
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44681
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8193
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 532
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 2.433682161109759e-4
allele num: 4109
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.479e0

MQRankSum
type: SiteQuality
SIO_000300: -1.39e-1

QD
type: SiteQuality
SIO_000300: 1.919e1

DP
type: SiteQuality
SIO_000300: 1.255541e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.29e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.283e0

FS
type: SiteQuality
SIO_000300: 3.677e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.3e-3

VQSLOD
type: SiteQuality
SIO_000300: 6.900000000000001e-2

GenotypeQuality
all individuals: 6263
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 454
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 9.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
all individuals: 279
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 875
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 664
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 2
allele frequency: 3.625815808556925e-4
allele num: 5516
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6439
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9045
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8196
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44726
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4114
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 533
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.47e0

MQ
type: SiteQuality
SIO_000300: 5.917e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.261292e6

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

GenotypeQuality
all individuals: 874
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 1

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 884
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 596
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variant carriers: 0

GenotypeQuality
all individuals: 703
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.23179413930859e-5
allele num: 44807
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 533
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8203
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6444
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4115
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9049
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5622
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.263701e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.02e0

QD
type: SiteQuality
SIO_000300: 2.414e1

VQSLOD
type: SiteQuality
SIO_000300: -1.933e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.23e-1

FS
type: SiteQuality
SIO_000300: 4.158e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.2e-3

MQ
type: SiteQuality
SIO_000300: 5.982e1

MQRankSum
type: SiteQuality
SIO_000300: 2.54e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.8e-1

GenotypeQuality
all individuals: 435
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 435
bin: 5.75e1
variant carriers: 2

GenotypeQuality
all individuals: 943
bin: 7.5e0
variant carriers: 3

GenotypeQuality
all individuals: 896
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variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 2

GenotypeQuality
all individuals: 264
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 367
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variant carriers: 2

GenotypeQuality
all individuals: 71
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variant carriers: 0

GenotypeQuality
all individuals: 167
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 5914
bin: 2.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 9
allele frequency: 1.992869954163991e-4
allele num: 45161
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 2
allele frequency: 4.932182490752158e-4
allele num: 4055
num of homozygotes: 0

African
type: Population
allele count: 6
allele frequency: 7.391893556732783e-4
allele num: 8117
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9077
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6510
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6359
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 532
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.17616e2

MQ
type: SiteQuality
SIO_000300: 5.993e1

VQSLOD
type: SiteQuality
SIO_000300: -7.009e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.864e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.2e-3

QD
type: SiteQuality
SIO_000300: 4.4e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.64e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.026e0

DP
type: SiteQuality
SIO_000300: 1.315741e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.88e0

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

GenotypeQuality
all individuals: 102
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variant carriers: 0

GenotypeQuality
all individuals: 306
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
all individuals: 4071
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variant carriers: 0

GenotypeQuality
all individuals: 5856
bin: 2.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9130
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6666
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4199
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 558
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6536
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.202790473899447e-4
allele num: 8314
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 45893
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

FS
type: SiteQuality
SIO_000300: 5.668e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.889e0

VQSLOD
type: SiteQuality
SIO_000300: -5.782e-1

MQ
type: SiteQuality
SIO_000300: 5.965e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.531e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.27e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.2e-1

DP
type: SiteQuality
SIO_000300: 1.309453e6

QD
type: SiteQuality
SIO_000300: 1.09e1

GenotypeQuality
all individuals: 70
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3987
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 859
bin: 2.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6535
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 573
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7336
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4194
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46201
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.871e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.78e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.85e-1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.375e-1

DP
type: SiteQuality
SIO_000300: 1.322611e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.85e-1

QD
type: SiteQuality
SIO_000300: 2.731e1

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 246
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3965
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 922
bin: 3.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8351
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6526
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4184
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9118
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46331
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 574
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 2.552974214960429e-4
allele num: 7834
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.18e-2

QD
type: SiteQuality
SIO_000300: 2.56e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.63e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.328288e6

GenotypeQuality
all individuals: 872
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 243
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 8.75e1
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GenotypeQuality
all individuals: 79
bin: 7.5e0
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GenotypeQuality
all individuals: 53
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 967
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 381
bin: 5.75e1
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GenotypeQuality
all individuals: 5649
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1000
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 165
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 49
bin: 9.25e1
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GenotypeQuality
all individuals: 44465
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3898
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 632
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.162250116225012e-4
allele num: 8604
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4158
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8338
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9088
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 585
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46338
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6488
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.446e0

DP
type: SiteQuality
SIO_000300: 1.329705e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.84e0

FS
type: SiteQuality
SIO_000300: 8.66e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.68e0

QD
type: SiteQuality
SIO_000300: 1.312e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.049e0

MQ
type: SiteQuality
SIO_000300: 5.977e1

VQSLOD
type: SiteQuality
SIO_000300: -2.806e-1

GenotypeQuality
all individuals: 1051
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 862
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 49
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 732
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 237
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 8.75e1
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GenotypeQuality
all individuals: 386
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8317
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8843
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9068
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.547029702970297e-4
allele num: 6464
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4151
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 46300
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 9.8e-2

DP
type: SiteQuality
SIO_000300: 1.326332e6

FS
type: SiteQuality
SIO_000300: 4.928e0

MQRankSum
type: SiteQuality
SIO_000300: 3.06e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.16e-1

MQ
type: SiteQuality
SIO_000300: 5.968e1

QD
type: SiteQuality
SIO_000300: 1.508e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.56e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.89e0

GenotypeQuality
all individuals: 835
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 589
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4123
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.168632893823733e-5
allele num: 46112
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9035
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9085
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8294
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 6.870000000000001e-1

FS
type: SiteQuality
SIO_000300: 5.86e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.74e-1

DP
type: SiteQuality
SIO_000300: 1.311455e6

ClippingRankSum
type: SiteQuality
SIO_000300: 8.999999999999999e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.689e0

MQRankSum
type: SiteQuality
SIO_000300: 9.09e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.187e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

GenotypeQuality
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variant carriers: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 9092
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8285
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.171599817585615e-5
allele num: 46049
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.55860349127182e-4
allele num: 6416
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4111
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9029
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.75e-1

QD
type: SiteQuality
SIO_000300: 1.768e1

BaseQRankSum
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SIO_000300: 1.08e0

DP
type: SiteQuality
SIO_000300: 1.305975e6

MQ
type: SiteQuality
SIO_000300: 5.686e1

MQRankSum
type: SiteQuality
SIO_000300: -1.116e0

FS
type: SiteQuality
SIO_000300: 7.17e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.27e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.72e-1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8259
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9006
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.571091908876669e-4
allele num: 6365
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4093
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 45841
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 582
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9168
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -9.66e-1

QD
type: SiteQuality
SIO_000300: 1.617e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.41e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 5.81e-1

DP
type: SiteQuality
SIO_000300: 1.290194e6

MQ
type: SiteQuality
SIO_000300: 5.593e1

FS
type: SiteQuality
SIO_000300: 1.085e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.66e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.34e-1

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 3
allele frequency: 3.255561584373304e-4
allele num: 9215
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6303
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4042
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8960
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 45467
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8221
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 579
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.19e0

MQRankSum
type: SiteQuality
SIO_000300: -6.18e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.02e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.254559e6

FS
type: SiteQuality
SIO_000300: 7.459e0

VQSLOD
type: SiteQuality
SIO_000300: -6.718e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.621e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.721e0

GenotypeQuality
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variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4019
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 45281
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 576
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6275
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9194
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8192
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.119444755401321e-4
allele num: 8933
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.395e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.14e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.11e-1

DP
type: SiteQuality
SIO_000300: 1.240017e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -2.085e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.27e-1

QD
type: SiteQuality
SIO_000300: 3.121e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.733e0

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

East Asian
type: Population
allele count: 3
allele frequency: 4.866180048661801e-4
allele num: 6165
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3929
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9049
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8828
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 569
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44568
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8079
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.699999999999999e-2

VQSLOD
type: SiteQuality
SIO_000300: -7.738e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

ClippingRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.177121e6

FS
type: SiteQuality
SIO_000300: 1.3143e1

MQ
type: SiteQuality
SIO_000300: 5.946e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.183e0

MQRankSum
type: SiteQuality
SIO_000300: -1.61e-1

QD
type: SiteQuality
SIO_000300: 1.565e1

GenotypeQuality
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variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3936
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8073
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8827
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6162
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44562
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 568
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South Asian
type: Population
allele count: 1
allele frequency: 1.104362230811706e-4
allele num: 9055
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

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

QD
type: SiteQuality
SIO_000300: 2.928e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

DP
type: SiteQuality
SIO_000300: 1.176694e6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1386
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variant carriers: 0

GenotypeQuality
all individuals: 4750
bin: 3.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8783
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 43780
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6092
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.258811681772407e-4
allele num: 7944
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8763
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3858
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 7.563e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.82e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

VQSLOD
type: SiteQuality
SIO_000300: -2.361e0

QD
type: SiteQuality
SIO_000300: 1.976e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.96e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.503e0

MQRankSum
type: SiteQuality
SIO_000300: -1.059e0

DP
type: SiteQuality
SIO_000300: 1.129311e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 43463
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7880
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6052
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8712
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 551
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.18e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.18e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.769e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.18e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.3e0

DP
type: SiteQuality
SIO_000300: 1.110676e6

GenotypeQuality
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variant carriers: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 8694
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8536
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7860
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.662510390689942e-4
allele num: 6015
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 43230
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3821
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 546
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.6e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.6e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.001e0

DP
type: SiteQuality
SIO_000300: 1.104747e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 2.927e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 3.2e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.598e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
all individuals: 424
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7848
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6035
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8708
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3814
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8530
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.30781657473864e-5
allele num: 43331
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 551
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.2e-3

MQ
type: SiteQuality
SIO_000300: 5.845e1

DP
type: SiteQuality
SIO_000300: 1.107003e6

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -6.43e-1

QD
type: SiteQuality
SIO_000300: 2.976e1

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 24144
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8727
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3815
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6039
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7811
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 553
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8466
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.312299119014036e-5
allele num: 43247
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.110733e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.733e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.29e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 1.658e1

MQRankSum
type: SiteQuality
SIO_000300: 3.02e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 2.915e0

VQSLOD
type: SiteQuality
SIO_000300: 2.27e-1

MQ
type: SiteQuality
SIO_000300: 5.883e1

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 1

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8753
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6060
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7812
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 2.360160490913382e-4
allele num: 8474
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3832
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 43353
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.51e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
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MQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.123461e6

BaseQRankSum
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VQSLOD
type: SiteQuality
SIO_000300: -3.227e-1

QD
type: SiteQuality
SIO_000300: 1.803e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

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

East Asian
type: Population
allele count: 4
allele frequency: 6.582195162086556e-4
allele num: 6077
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 555
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 43417
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3835
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8488
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 8763
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7829
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.94e0

FS
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -7.8e-2

MQ
type: SiteQuality
SIO_000300: 5.96e1

MQRankSum
type: SiteQuality
SIO_000300: 2.61e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.02e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -3.9e-2

DP
type: SiteQuality
SIO_000300: 1.129417e6

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.825e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 43412
num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
allele num: 553
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 4.936646371564917e-4
allele num: 6077
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 7820
num of homozygotes: 0

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

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

South Asian
type: Population
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allele frequency: 0.0e0
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MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
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BaseQRankSum
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QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -3.2e-3

ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 4.005e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.1e-2

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6099
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8781
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7821
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 554
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3848
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.596644449551827e-5
allele num: 43510
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.35e0

FS
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 7.15e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.226e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 3.82e-1

MQ
type: SiteQuality
SIO_000300: 5.86e1

DP
type: SiteQuality
SIO_000300: 1.142952e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.16e0

QD
type: SiteQuality
SIO_000300: 3.202e1

GenotypeQuality
all individuals: 165
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 224
bin: 8.25e1
variant carriers: 1

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 1

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1358
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 1

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11057
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 462
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.604805245420574e-4
allele num: 43619
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6104
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3850
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8781
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7826
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 558
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-2

DP
type: SiteQuality
SIO_000300: 1.167245e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.484e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.83e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.03e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 4.12e-1

MQ
type: SiteQuality
SIO_000300: 5.934e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.87e-1

QD
type: SiteQuality
SIO_000300: 2.357e1

GenotypeQuality
all individuals: 1235
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 1

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

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1044
bin: 4.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6113
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 557
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3856
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 43622
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8795
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7819
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.180498170227836e-4
allele num: 8471
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 2.131e0

QD
type: SiteQuality
SIO_000300: 5.9e0

VQSLOD
type: SiteQuality
SIO_000300: -1.281e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.35e-1

DP
type: SiteQuality
SIO_000300: 1.171445e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.6e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.06e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.905e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.12e-1

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 838
bin: 4.25e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31832
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6164
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7863
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8845
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44024
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3904
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.776198934280639e-3
allele num: 563
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

MQRankSum
type: SiteQuality
SIO_000300: -1.641e0

FS
type: SiteQuality
SIO_000300: 3.284e0

QD
type: SiteQuality
SIO_000300: 2.114e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.58e0

VQSLOD
type: SiteQuality
SIO_000300: -2.774e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.469e0

DP
type: SiteQuality
SIO_000300: 1.194472e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.434e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 293
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 36320
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variant carriers: 1

GenotypeQuality
all individuals: 51
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GenotypeQuality
all individuals: 131
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 9.75e1
variant carriers: 11

GenotypeQuality
all individuals: 255
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3968
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6261
num of homozygotes: 0

African
type: Population
allele count: 13
allele frequency: 1.644736842105263e-3
allele num: 7904
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8687
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8913
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 569
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44499
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.35e-2

MQ
type: SiteQuality
SIO_000300: 5.944e1

FS
type: SiteQuality
SIO_000300: 4.097e0

QD
type: SiteQuality
SIO_000300: 1.431e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.56e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.22e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.68e0

MQRankSum
type: SiteQuality
SIO_000300: 5.9e-1

DP
type: SiteQuality
SIO_000300: 1.24201e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.61e-1

GenotypeQuality
all individuals: 123
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 263
bin: 8.25e1
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
all individuals: 468
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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: 492
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 40004
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GenotypeQuality
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GenotypeQuality
all individuals: 681
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variant carriers: 0

GenotypeQuality
all individuals: 3813
bin: 6.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 572
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.257703433530374e-4
allele num: 7951
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44871
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6338
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8790
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4008
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8988
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.542e0

DP
type: SiteQuality
SIO_000300: 1.272075e6

MQRankSum
type: SiteQuality
SIO_000300: 1.62e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.991e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.31e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.39e-1

MQ
type: SiteQuality
SIO_000300: 5.777e1

QD
type: SiteQuality
SIO_000300: 1.655e1

GenotypeQuality
all individuals: 390
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 921
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variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 166
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GenotypeQuality
all individuals: 428
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GenotypeQuality
all individuals: 905
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 477
bin: 5.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8809
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.257387149503332e-4
allele num: 7953
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44947
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9001
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 572
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4011
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6346
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 6.09e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.62e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.2e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.94e-1

VQSLOD
type: SiteQuality
SIO_000300: -9.594e-1

MQ
type: SiteQuality
SIO_000300: 5.87e1

QD
type: SiteQuality
SIO_000300: 7.73e0

DP
type: SiteQuality
SIO_000300: 1.2765e6

FS
type: SiteQuality
SIO_000300: 3.938e0

GenotypeQuality
all individuals: 63
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1145
bin: 2.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8990
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.200849527917776e-5
allele num: 45437
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 574
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8013
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4083
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6449
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9080
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.315753e6

MQRankSum
type: SiteQuality
SIO_000300: -1.67e-1

MQ
type: SiteQuality
SIO_000300: 5.965e1

FS
type: SiteQuality
SIO_000300: 4.503e0

QD
type: SiteQuality
SIO_000300: 1.631e1

VQSLOD
type: SiteQuality
SIO_000300: 5.5e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.139e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.07e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -4.163e0

GenotypeQuality
all individuals: 6791
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 345
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 4293
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GenotypeQuality
all individuals: 167
bin: 9.75e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6493
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9120
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4143
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.195293291183702e-5
allele num: 45552
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7926
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8992
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 581
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.317159e6

VQSLOD
type: SiteQuality
SIO_000300: -1.913e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

FS
type: SiteQuality
SIO_000300: 1.075e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.18e-1

MQ
type: SiteQuality
SIO_000300: 5.941e1

MQRankSum
type: SiteQuality
SIO_000300: -1.447e0

QD
type: SiteQuality
SIO_000300: 1.235e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.24e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.224e0

GenotypeQuality
all individuals: 459
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variant carriers: 1

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 1

GenotypeQuality
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bin: 8.25e1
variant carriers: 2

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 15

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 604
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6491
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4148
num of homozygotes: 0

African
type: Population
allele count: 14
allele frequency: 1.789137380191693e-3
allele num: 7825
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8882
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 4.388370817334065e-4
allele num: 9115
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 579
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.204391147165153e-5
allele num: 45364
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.936e1

VQSLOD
type: SiteQuality
SIO_000300: 3.32e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.54e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.22e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.52e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.304365e6

ClippingRankSum
type: SiteQuality
SIO_000300: -4.33e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.01e-2

QD
type: SiteQuality
SIO_000300: 1.481e1

GenotypeQuality
all individuals: 128
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9114
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 580
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4156
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 45398
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6493
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.278445410380977e-4
allele num: 7822
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8888
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.91e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.0e-2

FS
type: SiteQuality
SIO_000300: 3.515e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.1e-1

DP
type: SiteQuality
SIO_000300: 1.305181e6

MQRankSum
type: SiteQuality
SIO_000300: 3.17e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.51e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.257e1

GenotypeQuality
all individuals: 751
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3921
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35943
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9095
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7485
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3813
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6480
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.23463687150838e-5
allele num: 44750
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8625
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.277e1

VQSLOD
type: SiteQuality
SIO_000300: 6.49e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.3e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.55e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.86e0

DP
type: SiteQuality
SIO_000300: 1.270713e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.28e-1

FS
type: SiteQuality
SIO_000300: 7.16e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.66e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 65
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9885
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 227
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 946
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7345
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.483299708585519e-5
allele num: 44610
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4196
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 565
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8576
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9085
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6478
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.5e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.736e0

MQ
type: SiteQuality
SIO_000300: 5.919e1

QD
type: SiteQuality
SIO_000300: 9.710000000000001e0

MQRankSum
type: SiteQuality
SIO_000300: -5.600000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.76e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -8.47e-2

DP
type: SiteQuality
SIO_000300: 1.251007e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.17e-1

GenotypeQuality
all individuals: 83
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 216
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2487
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 185
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 279
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4202
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7318
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44470
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9066
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8529
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 4.641089108910891e-4
allele num: 6464
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 565
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.667e0

FS
type: SiteQuality
SIO_000300: 1.2922e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.77e-1

QD
type: SiteQuality
SIO_000300: 2.352e1

DP
type: SiteQuality
SIO_000300: 1.242062e6

MQRankSum
type: SiteQuality
SIO_000300: 5.659999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.69e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.52e0

MQ
type: SiteQuality
SIO_000300: 5.958e1

GenotypeQuality
all individuals: 497
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1017
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3464
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 11005
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
all individuals: 2748
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 358
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 573
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 254
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3743
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 321
bin: 5.75e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3891
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8121
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 540
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 3.117206982543641e-4
allele num: 6416
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.29573681673133e-5
allele num: 43559
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9019
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7050
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.704e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.7e-2

VQSLOD
type: SiteQuality
SIO_000300: -4.714e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 3.79e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.73e-1

FS
type: SiteQuality
SIO_000300: 7.71e0

MQ
type: SiteQuality
SIO_000300: 5.952e1

DP
type: SiteQuality
SIO_000300: 1.18544e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.43e0

GenotypeQuality
all individuals: 2896
bin: 1.75e1
variant carriers: 2

GenotypeQuality
all individuals: 228
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3205
bin: 3.25e1
variant carriers: 2

GenotypeQuality
all individuals: 88
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2743
bin: 2.75e1
variant carriers: 3

GenotypeQuality
all individuals: 144
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 340
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1391
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1960
bin: 1.25e1
variant carriers: 3

GenotypeQuality
all individuals: 2625
bin: 7.5e0
variant carriers: 10

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18060
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 38
bin: 8.75e1
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GenotypeQuality
all individuals: 2071
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3146
bin: 3.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1553
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.772421127259837e-4
allele num: 5642
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 3.036283588887202e-4
allele num: 6587
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 397
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7717
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5596
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 2
allele frequency: 8.960573476702509e-4
allele num: 2232
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 1.087961703748028e-4
allele num: 36766
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.7015e1

MQRankSum
type: SiteQuality
SIO_000300: 2.17e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.274e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.94e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -5.92e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.18e-1

DP
type: SiteQuality
SIO_000300: 1.201721e6

QD
type: SiteQuality
SIO_000300: 1.79e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.1e-2

GenotypeQuality
all individuals: 1553
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 228
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2896
bin: 1.75e1
variant carriers: 5

GenotypeQuality
all individuals: 3013
bin: 4.75e1
variant carriers: 9

GenotypeQuality
all individuals: 88
bin: 8.25e1
variant carriers: 3

GenotypeQuality
all individuals: 7514
bin: 2.25e1
variant carriers: 7

GenotypeQuality
all individuals: 1391
bin: 5.75e1
variant carriers: 7

GenotypeQuality
all individuals: 3146
bin: 3.75e1
variant carriers: 7

GenotypeQuality
all individuals: 1960
bin: 1.25e1
variant carriers: 10

GenotypeQuality
all individuals: 3205
bin: 3.25e1
variant carriers: 8

GenotypeQuality
all individuals: 18060
bin: 6.25e1
variant carriers: 2

GenotypeQuality
all individuals: 2757
bin: 5.25e1
variant carriers: 3

GenotypeQuality
all individuals: 2743
bin: 2.75e1
variant carriers: 7

GenotypeQuality
all individuals: 38
bin: 8.75e1
variant carriers: 2

GenotypeQuality
all individuals: 340
bin: 7.25e1
variant carriers: 6

GenotypeQuality
all individuals: 28
bin: 9.25e1
variant carriers: 2

African
type: Population
allele count: 9
allele frequency: 1.608291636883488e-3
allele num: 5596
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 3.544842254519674e-4
allele num: 5642
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 2
allele frequency: 8.960573476702509e-4
allele num: 2232
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 51
allele frequency: 1.387151172278736e-3
allele num: 36766
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 2.591680704937152e-4
allele num: 7717
num of homozygotes: 0

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

Other
type: Population
allele count: 1
allele frequency: 2.518891687657431e-3
allele num: 397
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.201721e6

FS
type: SiteQuality
SIO_000300: 3.7015e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.92e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.274e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.18e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.1e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.94e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.17e-1

QD
type: SiteQuality
SIO_000300: 1.79e0

GenotypeQuality
all individuals: 2071
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2743
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18060
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2896
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7514
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 3013
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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Other
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allele frequency: 0.0e0
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African
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allele frequency: 1.78699070764832e-4
allele num: 5596
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European (Non-Finnish)
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allele frequency: 2.71990425937007e-5
allele num: 36766
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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VQSLOD
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InbreedingCoeff
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DP
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FS
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MQRankSum
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MQ
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BaseQRankSum
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ClippingRankSum
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QD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Non-Finnish)
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Other
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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Latino
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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 frequency: 1.564455569461827e-4
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ReadPosRankSum
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FS
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
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MQ
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DP
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QD
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MQRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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South Asian
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Other
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African
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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FS
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DP
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MQ
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QD
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VQSLOD
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

ClippingRankSum
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FS
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VQSLOD
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MQRankSum
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ReadPosRankSum
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BaseQRankSum
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QD
type: SiteQuality
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DP
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MQ
type: SiteQuality
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele frequency: 2.411323575510598e-5
allele num: 41471
num of homozygotes: 0

East Asian
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num of homozygotes: 0

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

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

African
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allele frequency: 0.0e0
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Other
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QD
type: SiteQuality
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FS
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MQ
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ClippingRankSum
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MQRankSum
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BaseQRankSum
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DP
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VQSLOD
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Finnish)
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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African
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Other
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 41491
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ClippingRankSum
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VQSLOD
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MQRankSum
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QD
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MQ
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DP
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BaseQRankSum
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ReadPosRankSum
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FS
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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African
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European (Finnish)
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allele frequency: 0.0e0
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East Asian
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European (Non-Finnish)
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Other
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South Asian
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BaseQRankSum
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ReadPosRankSum
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ClippingRankSum
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MQRankSum
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VQSLOD
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MQ
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InbreedingCoeff
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FS
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QD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Other
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European (Non-Finnish)
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Latino
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South Asian
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African
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European (Finnish)
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BaseQRankSum
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QD
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ReadPosRankSum
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DP
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MQ
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FS
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MQRankSum
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InbreedingCoeff
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VQSLOD
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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allele num: 467
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 5843
num of homozygotes: 0

European (Non-Finnish)
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allele count: 55
allele frequency: 1.414063504306466e-3
allele num: 38895
num of homozygotes: 0

African
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allele count: 3
allele frequency: 4.616805170821791e-4
allele num: 6498
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6320
num of homozygotes: 0

European (Finnish)
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allele count: 6
allele frequency: 1.774622892635315e-3
allele num: 3381
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 8249
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
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QD
type: SiteQuality
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FS
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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InbreedingCoeff
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SIO_000300: 4.15e-2

VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 3.19e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.65e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.58e-1

GenotypeQuality
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variant carriers: 0

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

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

African
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allele frequency: 1.556904873112253e-4
allele num: 6423
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 8102
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 38137
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 464
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3285
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
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QD
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DP
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ReadPosRankSum
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VQSLOD
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MQRankSum
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InbreedingCoeff
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FS
type: SiteQuality
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BaseQRankSum
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SIO_000300: -2.126e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

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

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 38034
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

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

ReadPosRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 462
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 2
allele frequency: 5.282620179609086e-5
allele num: 37860
num of homozygotes: 0

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: 9.9e-2

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.8e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 5.36e-1

QD
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DP
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 9.330000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.479e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.91e0

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

East Asian
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allele frequency: 0.0e0
allele num: 5640
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3183
num of homozygotes: 0

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

European (Non-Finnish)
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allele frequency: 2.680318421828513e-5
allele num: 37309
num of homozygotes: 0

African
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allele frequency: 0.0e0
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Other
type: Population
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allele frequency: 0.0e0
allele num: 454
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 5959
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FS
type: SiteQuality
SIO_000300: 2.392e0

MQ
type: SiteQuality
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BaseQRankSum
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DP
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -7.22e-1

ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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InbreedingCoeff
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QD
type: SiteQuality
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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num of homozygotes: 0

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

African
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allele num: 6325
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East Asian
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Other
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South Asian
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MQRankSum
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MQ
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ReadPosRankSum
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InbreedingCoeff
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ClippingRankSum
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FS
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DP
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VQSLOD
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QD
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele frequency: 0.0e0
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Other
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South Asian
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East Asian
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Latino
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African
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European (Non-Finnish)
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allele frequency: 5.486968449931413e-5
allele num: 36450
num of homozygotes: 0

FS
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MQRankSum
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QD
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InbreedingCoeff
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MQ
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VQSLOD
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DP
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ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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South Asian
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Latino
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African
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Other
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European (Finnish)
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European (Non-Finnish)
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FS
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VQSLOD
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BaseQRankSum
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DP
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MQRankSum
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InbreedingCoeff
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QD
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ClippingRankSum
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MQ
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 0.0e0
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European (Finnish)
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South Asian
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 5496
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6192
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 5.553395901593825e-5
allele num: 36014
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 8.94099e5

QD
type: SiteQuality
SIO_000300: 2.106e1

FS
type: SiteQuality
SIO_000300: 3.452e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.8e-3

MQRankSum
type: SiteQuality
SIO_000300: 5.49e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.19e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.517e0

VQSLOD
type: SiteQuality
SIO_000300: -1.693e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.22e-1

GenotypeQuality
all individuals: 319
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3445
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4464
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22389
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 49
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1682
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4500
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 842
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 351
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1749
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 926
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13894
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1026
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 430
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5494
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6193
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7745
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3012
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 445
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 35918
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5821
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.36e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.41e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.331e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.6e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.3e-2

QD
type: SiteQuality
SIO_000300: 2.41e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 8.92343e5

MQRankSum
type: SiteQuality
SIO_000300: 5.669999999999999e-1

GenotypeQuality
all individuals: 1692
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1283
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4505
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 314
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 408
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1819
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2480
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13699
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 318
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 890
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 162
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 834
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4506
bin: 3.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 437
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.786058562950993e-5
allele num: 35893
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6173
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5469
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7716
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5838
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3012
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.8e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.500000000000001e-3

DP
type: SiteQuality
SIO_000300: 8.88665e5

QD
type: SiteQuality
SIO_000300: 2.759e1

GenotypeQuality
all individuals: 1776
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1344
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4489
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 905
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 304
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 484
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3630
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2509
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1665
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 384
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 860
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22588
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13289
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5763
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 434
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2975
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6138
num of homozygotes: 0