1-95699829-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95699829
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 95699829
    reference: chr 1
allele count: 686
allele frequency: 1.549022264372488e-2
allele num: 44286
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000359221
  ensembl transcript: ENST00000370202
  gene symbol: RWDD3
  hgvsc: ENST00000370202.4:c.43A>G
  hgvsp: ENSP00000359221.4:p.Ile15Val
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000475025
  ensembl transcript: ENST00000604534
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604534.1:c.566+3279A>G
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000473397
  gene symbol: RWDD3
  hgvsc: ENST00000473397.1:n.6A>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000497058
  gene symbol: RWDD3
  hgvsc: ENST00000497058.1:n.49A>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000495272
  gene symbol: RWDD3
  hgvsc: ENST00000495272.1:n.53A>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000397398
  ensembl transcript: ENST00000429514
  gene symbol: RWDD3
  hgvsc: ENST00000429514.2:c.-136A>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000263893
  ensembl transcript: ENST00000263893
  gene symbol: RWDD3
  hgvsc: ENST00000263893.6:c.43A>G
  hgvsp: ENSP00000263893.6:p.Ile15Val
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000492639
  gene symbol: RWDD3
  hgvsc: ENST00000492639.1:n.60A>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000474793
  ensembl transcript: ENST00000604203
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604203.1:c.210+3279A>G
  variant of: http://identifiers.org/hgnc/49388
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1223
  bin: 1.75e1
  variant carriers: 186
genotype depth: GenotypeDepth
  all individuals: 31691
  bin: 7.5e0
  variant carriers: 134
genotype depth: GenotypeDepth
  all individuals: 10436
  bin: 2.25e1
  variant carriers: 99
genotype depth: GenotypeDepth
  all individuals: 5720
  bin: 2.5e0
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 2804
  bin: 2.75e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 5462
  bin: 1.25e1
  variant carriers: 247
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1238
  bin: 3.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.75e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 3.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 5.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 442
  bin: 5.25e1
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 489
  bin: 3.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 367
  bin: 2.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 218
  bin: 8.75e1
  variant carriers: 15
genotype quality: GenotypeQuality
  all individuals: 292
  bin: 5.75e1
  variant carriers: 13
hgvs: p.Ile15Val
num of homozygotes: 6
population: South Asian
population: African
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP

1-95699840-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95699840
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 95699840
    reference: chr 1
allele count: 2
allele frequency: 4.546694553059925e-5
allele num: 43988
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000495272
  gene symbol: RWDD3
  hgvsc: ENST00000495272.1:n.64G>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000263893
  ensembl transcript: ENST00000263893
  gene symbol: RWDD3
  hgvsc: ENST00000263893.6:c.54G>T
  hgvsp: ENSP00000263893.6:p.Arg18Ser
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000475025
  ensembl transcript: ENST00000604534
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604534.1:c.566+3290G>T
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000359221
  ensembl transcript: ENST00000370202
  gene symbol: RWDD3
  hgvsc: ENST00000370202.4:c.54G>T
  hgvsp: ENSP00000359221.4:p.Arg18Ser
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000497058
  gene symbol: RWDD3
  hgvsc: ENST00000497058.1:n.60G>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000474793
  ensembl transcript: ENST00000604203
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604203.1:c.210+3290G>T
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000492639
  gene symbol: RWDD3
  hgvsc: ENST00000492639.1:n.71G>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000473397
  gene symbol: RWDD3
  hgvsc: ENST00000473397.1:n.17G>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000397398
  ensembl transcript: ENST00000429514
  gene symbol: RWDD3
  hgvsc: ENST00000429514.2:c.-125G>T
  variant of: http://identifiers.org/hgnc/21393
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6407
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9431
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1171
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2848
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31287
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6225
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 501
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 658
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 319
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 229
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1066
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Arg18Ser
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: DP

1-95699841-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95699841
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 95699841
    reference: chr 1
allele count: 15
allele frequency: 3.412037668895864e-4
allele num: 43962
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000497058
  gene symbol: RWDD3
  hgvsc: ENST00000497058.1:n.61C>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000492639
  gene symbol: RWDD3
  hgvsc: ENST00000492639.1:n.72C>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000397398
  ensembl transcript: ENST00000429514
  gene symbol: RWDD3
  hgvsc: ENST00000429514.2:c.-124C>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000473397
  gene symbol: RWDD3
  hgvsc: ENST00000473397.1:n.18C>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000495272
  gene symbol: RWDD3
  hgvsc: ENST00000495272.1:n.65C>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000474793
  ensembl transcript: ENST00000604203
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604203.1:c.210+3291C>T
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000359221
  ensembl transcript: ENST00000370202
  gene symbol: RWDD3
  hgvsc: ENST00000370202.4:c.55C>T
  hgvsp: ENSP00000359221.4:p.Pro19Ser
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000263893
  ensembl transcript: ENST00000263893
  gene symbol: RWDD3
  hgvsc: ENST00000263893.6:c.55C>T
  hgvsp: ENSP00000263893.6:p.Pro19Ser
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000475025
  ensembl transcript: ENST00000604534
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604534.1:c.566+3291C>T
  variant of: http://identifiers.org/hgnc/49388
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1249
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9349
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1190
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6267
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31211
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2831
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6510
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 688
  bin: 9.75e1
  variant carriers: 13
genotype quality: GenotypeQuality
  all individuals: 1395
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 515
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1231
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 568
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Pro19Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: Other
population: South Asian
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ

1-95699843-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95699843
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 95699843
    reference: chr 1
allele count: 1
allele frequency: 2.27396761870111e-5
allele num: 43976
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000359221
  ensembl transcript: ENST00000370202
  gene symbol: RWDD3
  hgvsc: ENST00000370202.4:c.57C>T
  hgvsp: ENST00000370202.4:c.57C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000492639
  gene symbol: RWDD3
  hgvsc: ENST00000492639.1:n.74C>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000263893
  ensembl transcript: ENST00000263893
  gene symbol: RWDD3
  hgvsc: ENST00000263893.6:c.57C>T
  hgvsp: ENST00000263893.6:c.57C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000475025
  ensembl transcript: ENST00000604534
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604534.1:c.566+3293C>T
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000397398
  ensembl transcript: ENST00000429514
  gene symbol: RWDD3
  hgvsc: ENST00000429514.2:c.-122C>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000473397
  gene symbol: RWDD3
  hgvsc: ENST00000473397.1:n.20C>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000497058
  gene symbol: RWDD3
  hgvsc: ENST00000497058.1:n.63C>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000495272
  gene symbol: RWDD3
  hgvsc: ENST00000495272.1:n.67C>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000474793
  ensembl transcript: ENST00000604203
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604203.1:c.210+3293C>T
  variant of: http://identifiers.org/hgnc/49388
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 6360
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9201
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31134
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6694
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2806
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1253
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 350
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 227
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 655
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 184
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 500
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Pro19Pro
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ

1-95699851-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95699851
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 95699851
    reference: chr 1
allele count: 1
allele frequency: 2.323852017103551e-5
allele num: 43032
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000475025
  ensembl transcript: ENST00000604534
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604534.1:c.566+3301G>T
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000263893
  ensembl transcript: ENST00000263893
  gene symbol: RWDD3
  hgvsc: ENST00000263893.6:c.65G>T
  hgvsp: ENSP00000263893.6:p.Trp22Leu
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000497058
  gene symbol: RWDD3
  hgvsc: ENST00000497058.1:n.71G>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000495272
  gene symbol: RWDD3
  hgvsc: ENST00000495272.1:n.75G>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000397398
  ensembl transcript: ENST00000429514
  gene symbol: RWDD3
  hgvsc: ENST00000429514.2:c.-114G>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000473397
  gene symbol: RWDD3
  hgvsc: ENST00000473397.1:n.28G>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000474793
  ensembl transcript: ENST00000604203
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604203.1:c.210+3301G>T
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000359221
  ensembl transcript: ENST00000370202
  gene symbol: RWDD3
  hgvsc: ENST00000370202.4:c.65G>T
  hgvsp: ENSP00000359221.4:p.Trp22Leu
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000492639
  gene symbol: RWDD3
  hgvsc: ENST00000492639.1:n.82G>T
  variant of: http://identifiers.org/hgnc/21393
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30599
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1199
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2746
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1245
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7555
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7349
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7834
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33462
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 202
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7382
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1355
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 379
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Trp22Leu
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Latino
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

1-95699856-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95699856
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 95699856
    reference: chr 1
allele count: 1
allele frequency: 2.356489772834386e-5
allele num: 42436
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000263893
  ensembl transcript: ENST00000263893
  gene symbol: RWDD3
  hgvsc: ENST00000263893.6:c.70G>C
  hgvsp: ENSP00000263893.6:p.Val24Leu
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000473397
  gene symbol: RWDD3
  hgvsc: ENST00000473397.1:n.33G>C
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000474793
  ensembl transcript: ENST00000604203
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604203.1:c.210+3306G>C
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000475025
  ensembl transcript: ENST00000604534
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604534.1:c.566+3306G>C
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000359221
  ensembl transcript: ENST00000370202
  gene symbol: RWDD3
  hgvsc: ENST00000370202.4:c.70G>C
  hgvsp: ENSP00000359221.4:p.Val24Leu
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000397398
  ensembl transcript: ENST00000429514
  gene symbol: RWDD3
  hgvsc: ENST00000429514.2:c.-109G>C
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000495272
  gene symbol: RWDD3
  hgvsc: ENST00000495272.1:n.80G>C
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000497058
  gene symbol: RWDD3
  hgvsc: ENST00000497058.1:n.76G>C
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000492639
  gene symbol: RWDD3
  hgvsc: ENST00000492639.1:n.87G>C
  variant of: http://identifiers.org/hgnc/21393
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1146
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7088
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8087
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2679
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8093
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30150
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1238
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 229
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 531
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 174
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8145
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 226
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Val24Leu
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: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

1-95699864-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95699864
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 95699864
    reference: chr 1
allele count: 4
allele frequency: 9.729992702505473e-5
allele num: 41110
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000263893
  ensembl transcript: ENST00000263893
  gene symbol: RWDD3
  hgvsc: ENST00000263893.6:c.78C>T
  hgvsp: ENST00000263893.6:c.78C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000475025
  ensembl transcript: ENST00000604534
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604534.1:c.566+3314C>T
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000492639
  gene symbol: RWDD3
  hgvsc: ENST00000492639.1:n.95C>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000497058
  gene symbol: RWDD3
  hgvsc: ENST00000497058.1:n.84C>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000474793
  ensembl transcript: ENST00000604203
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604203.1:c.210+3314C>T
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000495272
  gene symbol: RWDD3
  hgvsc: ENST00000495272.1:n.88C>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000473397
  gene symbol: RWDD3
  hgvsc: ENST00000473397.1:n.41C>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000397398
  ensembl transcript: ENST00000429514
  gene symbol: RWDD3
  hgvsc: ENST00000429514.2:c.-101C>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000359221
  ensembl transcript: ENST00000370202
  gene symbol: RWDD3
  hgvsc: ENST00000370202.4:c.78C>T
  hgvsp: ENST00000370202.4:c.78C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21393
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1155
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2617
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9572
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8799
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5951
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29050
  bin: 7.5e0
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1237
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1287
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 829
  bin: 1.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 230
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1054
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ser26Ser
num of homozygotes: 0
population: Other
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum

1-95699868-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95699868
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 95699868
    reference: chr 1
allele count: 1
allele frequency: 2.466091245376079e-5
allele num: 40550
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000495272
  gene symbol: RWDD3
  hgvsc: ENST00000495272.1:n.92T>A
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000263893
  ensembl transcript: ENST00000263893
  gene symbol: RWDD3
  hgvsc: ENST00000263893.6:c.82T>A
  hgvsp: ENSP00000263893.6:p.Ser28Thr
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000397398
  ensembl transcript: ENST00000429514
  gene symbol: RWDD3
  hgvsc: ENST00000429514.2:c.-97T>A
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000474793
  ensembl transcript: ENST00000604203
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604203.1:c.210+3318T>A
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000492639
  gene symbol: RWDD3
  hgvsc: ENST00000492639.1:n.99T>A
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000475025
  ensembl transcript: ENST00000604534
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604534.1:c.566+3318T>A
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000473397
  gene symbol: RWDD3
  hgvsc: ENST00000473397.1:n.45T>A
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000359221
  ensembl transcript: ENST00000370202
  gene symbol: RWDD3
  hgvsc: ENST00000370202.4:c.82T>A
  hgvsp: ENSP00000359221.4:p.Ser28Thr
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000497058
  gene symbol: RWDD3
  hgvsc: ENST00000497058.1:n.88T>A
  variant of: http://identifiers.org/hgnc/21393
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10553
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1032
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1232
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9083
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5420
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2532
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28466
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 475
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 864
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1400
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ser28Thr
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

1-95699876-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95699876
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 95699876
    reference: chr 1
allele count: 1
allele frequency: 2.607425949103045e-5
allele num: 38352
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000397398
  ensembl transcript: ENST00000429514
  gene symbol: RWDD3
  hgvsc: ENST00000429514.2:c.-94+5C>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000474793
  ensembl transcript: ENST00000604203
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604203.1:c.210+3326C>G
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000497058
  gene symbol: RWDD3
  hgvsc: ENST00000497058.1:n.91+5C>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000475025
  ensembl transcript: ENST00000604534
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604534.1:c.566+3326C>G
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000359221
  ensembl transcript: ENST00000370202
  gene symbol: RWDD3
  hgvsc: ENST00000370202.4:c.85+5C>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000492639
  gene symbol: RWDD3
  hgvsc: ENST00000492639.1:n.102+5C>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000495272
  gene symbol: RWDD3
  hgvsc: ENST00000495272.1:n.95+5C>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000263893
  ensembl transcript: ENST00000263893
  gene symbol: RWDD3
  hgvsc: ENST00000263893.6:c.85+5C>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000473397
  gene symbol: RWDD3
  hgvsc: ENST00000473397.1:n.48+5C>G
  variant of: http://identifiers.org/hgnc/21393
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26340
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 13450
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9244
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1079
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2359
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4344
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1227
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29866
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1228
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1402
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 4.75e1
  variant carriers: 0
hgvs: c.85+5C>G
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

1-95699878-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95699878
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 95699878
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 37440
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000492639
  gene symbol: RWDD3
  hgvsc: ENST00000492639.1:n.102+7A>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000397398
  ensembl transcript: ENST00000429514
  gene symbol: RWDD3
  hgvsc: ENST00000429514.2:c.-94+7A>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000497058
  gene symbol: RWDD3
  hgvsc: ENST00000497058.1:n.91+7A>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000359221
  ensembl transcript: ENST00000370202
  gene symbol: RWDD3
  hgvsc: ENST00000370202.4:c.85+7A>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000495272
  gene symbol: RWDD3
  hgvsc: ENST00000495272.1:n.95+7A>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000263893
  ensembl transcript: ENST00000263893
  gene symbol: RWDD3
  hgvsc: ENST00000263893.6:c.85+7A>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000473397
  gene symbol: RWDD3
  hgvsc: ENST00000473397.1:n.48+7A>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000475025
  ensembl transcript: ENST00000604534
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604534.1:c.566+3328A>G
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000474793
  ensembl transcript: ENST00000604203
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604203.1:c.210+3328A>G
  variant of: http://identifiers.org/hgnc/49388
canonical: true
consequence: splice region
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25667
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2334
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14191
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4182
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9311
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28386
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 677
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1218
  bin: 6.75e1
  variant carriers: 0
hgvs: c.85+7A>G
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum

1-95699881-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95699881
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 95699881
    reference: chr 1
allele count: 2
allele frequency: 5.461794745753454e-5
allele num: 36618
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000497058
  gene symbol: RWDD3
  hgvsc: ENST00000497058.1:n.91+10C>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000397398
  ensembl transcript: ENST00000429514
  gene symbol: RWDD3
  hgvsc: ENST00000429514.2:c.-94+10C>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000359221
  ensembl transcript: ENST00000370202
  gene symbol: RWDD3
  hgvsc: ENST00000370202.4:c.85+10C>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000492639
  gene symbol: RWDD3
  hgvsc: ENST00000492639.1:n.102+10C>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000474793
  ensembl transcript: ENST00000604203
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604203.1:c.210+3331C>G
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000475025
  ensembl transcript: ENST00000604534
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604534.1:c.566+3331C>G
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000263893
  ensembl transcript: ENST00000263893
  gene symbol: RWDD3
  hgvsc: ENST00000263893.6:c.85+10C>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000495272
  gene symbol: RWDD3
  hgvsc: ENST00000495272.1:n.95+10C>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000473397
  gene symbol: RWDD3
  hgvsc: ENST00000473397.1:n.48+10C>G
  variant of: http://identifiers.org/hgnc/21393
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15623
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24703
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2293
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9051
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4000
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1224
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 546
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16047
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27838
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1574
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 789
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 529
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum

1-95699883-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95699883
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 95699883
    reference: chr 1
allele count: 1
allele frequency: 2.774386860503829e-5
allele num: 36044
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000473397
  gene symbol: RWDD3
  hgvsc: ENST00000473397.1:n.48+12C>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000263893
  ensembl transcript: ENST00000263893
  gene symbol: RWDD3
  hgvsc: ENST00000263893.6:c.85+12C>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000397398
  ensembl transcript: ENST00000429514
  gene symbol: RWDD3
  hgvsc: ENST00000429514.2:c.-94+12C>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000497058
  gene symbol: RWDD3
  hgvsc: ENST00000497058.1:n.91+12C>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000492639
  gene symbol: RWDD3
  hgvsc: ENST00000492639.1:n.102+12C>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000359221
  ensembl transcript: ENST00000370202
  gene symbol: RWDD3
  hgvsc: ENST00000370202.4:c.85+12C>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000475025
  ensembl transcript: ENST00000604534
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604534.1:c.566+3333C>T
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000495272
  gene symbol: RWDD3
  hgvsc: ENST00000495272.1:n.95+12C>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000474793
  ensembl transcript: ENST00000604203
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604203.1:c.210+3333C>T
  variant of: http://identifiers.org/hgnc/49388
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2271
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16590
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8892
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1216
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24071
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3871
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1314
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 546
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 530
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 735
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1443
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 472
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ClippingRankSum

1-95699887-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95699887
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 95699887
    reference: chr 1
allele count: 1
allele frequency: 2.90596303615018e-5
allele num: 34412
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000263893
  ensembl transcript: ENST00000263893
  gene symbol: RWDD3
  hgvsc: ENST00000263893.6:c.85+16C>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000475025
  ensembl transcript: ENST00000604534
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604534.1:c.566+3337C>T
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000497058
  gene symbol: RWDD3
  hgvsc: ENST00000497058.1:n.91+16C>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000492639
  gene symbol: RWDD3
  hgvsc: ENST00000492639.1:n.102+16C>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000473397
  gene symbol: RWDD3
  hgvsc: ENST00000473397.1:n.48+16C>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000359221
  ensembl transcript: ENST00000370202
  gene symbol: RWDD3
  hgvsc: ENST00000370202.4:c.85+16C>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000397398
  ensembl transcript: ENST00000429514
  gene symbol: RWDD3
  hgvsc: ENST00000429514.2:c.-94+16C>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000495272
  gene symbol: RWDD3
  hgvsc: ENST00000495272.1:n.95+16C>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000474793
  ensembl transcript: ENST00000604203
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604203.1:c.210+3337C>T
  variant of: http://identifiers.org/hgnc/49388
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2235
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22593
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8518
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18641
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3647
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 521
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 676
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 924
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1734
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: DP

1-95699895-ACAGGGCGCCCT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95699895
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 95699884
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 29932
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000492639
  gene symbol: RWDD3
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000263893
  ensembl transcript: ENST00000263893
  gene symbol: RWDD3
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000359221
  ensembl transcript: ENST00000370202
  gene symbol: RWDD3
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000397398
  ensembl transcript: ENST00000429514
  gene symbol: RWDD3
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000497058
  gene symbol: RWDD3
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000495272
  gene symbol: RWDD3
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000474793
  ensembl transcript: ENST00000604203
  gene symbol: TMEM56-RWDD3
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000475025
  ensembl transcript: ENST00000604534
  gene symbol: TMEM56-RWDD3
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000473397
  gene symbol: RWDD3
  variant of: http://identifiers.org/hgnc/21393
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 6685
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23173
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1228
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3308
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19747
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2192
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 676
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 538
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18568
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 953
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1805
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 202
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1146
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: ACAGGGCGCCCT
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP

1-95699902-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95699902
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 95699902
    reference: chr 1
allele count: 1
allele frequency: 4.140786749482401e-5
allele num: 24150
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000473397
  gene symbol: RWDD3
  hgvsc: ENST00000473397.1:n.48+31G>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000359221
  ensembl transcript: ENST00000370202
  gene symbol: RWDD3
  hgvsc: ENST00000370202.4:c.85+31G>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000263893
  ensembl transcript: ENST00000263893
  gene symbol: RWDD3
  hgvsc: ENST00000263893.6:c.85+31G>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000474793
  ensembl transcript: ENST00000604203
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604203.1:c.210+3352G>T
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000495272
  gene symbol: RWDD3
  hgvsc: ENST00000495272.1:n.95+31G>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000497058
  gene symbol: RWDD3
  hgvsc: ENST00000497058.1:n.91+31G>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000397398
  ensembl transcript: ENST00000429514
  gene symbol: RWDD3
  hgvsc: ENST00000429514.2:c.-94+31G>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000492639
  gene symbol: RWDD3
  hgvsc: ENST00000492639.1:n.102+31G>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000475025
  ensembl transcript: ENST00000604534
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604534.1:c.566+3352G>T
  variant of: http://identifiers.org/hgnc/49388
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26180
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2106
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2988
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18165
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4337
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10598
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26946
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 713
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum

1-95699907-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95699907
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 95699907
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 23358
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000359221
  ensembl transcript: ENST00000370202
  gene symbol: RWDD3
  hgvsc: ENST00000370202.4:c.85+36C>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000473397
  gene symbol: RWDD3
  hgvsc: ENST00000473397.1:n.48+36C>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000497058
  gene symbol: RWDD3
  hgvsc: ENST00000497058.1:n.91+36C>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000397398
  ensembl transcript: ENST00000429514
  gene symbol: RWDD3
  hgvsc: ENST00000429514.2:c.-94+36C>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000495272
  gene symbol: RWDD3
  hgvsc: ENST00000495272.1:n.95+36C>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000492639
  gene symbol: RWDD3
  hgvsc: ENST00000492639.1:n.102+36C>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000475025
  ensembl transcript: ENST00000604534
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604534.1:c.566+3357C>T
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000474793
  ensembl transcript: ENST00000604203
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604203.1:c.210+3357C>T
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000263893
  ensembl transcript: ENST00000263893
  gene symbol: RWDD3
  hgvsc: ENST00000263893.6:c.85+36C>T
  variant of: http://identifiers.org/hgnc/21393
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26745
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18035
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3733
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2915
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2094
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 599
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 508
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 469
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2528
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: BaseQRankSum

1-95699909-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95699909
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 95699909
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 22386
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000497058
  gene symbol: RWDD3
  hgvsc: ENST00000497058.1:n.91+38G>A
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000359221
  ensembl transcript: ENST00000370202
  gene symbol: RWDD3
  hgvsc: ENST00000370202.4:c.85+38G>A
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000473397
  gene symbol: RWDD3
  hgvsc: ENST00000473397.1:n.48+38G>A
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000397398
  ensembl transcript: ENST00000429514
  gene symbol: RWDD3
  hgvsc: ENST00000429514.2:c.-94+38G>A
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000263893
  ensembl transcript: ENST00000263893
  gene symbol: RWDD3
  hgvsc: ENST00000263893.6:c.85+38G>A
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000475025
  ensembl transcript: ENST00000604534
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604534.1:c.566+3359G>A
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000495272
  gene symbol: RWDD3
  hgvsc: ENST00000495272.1:n.95+38G>A
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000474793
  ensembl transcript: ENST00000604203
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604203.1:c.210+3359G>A
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000492639
  gene symbol: RWDD3
  hgvsc: ENST00000492639.1:n.102+38G>A
  variant of: http://identifiers.org/hgnc/21393
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1204
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3246
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2051
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26873
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18114
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2865
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 603
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 531
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
reference allele: G
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

1-95699920-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95699920
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 95699920
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 20186
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000495272
  gene symbol: RWDD3
  hgvsc: ENST00000495272.1:n.95+49C>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000492639
  gene symbol: RWDD3
  hgvsc: ENST00000492639.1:n.102+49C>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000359221
  ensembl transcript: ENST00000370202
  gene symbol: RWDD3
  hgvsc: ENST00000370202.4:c.85+49C>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000397398
  ensembl transcript: ENST00000429514
  gene symbol: RWDD3
  hgvsc: ENST00000429514.2:c.-94+49C>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000473397
  gene symbol: RWDD3
  hgvsc: ENST00000473397.1:n.48+49C>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000474793
  ensembl transcript: ENST00000604203
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604203.1:c.210+3370C>T
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000475025
  ensembl transcript: ENST00000604534
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604534.1:c.566+3370C>T
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000497058
  gene symbol: RWDD3
  hgvsc: ENST00000497058.1:n.91+49C>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000263893
  ensembl transcript: ENST00000263893
  gene symbol: RWDD3
  hgvsc: ENST00000263893.6:c.85+49C>T
  variant of: http://identifiers.org/hgnc/21393
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18276
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2868
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2028
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26943
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2211
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2775
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 225
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6287
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 231
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 537
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 237
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: QD
site quality: FS
site quality: InbreedingCoeff

1-95705412-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95705412
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 95705412
    reference: chr 1
allele count: 19
allele frequency: 1.544715447154472e-3
allele num: 12300
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000263893
  ensembl transcript: ENST00000263893
  gene symbol: RWDD3
  hgvsc: ENST00000263893.6:c.86-4355C>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000473397
  gene symbol: RWDD3
  hgvsc: ENST00000473397.1:n.48+5541C>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000397398
  ensembl transcript: ENST00000429514
  gene symbol: RWDD3
  hgvsc: ENST00000429514.2:c.-14C>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000497058
  gene symbol: RWDD3
  hgvsc: ENST00000497058.1:n.125+46C>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000474793
  ensembl transcript: ENST00000604203
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604203.1:c.211-6900C>T
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000495272
  gene symbol: RWDD3
  hgvsc: ENST00000495272.1:n.175C>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000359221
  ensembl transcript: ENST00000370202
  gene symbol: RWDD3
  hgvsc: ENST00000370202.4:c.86-4355C>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000492639
  gene symbol: RWDD3
  hgvsc: ENST00000492639.1:n.295C>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000475025
  ensembl transcript: ENST00000604534
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604534.1:c.567-4355C>T
  variant of: http://identifiers.org/hgnc/49388
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1857
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1567
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1967
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 3.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 682
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 367
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum

1-95705448-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95705448
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 95705448
    reference: chr 1
allele count: 11
allele frequency: 8.938729075247847e-4
allele num: 12306
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000263893
  ensembl transcript: ENST00000263893
  gene symbol: RWDD3
  hgvsc: ENST00000263893.6:c.86-4319T>C
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000492639
  gene symbol: RWDD3
  hgvsc: ENST00000492639.1:n.331T>C
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000473397
  gene symbol: RWDD3
  hgvsc: ENST00000473397.1:n.48+5577T>C
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000475025
  ensembl transcript: ENST00000604534
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604534.1:c.567-4319T>C
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000397398
  ensembl transcript: ENST00000429514
  gene symbol: RWDD3
  hgvsc: ENST00000429514.2:c.23T>C
  hgvsp: ENSP00000397398.2:p.Leu8Pro
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000359221
  ensembl transcript: ENST00000370202
  gene symbol: RWDD3
  hgvsc: ENST00000370202.4:c.86-4319T>C
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000495272
  gene symbol: RWDD3
  hgvsc: ENST00000495272.1:n.211T>C
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000497058
  gene symbol: RWDD3
  hgvsc: ENST00000497058.1:n.125+82T>C
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000474793
  ensembl transcript: ENST00000604203
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604203.1:c.211-6864T>C
  variant of: http://identifiers.org/hgnc/49388
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1570
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1868
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1946
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 678
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 368
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Leu8Pro
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum

1-95705452-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95705452
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 95705452
    reference: chr 1
allele count: 1
allele frequency: 8.126117341134406e-5
allele num: 12306
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000475025
  ensembl transcript: ENST00000604534
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604534.1:c.567-4315C>G
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000397398
  ensembl transcript: ENST00000429514
  gene symbol: RWDD3
  hgvsc: ENST00000429514.2:c.27C>G
  hgvsp: ENSP00000397398.2:p.His9Gln
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000492639
  gene symbol: RWDD3
  hgvsc: ENST00000492639.1:n.335C>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000359221
  ensembl transcript: ENST00000370202
  gene symbol: RWDD3
  hgvsc: ENST00000370202.4:c.86-4315C>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000474793
  ensembl transcript: ENST00000604203
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604203.1:c.211-6860C>G
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000497058
  gene symbol: RWDD3
  hgvsc: ENST00000497058.1:n.125+86C>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000495272
  gene symbol: RWDD3
  hgvsc: ENST00000495272.1:n.215C>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000263893
  ensembl transcript: ENST00000263893
  gene symbol: RWDD3
  hgvsc: ENST00000263893.6:c.86-4315C>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000473397
  gene symbol: RWDD3
  hgvsc: ENST00000473397.1:n.48+5581C>G
  variant of: http://identifiers.org/hgnc/21393
canonical: false
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1872
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1571
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1893
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 462
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 675
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.25e1
  variant carriers: 0
hgvs: p.His9Gln
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ReadPosRankSum

1-95705464-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95705464
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 95705464
    reference: chr 1
allele count: 2
allele frequency: 1.625487646293888e-4
allele num: 12304
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000397398
  ensembl transcript: ENST00000429514
  gene symbol: RWDD3
  hgvsc: ENST00000429514.2:c.39C>T
  hgvsp: ENST00000429514.2:c.39C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000497058
  gene symbol: RWDD3
  hgvsc: ENST00000497058.1:n.125+98C>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000492639
  gene symbol: RWDD3
  hgvsc: ENST00000492639.1:n.347C>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000474793
  ensembl transcript: ENST00000604203
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604203.1:c.211-6848C>T
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000359221
  ensembl transcript: ENST00000370202
  gene symbol: RWDD3
  hgvsc: ENST00000370202.4:c.86-4303C>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000495272
  gene symbol: RWDD3
  hgvsc: ENST00000495272.1:n.227C>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000475025
  ensembl transcript: ENST00000604534
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604534.1:c.567-4303C>T
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000473397
  gene symbol: RWDD3
  hgvsc: ENST00000473397.1:n.48+5593C>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000263893
  ensembl transcript: ENST00000263893
  gene symbol: RWDD3
  hgvsc: ENST00000263893.6:c.86-4303C>T
  variant of: http://identifiers.org/hgnc/21393
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1566
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1910
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1871
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 225
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 369
  bin: 9.25e1
  variant carriers: 0
hgvs: n.347C>T
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: Latino
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum

1-95705481-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95705481
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 95705481
    reference: chr 1
allele count: 1
allele frequency: 8.128759551292472e-5
allele num: 12302
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000495272
  gene symbol: RWDD3
  hgvsc: ENST00000495272.1:n.228+16G>A
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000397398
  ensembl transcript: ENST00000429514
  gene symbol: RWDD3
  hgvsc: ENST00000429514.2:c.40+16G>A
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000263893
  ensembl transcript: ENST00000263893
  gene symbol: RWDD3
  hgvsc: ENST00000263893.6:c.86-4286G>A
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000497058
  gene symbol: RWDD3
  hgvsc: ENST00000497058.1:n.125+115G>A
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000473397
  gene symbol: RWDD3
  hgvsc: ENST00000473397.1:n.48+5610G>A
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000475025
  ensembl transcript: ENST00000604534
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604534.1:c.567-4286G>A
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000492639
  gene symbol: RWDD3
  hgvsc: ENST00000492639.1:n.348+16G>A
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000359221
  ensembl transcript: ENST00000370202
  gene symbol: RWDD3
  hgvsc: ENST00000370202.4:c.86-4286G>A
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000474793
  ensembl transcript: ENST00000604203
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604203.1:c.211-6831G>A
  variant of: http://identifiers.org/hgnc/49388
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1930
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  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 depth: GenotypeDepth
  all individuals: 75
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1555
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1862
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 940
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 549
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1989
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1620
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: MQ

1-95705491-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95705491
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 95705491
    reference: chr 1
allele count: 9
allele frequency: 7.31826313221662e-4
allele num: 12298
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000495272
  gene symbol: RWDD3
  hgvsc: ENST00000495272.1:n.228+26G>C
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000473397
  gene symbol: RWDD3
  hgvsc: ENST00000473397.1:n.48+5620G>C
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000474793
  ensembl transcript: ENST00000604203
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604203.1:c.211-6821G>C
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000359221
  ensembl transcript: ENST00000370202
  gene symbol: RWDD3
  hgvsc: ENST00000370202.4:c.86-4276G>C
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000397398
  ensembl transcript: ENST00000429514
  gene symbol: RWDD3
  hgvsc: ENST00000429514.2:c.40+26G>C
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000492639
  gene symbol: RWDD3
  hgvsc: ENST00000492639.1:n.348+26G>C
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000263893
  ensembl transcript: ENST00000263893
  gene symbol: RWDD3
  hgvsc: ENST00000263893.6:c.86-4276G>C
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000497058
  gene symbol: RWDD3
  hgvsc: ENST00000497058.1:n.125+125G>C
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000475025
  ensembl transcript: ENST00000604534
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604534.1:c.567-4276G>C
  variant of: http://identifiers.org/hgnc/49388
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 921
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2033
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1840
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1541
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 268
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 448
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 666
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 366
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: QD

1-95705512-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95705512
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 95705512
    reference: chr 1
allele count: 1
allele frequency: 8.138020833333333e-5
allele num: 12288
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000492639
  gene symbol: RWDD3
  hgvsc: ENST00000492639.1:n.348+47G>A
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000497058
  gene symbol: RWDD3
  hgvsc: ENST00000497058.1:n.125+146G>A
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000495272
  gene symbol: RWDD3
  hgvsc: ENST00000495272.1:n.228+47G>A
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000359221
  ensembl transcript: ENST00000370202
  gene symbol: RWDD3
  hgvsc: ENST00000370202.4:c.86-4255G>A
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000473397
  gene symbol: RWDD3
  hgvsc: ENST00000473397.1:n.48+5641G>A
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000263893
  ensembl transcript: ENST00000263893
  gene symbol: RWDD3
  hgvsc: ENST00000263893.6:c.86-4255G>A
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000474793
  ensembl transcript: ENST00000604203
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604203.1:c.211-6800G>A
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000397398
  ensembl transcript: ENST00000429514
  gene symbol: RWDD3
  hgvsc: ENST00000429514.2:c.40+47G>A
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000475025
  ensembl transcript: ENST00000604534
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604534.1:c.567-4255G>A
  variant of: http://identifiers.org/hgnc/49388
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2205
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1017
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1588
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1430
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 666
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 427
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 757
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum

1-95709722-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95709722
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 95709722
    reference: chr 1
allele count: 3
allele frequency: 2.600960621456191e-5
allele num: 115342
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000474793
  ensembl transcript: ENST00000604203
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604203.1:c.211-2590A>G
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000397398
  ensembl transcript: ENST00000429514
  gene symbol: RWDD3
  hgvsc: ENST00000429514.2:c.41-45A>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000495272
  gene symbol: RWDD3
  hgvsc: ENST00000495272.1:n.229-45A>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000359221
  ensembl transcript: ENST00000370202
  gene symbol: RWDD3
  hgvsc: ENST00000370202.4:c.86-45A>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000473397
  gene symbol: RWDD3
  hgvsc: ENST00000473397.1:n.49-2590A>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000492639
  gene symbol: RWDD3
  hgvsc: ENST00000492639.1:n.349-45A>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000263893
  ensembl transcript: ENST00000263893
  gene symbol: RWDD3
  hgvsc: ENST00000263893.6:c.86-45A>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000497058
  gene symbol: RWDD3
  hgvsc: ENST00000497058.1:n.126-399A>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000228852
  ensembl transcript: ENST00000444665
  gene symbol: RP11-57H12.5
  hgvsc: ENST00000444665.1:n.71-641T>C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000475025
  ensembl transcript: ENST00000604534
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604534.1:c.567-45A>G
  variant of: http://identifiers.org/hgnc/49388
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1308
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4650
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2257
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3557
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5432
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1846
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2294
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5660
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4481
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5271
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6010
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3489
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2680
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2397
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1477
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4943
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 474
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 280
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 734
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1894
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum

1-95709728-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95709728
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 95709728
    reference: chr 1
allele count: 1
allele frequency: 8.660408078428655e-6
allele num: 115468
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000475025
  ensembl transcript: ENST00000604534
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604534.1:c.567-39A>G
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000474793
  ensembl transcript: ENST00000604203
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604203.1:c.211-2584A>G
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000228852
  ensembl transcript: ENST00000444665
  gene symbol: RP11-57H12.5
  hgvsc: ENST00000444665.1:n.71-647T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000473397
  gene symbol: RWDD3
  hgvsc: ENST00000473397.1:n.49-2584A>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000397398
  ensembl transcript: ENST00000429514
  gene symbol: RWDD3
  hgvsc: ENST00000429514.2:c.41-39A>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000495272
  gene symbol: RWDD3
  hgvsc: ENST00000495272.1:n.229-39A>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000492639
  gene symbol: RWDD3
  hgvsc: ENST00000492639.1:n.349-39A>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000263893
  ensembl transcript: ENST00000263893
  gene symbol: RWDD3
  hgvsc: ENST00000263893.6:c.86-39A>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000359221
  ensembl transcript: ENST00000370202
  gene symbol: RWDD3
  hgvsc: ENST00000370202.4:c.86-39A>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000497058
  gene symbol: RWDD3
  hgvsc: ENST00000497058.1:n.126-393A>G
  variant of: http://identifiers.org/hgnc/21393
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 841
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2398
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5660
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5271
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2292
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4481
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6011
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4943
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2680
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1496
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3492
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1846
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2253
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5432
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3557
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1308
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4650
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 480
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2106
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 961
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 190
  bin: 1.25e1
  variant carriers: 1
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: A
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

1-95709739-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95709739
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 95709739
    reference: chr 1
allele count: 1
allele frequency: 8.627978809684043e-6
allele num: 115902
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000495272
  gene symbol: RWDD3
  hgvsc: ENST00000495272.1:n.229-28C>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000492639
  gene symbol: RWDD3
  hgvsc: ENST00000492639.1:n.349-28C>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000397398
  ensembl transcript: ENST00000429514
  gene symbol: RWDD3
  hgvsc: ENST00000429514.2:c.41-28C>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000475025
  ensembl transcript: ENST00000604534
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604534.1:c.567-28C>G
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000359221
  ensembl transcript: ENST00000370202
  gene symbol: RWDD3
  hgvsc: ENST00000370202.4:c.86-28C>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000473397
  gene symbol: RWDD3
  hgvsc: ENST00000473397.1:n.49-2573C>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000497058
  gene symbol: RWDD3
  hgvsc: ENST00000497058.1:n.126-382C>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000474793
  ensembl transcript: ENST00000604203
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604203.1:c.211-2573C>G
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000228852
  ensembl transcript: ENST00000444665
  gene symbol: RP11-57H12.5
  hgvsc: ENST00000444665.1:n.71-658G>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000263893
  ensembl transcript: ENST00000263893
  gene symbol: RWDD3
  hgvsc: ENST00000263893.6:c.86-28C>G
  variant of: http://identifiers.org/hgnc/21393
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2680
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1308
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5660
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4944
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5432
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3493
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2403
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1861
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2185
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5272
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6012
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4481
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1521
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1846
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1623
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4649
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3557
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51104
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 430
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 610
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum

1-95709747-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95709747
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 95709747
    reference: chr 1
allele count: 98
allele frequency: 8.39386049061258e-4
allele num: 116752
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000397398
  ensembl transcript: ENST00000429514
  gene symbol: RWDD3
  hgvsc: ENST00000429514.2:c.41-20T>A
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000474793
  ensembl transcript: ENST00000604203
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604203.1:c.211-2565T>A
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000492639
  gene symbol: RWDD3
  hgvsc: ENST00000492639.1:n.349-20T>A
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000495272
  gene symbol: RWDD3
  hgvsc: ENST00000495272.1:n.229-20T>A
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000497058
  gene symbol: RWDD3
  hgvsc: ENST00000497058.1:n.126-374T>A
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000359221
  ensembl transcript: ENST00000370202
  gene symbol: RWDD3
  hgvsc: ENST00000370202.4:c.86-20T>A
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000475025
  ensembl transcript: ENST00000604534
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604534.1:c.567-20T>A
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000263893
  ensembl transcript: ENST00000263893
  gene symbol: RWDD3
  hgvsc: ENST00000263893.6:c.86-20T>A
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000473397
  gene symbol: RWDD3
  hgvsc: ENST00000473397.1:n.49-2565T>A
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000228852
  ensembl transcript: ENST00000444665
  gene symbol: RP11-57H12.5
  hgvsc: ENST00000444665.1:n.71-666A>T
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5997
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5422
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5650
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2549
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4987
  bin: 9.75e1
  variant carriers: 51
genotype depth: GenotypeDepth
  all individuals: 4478
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1541
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1310
  bin: 9.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1852
  bin: 8.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1917
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5261
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2687
  bin: 8.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 4648
  bin: 7.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 3558
  bin: 7.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 2403
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3489
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 627
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 275
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 1
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

1-95709750-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95709750
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 95709750
    reference: chr 1
allele count: 1
allele frequency: 8.540147232138282e-6
allele num: 117094
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000495272
  gene symbol: RWDD3
  hgvsc: ENST00000495272.1:n.229-17T>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000497058
  gene symbol: RWDD3
  hgvsc: ENST00000497058.1:n.126-371T>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000359221
  ensembl transcript: ENST00000370202
  gene symbol: RWDD3
  hgvsc: ENST00000370202.4:c.86-17T>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000228852
  ensembl transcript: ENST00000444665
  gene symbol: RP11-57H12.5
  hgvsc: ENST00000444665.1:n.71-669A>C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000475025
  ensembl transcript: ENST00000604534
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604534.1:c.567-17T>G
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000474793
  ensembl transcript: ENST00000604203
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604203.1:c.211-2562T>G
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000492639
  gene symbol: RWDD3
  hgvsc: ENST00000492639.1:n.349-17T>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000473397
  gene symbol: RWDD3
  hgvsc: ENST00000473397.1:n.49-2562T>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000263893
  ensembl transcript: ENST00000263893
  gene symbol: RWDD3
  hgvsc: ENST00000263893.6:c.86-17T>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000397398
  ensembl transcript: ENST00000429514
  gene symbol: RWDD3
  hgvsc: ENST00000429514.2:c.41-17T>G
  variant of: http://identifiers.org/hgnc/21393
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4987
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5422
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1127
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1751
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5650
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2913
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3557
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1553
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1853
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4478
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5997
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4650
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2685
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5261
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3490
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1309
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2404
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 634
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 471
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ

1-95709758-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95709758
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 95709758
    reference: chr 1
allele count: 1520
allele frequency: 1.286086573933056e-2
allele num: 118188
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000474793
  ensembl transcript: ENST00000604203
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604203.1:c.211-2554G>T
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000473397
  gene symbol: RWDD3
  hgvsc: ENST00000473397.1:n.49-2554G>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000263893
  ensembl transcript: ENST00000263893
  gene symbol: RWDD3
  hgvsc: ENST00000263893.6:c.86-9G>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000495272
  gene symbol: RWDD3
  hgvsc: ENST00000495272.1:n.229-9G>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000359221
  ensembl transcript: ENST00000370202
  gene symbol: RWDD3
  hgvsc: ENST00000370202.4:c.86-9G>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000228852
  ensembl transcript: ENST00000444665
  gene symbol: RP11-57H12.5
  hgvsc: ENST00000444665.1:n.71-677C>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000492639
  gene symbol: RWDD3
  hgvsc: ENST00000492639.1:n.349-9G>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000475025
  ensembl transcript: ENST00000604534
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604534.1:c.567-9G>T
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000497058
  gene symbol: RWDD3
  hgvsc: ENST00000497058.1:n.126-363G>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000397398
  ensembl transcript: ENST00000429514
  gene symbol: RWDD3
  hgvsc: ENST00000429514.2:c.41-9G>T
  variant of: http://identifiers.org/hgnc/21393
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2326
  bin: 3.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 3369
  bin: 4.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 4353
  bin: 4.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 2.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 5390
  bin: 6.75e1
  variant carriers: 69
genotype depth: GenotypeDepth
  all individuals: 5122
  bin: 5.25e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 1562
  bin: 3.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 1381
  bin: 9.25e1
  variant carriers: 90
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 1.75e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 3672
  bin: 2.25e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 1.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 5568
  bin: 6.25e1
  variant carriers: 47
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1242
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2726
  bin: 8.25e1
  variant carriers: 81
genotype depth: GenotypeDepth
  all individuals: 4673
  bin: 7.25e1
  variant carriers: 92
genotype depth: GenotypeDepth
  all individuals: 1912
  bin: 8.75e1
  variant carriers: 83
genotype depth: GenotypeDepth
  all individuals: 5601
  bin: 9.75e1
  variant carriers: 720
genotype depth: GenotypeDepth
  all individuals: 5878
  bin: 5.75e1
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 3587
  bin: 7.75e1
  variant carriers: 91
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 266
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 227
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 12
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum

1-95709761-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95709761
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 95709761
    reference: chr 1
allele count: 2
allele frequency: 1.68335998653312e-5
allele num: 118810
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000359221
  ensembl transcript: ENST00000370202
  gene symbol: RWDD3
  hgvsc: ENST00000370202.4:c.86-6T>C
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000397398
  ensembl transcript: ENST00000429514
  gene symbol: RWDD3
  hgvsc: ENST00000429514.2:c.41-6T>C
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000474793
  ensembl transcript: ENST00000604203
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604203.1:c.211-2551T>C
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000475025
  ensembl transcript: ENST00000604534
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604534.1:c.567-6T>C
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000228852
  ensembl transcript: ENST00000444665
  gene symbol: RP11-57H12.5
  hgvsc: ENST00000444665.1:n.71-680A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000495272
  gene symbol: RWDD3
  hgvsc: ENST00000495272.1:n.229-6T>C
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000497058
  gene symbol: RWDD3
  hgvsc: ENST00000497058.1:n.126-360T>C
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000263893
  ensembl transcript: ENST00000263893
  gene symbol: RWDD3
  hgvsc: ENST00000263893.6:c.86-6T>C
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000473397
  gene symbol: RWDD3
  hgvsc: ENST00000473397.1:n.49-2551T>C
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000492639
  gene symbol: RWDD3
  hgvsc: ENST00000492639.1:n.349-6T>C
  variant of: http://identifiers.org/hgnc/21393
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2733
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3915
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1338
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5589
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4685
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1911
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1626
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4359
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3376
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3597
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1385
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5388
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5527
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5884
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2322
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5127
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 609
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 4.25e1
  variant carriers: 0
hgvs: c.567-6T>C
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD

1-95709766-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95709766
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 95709766
    reference: chr 1
allele count: 1
allele frequency: 8.358548287333457e-6
allele num: 119638
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000492639
  gene symbol: RWDD3
  hgvsc: ENST00000492639.1:n.349-1G>A
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000228852
  ensembl transcript: ENST00000444665
  gene symbol: RP11-57H12.5
  hgvsc: ENST00000444665.1:n.71-685C>T
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000359221
  ensembl transcript: ENST00000370202
  gene symbol: RWDD3
  hgvsc: ENST00000370202.4:c.86-1G>A
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000497058
  gene symbol: RWDD3
  hgvsc: ENST00000497058.1:n.126-355G>A
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000475025
  ensembl transcript: ENST00000604534
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604534.1:c.567-1G>A
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000263893
  ensembl transcript: ENST00000263893
  gene symbol: RWDD3
  hgvsc: ENST00000263893.6:c.86-1G>A
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000397398
  ensembl transcript: ENST00000429514
  gene symbol: RWDD3
  hgvsc: ENST00000429514.2:c.41-1G>A
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000473397
  gene symbol: RWDD3
  hgvsc: ENST00000473397.1:n.49-2546G>A
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000495272
  gene symbol: RWDD3
  hgvsc: ENST00000495272.1:n.229-1G>A
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000474793
  ensembl transcript: ENST00000604203
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604203.1:c.211-2546G>A
  variant of: http://identifiers.org/hgnc/49388
canonical: true
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4360
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1911
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5884
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5589
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1385
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2324
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3598
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1472
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3379
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5127
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2733
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5527
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4685
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5388
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4357
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1728
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 503
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 594
  bin: 2.25e1
  variant carriers: 0
hgvs: c.567-1G>A
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ

1-95709767-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95709767
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 95709767
    reference: chr 1
allele count: 1
allele frequency: 8.354079296920687e-6
allele num: 119702
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000497058
  gene symbol: RWDD3
  hgvsc: ENST00000497058.1:n.126-354A>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000359221
  ensembl transcript: ENST00000370202
  gene symbol: RWDD3
  hgvsc: ENST00000370202.4:c.86A>G
  hgvsp: ENSP00000359221.4:p.Glu29Gly
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000473397
  gene symbol: RWDD3
  hgvsc: ENST00000473397.1:n.49-2545A>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000495272
  gene symbol: RWDD3
  hgvsc: ENST00000495272.1:n.229A>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000397398
  ensembl transcript: ENST00000429514
  gene symbol: RWDD3
  hgvsc: ENST00000429514.2:c.41A>G
  hgvsp: ENSP00000397398.2:p.Glu14Gly
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000492639
  gene symbol: RWDD3
  hgvsc: ENST00000492639.1:n.349A>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000474793
  ensembl transcript: ENST00000604203
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604203.1:c.211-2545A>G
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000475025
  ensembl transcript: ENST00000604534
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604534.1:c.567A>G
  hgvsp: ENST00000604534.1:c.567A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000263893
  ensembl transcript: ENST00000263893
  gene symbol: RWDD3
  hgvsc: ENST00000263893.6:c.86A>G
  hgvsp: ENSP00000263893.6:p.Glu29Gly
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000228852
  ensembl transcript: ENST00000444665
  gene symbol: RP11-57H12.5
  hgvsc: ENST00000444665.1:n.71-686T>C
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1477
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4404
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5589
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3598
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5884
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5388
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5127
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4360
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4686
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3378
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1739
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2326
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5527
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2733
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1911
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1385
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 710
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Glu29Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff

1-95709767-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95709767
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 95709767
    reference: chr 1
allele count: 1
allele frequency: 8.354079296920687e-6
allele num: 119702
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000474793
  ensembl transcript: ENST00000604203
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604203.1:c.211-2545A>T
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000397398
  ensembl transcript: ENST00000429514
  gene symbol: RWDD3
  hgvsc: ENST00000429514.2:c.41A>T
  hgvsp: ENSP00000397398.2:p.Glu14Val
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000263893
  ensembl transcript: ENST00000263893
  gene symbol: RWDD3
  hgvsc: ENST00000263893.6:c.86A>T
  hgvsp: ENSP00000263893.6:p.Glu29Val
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000228852
  ensembl transcript: ENST00000444665
  gene symbol: RP11-57H12.5
  hgvsc: ENST00000444665.1:n.71-686T>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000497058
  gene symbol: RWDD3
  hgvsc: ENST00000497058.1:n.126-354A>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000495272
  gene symbol: RWDD3
  hgvsc: ENST00000495272.1:n.229A>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000473397
  gene symbol: RWDD3
  hgvsc: ENST00000473397.1:n.49-2545A>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000359221
  ensembl transcript: ENST00000370202
  gene symbol: RWDD3
  hgvsc: ENST00000370202.4:c.86A>T
  hgvsp: ENSP00000359221.4:p.Glu29Val
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000492639
  gene symbol: RWDD3
  hgvsc: ENST00000492639.1:n.349A>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000475025
  ensembl transcript: ENST00000604534
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604534.1:c.567A>T
  hgvsp: ENSP00000475025.1:p.Gln189His
  variant of: http://identifiers.org/hgnc/49388
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3598
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1477
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4360
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5884
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1739
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2733
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2326
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4686
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5127
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4404
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1385
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5527
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5388
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5589
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1911
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3378
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Gln189His
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Latino
reference allele: A
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

1-95709773-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95709773
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 95709773
    reference: chr 1
allele count: 3
allele frequency: 2.498417668809754e-5
allele num: 120076
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000228852
  ensembl transcript: ENST00000444665
  gene symbol: RP11-57H12.5
  hgvsc: ENST00000444665.1:n.71-692T>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000263893
  ensembl transcript: ENST00000263893
  gene symbol: RWDD3
  hgvsc: ENST00000263893.6:c.92A>G
  hgvsp: ENSP00000263893.6:p.Asp31Gly
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000497058
  gene symbol: RWDD3
  hgvsc: ENST00000497058.1:n.126-348A>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000495272
  gene symbol: RWDD3
  hgvsc: ENST00000495272.1:n.235A>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000359221
  ensembl transcript: ENST00000370202
  gene symbol: RWDD3
  hgvsc: ENST00000370202.4:c.92A>G
  hgvsp: ENSP00000359221.4:p.Asp31Gly
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000492639
  gene symbol: RWDD3
  hgvsc: ENST00000492639.1:n.355A>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000473397
  gene symbol: RWDD3
  hgvsc: ENST00000473397.1:n.49-2539A>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000397398
  ensembl transcript: ENST00000429514
  gene symbol: RWDD3
  hgvsc: ENST00000429514.2:c.47A>G
  hgvsp: ENSP00000397398.2:p.Asp16Gly
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000475025
  ensembl transcript: ENST00000604534
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604534.1:c.573A>G
  hgvsp: ENST00000604534.1:c.573A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000474793
  ensembl transcript: ENST00000604203
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604203.1:c.211-2539A>G
  variant of: http://identifiers.org/hgnc/49388
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3597
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5128
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4473
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1913
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5588
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3379
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5528
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1629
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2733
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2331
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5882
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1810
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4685
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1385
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5389
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4360
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 524
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Asp31Gly
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: QD

1-95709776-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95709776
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 95709776
    reference: chr 1
allele count: 1
allele frequency: 8.320575118152166e-6
allele num: 120184
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000228852
  ensembl transcript: ENST00000444665
  gene symbol: RP11-57H12.5
  hgvsc: ENST00000444665.1:n.71-695C>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000497058
  gene symbol: RWDD3
  hgvsc: ENST00000497058.1:n.126-345G>C
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000263893
  ensembl transcript: ENST00000263893
  gene symbol: RWDD3
  hgvsc: ENST00000263893.6:c.95G>C
  hgvsp: ENSP00000263893.6:p.Gly32Ala
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000473397
  gene symbol: RWDD3
  hgvsc: ENST00000473397.1:n.49-2536G>C
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000397398
  ensembl transcript: ENST00000429514
  gene symbol: RWDD3
  hgvsc: ENST00000429514.2:c.50G>C
  hgvsp: ENSP00000397398.2:p.Gly17Ala
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000359221
  ensembl transcript: ENST00000370202
  gene symbol: RWDD3
  hgvsc: ENST00000370202.4:c.95G>C
  hgvsp: ENSP00000359221.4:p.Gly32Ala
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000474793
  ensembl transcript: ENST00000604203
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604203.1:c.211-2536G>C
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000475025
  ensembl transcript: ENST00000604534
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604534.1:c.576G>C
  hgvsp: ENSP00000475025.1:p.Trp192Cys
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000492639
  gene symbol: RWDD3
  hgvsc: ENST00000492639.1:n.358G>C
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000495272
  gene symbol: RWDD3
  hgvsc: ENST00000495272.1:n.238G>C
  variant of: http://identifiers.org/hgnc/21393
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2334
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5128
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4359
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4487
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3378
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1911
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1680
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5389
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4685
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5882
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5588
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1841
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3597
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1386
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5528
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2735
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 304
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Trp192Cys
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff

1-95709780-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95709780
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 95709780
    reference: chr 1
allele count: 23
allele frequency: 1.910997374455781e-4
allele num: 120356
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000228852
  ensembl transcript: ENST00000444665
  gene symbol: RP11-57H12.5
  hgvsc: ENST00000444665.1:n.71-699G>A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000397398
  ensembl transcript: ENST00000429514
  gene symbol: RWDD3
  hgvsc: ENST00000429514.2:c.54C>T
  hgvsp: ENST00000429514.2:c.54C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000497058
  gene symbol: RWDD3
  hgvsc: ENST00000497058.1:n.126-341C>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000495272
  gene symbol: RWDD3
  hgvsc: ENST00000495272.1:n.242C>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000475025
  ensembl transcript: ENST00000604534
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604534.1:c.580C>T
  hgvsp: ENSP00000475025.1:p.Arg194Cys
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000359221
  ensembl transcript: ENST00000370202
  gene symbol: RWDD3
  hgvsc: ENST00000370202.4:c.99C>T
  hgvsp: ENST00000370202.4:c.99C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000263893
  ensembl transcript: ENST00000263893
  gene symbol: RWDD3
  hgvsc: ENST00000263893.6:c.99C>T
  hgvsp: ENST00000263893.6:c.99C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000492639
  gene symbol: RWDD3
  hgvsc: ENST00000492639.1:n.362C>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000474793
  ensembl transcript: ENST00000604203
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604203.1:c.211-2532C>T
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000473397
  gene symbol: RWDD3
  hgvsc: ENST00000473397.1:n.49-2532C>T
  variant of: http://identifiers.org/hgnc/21393
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3380
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2347
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4684
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5585
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1765
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5126
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1940
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3599
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5880
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1913
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4419
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1386
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4359
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5539
  bin: 9.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 5390
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2734
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 767
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 837
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Arg194Cys
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: South Asian
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD

1-95709781-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95709781
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 95709781
    reference: chr 1
allele count: 5
allele frequency: 4.151927324664109e-5
allele num: 120426
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000495272
  gene symbol: RWDD3
  hgvsc: ENST00000495272.1:n.243G>A
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000492639
  gene symbol: RWDD3
  hgvsc: ENST00000492639.1:n.363G>A
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000359221
  ensembl transcript: ENST00000370202
  gene symbol: RWDD3
  hgvsc: ENST00000370202.4:c.100G>A
  hgvsp: ENSP00000359221.4:p.Val34Met
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000397398
  ensembl transcript: ENST00000429514
  gene symbol: RWDD3
  hgvsc: ENST00000429514.2:c.55G>A
  hgvsp: ENSP00000397398.2:p.Val19Met
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000497058
  gene symbol: RWDD3
  hgvsc: ENST00000497058.1:n.126-340G>A
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000473397
  gene symbol: RWDD3
  hgvsc: ENST00000473397.1:n.49-2531G>A
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000263893
  ensembl transcript: ENST00000263893
  gene symbol: RWDD3
  hgvsc: ENST00000263893.6:c.100G>A
  hgvsp: ENSP00000263893.6:p.Val34Met
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000475025
  ensembl transcript: ENST00000604534
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604534.1:c.581G>A
  hgvsp: ENSP00000475025.1:p.Arg194His
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000474793
  ensembl transcript: ENST00000604203
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604203.1:c.211-2531G>A
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000228852
  ensembl transcript: ENST00000444665
  gene symbol: RP11-57H12.5
  hgvsc: ENST00000444665.1:n.71-700C>T
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5880
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5584
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2737
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3599
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5125
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2351
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4685
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3382
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4434
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1776
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1958
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5540
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4358
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1387
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5389
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1910
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 783
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg194His
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP

1-95709782-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95709782
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 95709782
    reference: chr 1
allele count: 3
allele frequency: 2.490411914130597e-5
allele num: 120462
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000492639
  gene symbol: RWDD3
  hgvsc: ENST00000492639.1:n.364T>C
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000497058
  gene symbol: RWDD3
  hgvsc: ENST00000497058.1:n.126-339T>C
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000263893
  ensembl transcript: ENST00000263893
  gene symbol: RWDD3
  hgvsc: ENST00000263893.6:c.101T>C
  hgvsp: ENSP00000263893.6:p.Val34Ala
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000474793
  ensembl transcript: ENST00000604203
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604203.1:c.211-2530T>C
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000473397
  gene symbol: RWDD3
  hgvsc: ENST00000473397.1:n.49-2530T>C
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000397398
  ensembl transcript: ENST00000429514
  gene symbol: RWDD3
  hgvsc: ENST00000429514.2:c.56T>C
  hgvsp: ENSP00000397398.2:p.Val19Ala
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000359221
  ensembl transcript: ENST00000370202
  gene symbol: RWDD3
  hgvsc: ENST00000370202.4:c.101T>C
  hgvsp: ENSP00000359221.4:p.Val34Ala
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000228852
  ensembl transcript: ENST00000444665
  gene symbol: RP11-57H12.5
  hgvsc: ENST00000444665.1:n.71-701A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000495272
  gene symbol: RWDD3
  hgvsc: ENST00000495272.1:n.244T>C
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000475025
  ensembl transcript: ENST00000604534
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604534.1:c.582T>C
  hgvsp: ENST00000604534.1:c.582T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/49388
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5880
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5125
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4685
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1786
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1965
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4449
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2737
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5539
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5389
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3382
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4358
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3599
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1910
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1388
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2353
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5584
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4203
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 796
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Val34Ala
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum

1-95709786-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95709786
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 95709786
    reference: chr 1
allele count: 2
allele frequency: 1.658897496723677e-5
allele num: 120562
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000263893
  ensembl transcript: ENST00000263893
  gene symbol: RWDD3
  hgvsc: ENST00000263893.6:c.105C>T
  hgvsp: ENST00000263893.6:c.105C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000359221
  ensembl transcript: ENST00000370202
  gene symbol: RWDD3
  hgvsc: ENST00000370202.4:c.105C>T
  hgvsp: ENST00000370202.4:c.105C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000497058
  gene symbol: RWDD3
  hgvsc: ENST00000497058.1:n.126-335C>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000228852
  ensembl transcript: ENST00000444665
  gene symbol: RP11-57H12.5
  hgvsc: ENST00000444665.1:n.71-705G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000474793
  ensembl transcript: ENST00000604203
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604203.1:c.211-2526C>T
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000397398
  ensembl transcript: ENST00000429514
  gene symbol: RWDD3
  hgvsc: ENST00000429514.2:c.60C>T
  hgvsp: ENST00000429514.2:c.60C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000475025
  ensembl transcript: ENST00000604534
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604534.1:c.586C>T
  hgvsp: ENSP00000475025.1:p.Gln196Ter
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000492639
  gene symbol: RWDD3
  hgvsc: ENST00000492639.1:n.368C>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000473397
  gene symbol: RWDD3
  hgvsc: ENST00000473397.1:n.49-2526C>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000495272
  gene symbol: RWDD3
  hgvsc: ENST00000495272.1:n.248C>T
  variant of: http://identifiers.org/hgnc/21393
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4357
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1804
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5880
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5540
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4686
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4486
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3383
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2356
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1910
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1994
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2737
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1388
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5389
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3599
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5584
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5125
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 804
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 527
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1025
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Gln196Ter
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD

1-95709819-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95709819
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 95709819
    reference: chr 1
allele count: 6
allele frequency: 4.968861799390487e-5
allele num: 120752
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000359221
  ensembl transcript: ENST00000370202
  gene symbol: RWDD3
  hgvsc: ENST00000370202.4:c.138T>G
  hgvsp: ENSP00000359221.4:p.Asp46Glu
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000397398
  ensembl transcript: ENST00000429514
  gene symbol: RWDD3
  hgvsc: ENST00000429514.2:c.93T>G
  hgvsp: ENSP00000397398.2:p.Asp31Glu
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000492639
  gene symbol: RWDD3
  hgvsc: ENST00000492639.1:n.401T>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000263893
  ensembl transcript: ENST00000263893
  gene symbol: RWDD3
  hgvsc: ENST00000263893.6:c.138T>G
  hgvsp: ENSP00000263893.6:p.Asp46Glu
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000475025
  ensembl transcript: ENST00000604534
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604534.1:c.*13T>G
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000228852
  ensembl transcript: ENST00000444665
  gene symbol: RP11-57H12.5
  hgvsc: ENST00000444665.1:n.71-738A>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000495272
  gene symbol: RWDD3
  hgvsc: ENST00000495272.1:n.281T>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000473397
  gene symbol: RWDD3
  hgvsc: ENST00000473397.1:n.49-2493T>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000474793
  ensembl transcript: ENST00000604203
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604203.1:c.211-2493T>G
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000497058
  gene symbol: RWDD3
  hgvsc: ENST00000497058.1:n.126-302T>G
  variant of: http://identifiers.org/hgnc/21393
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3599
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4466
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5389
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1388
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5881
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1910
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3398
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2381
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5542
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4359
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4687
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5584
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1851
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5126
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2061
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2737
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51328
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Asp46Glu
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum

1-95709821-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95709821
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 95709821
    reference: chr 1
allele count: 120230
allele frequency: 9.955286909000579e-1
allele num: 120770
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000492639
  gene symbol: RWDD3
  hgvsc: ENST00000492639.1:n.403T>C
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000228852
  ensembl transcript: ENST00000444665
  gene symbol: RP11-57H12.5
  hgvsc: ENST00000444665.1:n.71-740A>G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000263893
  ensembl transcript: ENST00000263893
  gene symbol: RWDD3
  hgvsc: ENST00000263893.6:c.140T>C
  hgvsp: ENSP00000263893.6:p.Val47Ala
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000497058
  gene symbol: RWDD3
  hgvsc: ENST00000497058.1:n.126-300T>C
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000397398
  ensembl transcript: ENST00000429514
  gene symbol: RWDD3
  hgvsc: ENST00000429514.2:c.95T>C
  hgvsp: ENSP00000397398.2:p.Val32Ala
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000475025
  ensembl transcript: ENST00000604534
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604534.1:c.*15T>C
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000359221
  ensembl transcript: ENST00000370202
  gene symbol: RWDD3
  hgvsc: ENST00000370202.4:c.140T>C
  hgvsp: ENSP00000359221.4:p.Val47Ala
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000495272
  gene symbol: RWDD3
  hgvsc: ENST00000495272.1:n.283T>C
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000474793
  ensembl transcript: ENST00000604203
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604203.1:c.211-2491T>C
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000473397
  gene symbol: RWDD3
  hgvsc: ENST00000473397.1:n.49-2491T>C
  variant of: http://identifiers.org/hgnc/21393
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2422
  bin: 6.75e1
  variant carriers: 2422
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 3.25e1
  variant carriers: 97
genotype depth: GenotypeDepth
  all individuals: 2969
  bin: 7.25e1
  variant carriers: 2969
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 3442
  bin: 8.25e1
  variant carriers: 3442
genotype depth: GenotypeDepth
  all individuals: 1434
  bin: 5.75e1
  variant carriers: 1432
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 4.25e1
  variant carriers: 382
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.25e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 3.75e1
  variant carriers: 203
genotype depth: GenotypeDepth
  all individuals: 35050
  bin: 9.75e1
  variant carriers: 35050
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 4.75e1
  variant carriers: 639
genotype depth: GenotypeDepth
  all individuals: 3744
  bin: 9.25e1
  variant carriers: 3744
genotype depth: GenotypeDepth
  all individuals: 3202
  bin: 7.75e1
  variant carriers: 3202
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 5.25e1
  variant carriers: 1000
genotype depth: GenotypeDepth
  all individuals: 1982
  bin: 6.25e1
  variant carriers: 1982
genotype depth: GenotypeDepth
  all individuals: 3704
  bin: 8.75e1
  variant carriers: 3704
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.75e1
  variant carriers: 49
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 8.75e1
  variant carriers: 21
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.25e1
  variant carriers: 3
hgvs: p.Val47Ala
num of homozygotes: 59858
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
reference allele: T
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD

1-95709822-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95709822
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 95709822
    reference: chr 1
allele count: 1
allele frequency: 8.280750567231414e-6
allele num: 120762
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000492639
  gene symbol: RWDD3
  hgvsc: ENST00000492639.1:n.404G>A
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000263893
  ensembl transcript: ENST00000263893
  gene symbol: RWDD3
  hgvsc: ENST00000263893.6:c.141G>A
  hgvsp: ENST00000263893.6:c.141G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000473397
  gene symbol: RWDD3
  hgvsc: ENST00000473397.1:n.49-2490G>A
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000228852
  ensembl transcript: ENST00000444665
  gene symbol: RP11-57H12.5
  hgvsc: ENST00000444665.1:n.71-741C>T
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000475025
  ensembl transcript: ENST00000604534
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604534.1:c.*16G>A
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000495272
  gene symbol: RWDD3
  hgvsc: ENST00000495272.1:n.284G>A
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000474793
  ensembl transcript: ENST00000604203
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604203.1:c.211-2490G>A
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000397398
  ensembl transcript: ENST00000429514
  gene symbol: RWDD3
  hgvsc: ENST00000429514.2:c.96G>A
  hgvsp: ENST00000429514.2:c.96G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000359221
  ensembl transcript: ENST00000370202
  gene symbol: RWDD3
  hgvsc: ENST00000370202.4:c.141G>A
  hgvsp: ENST00000370202.4:c.141G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000497058
  gene symbol: RWDD3
  hgvsc: ENST00000497058.1:n.126-299G>A
  variant of: http://identifiers.org/hgnc/21393
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5435
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4935
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5624
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4068
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2143
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3164
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4927
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1386
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13910
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4121
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3294
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5557
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Val47Val
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ

1-95709823-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95709823
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 95709823
    reference: chr 1
allele count: 1
allele frequency: 8.280613427842734e-6
allele num: 120764
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000228852
  ensembl transcript: ENST00000444665
  gene symbol: RP11-57H12.5
  hgvsc: ENST00000444665.1:n.71-742C>T
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000475025
  ensembl transcript: ENST00000604534
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604534.1:c.*17G>A
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000474793
  ensembl transcript: ENST00000604203
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604203.1:c.211-2489G>A
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000495272
  gene symbol: RWDD3
  hgvsc: ENST00000495272.1:n.285G>A
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000397398
  ensembl transcript: ENST00000429514
  gene symbol: RWDD3
  hgvsc: ENST00000429514.2:c.97G>A
  hgvsp: ENSP00000397398.2:p.Asp33Asn
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000492639
  gene symbol: RWDD3
  hgvsc: ENST00000492639.1:n.405G>A
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000263893
  ensembl transcript: ENST00000263893
  gene symbol: RWDD3
  hgvsc: ENST00000263893.6:c.142G>A
  hgvsp: ENSP00000263893.6:p.Asp48Asn
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000359221
  ensembl transcript: ENST00000370202
  gene symbol: RWDD3
  hgvsc: ENST00000370202.4:c.142G>A
  hgvsp: ENSP00000359221.4:p.Asp48Asn
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000497058
  gene symbol: RWDD3
  hgvsc: ENST00000497058.1:n.126-298G>A
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000473397
  gene symbol: RWDD3
  hgvsc: ENST00000473397.1:n.49-2489G>A
  variant of: http://identifiers.org/hgnc/21393
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4935
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3294
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5555
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13909
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4070
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2143
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1386
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3165
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4927
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4121
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5624
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5435
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 241
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Asp48Asn
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

http://identifiers.org/exac.variant/1-95709830-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95709830
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 95709830
    reference: chr 1
allele count: 1
allele frequency: 8.281024859636628e-6
allele num: 120758
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000473397
  gene symbol: RWDD3
  hgvsc: ENST00000473397.1:n.49-2482C>A
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000492639
  gene symbol: RWDD3
  hgvsc: ENST00000492639.1:n.412C>A
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000397398
  ensembl transcript: ENST00000429514
  gene symbol: RWDD3
  hgvsc: ENST00000429514.2:c.104C>A
  hgvsp: ENSP00000397398.2:p.Pro35His
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000359221
  ensembl transcript: ENST00000370202
  gene symbol: RWDD3
  hgvsc: ENST00000370202.4:c.149C>A
  hgvsp: ENSP00000359221.4:p.Pro50His
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000475025
  ensembl transcript: ENST00000604534
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604534.1:c.*24C>A
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000495272
  gene symbol: RWDD3
  hgvsc: ENST00000495272.1:n.292C>A
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000474793
  ensembl transcript: ENST00000604203
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604203.1:c.211-2482C>A
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000263893
  ensembl transcript: ENST00000263893
  gene symbol: RWDD3
  hgvsc: ENST00000263893.6:c.149C>A
  hgvsp: ENSP00000263893.6:p.Pro50His
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000228852
  ensembl transcript: ENST00000444665
  gene symbol: RP11-57H12.5
  hgvsc: ENST00000444665.1:n.71-749G>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000497058
  gene symbol: RWDD3
  hgvsc: ENST00000497058.1:n.126-291C>A
  variant of: http://identifiers.org/hgnc/21393
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3164
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4935
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1388
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2142
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13908
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5436
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3294
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5556
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4069
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4121
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5625
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4926
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 410
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 270
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Pro50His
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: European (Finnish)
population: East Asian
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

1-95709836-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95709836
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 95709836
    reference: chr 1
allele count: 1
allele frequency: 8.280476292996373e-6
allele num: 120766
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000475025
  ensembl transcript: ENST00000604534
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604534.1:c.*30A>G
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000263893
  ensembl transcript: ENST00000263893
  gene symbol: RWDD3
  hgvsc: ENST00000263893.6:c.155A>G
  hgvsp: ENSP00000263893.6:p.Glu52Gly
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000473397
  gene symbol: RWDD3
  hgvsc: ENST00000473397.1:n.49-2476A>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000495272
  gene symbol: RWDD3
  hgvsc: ENST00000495272.1:n.298A>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000497058
  gene symbol: RWDD3
  hgvsc: ENST00000497058.1:n.126-285A>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000359221
  ensembl transcript: ENST00000370202
  gene symbol: RWDD3
  hgvsc: ENST00000370202.4:c.155A>G
  hgvsp: ENSP00000359221.4:p.Glu52Gly
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000397398
  ensembl transcript: ENST00000429514
  gene symbol: RWDD3
  hgvsc: ENST00000429514.2:c.110A>G
  hgvsp: ENSP00000397398.2:p.Glu37Gly
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000228852
  ensembl transcript: ENST00000444665
  gene symbol: RP11-57H12.5
  hgvsc: ENST00000444665.1:n.71-755T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000492639
  gene symbol: RWDD3
  hgvsc: ENST00000492639.1:n.418A>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000474793
  ensembl transcript: ENST00000604203
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604203.1:c.211-2476A>G
  variant of: http://identifiers.org/hgnc/49388
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3165
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4070
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1389
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4121
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4933
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5623
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13908
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5550
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4925
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3294
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5436
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2149
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 443
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Glu52Gly
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: QD

1-95709838-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95709838
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 95709838
    reference: chr 1
allele count: 122
allele frequency: 1.010234838196814e-3
allele num: 120764
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000228852
  ensembl transcript: ENST00000444665
  gene symbol: RP11-57H12.5
  hgvsc: ENST00000444665.1:n.71-757A>G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000263893
  ensembl transcript: ENST00000263893
  gene symbol: RWDD3
  hgvsc: ENST00000263893.6:c.157T>C
  hgvsp: ENST00000263893.6:c.157T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000359221
  ensembl transcript: ENST00000370202
  gene symbol: RWDD3
  hgvsc: ENST00000370202.4:c.157T>C
  hgvsp: ENST00000370202.4:c.157T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000397398
  ensembl transcript: ENST00000429514
  gene symbol: RWDD3
  hgvsc: ENST00000429514.2:c.112T>C
  hgvsp: ENST00000429514.2:c.112T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000497058
  gene symbol: RWDD3
  hgvsc: ENST00000497058.1:n.126-283T>C
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000492639
  gene symbol: RWDD3
  hgvsc: ENST00000492639.1:n.420T>C
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000475025
  ensembl transcript: ENST00000604534
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604534.1:c.*32T>C
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000473397
  gene symbol: RWDD3
  hgvsc: ENST00000473397.1:n.49-2474T>C
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000495272
  gene symbol: RWDD3
  hgvsc: ENST00000495272.1:n.300T>C
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000474793
  ensembl transcript: ENST00000604203
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604203.1:c.211-2474T>C
  variant of: http://identifiers.org/hgnc/49388
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3164
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4128
  bin: 8.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 4065
  bin: 5.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1389
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5548
  bin: 6.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 3296
  bin: 9.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2148
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4915
  bin: 6.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 5612
  bin: 7.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 13932
  bin: 9.75e1
  variant carriers: 46
genotype depth: GenotypeDepth
  all individuals: 5433
  bin: 7.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4935
  bin: 8.25e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 315
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Leu53Leu
num of homozygotes: 1
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/1-95709848-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95709848
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 95709848
    reference: chr 1
allele count: 1
allele frequency: 8.280750567231414e-6
allele num: 120762
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000475025
  ensembl transcript: ENST00000604534
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604534.1:c.*42A>C
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000397398
  ensembl transcript: ENST00000429514
  gene symbol: RWDD3
  hgvsc: ENST00000429514.2:c.122A>C
  hgvsp: ENSP00000397398.2:p.His41Pro
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000473397
  gene symbol: RWDD3
  hgvsc: ENST00000473397.1:n.49-2464A>C
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000263893
  ensembl transcript: ENST00000263893
  gene symbol: RWDD3
  hgvsc: ENST00000263893.6:c.167A>C
  hgvsp: ENSP00000263893.6:p.His56Pro
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000492639
  gene symbol: RWDD3
  hgvsc: ENST00000492639.1:n.430A>C
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000497058
  gene symbol: RWDD3
  hgvsc: ENST00000497058.1:n.126-273A>C
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000474793
  ensembl transcript: ENST00000604203
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604203.1:c.211-2464A>C
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000359221
  ensembl transcript: ENST00000370202
  gene symbol: RWDD3
  hgvsc: ENST00000370202.4:c.167A>C
  hgvsp: ENSP00000359221.4:p.His56Pro
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000495272
  gene symbol: RWDD3
  hgvsc: ENST00000495272.1:n.310A>C
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000228852
  ensembl transcript: ENST00000444665
  gene symbol: RP11-57H12.5
  hgvsc: ENST00000444665.1:n.71-767T>G
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2145
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3172
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4123
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5610
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4069
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1389
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4939
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13925
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4922
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5429
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3296
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5540
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 412
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58270
  bin: 9.75e1
  variant carriers: 1
hgvs: p.His56Pro
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: A
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum

1-95709852-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95709852
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 95709852
    reference: chr 1
allele count: 4
allele frequency: 3.312355084465055e-5
allele num: 120760
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000492639
  gene symbol: RWDD3
  hgvsc: ENST00000492639.1:n.434G>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000397398
  ensembl transcript: ENST00000429514
  gene symbol: RWDD3
  hgvsc: ENST00000429514.2:c.126G>T
  hgvsp: ENSP00000397398.2:p.Leu42Phe
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000474793
  ensembl transcript: ENST00000604203
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604203.1:c.211-2460G>T
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000495272
  gene symbol: RWDD3
  hgvsc: ENST00000495272.1:n.314G>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000263893
  ensembl transcript: ENST00000263893
  gene symbol: RWDD3
  hgvsc: ENST00000263893.6:c.171G>T
  hgvsp: ENSP00000263893.6:p.Leu57Phe
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000359221
  ensembl transcript: ENST00000370202
  gene symbol: RWDD3
  hgvsc: ENST00000370202.4:c.171G>T
  hgvsp: ENSP00000359221.4:p.Leu57Phe
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000497058
  gene symbol: RWDD3
  hgvsc: ENST00000497058.1:n.126-269G>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000473397
  gene symbol: RWDD3
  hgvsc: ENST00000473397.1:n.49-2460G>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000475025
  ensembl transcript: ENST00000604534
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604534.1:c.*46G>T
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000228852
  ensembl transcript: ENST00000444665
  gene symbol: RP11-57H12.5
  hgvsc: ENST00000444665.1:n.71-771C>A
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5540
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5610
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2145
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4922
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4070
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1389
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3171
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5429
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4940
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13925
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3296
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4122
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 238
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Leu57Phe
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: African
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: DP

1-95709852-GC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95709852
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 95709851
    reference: chr 1
allele count: 1
allele frequency: 8.280887711162637e-6
allele num: 120760
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000492639
  gene symbol: RWDD3
  hgvsc: ENST00000492639.1:n.436delC
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000359221
  ensembl transcript: ENST00000370202
  gene symbol: RWDD3
  hgvsc: ENST00000370202.4:c.173delC
  hgvsp: ENSP00000359221.4:p.Pro58GlnfsTer18
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000263893
  ensembl transcript: ENST00000263893
  gene symbol: RWDD3
  hgvsc: ENST00000263893.6:c.173delC
  hgvsp: ENSP00000263893.6:p.Pro58GlnfsTer18
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000474793
  ensembl transcript: ENST00000604203
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604203.1:c.211-2458delC
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000497058
  gene symbol: RWDD3
  hgvsc: ENST00000497058.1:n.126-267delC
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000397398
  ensembl transcript: ENST00000429514
  gene symbol: RWDD3
  hgvsc: ENST00000429514.2:c.128delC
  hgvsp: ENSP00000397398.2:p.Pro43GlnfsTer18
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000473397
  gene symbol: RWDD3
  hgvsc: ENST00000473397.1:n.49-2458delC
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000495272
  gene symbol: RWDD3
  hgvsc: ENST00000495272.1:n.316delC
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000228852
  ensembl transcript: ENST00000444665
  gene symbol: RP11-57H12.5
  hgvsc: ENST00000444665.1:n.71-772delG
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000475025
  ensembl transcript: ENST00000604534
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604534.1:c.*48delC
  variant of: http://identifiers.org/hgnc/49388
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2145
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5429
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3296
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5610
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1389
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13925
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4922
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3171
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5540
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4070
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4940
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4122
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Pro58GlnfsTer18
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: GC
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD

1-95709853-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95709853
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 95709853
    reference: chr 1
allele count: 1
allele frequency: 8.281024859636628e-6
allele num: 120758
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000492639
  gene symbol: RWDD3
  hgvsc: ENST00000492639.1:n.435C>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000228852
  ensembl transcript: ENST00000444665
  gene symbol: RP11-57H12.5
  hgvsc: ENST00000444665.1:n.71-772G>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000263893
  ensembl transcript: ENST00000263893
  gene symbol: RWDD3
  hgvsc: ENST00000263893.6:c.172C>T
  hgvsp: ENSP00000263893.6:p.Pro58Ser
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000397398
  ensembl transcript: ENST00000429514
  gene symbol: RWDD3
  hgvsc: ENST00000429514.2:c.127C>T
  hgvsp: ENSP00000397398.2:p.Pro43Ser
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000359221
  ensembl transcript: ENST00000370202
  gene symbol: RWDD3
  hgvsc: ENST00000370202.4:c.172C>T
  hgvsp: ENSP00000359221.4:p.Pro58Ser
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000473397
  gene symbol: RWDD3
  hgvsc: ENST00000473397.1:n.49-2459C>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000497058
  gene symbol: RWDD3
  hgvsc: ENST00000497058.1:n.126-268C>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000474793
  ensembl transcript: ENST00000604203
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604203.1:c.211-2459C>T
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000495272
  gene symbol: RWDD3
  hgvsc: ENST00000495272.1:n.315C>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000475025
  ensembl transcript: ENST00000604534
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604534.1:c.*47C>T
  variant of: http://identifiers.org/hgnc/49388
canonical: true
consequence: missense
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 1390
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5609
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4939
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13925
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2146
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4122
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3295
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5539
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5430
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3171
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4922
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4070
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 412
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Pro58Ser
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: QD

1-95709853-CCAGT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95709853
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 95709849
    reference: chr 1
allele count: 1
allele frequency: 8.281024859636628e-6
allele num: 120758
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000473397
  gene symbol: RWDD3
  hgvsc: ENST00000473397.1:n.49-2456_49-2453delGTCA
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000492639
  gene symbol: RWDD3
  hgvsc: ENST00000492639.1:n.438_441delGTCA
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000263893
  ensembl transcript: ENST00000263893
  gene symbol: RWDD3
  hgvsc: ENST00000263893.6:c.175_178delGTCA
  hgvsp: ENSP00000263893.6:p.Val59IlefsTer16
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000228852
  ensembl transcript: ENST00000444665
  gene symbol: RP11-57H12.5
  hgvsc: ENST00000444665.1:n.71-776_71-773delACTG
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000397398
  ensembl transcript: ENST00000429514
  gene symbol: RWDD3
  hgvsc: ENST00000429514.2:c.130_133delGTCA
  hgvsp: ENSP00000397398.2:p.Val44IlefsTer16
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000475025
  ensembl transcript: ENST00000604534
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604534.1:c.*50_*53delGTCA
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000359221
  ensembl transcript: ENST00000370202
  gene symbol: RWDD3
  hgvsc: ENST00000370202.4:c.175_178delGTCA
  hgvsp: ENSP00000359221.4:p.Val59IlefsTer16
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000497058
  gene symbol: RWDD3
  hgvsc: ENST00000497058.1:n.126-265_126-262delGTCA
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000474793
  ensembl transcript: ENST00000604203
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604203.1:c.211-2456_211-2453delGTCA
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000495272
  gene symbol: RWDD3
  hgvsc: ENST00000495272.1:n.318_321delGTCA
  variant of: http://identifiers.org/hgnc/21393
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 5539
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1390
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4070
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4939
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3171
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4122
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2146
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3295
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4922
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5609
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13925
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5430
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 439
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 270
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Val59IlefsTer16
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: CCAGT
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP

http://identifiers.org/exac.variant/1-95709863-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95709863
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 95709863
    reference: chr 1
allele count: 5
allele frequency: 4.140238146498186e-5
allele num: 120766
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000495272
  gene symbol: RWDD3
  hgvsc: ENST00000495272.1:n.325A>C
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000492639
  gene symbol: RWDD3
  hgvsc: ENST00000492639.1:n.445A>C
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000228852
  ensembl transcript: ENST00000444665
  gene symbol: RP11-57H12.5
  hgvsc: ENST00000444665.1:n.71-782T>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000474793
  ensembl transcript: ENST00000604203
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604203.1:c.211-2449A>C
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000397398
  ensembl transcript: ENST00000429514
  gene symbol: RWDD3
  hgvsc: ENST00000429514.2:c.137A>C
  hgvsp: ENSP00000397398.2:p.Tyr46Ser
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000473397
  gene symbol: RWDD3
  hgvsc: ENST00000473397.1:n.49-2449A>C
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000475025
  ensembl transcript: ENST00000604534
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604534.1:c.*57A>C
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000497058
  gene symbol: RWDD3
  hgvsc: ENST00000497058.1:n.126-258A>C
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000359221
  ensembl transcript: ENST00000370202
  gene symbol: RWDD3
  hgvsc: ENST00000370202.4:c.182A>C
  hgvsp: ENSP00000359221.4:p.Tyr61Ser
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000263893
  ensembl transcript: ENST00000263893
  gene symbol: RWDD3
  hgvsc: ENST00000263893.6:c.182A>C
  hgvsp: ENSP00000263893.6:p.Tyr61Ser
  variant of: http://identifiers.org/hgnc/21393
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4122
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4939
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13925
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4069
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4922
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5609
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5430
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3172
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3295
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2146
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5539
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1390
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 316
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Tyr61Ser
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: QD

1-95709863-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95709863
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 95709863
    reference: chr 1
allele count: 1
allele frequency: 8.280476292996373e-6
allele num: 120766
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000397398
  ensembl transcript: ENST00000429514
  gene symbol: RWDD3
  hgvsc: ENST00000429514.2:c.137A>G
  hgvsp: ENSP00000397398.2:p.Tyr46Cys
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000474793
  ensembl transcript: ENST00000604203
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604203.1:c.211-2449A>G
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000492639
  gene symbol: RWDD3
  hgvsc: ENST00000492639.1:n.445A>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000475025
  ensembl transcript: ENST00000604534
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604534.1:c.*57A>G
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000359221
  ensembl transcript: ENST00000370202
  gene symbol: RWDD3
  hgvsc: ENST00000370202.4:c.182A>G
  hgvsp: ENSP00000359221.4:p.Tyr61Cys
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000228852
  ensembl transcript: ENST00000444665
  gene symbol: RP11-57H12.5
  hgvsc: ENST00000444665.1:n.71-782T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000495272
  gene symbol: RWDD3
  hgvsc: ENST00000495272.1:n.325A>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000263893
  ensembl transcript: ENST00000263893
  gene symbol: RWDD3
  hgvsc: ENST00000263893.6:c.182A>G
  hgvsp: ENSP00000263893.6:p.Tyr61Cys
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000497058
  gene symbol: RWDD3
  hgvsc: ENST00000497058.1:n.126-258A>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000473397
  gene symbol: RWDD3
  hgvsc: ENST00000473397.1:n.49-2449A>G
  variant of: http://identifiers.org/hgnc/21393
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13925
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4122
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4069
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3295
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5430
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4939
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3172
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1390
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4922
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2146
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5539
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5609
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 316
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 450
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Tyr61Cys
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

1-95709873-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95709873
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 95709873
    reference: chr 1
allele count: 1
allele frequency: 8.280750567231414e-6
allele num: 120762
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000495272
  gene symbol: RWDD3
  hgvsc: ENST00000495272.1:n.335T>C
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000497058
  gene symbol: RWDD3
  hgvsc: ENST00000497058.1:n.126-248T>C
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000397398
  ensembl transcript: ENST00000429514
  gene symbol: RWDD3
  hgvsc: ENST00000429514.2:c.147T>C
  hgvsp: ENST00000429514.2:c.147T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000473397
  gene symbol: RWDD3
  hgvsc: ENST00000473397.1:n.49-2439T>C
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000475025
  ensembl transcript: ENST00000604534
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604534.1:c.*67T>C
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000263893
  ensembl transcript: ENST00000263893
  gene symbol: RWDD3
  hgvsc: ENST00000263893.6:c.192T>C
  hgvsp: ENST00000263893.6:c.192T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000359221
  ensembl transcript: ENST00000370202
  gene symbol: RWDD3
  hgvsc: ENST00000370202.4:c.192T>C
  hgvsp: ENST00000370202.4:c.192T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000492639
  gene symbol: RWDD3
  hgvsc: ENST00000492639.1:n.455T>C
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000474793
  ensembl transcript: ENST00000604203
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604203.1:c.211-2439T>C
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000228852
  ensembl transcript: ENST00000444665
  gene symbol: RP11-57H12.5
  hgvsc: ENST00000444665.1:n.71-792A>G
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3173
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2146
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4939
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1393
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4120
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5540
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5429
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13925
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4071
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3296
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4921
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5609
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58267
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 238
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Cys64Cys
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum

1-95709873-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95709873
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 95709873
    reference: chr 1
allele count: 1
allele frequency: 8.280750567231414e-6
allele num: 120762
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000497058
  gene symbol: RWDD3
  hgvsc: ENST00000497058.1:n.126-248T>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000263893
  ensembl transcript: ENST00000263893
  gene symbol: RWDD3
  hgvsc: ENST00000263893.6:c.192T>G
  hgvsp: ENSP00000263893.6:p.Cys64Trp
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000495272
  gene symbol: RWDD3
  hgvsc: ENST00000495272.1:n.335T>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000473397
  gene symbol: RWDD3
  hgvsc: ENST00000473397.1:n.49-2439T>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000397398
  ensembl transcript: ENST00000429514
  gene symbol: RWDD3
  hgvsc: ENST00000429514.2:c.147T>G
  hgvsp: ENSP00000397398.2:p.Cys49Trp
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000475025
  ensembl transcript: ENST00000604534
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604534.1:c.*67T>G
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000492639
  gene symbol: RWDD3
  hgvsc: ENST00000492639.1:n.455T>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000359221
  ensembl transcript: ENST00000370202
  gene symbol: RWDD3
  hgvsc: ENST00000370202.4:c.192T>G
  hgvsp: ENSP00000359221.4:p.Cys64Trp
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000474793
  ensembl transcript: ENST00000604203
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604203.1:c.211-2439T>G
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000228852
  ensembl transcript: ENST00000444665
  gene symbol: RP11-57H12.5
  hgvsc: ENST00000444665.1:n.71-792A>C
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2146
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5540
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4120
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4939
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3296
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1393
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4921
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5609
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5429
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3173
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13925
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4071
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 238
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 245
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 315
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Cys64Trp
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
reference allele: T
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

1-95709887-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95709887
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 95709887
    reference: chr 1
allele count: 2
allele frequency: 1.656150113446283e-5
allele num: 120762
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000359221
  ensembl transcript: ENST00000370202
  gene symbol: RWDD3
  hgvsc: ENST00000370202.4:c.206C>G
  hgvsp: ENSP00000359221.4:p.Ser69Trp
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000492639
  gene symbol: RWDD3
  hgvsc: ENST00000492639.1:n.469C>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000495272
  gene symbol: RWDD3
  hgvsc: ENST00000495272.1:n.349C>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000263893
  ensembl transcript: ENST00000263893
  gene symbol: RWDD3
  hgvsc: ENST00000263893.6:c.206C>G
  hgvsp: ENSP00000263893.6:p.Ser69Trp
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000497058
  gene symbol: RWDD3
  hgvsc: ENST00000497058.1:n.126-234C>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000474793
  ensembl transcript: ENST00000604203
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604203.1:c.211-2425C>G
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000228852
  ensembl transcript: ENST00000444665
  gene symbol: RP11-57H12.5
  hgvsc: ENST00000444665.1:n.71-806G>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000397398
  ensembl transcript: ENST00000429514
  gene symbol: RWDD3
  hgvsc: ENST00000429514.2:c.161C>G
  hgvsp: ENSP00000397398.2:p.Ser54Trp
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000475025
  ensembl transcript: ENST00000604534
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604534.1:c.*81C>G
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000473397
  gene symbol: RWDD3
  hgvsc: ENST00000473397.1:n.49-2425C>G
  variant of: http://identifiers.org/hgnc/21393
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4070
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1393
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4922
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5608
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13925
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2145
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4121
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4939
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5540
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5430
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3172
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3295
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ser69Trp
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: African
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff

1-95709887-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95709887
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 95709887
    reference: chr 1
allele count: 1
allele frequency: 8.280750567231414e-6
allele num: 120762
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000359221
  ensembl transcript: ENST00000370202
  gene symbol: RWDD3
  hgvsc: ENST00000370202.4:c.206C>T
  hgvsp: ENSP00000359221.4:p.Ser69Leu
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000495272
  gene symbol: RWDD3
  hgvsc: ENST00000495272.1:n.349C>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000475025
  ensembl transcript: ENST00000604534
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604534.1:c.*81C>T
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000397398
  ensembl transcript: ENST00000429514
  gene symbol: RWDD3
  hgvsc: ENST00000429514.2:c.161C>T
  hgvsp: ENSP00000397398.2:p.Ser54Leu
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000497058
  gene symbol: RWDD3
  hgvsc: ENST00000497058.1:n.126-234C>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000263893
  ensembl transcript: ENST00000263893
  gene symbol: RWDD3
  hgvsc: ENST00000263893.6:c.206C>T
  hgvsp: ENSP00000263893.6:p.Ser69Leu
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000492639
  gene symbol: RWDD3
  hgvsc: ENST00000492639.1:n.469C>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000473397
  gene symbol: RWDD3
  hgvsc: ENST00000473397.1:n.49-2425C>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000474793
  ensembl transcript: ENST00000604203
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604203.1:c.211-2425C>T
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000228852
  ensembl transcript: ENST00000444665
  gene symbol: RP11-57H12.5
  hgvsc: ENST00000444665.1:n.71-806G>A
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2145
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4070
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1393
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5608
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4939
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3172
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3295
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5430
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5540
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4922
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4121
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13925
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ser69Leu
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum

1-95709888-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95709888
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 95709888
    reference: chr 1
allele count: 1
allele frequency: 8.280613427842734e-6
allele num: 120764
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000497058
  gene symbol: RWDD3
  hgvsc: ENST00000497058.1:n.126-233G>A
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000228852
  ensembl transcript: ENST00000444665
  gene symbol: RP11-57H12.5
  hgvsc: ENST00000444665.1:n.71-807C>T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000359221
  ensembl transcript: ENST00000370202
  gene symbol: RWDD3
  hgvsc: ENST00000370202.4:c.207G>A
  hgvsp: ENST00000370202.4:c.207G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000475025
  ensembl transcript: ENST00000604534
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604534.1:c.*82G>A
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000474793
  ensembl transcript: ENST00000604203
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604203.1:c.211-2424G>A
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000492639
  gene symbol: RWDD3
  hgvsc: ENST00000492639.1:n.470G>A
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000397398
  ensembl transcript: ENST00000429514
  gene symbol: RWDD3
  hgvsc: ENST00000429514.2:c.162G>A
  hgvsp: ENST00000429514.2:c.162G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000473397
  gene symbol: RWDD3
  hgvsc: ENST00000473397.1:n.49-2424G>A
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000263893
  ensembl transcript: ENST00000263893
  gene symbol: RWDD3
  hgvsc: ENST00000263893.6:c.207G>A
  hgvsp: ENST00000263893.6:c.207G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000495272
  gene symbol: RWDD3
  hgvsc: ENST00000495272.1:n.350G>A
  variant of: http://identifiers.org/hgnc/21393
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4939
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4921
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4071
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3295
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5609
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3172
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1393
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2145
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4121
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13925
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5429
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5540
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ser69Ser
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: MQ

1-95709897-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95709897
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 95709897
    reference: chr 1
allele count: 2
allele frequency: 1.656122685568547e-5
allele num: 120764
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000497058
  gene symbol: RWDD3
  hgvsc: ENST00000497058.1:n.126-224T>C
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000492639
  gene symbol: RWDD3
  hgvsc: ENST00000492639.1:n.479T>C
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000397398
  ensembl transcript: ENST00000429514
  gene symbol: RWDD3
  hgvsc: ENST00000429514.2:c.171T>C
  hgvsp: ENST00000429514.2:c.171T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000475025
  ensembl transcript: ENST00000604534
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604534.1:c.*91T>C
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000228852
  ensembl transcript: ENST00000444665
  gene symbol: RP11-57H12.5
  hgvsc: ENST00000444665.1:n.71-816A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000495272
  gene symbol: RWDD3
  hgvsc: ENST00000495272.1:n.359T>C
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000359221
  ensembl transcript: ENST00000370202
  gene symbol: RWDD3
  hgvsc: ENST00000370202.4:c.216T>C
  hgvsp: ENST00000370202.4:c.216T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000473397
  gene symbol: RWDD3
  hgvsc: ENST00000473397.1:n.49-2415T>C
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000474793
  ensembl transcript: ENST00000604203
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604203.1:c.211-2415T>C
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000263893
  ensembl transcript: ENST00000263893
  gene symbol: RWDD3
  hgvsc: ENST00000263893.6:c.216T>C
  hgvsp: ENST00000263893.6:c.216T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21393
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1393
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2145
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4939
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4921
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5428
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3172
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3295
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4071
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5540
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4123
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 13925
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5608
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 417
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ser72Ser
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

1-95709898-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95709898
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 95709898
    reference: chr 1
allele count: 1
allele frequency: 8.280887711162637e-6
allele num: 120760
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000474793
  ensembl transcript: ENST00000604203
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604203.1:c.211-2414G>T
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000359221
  ensembl transcript: ENST00000370202
  gene symbol: RWDD3
  hgvsc: ENST00000370202.4:c.217G>T
  hgvsp: ENSP00000359221.4:p.Glu73Ter
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000397398
  ensembl transcript: ENST00000429514
  gene symbol: RWDD3
  hgvsc: ENST00000429514.2:c.172G>T
  hgvsp: ENSP00000397398.2:p.Glu58Ter
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000492639
  gene symbol: RWDD3
  hgvsc: ENST00000492639.1:n.480G>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000263893
  ensembl transcript: ENST00000263893
  gene symbol: RWDD3
  hgvsc: ENST00000263893.6:c.217G>T
  hgvsp: ENSP00000263893.6:p.Glu73Ter
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000473397
  gene symbol: RWDD3
  hgvsc: ENST00000473397.1:n.49-2414G>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000495272
  gene symbol: RWDD3
  hgvsc: ENST00000495272.1:n.360G>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000497058
  gene symbol: RWDD3
  hgvsc: ENST00000497058.1:n.126-223G>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000228852
  ensembl transcript: ENST00000444665
  gene symbol: RP11-57H12.5
  hgvsc: ENST00000444665.1:n.71-817C>A
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000475025
  ensembl transcript: ENST00000604534
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604534.1:c.*92G>T
  variant of: http://identifiers.org/hgnc/49388
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2145
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5609
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4921
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5540
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1393
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4121
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4071
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5429
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4939
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3172
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3295
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13925
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 269
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 243
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Glu73Ter
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

1-95709917-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95709917
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 95709917
    reference: chr 1
allele count: 1
allele frequency: 8.281024859636628e-6
allele num: 120758
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000263893
  ensembl transcript: ENST00000263893
  gene symbol: RWDD3
  hgvsc: ENST00000263893.6:c.236A>T
  hgvsp: ENSP00000263893.6:p.Gln79Leu
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000397398
  ensembl transcript: ENST00000429514
  gene symbol: RWDD3
  hgvsc: ENST00000429514.2:c.191A>T
  hgvsp: ENSP00000397398.2:p.Gln64Leu
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000492639
  gene symbol: RWDD3
  hgvsc: ENST00000492639.1:n.499A>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000474793
  ensembl transcript: ENST00000604203
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604203.1:c.211-2395A>T
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000228852
  ensembl transcript: ENST00000444665
  gene symbol: RP11-57H12.5
  hgvsc: ENST00000444665.1:n.71-836T>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000495272
  gene symbol: RWDD3
  hgvsc: ENST00000495272.1:n.379A>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000359221
  ensembl transcript: ENST00000370202
  gene symbol: RWDD3
  hgvsc: ENST00000370202.4:c.236A>T
  hgvsp: ENSP00000359221.4:p.Gln79Leu
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000473397
  gene symbol: RWDD3
  hgvsc: ENST00000473397.1:n.49-2395A>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000475025
  ensembl transcript: ENST00000604534
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604534.1:c.*111A>T
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000497058
  gene symbol: RWDD3
  hgvsc: ENST00000497058.1:n.126-204A>T
  variant of: http://identifiers.org/hgnc/21393
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4939
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5427
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5539
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13925
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5609
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3295
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4074
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1387
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2149
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3174
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4918
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4121
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 265
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Gln79Leu
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ

1-95709918-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95709918
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 95709918
    reference: chr 1
allele count: 1
allele frequency: 8.281162012653616e-6
allele num: 120756
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000263893
  ensembl transcript: ENST00000263893
  gene symbol: RWDD3
  hgvsc: ENST00000263893.6:c.237G>A
  hgvsp: ENST00000263893.6:c.237G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000228852
  ensembl transcript: ENST00000444665
  gene symbol: RP11-57H12.5
  hgvsc: ENST00000444665.1:n.71-837C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000495272
  gene symbol: RWDD3
  hgvsc: ENST00000495272.1:n.380G>A
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000474793
  ensembl transcript: ENST00000604203
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604203.1:c.211-2394G>A
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000473397
  gene symbol: RWDD3
  hgvsc: ENST00000473397.1:n.49-2394G>A
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000397398
  ensembl transcript: ENST00000429514
  gene symbol: RWDD3
  hgvsc: ENST00000429514.2:c.192G>A
  hgvsp: ENST00000429514.2:c.192G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000359221
  ensembl transcript: ENST00000370202
  gene symbol: RWDD3
  hgvsc: ENST00000370202.4:c.237G>A
  hgvsp: ENST00000370202.4:c.237G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000475025
  ensembl transcript: ENST00000604534
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604534.1:c.*112G>A
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000497058
  gene symbol: RWDD3
  hgvsc: ENST00000497058.1:n.126-203G>A
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000492639
  gene symbol: RWDD3
  hgvsc: ENST00000492639.1:n.500G>A
  variant of: http://identifiers.org/hgnc/21393
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4121
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3295
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1388
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4939
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4918
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5539
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5427
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3174
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5609
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2149
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4074
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13925
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 245
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Gln79Gln
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: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum

1-95709923-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95709923
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 95709923
    reference: chr 1
allele count: 1
allele frequency: 8.281299170213822e-6
allele num: 120754
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000228852
  ensembl transcript: ENST00000444665
  gene symbol: RP11-57H12.5
  hgvsc: ENST00000444665.1:n.71-842A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000495272
  gene symbol: RWDD3
  hgvsc: ENST00000495272.1:n.385T>C
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000263893
  ensembl transcript: ENST00000263893
  gene symbol: RWDD3
  hgvsc: ENST00000263893.6:c.242T>C
  hgvsp: ENSP00000263893.6:p.Val81Ala
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000473397
  gene symbol: RWDD3
  hgvsc: ENST00000473397.1:n.49-2389T>C
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000474793
  ensembl transcript: ENST00000604203
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604203.1:c.211-2389T>C
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000359221
  ensembl transcript: ENST00000370202
  gene symbol: RWDD3
  hgvsc: ENST00000370202.4:c.242T>C
  hgvsp: ENSP00000359221.4:p.Val81Ala
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000492639
  gene symbol: RWDD3
  hgvsc: ENST00000492639.1:n.505T>C
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000397398
  ensembl transcript: ENST00000429514
  gene symbol: RWDD3
  hgvsc: ENST00000429514.2:c.197T>C
  hgvsp: ENSP00000397398.2:p.Val66Ala
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000475025
  ensembl transcript: ENST00000604534
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604534.1:c.*117T>C
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000497058
  gene symbol: RWDD3
  hgvsc: ENST00000497058.1:n.126-198T>C
  variant of: http://identifiers.org/hgnc/21393
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4939
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5540
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3295
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4917
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4074
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4121
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3176
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5608
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1387
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13925
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2148
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5427
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 248
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Val81Ala
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: African
reference allele: T
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD

1-95709936-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95709936
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 95709936
    reference: chr 1
allele count: 1
allele frequency: 8.281162012653616e-6
allele num: 120756
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000263893
  ensembl transcript: ENST00000263893
  gene symbol: RWDD3
  hgvsc: ENST00000263893.6:c.255G>T
  hgvsp: ENSP00000263893.6:p.Glu85Asp
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000495272
  gene symbol: RWDD3
  hgvsc: ENST00000495272.1:n.398G>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000492639
  gene symbol: RWDD3
  hgvsc: ENST00000492639.1:n.518G>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000497058
  gene symbol: RWDD3
  hgvsc: ENST00000497058.1:n.126-185G>T
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000359221
  ensembl transcript: ENST00000370202
  gene symbol: RWDD3
  hgvsc: ENST00000370202.4:c.255G>T
  hgvsp: ENSP00000359221.4:p.Glu85Asp
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000475025
  ensembl transcript: ENST00000604534
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604534.1:c.*130G>T
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000397398
  ensembl transcript: ENST00000429514
  gene symbol: RWDD3
  hgvsc: ENST00000429514.2:c.210G>T
  hgvsp: ENSP00000397398.2:p.Glu70Asp
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000228852
  ensembl transcript: ENST00000444665
  gene symbol: RP11-57H12.5
  hgvsc: ENST00000444665.1:n.71-855C>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000474793
  ensembl transcript: ENST00000604203
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604203.1:c.211-2376G>T
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000473397
  gene symbol: RWDD3
  hgvsc: ENST00000473397.1:n.49-2376G>T
  variant of: http://identifiers.org/hgnc/21393
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3295
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1389
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2147
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13924
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4917
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5426
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5608
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5540
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4121
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3176
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4941
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4075
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 411
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Glu85Asp
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: BaseQRankSum

1-95709939-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95709939
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 95709939
    reference: chr 1
allele count: 1
allele frequency: 8.282670995742708e-6
allele num: 120734
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000492639
  gene symbol: RWDD3
  hgvsc: ENST00000492639.1:n.521T>A
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000497058
  gene symbol: RWDD3
  hgvsc: ENST00000497058.1:n.126-182T>A
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000263893
  ensembl transcript: ENST00000263893
  gene symbol: RWDD3
  hgvsc: ENST00000263893.6:c.258T>A
  hgvsp: ENSP00000263893.6:p.Asn86Lys
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000228852
  ensembl transcript: ENST00000444665
  gene symbol: RP11-57H12.5
  hgvsc: ENST00000444665.1:n.71-858A>T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000359221
  ensembl transcript: ENST00000370202
  gene symbol: RWDD3
  hgvsc: ENST00000370202.4:c.258T>A
  hgvsp: ENSP00000359221.4:p.Asn86Lys
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000475025
  ensembl transcript: ENST00000604534
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604534.1:c.*133T>A
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000473397
  gene symbol: RWDD3
  hgvsc: ENST00000473397.1:n.49-2373T>A
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000474793
  ensembl transcript: ENST00000604203
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604203.1:c.211-2373T>A
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000397398
  ensembl transcript: ENST00000429514
  gene symbol: RWDD3
  hgvsc: ENST00000429514.2:c.213T>A
  hgvsp: ENSP00000397398.2:p.Asn71Lys
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000495272
  gene symbol: RWDD3
  hgvsc: ENST00000495272.1:n.401T>A
  variant of: http://identifiers.org/hgnc/21393
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3483
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4902
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21277
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4734
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1409
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3827
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4405
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2187
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4176
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3066
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4642
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 264
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Asn86Lys
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
reference allele: T
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum

1-95709939-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95709939
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 95709939
    reference: chr 1
allele count: 103205
allele frequency: 8.548130601156261e-1
allele num: 120734
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000492639
  gene symbol: RWDD3
  hgvsc: ENST00000492639.1:n.521T>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000474793
  ensembl transcript: ENST00000604203
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604203.1:c.211-2373T>G
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000359221
  ensembl transcript: ENST00000370202
  gene symbol: RWDD3
  hgvsc: ENST00000370202.4:c.258T>G
  hgvsp: ENSP00000359221.4:p.Asn86Lys
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000228852
  ensembl transcript: ENST00000444665
  gene symbol: RP11-57H12.5
  hgvsc: ENST00000444665.1:n.71-858A>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000397398
  ensembl transcript: ENST00000429514
  gene symbol: RWDD3
  hgvsc: ENST00000429514.2:c.213T>G
  hgvsp: ENSP00000397398.2:p.Asn71Lys
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000475025
  ensembl transcript: ENST00000604534
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604534.1:c.*133T>G
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000263893
  ensembl transcript: ENST00000263893
  gene symbol: RWDD3
  hgvsc: ENST00000263893.6:c.258T>G
  hgvsp: ENSP00000263893.6:p.Asn86Lys
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000473397
  gene symbol: RWDD3
  hgvsc: ENST00000473397.1:n.49-2373T>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000497058
  gene symbol: RWDD3
  hgvsc: ENST00000497058.1:n.126-182T>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000495272
  gene symbol: RWDD3
  hgvsc: ENST00000495272.1:n.401T>G
  variant of: http://identifiers.org/hgnc/21393
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21277
  bin: 9.75e1
  variant carriers: 21225
genotype depth: GenotypeDepth
  all individuals: 3066
  bin: 5.75e1
  variant carriers: 2916
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 3.25e1
  variant carriers: 204
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 4.25e1
  variant carriers: 767
genotype depth: GenotypeDepth
  all individuals: 4176
  bin: 8.75e1
  variant carriers: 4160
genotype depth: GenotypeDepth
  all individuals: 4902
  bin: 7.75e1
  variant carriers: 4874
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 2.25e1
  variant carriers: 47
genotype depth: GenotypeDepth
  all individuals: 1409
  bin: 4.75e1
  variant carriers: 1260
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 2.75e1
  variant carriers: 92
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 3483
  bin: 9.25e1
  variant carriers: 3478
genotype depth: GenotypeDepth
  all individuals: 4734
  bin: 8.25e1
  variant carriers: 4707
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 3.75e1
  variant carriers: 423
genotype depth: GenotypeDepth
  all individuals: 4642
  bin: 7.25e1
  variant carriers: 4597
genotype depth: GenotypeDepth
  all individuals: 2187
  bin: 5.25e1
  variant carriers: 2039
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 3827
  bin: 6.25e1
  variant carriers: 3744
genotype depth: GenotypeDepth
  all individuals: 4405
  bin: 6.75e1
  variant carriers: 4324
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 8.25e1
  variant carriers: 36
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 7.25e1
  variant carriers: 13
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.25e1
  variant carriers: 5
hgvs: p.Asn86Lys
num of homozygotes: 44327
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: MQ
site quality: FS
site quality: ClippingRankSum

1-95709954-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95709954
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 95709954
    reference: chr 1
allele count: 2
allele frequency: 1.656177542232527e-5
allele num: 120760
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000495272
  gene symbol: RWDD3
  hgvsc: ENST00000495272.1:n.416A>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000497058
  gene symbol: RWDD3
  hgvsc: ENST00000497058.1:n.126-167A>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000492639
  gene symbol: RWDD3
  hgvsc: ENST00000492639.1:n.536A>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000228852
  ensembl transcript: ENST00000444665
  gene symbol: RP11-57H12.5
  hgvsc: ENST00000444665.1:n.71-873T>C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000397398
  ensembl transcript: ENST00000429514
  gene symbol: RWDD3
  hgvsc: ENST00000429514.2:c.228A>G
  hgvsp: ENST00000429514.2:c.228A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000475025
  ensembl transcript: ENST00000604534
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604534.1:c.*148A>G
  variant of: http://identifiers.org/hgnc/49388
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000263893
  ensembl transcript: ENST00000263893
  gene symbol: RWDD3
  hgvsc: ENST00000263893.6:c.273A>G
  hgvsp: ENST00000263893.6:c.273A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000122481
  ensembl protein: ENSP00000359221
  ensembl transcript: ENST00000370202
  gene symbol: RWDD3
  hgvsc: ENST00000370202.4:c.273A>G
  hgvsp: ENST00000370202.4:c.273A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122481
  ensembl transcript: ENST00000473397
  gene symbol: RWDD3
  hgvsc: ENST00000473397.1:n.49-2358A>G
  variant of: http://identifiers.org/hgnc/21393
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000271092
  ensembl protein: ENSP00000474793
  ensembl transcript: ENST00000604203
  gene symbol: TMEM56-RWDD3
  hgvsc: ENST00000604203.1:c.211-2358A>G
  variant of: http://identifiers.org/hgnc/49388
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5674
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8375
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2322
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1841
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4956
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5898
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6277
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6901
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2622
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3774
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2764
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5858
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1200
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 841
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1781
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2653
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ala91Ala
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: ReadPosRankSum

GenotypeQuality
all individuals: 32581
bin: 2.25e1
variant carriers: 9

GenotypeQuality
all individuals: 1273
bin: 1.75e1
variant carriers: 12

GenotypeQuality
all individuals: 1137
bin: 2.75e1
variant carriers: 4

GenotypeQuality
all individuals: 575
bin: 7.25e1
variant carriers: 17

GenotypeQuality
all individuals: 252
bin: 9.25e1
variant carriers: 24

GenotypeQuality
all individuals: 662
bin: 1.25e1
variant carriers: 9

GenotypeQuality
all individuals: 5636
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 489
bin: 8.25e1
variant carriers: 15

GenotypeQuality
all individuals: 1402
bin: 6.75e1
variant carriers: 10

GenotypeQuality
all individuals: 354
bin: 4.75e1
variant carriers: 12

GenotypeQuality
all individuals: 10620
bin: 6.25e1
variant carriers: 15

GenotypeQuality
all individuals: 569
bin: 7.75e1
variant carriers: 11

GenotypeQuality
all individuals: 176
bin: 4.25e1
variant carriers: 6

GenotypeQuality
all individuals: 1006
bin: 3.25e1
variant carriers: 5

GenotypeQuality
all individuals: 1289
bin: 9.75e1
variant carriers: 630

South Asian
type: Population
allele count: 34
allele frequency: 3.562447611064543e-3
allele num: 9544
num of homozygotes: 1

African
type: Population
allele count: 14
allele frequency: 3.737319807794981e-3
allele num: 3746
num of homozygotes: 0

Other
type: Population
allele count: 5
allele frequency: 1.54320987654321e-2
allele num: 324
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3274
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 7
allele frequency: 9.408602150537635e-3
allele num: 744
num of homozygotes: 0

Latino
type: Population
allele count: 35
allele frequency: 1.092384519350812e-2
allele num: 3204
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 591
allele frequency: 2.520255863539446e-2
allele num: 23450
num of homozygotes: 5

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.9e-3

VQSLOD
type: SiteQuality
SIO_000300: 5.31e0

MQRankSum
type: SiteQuality
SIO_000300: 2.64e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.71e-1

QD
type: SiteQuality
SIO_000300: 1.208e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.95e-1

DP
type: SiteQuality
SIO_000300: 7.34257e5

GenotypeQuality
all individuals: 568
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 480
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6199
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9753
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1396
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1504
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 321
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 33206
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 568
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 678
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 270
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 203
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 476
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1245
bin: 2.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3250
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 312
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3154
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3720
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 8.605851979345956e-5
allele num: 23240
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 762
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.48e0

MQ
type: SiteQuality
SIO_000300: 5.82e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.81e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.354e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.61e-1

FS
type: SiteQuality
SIO_000300: 1.97e0

VQSLOD
type: SiteQuality
SIO_000300: -1.98e0

QD
type: SiteQuality
SIO_000300: 8.630000000000001e0

DP
type: SiteQuality
SIO_000300: 7.1631e5

GenotypeQuality
all individuals: 469
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 565
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 274
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1497
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 365
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 229
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 315
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 652
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6267
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1062
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 203
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 33194
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 479
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9667
bin: 6.25e1
variant carriers: 3

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 23220
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3244
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 9.46969696969697e-4
allele num: 3168
num of homozygotes: 0

African
type: Population
allele count: 12
allele frequency: 3.232758620689655e-3
allele num: 3712
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 312
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9548
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 758
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.43e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.48e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.215e1

FS
type: SiteQuality
SIO_000300: 5.21e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.15e0

MQRankSum
type: SiteQuality
SIO_000300: 4.7e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -6.34e-1

DP
type: SiteQuality
SIO_000300: 7.15502e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 9619
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1389
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33413
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 563
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1247
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 562
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1043
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 295
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6350
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1382
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 415
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 479
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 229
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 676
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 202
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3170
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9560
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 770
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3204
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 308
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.299965600275198e-5
allele num: 23256
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3708
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.85e0

DP
type: SiteQuality
SIO_000300: 7.12788e5

BaseQRankSum
type: SiteQuality
SIO_000300: -1.85e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.997e0

FS
type: SiteQuality
SIO_000300: 1.623e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.51e-2

QD
type: SiteQuality
SIO_000300: 2.943e1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.85e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 685
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1076
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 479
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 558
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1541
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 312
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 225
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 521
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 557
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 254
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 180
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8302
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 677
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1339
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 229
bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 294
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 22650
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3142
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3638
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 738
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.055074910318633e-4
allele num: 9478
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3092
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -5.698e-1

QD
type: SiteQuality
SIO_000300: 8.02e0

FS
type: SiteQuality
SIO_000300: 6.319e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.96e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.96e-1

MQ
type: SiteQuality
SIO_000300: 5.938e1

DP
type: SiteQuality
SIO_000300: 6.91792e5

MQRankSum
type: SiteQuality
SIO_000300: 2.96e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.68e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.209e0

GenotypeQuality
all individuals: 477
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1086
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1460
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 743
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1324
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1399
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 554
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 203
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 554
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 304
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 33455
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7691
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 214
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 221
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 678
bin: 9.75e1
variant carriers: 2

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3094
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9448
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3016
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 22274
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 2.782415136338342e-4
allele num: 3594
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 292
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 718
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 8.99e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.76e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.81e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.4e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.16e0

FS
type: SiteQuality
SIO_000300: 5.21e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.8e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.35e-1

DP
type: SiteQuality
SIO_000300: 6.77353e5

GenotypeQuality
all individuals: 146
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1542
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 499
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9677
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 522
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 681
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 545
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 548
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1381
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 478
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 203
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 160
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32821
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6650
bin: 6.25e1
variant carriers: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 288
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 8.479366873940079e-4
allele num: 3538
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2868
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 674
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 21444
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2966
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.071581654522075e-4
allele num: 9332
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.51e-1

FS
type: SiteQuality
SIO_000300: 4.35e-1

DP
type: SiteQuality
SIO_000300: 6.5563e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.11e-2

MQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.21e-1

QD
type: SiteQuality
SIO_000300: 1.198e1

VQSLOD
type: SiteQuality
SIO_000300: 3.17e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.06e-1

GenotypeQuality
all individuals: 1007
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 544
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 202
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1266
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 372
bin: 2.5e0
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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East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2794
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 3508
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 4.737540269092287e-5
allele num: 21108
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

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

FS
type: SiteQuality
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MQRankSum
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QD
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ClippingRankSum
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MQ
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
type: SiteQuality
SIO_000300: 3.86e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.003e0

DP
type: SiteQuality
SIO_000300: 6.41298e5

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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num of homozygotes: 0

African
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allele frequency: 3.03030303030303e-4
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South Asian
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allele frequency: 0.0e0
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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 frequency: 0.0e0
allele num: 19800
num of homozygotes: 0

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

European (Finnish)
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allele frequency: 0.0e0
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BaseQRankSum
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SIO_000300: -6.12e-1

FS
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ClippingRankSum
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QD
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MQRankSum
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MQ
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InbreedingCoeff
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VQSLOD
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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

East Asian
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allele frequency: 0.0e0
allele num: 2554
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

African
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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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South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 19234
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Other
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allele frequency: 0.0e0
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num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.31e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.76e-1

DP
type: SiteQuality
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VQSLOD
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InbreedingCoeff
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QD
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MQ
type: SiteQuality
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BaseQRankSum
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ClippingRankSum
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SIO_000300: -1.652e0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 3178
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 258
num of homozygotes: 0

East Asian
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allele frequency: 8.176614881439084e-4
allele num: 2446
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 9076
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 2362
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 18752
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 546
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 5.88266e5

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.67e-2

FS
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -8.672e-1

MQRankSum
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ClippingRankSum
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QD
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BaseQRankSum
type: SiteQuality
SIO_000300: 1.43e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 520
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 1.10938540048813e-4
allele num: 9014
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East Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 3156
num of homozygotes: 0

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

Other
type: Population
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: 3.94e-1

DP
type: SiteQuality
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ReadPosRankSum
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MQ
type: SiteQuality
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BaseQRankSum
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InbreedingCoeff
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SIO_000300: -3.35e-2

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
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QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 1.97e-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

European (Non-Finnish)
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allele count: 1
allele frequency: 5.737893045673629e-5
allele num: 17428
num of homozygotes: 0

Other
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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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East Asian
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South Asian
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InbreedingCoeff
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VQSLOD
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ClippingRankSum
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MQRankSum
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QD
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ReadPosRankSum
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FS
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MQ
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BaseQRankSum
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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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Latino
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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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East Asian
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South Asian
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European (Non-Finnish)
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Other
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num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.184e1

ReadPosRankSum
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QD
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FS
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MQRankSum
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VQSLOD
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BaseQRankSum
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ClippingRankSum
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InbreedingCoeff
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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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African
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Latino
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South Asian
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European (Non-Finnish)
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European (Finnish)
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East Asian
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MQ
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BaseQRankSum
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VQSLOD
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ReadPosRankSum
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QD
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FS
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DP
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InbreedingCoeff
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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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African
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num of homozygotes: 0

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

South Asian
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Latino
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Other
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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

InbreedingCoeff
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ClippingRankSum
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VQSLOD
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SIO_000300: -1.451e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.5e-1

DP
type: SiteQuality
SIO_000300: 4.63663e5

MQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 9.85e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.537e0

GenotypeQuality
all individuals: 5049
bin: 1.25e1
variant carriers: 1

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 332
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 650
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 509
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1087
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8064
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 116
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 994
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 732
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10172
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2114
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 194
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.84e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.47e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.71e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -7.543e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.47e-1

MQ
type: SiteQuality
SIO_000300: 5.79e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.47e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.47e-1

DP
type: SiteQuality
SIO_000300: 4.54909e5

GenotypeQuality
all individuals: 513
bin: 7.25e1
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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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 564
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 675
bin: 9.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1928
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 70
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 746
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7928
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 190
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8790
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 534
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.53e0

DP
type: SiteQuality
SIO_000300: 4.42367e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.712e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.24e-2

GenotypeQuality
all individuals: 868
bin: 9.75e1
variant carriers: 19

GenotypeQuality
all individuals: 2
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 271
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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 893
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 463
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.785714285714286e-3
allele num: 560
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.942286348501665e-3
allele num: 3604
num of homozygotes: 0

South Asian
type: Population
allele count: 11
allele frequency: 1.444327731092437e-3
allele num: 7616
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.171e1

MQ
type: SiteQuality
SIO_000300: 5.987e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

FS
type: SiteQuality
SIO_000300: 1.12e0

VQSLOD
type: SiteQuality
SIO_000300: 1.27e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.89e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.2e-2

DP
type: SiteQuality
SIO_000300: 1.97734e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.28e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 8.9e-2

GenotypeQuality
all individuals: 463
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 860
bin: 9.75e1
variant carriers: 11

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 162
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 2044
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variant carriers: 0

GenotypeQuality
all individuals: 897
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variant carriers: 0

GenotypeQuality
all individuals: 550
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

South Asian
type: Population
allele count: 11
allele frequency: 1.443948542924652e-3
allele num: 7618
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3608
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.8e-2

FS
type: SiteQuality
SIO_000300: 1.1e0

MQ
type: SiteQuality
SIO_000300: 5.966e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.54e0

MQRankSum
type: SiteQuality
SIO_000300: -1.71e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.7e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.84e-1

QD
type: SiteQuality
SIO_000300: 9.949999999999999e0

DP
type: SiteQuality
SIO_000300: 1.98141e5

ClippingRankSum
type: SiteQuality
SIO_000300: -1.243e0

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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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 276
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3608
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.312680493567866e-4
allele num: 7618
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.69e-2

MQRankSum
type: SiteQuality
SIO_000300: 5.34e-1

MQ
type: SiteQuality
SIO_000300: 5.834e1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.5e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.96e-1

QD
type: SiteQuality
SIO_000300: 5.09e0

VQSLOD
type: SiteQuality
SIO_000300: -2.98e0

FS
type: SiteQuality
SIO_000300: 2.873e0

DP
type: SiteQuality
SIO_000300: 1.97639e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.067e0

GenotypeQuality
all individuals: 552
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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GenotypeQuality
all individuals: 8
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 7
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.771618625277162e-4
allele num: 3608
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.792114695340502e-3
allele num: 558
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7618
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.25e-1

QD
type: SiteQuality
SIO_000300: 1.106e1

DP
type: SiteQuality
SIO_000300: 1.97491e5

ClippingRankSum
type: SiteQuality
SIO_000300: 5.38e-1

FS
type: SiteQuality
SIO_000300: 5.48e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.71e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.76e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.47e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.25e-1

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
all individuals: 271
bin: 8.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3608
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.313025210084034e-4
allele num: 7616
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.036e0

MQRankSum
type: SiteQuality
SIO_000300: 9.9e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.41e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.89e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.79e-2

DP
type: SiteQuality
SIO_000300: 1.96867e5

QD
type: SiteQuality
SIO_000300: 9.44e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.578e0

MQ
type: SiteQuality
SIO_000300: 5.97e1

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
all individuals: 15
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GenotypeQuality
all individuals: 28
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
all individuals: 20
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 9

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7614
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

African
type: Population
allele count: 9
allele frequency: 1.612903225806452e-2
allele num: 558
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3606
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.33e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.1e-2

ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 3.8e0

FS
type: SiteQuality
SIO_000300: 6.75e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.21e-1

MQ
type: SiteQuality
SIO_000300: 5.973e1

DP
type: SiteQuality
SIO_000300: 1.96419e5

QD
type: SiteQuality
SIO_000300: 1.445e1

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 541
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GenotypeQuality
all individuals: 364
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variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.792114695340502e-3
allele num: 558
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3600
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7610
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.084e0

VQSLOD
type: SiteQuality
SIO_000300: -1.586e0

FS
type: SiteQuality
SIO_000300: 1.1847e1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.985e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.59e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.17e0

DP
type: SiteQuality
SIO_000300: 1.92842e5

BaseQRankSum
type: SiteQuality
SIO_000300: -1.38e0

GenotypeQuality
all individuals: 963
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 284
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 350
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 2.5e0
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GenotypeQuality
all individuals: 269
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 222
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 593
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51099
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 265
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 750
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 600
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 454
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 408
bin: 6.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.592352202798273e-5
allele num: 65326
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11522
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12744
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9722
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 850
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.22e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.16e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.06e-1

FS
type: SiteQuality
SIO_000300: 2.514e0

QD
type: SiteQuality
SIO_000300: 1.332e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.71e0

DP
type: SiteQuality
SIO_000300: 3.627642e6

MQ
type: SiteQuality
SIO_000300: 5.976e1

MQRankSum
type: SiteQuality
SIO_000300: -2.31e-1

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

GenotypeQuality
all individuals: 198
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 599
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 800
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 460
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 421
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51099
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 278
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 202
bin: 4.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12826
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8572
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11522
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.53003457878148e-5
allele num: 65358
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9726
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.265e0

MQ
type: SiteQuality
SIO_000300: 5.805e1

DP
type: SiteQuality
SIO_000300: 3.630322e6

QD
type: SiteQuality
SIO_000300: 6.25e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.66e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.94e-1

FS
type: SiteQuality
SIO_000300: 1.287e0

MQRankSum
type: SiteQuality
SIO_000300: 1.73e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.25e-1

GenotypeQuality
all individuals: 463
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 71
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variant carriers: 0

GenotypeQuality
all individuals: 760
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variant carriers: 0

GenotypeQuality
all individuals: 147
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variant carriers: 0

GenotypeQuality
all individuals: 64
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variant carriers: 0

GenotypeQuality
all individuals: 302
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variant carriers: 0

GenotypeQuality
all individuals: 616
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 499
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variant carriers: 0

GenotypeQuality
all individuals: 2190
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 110
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variant carriers: 0

GenotypeQuality
all individuals: 1437
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 795
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variant carriers: 0

GenotypeQuality
all individuals: 484
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variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 5.75e1
variant carriers: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13126
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11526
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.027749229188078e-4
allele num: 9730
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65468
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.032e1

VQSLOD
type: SiteQuality
SIO_000300: -1.67e0

FS
type: SiteQuality
SIO_000300: 1.1501e1

MQRankSum
type: SiteQuality
SIO_000300: 1.16e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.35e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-3

MQ
type: SiteQuality
SIO_000300: 5.893e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.070000000000001e-1

DP
type: SiteQuality
SIO_000300: 3.640814e6

ClippingRankSum
type: SiteQuality
SIO_000300: -9.27e-1

GenotypeQuality
all individuals: 85
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 325
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 34
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1972
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variant carriers: 0

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

GenotypeQuality
all individuals: 564
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 763
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 571
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 467
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51109
bin: 9.75e1
variant carriers: 97

GenotypeQuality
all individuals: 522
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2244
bin: 6.25e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 66
allele frequency: 9.978832778953735e-3
allele num: 6614
num of homozygotes: 0

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

Latino
type: Population
allele count: 4
allele frequency: 3.466805338880222e-4
allele num: 11538
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13738
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 26
allele frequency: 3.960878705706712e-4
allele num: 65642
num of homozygotes: 1

Other
type: Population
allele count: 2
allele frequency: 2.314814814814815e-3
allele num: 864
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.14e-2

MQ
type: SiteQuality
SIO_000300: 5.973e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 5.78e0

DP
type: SiteQuality
SIO_000300: 3.655832e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.131e0

QD
type: SiteQuality
SIO_000300: 1.309e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.15e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.69e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.24e-1

GenotypeQuality
all individuals: 75
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 7.5e0
variant carriers: 0

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

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

GenotypeQuality
all individuals: 477
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variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1813
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 604
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 763
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 403
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variant carriers: 0

GenotypeQuality
all individuals: 2631
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variant carriers: 0

GenotypeQuality
all individuals: 47
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GenotypeQuality
all individuals: 51108
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variant carriers: 1

GenotypeQuality
all individuals: 230
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 329
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 530
bin: 7.75e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13956
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.664009703690868e-5
allele num: 11542
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65748
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.7e-1

QD
type: SiteQuality
SIO_000300: 1.49e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.66e-1

FS
type: SiteQuality
SIO_000300: 2.403e0

DP
type: SiteQuality
SIO_000300: 3.660765e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.11e-2

VQSLOD
type: SiteQuality
SIO_000300: -6.876e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.99e0

MQRankSum
type: SiteQuality
SIO_000300: -1.463e0

MQ
type: SiteQuality
SIO_000300: 5.913e1

GenotypeQuality
all individuals: 3294
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 626
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1303
bin: 2.25e1
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GenotypeQuality
all individuals: 541
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variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 7.5e0
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GenotypeQuality
all individuals: 74
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variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 2.5e0
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GenotypeQuality
all individuals: 680
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 91
bin: 5.75e1
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GenotypeQuality
all individuals: 23
bin: 1.75e1
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GenotypeQuality
all individuals: 58
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variant carriers: 0

GenotypeQuality
all individuals: 745
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 462
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51385
bin: 9.75e1
variant carriers: 1505

GenotypeQuality
all individuals: 360
bin: 7.25e1
variant carriers: 1

African
type: Population
allele count: 32
allele frequency: 3.272652894252403e-3
allele num: 9778
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1192
allele frequency: 1.804693414080242e-2
allele num: 66050
num of homozygotes: 9

European (Finnish)
type: Population
allele count: 96
allele frequency: 1.451466586029634e-2
allele num: 6614
num of homozygotes: 2

South Asian
type: Population
allele count: 100
allele frequency: 6.799020940984498e-3
allele num: 14708
num of homozygotes: 1

Latino
type: Population
allele count: 87
allele frequency: 7.535077082972458e-3
allele num: 11546
num of homozygotes: 0

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

Other
type: Population
allele count: 13
allele frequency: 1.484018264840183e-2
allele num: 876
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.06e-1

DP
type: SiteQuality
SIO_000300: 3.736428e6

QD
type: SiteQuality
SIO_000300: 1.182e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.8e-3

FS
type: SiteQuality
SIO_000300: 5.649999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.02e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.4e0

MQ
type: SiteQuality
SIO_000300: 5.964e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.949e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.54e-1

GenotypeQuality
all individuals: 111
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1013
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51270
bin: 9.75e1
variant carriers: 2

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

GenotypeQuality
all individuals: 33
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GenotypeQuality
all individuals: 3644
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GenotypeQuality
all individuals: 794
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 194
bin: 3.25e1
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GenotypeQuality
all individuals: 400
bin: 7.25e1
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GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 2.5e0
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GenotypeQuality
all individuals: 26
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 767
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 678
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 478
bin: 8.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 882
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9786
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11554
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15156
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.021148036253776e-5
allele num: 66200
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.2e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 1.33e0

DP
type: SiteQuality
SIO_000300: 3.737823e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.71e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 5.494e0

QD
type: SiteQuality
SIO_000300: 1.698e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.82e0

MQRankSum
type: SiteQuality
SIO_000300: 7.84e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.802e-1

GenotypeQuality
all individuals: 116
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 796
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 884
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4030
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 670
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 54
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 433
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 51276
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 26
bin: 7.5e0
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9792
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11558
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.337135614702154e-5
allele num: 15780
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66378
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -9.53e-1

FS
type: SiteQuality
SIO_000300: 1.891e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.649999999999999e-1

DP
type: SiteQuality
SIO_000300: 3.747901e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.022e0

QD
type: SiteQuality
SIO_000300: 1.79e1

VQSLOD
type: SiteQuality
SIO_000300: -4.504e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -5.15e-1

MQ
type: SiteQuality
SIO_000300: 5.97e1

GenotypeQuality
all individuals: 7
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51277
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 44
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 64
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 891
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 108
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 439
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 2.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 558
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 797
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4093
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 676
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 506
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66396
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.319514661274014e-5
allele num: 15824
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11558
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 4.26e-1

FS
type: SiteQuality
SIO_000300: 6.209e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.38e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.46e-1

DP
type: SiteQuality
SIO_000300: 3.748821e6

MQRankSum
type: SiteQuality
SIO_000300: 1.82e-1

QD
type: SiteQuality
SIO_000300: 1.53e1

MQ
type: SiteQuality
SIO_000300: 5.975e1

VQSLOD
type: SiteQuality
SIO_000300: 5.54e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

GenotypeQuality
all individuals: 108
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 64
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 891
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 797
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 34
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
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variant carriers: 0

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

GenotypeQuality
all individuals: 710
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variant carriers: 0

GenotypeQuality
all individuals: 558
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 439
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 506
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51277
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 676
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4093
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66396
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.319514661274014e-5
allele num: 15824
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11558
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.54e-1

FS
type: SiteQuality
SIO_000300: 6.209e0

MQRankSum
type: SiteQuality
SIO_000300: 1.82e-1

MQ
type: SiteQuality
SIO_000300: 5.975e1

DP
type: SiteQuality
SIO_000300: 3.748821e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.46e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.26e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.38e0

QD
type: SiteQuality
SIO_000300: 1.53e1

GenotypeQuality
all individuals: 69
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 725
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variant carriers: 0

GenotypeQuality
all individuals: 926
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variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 761
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4184
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 48
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51281
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 368
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 481
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 810
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 5.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.64902266043937e-5
allele num: 11562
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.021033285685113e-4
allele num: 9794
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503533303262667e-5
allele num: 66510
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16078
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.96e1

DP
type: SiteQuality
SIO_000300: 3.754236e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.38e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 6.65e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.15e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.34e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.61e-1

FS
type: SiteQuality
SIO_000300: 5.33e-1

QD
type: SiteQuality
SIO_000300: 1.299e1

GenotypeQuality
all individuals: 8
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4210
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 24
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 955
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variant carriers: 0

GenotypeQuality
all individuals: 530
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variant carriers: 0

GenotypeQuality
all individuals: 6
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variant carriers: 0

GenotypeQuality
all individuals: 813
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 487
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variant carriers: 0

GenotypeQuality
all individuals: 741
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 767
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51284
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 35
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.02082482645978e-4
allele num: 9796
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16158
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66536
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.324e1

MQ
type: SiteQuality
SIO_000300: 5.968e1

FS
type: SiteQuality
SIO_000300: 6.229e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.07e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.467e-1

DP
type: SiteQuality
SIO_000300: 3.756078e6

BaseQRankSum
type: SiteQuality
SIO_000300: 6.98e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.34e0

MQRankSum
type: SiteQuality
SIO_000300: -1.784e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

GenotypeQuality
all individuals: 545
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 29
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variant carriers: 0

GenotypeQuality
all individuals: 36
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variant carriers: 0

GenotypeQuality
all individuals: 46
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variant carriers: 0

GenotypeQuality
all individuals: 27
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variant carriers: 0

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 38
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variant carriers: 0

GenotypeQuality
all individuals: 54
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variant carriers: 0

GenotypeQuality
all individuals: 982
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variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 4150
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 805
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variant carriers: 0

GenotypeQuality
all individuals: 51293
bin: 9.75e1
variant carriers: 23

GenotypeQuality
all individuals: 510
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variant carriers: 0

GenotypeQuality
all individuals: 207
bin: 2.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66580
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.646031471554557e-5
allele num: 11566
num of homozygotes: 0

African
type: Population
allele count: 22
allele frequency: 2.245356195141866e-3
allele num: 9798
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16280
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -3.81e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.91e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.09e0

MQ
type: SiteQuality
SIO_000300: 5.967e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.34e-1

DP
type: SiteQuality
SIO_000300: 3.760802e6

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.92e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.5e-3

QD
type: SiteQuality
SIO_000300: 1.241e1

GenotypeQuality
all individuals: 22
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 173
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4184
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 843
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GenotypeQuality
all individuals: 551
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variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 7.5e0
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GenotypeQuality
all individuals: 1002
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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: 5

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 519
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variant carriers: 0

GenotypeQuality
all individuals: 823
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.319647413593134e-4
allele num: 8622
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.020199959192002e-4
allele num: 9802
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16332
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.729505361466621e-4
allele num: 11564
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66596
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.111e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.37e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.16e-1

MQ
type: SiteQuality
SIO_000300: 5.955e1

VQSLOD
type: SiteQuality
SIO_000300: 3.47e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 2.57e-1

QD
type: SiteQuality
SIO_000300: 1.218e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.0e-3

DP
type: SiteQuality
SIO_000300: 3.761708e6

GenotypeQuality
all individuals: 15
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 846
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variant carriers: 0

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
all individuals: 22
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GenotypeQuality
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GenotypeQuality
all individuals: 5
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GenotypeQuality
all individuals: 824
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 519
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GenotypeQuality
all individuals: 158
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
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variant carriers: 0

GenotypeQuality
all individuals: 555
bin: 8.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66608
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.834637964774951e-4
allele num: 16352
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.99e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.48e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.938e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.76e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.05e-1

DP
type: SiteQuality
SIO_000300: 3.762199e6

VQSLOD
type: SiteQuality
SIO_000300: 2.66e0

QD
type: SiteQuality
SIO_000300: 1.519e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.39e0

GenotypeQuality
all individuals: 833
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 22
bin: 5.75e1
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GenotypeQuality
all individuals: 560
bin: 8.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 26
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variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 851
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51304
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 17
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4246
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 5.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.5008254539997e-5
allele num: 66630
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.087168249330411e-5
allele num: 16428
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.763842e6

MQRankSum
type: SiteQuality
SIO_000300: 9.14e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.583e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.48e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.69e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.409999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.52e-1

QD
type: SiteQuality
SIO_000300: 1.451e1

GenotypeQuality
all individuals: 24
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 869
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 582
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4245
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 550
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 839
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 867
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1061
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.493330935467435e-5
allele num: 66726
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.638562543192812e-5
allele num: 11576
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

East 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: 6614
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.120000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.72e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.38e0

MQ
type: SiteQuality
SIO_000300: 5.976e1

QD
type: SiteQuality
SIO_000300: 1.374e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.32e-2

DP
type: SiteQuality
SIO_000300: 3.767549e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.13e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.77e0

GenotypeQuality
all individuals: 17
bin: 7.75e1
variant carriers: 16

GenotypeQuality
all individuals: 18
bin: 6.75e1
variant carriers: 18

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

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

GenotypeQuality
all individuals: 5
bin: 5.25e1
variant carriers: 5

GenotypeQuality
all individuals: 4
bin: 1.75e1
variant carriers: 4

GenotypeQuality
all individuals: 5
bin: 3.75e1
variant carriers: 5

GenotypeQuality
all individuals: 60235
bin: 9.75e1
variant carriers: 60231

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 3

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

GenotypeQuality
all individuals: 22
bin: 8.25e1
variant carriers: 19

GenotypeQuality
all individuals: 14
bin: 6.25e1
variant carriers: 11

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

GenotypeQuality
all individuals: 1
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2
bin: 4.25e1
variant carriers: 2

GenotypeQuality
all individuals: 24
bin: 9.25e1
variant carriers: 24

GenotypeQuality
all individuals: 11
bin: 7.25e1
variant carriers: 9

European (Non-Finnish)
type: Population
allele count: 66710
allele frequency: 9.995504944560983e-1
allele num: 66740
num of homozygotes: 33341

African
type: Population
allele count: 9320
allele frequency: 9.508263619669455e-1
allele num: 9802
num of homozygotes: 4431

Latino
type: Population
allele count: 11553
allele frequency: 9.980131306150657e-1
allele num: 11576
num of homozygotes: 5765

European (Finnish)
type: Population
allele count: 6614
allele frequency: 1.0e0
allele num: 6614
num of homozygotes: 3307

South Asian
type: Population
allele count: 16509
allele frequency: 9.998183139534884e-1
allele num: 16512
num of homozygotes: 8253

Other
type: Population
allele count: 898
allele frequency: 9.977777777777778e-1
allele num: 900
num of homozygotes: 448

East Asian
type: Population
allele count: 8626
allele frequency: 1.0e0
allele num: 8626
num of homozygotes: 4313

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.510000000000001e-2

QD
type: SiteQuality
SIO_000300: 3.418e1

DP
type: SiteQuality
SIO_000300: 6.518342e6

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.7e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.51e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.5e-2

MQ
type: SiteQuality
SIO_000300: 5.969e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.05e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.25e0

GenotypeQuality
all individuals: 409
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 425
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 314
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 240
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 268
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58277
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 251
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.25e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.159285879897983e-4
allele num: 8626
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66734
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 3.009e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.524e0

DP
type: SiteQuality
SIO_000300: 5.033341e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.76e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -2.635e0

FS
type: SiteQuality
SIO_000300: 4.095e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.35e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.38e-1

MQ
type: SiteQuality
SIO_000300: 5.933e1

GenotypeQuality
all individuals: 10
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 314
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 159
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 269
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 250
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 428
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 409
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58275
bin: 9.75e1
variant carriers: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498441620714457e-5
allele num: 66736
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 9.29e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.09e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.15e0

FS
type: SiteQuality
SIO_000300: 4.095e0

DP
type: SiteQuality
SIO_000300: 5.033233e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.955e1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.1e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.13e0

QD
type: SiteQuality
SIO_000300: 1.122e1

GenotypeQuality
all individuals: 5
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 433
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 239
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 11
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 248
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 58274
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 314
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 3.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66730
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.640055296353897e-5
allele num: 11574
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 5.033206e6

VQSLOD
type: SiteQuality
SIO_000300: -1.641e0

MQ
type: SiteQuality
SIO_000300: 5.975e1

MQRankSum
type: SiteQuality
SIO_000300: 2.34e-1

FS
type: SiteQuality
SIO_000300: 1.334e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.477e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.14e-2

QD
type: SiteQuality
SIO_000300: 1.33e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.5e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 9.5e-2

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

GenotypeQuality
all individuals: 2
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 14
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 239
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 413
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 247
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 5
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58272
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 270
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66738
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.159285879897983e-4
allele num: 8626
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.42e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -7.77e-1

FS
type: SiteQuality
SIO_000300: 2.675e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.28e-1

DP
type: SiteQuality
SIO_000300: 5.03293e6

VQSLOD
type: SiteQuality
SIO_000300: 1.54e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.53e0

QD
type: SiteQuality
SIO_000300: 8.869999999999999e0

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58273
bin: 9.75e1
variant carriers: 121

GenotypeQuality
all individuals: 248
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 12
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 413
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 239
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 441
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 269
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 121
allele frequency: 7.328003875968992e-3
allele num: 16512
num of homozygotes: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.111111111111111e-3
allele num: 900
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.46e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.22e-1

QD
type: SiteQuality
SIO_000300: 1.493e1

DP
type: SiteQuality
SIO_000300: 5.034268e6

MQ
type: SiteQuality
SIO_000300: 5.975e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.61e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.04e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.3e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.08e0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 439
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 248
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 269
bin: 8.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498441620714457e-5
allele num: 66736
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -4.668e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.14e0

MQ
type: SiteQuality
SIO_000300: 5.924e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.89e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.461e1

MQRankSum
type: SiteQuality
SIO_000300: 1.28e0

FS
type: SiteQuality
SIO_000300: 2.851e0

DP
type: SiteQuality
SIO_000300: 5.033501e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.045e0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 4

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 5.993946114424431e-5
allele num: 66734
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.941e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.61e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 5.1e-2

FS
type: SiteQuality
SIO_000300: 5.24e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 1.67e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.31e0

QD
type: SiteQuality
SIO_000300: 1.195e1

DP
type: SiteQuality
SIO_000300: 5.033492e6

GenotypeQuality
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498486528606108e-5
allele num: 66734
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.941e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.61e-1

FS
type: SiteQuality
SIO_000300: 5.24e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.67e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 5.1e-2

DP
type: SiteQuality
SIO_000300: 5.033492e6

QD
type: SiteQuality
SIO_000300: 1.195e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 3.31e0

GenotypeQuality
all individuals: 0
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
all individuals: 270
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 245
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498531439189594e-5
allele num: 66732
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.26e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.1e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.422e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

FS
type: SiteQuality
SIO_000300: 2.7349e1

MQRankSum
type: SiteQuality
SIO_000300: -5.9e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.053e0

DP
type: SiteQuality
SIO_000300: 5.033345e6

MQ
type: SiteQuality
SIO_000300: 5.957e1

QD
type: SiteQuality
SIO_000300: 1.641e1

GenotypeQuality
all individuals: 7
bin: 2.25e1
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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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 245
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66732
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 2.7349e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

MQ
type: SiteQuality
SIO_000300: 5.957e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.26e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.1e-2

QD
type: SiteQuality
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VQSLOD
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BaseQRankSum
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SIO_000300: -2.422e0

MQRankSum
type: SiteQuality
SIO_000300: -5.9e-1

DP
type: SiteQuality
SIO_000300: 5.033345e6

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.491983577571999e-5
allele num: 66738
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9802
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

MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
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SIO_000300: 5.4e0

FS
type: SiteQuality
SIO_000300: 1.737e0

DP
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

QD
type: SiteQuality
SIO_000300: 1.401e1

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 9802
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.4983967155144e-5
allele num: 66738
num of homozygotes: 0

DP
type: SiteQuality
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FS
type: SiteQuality
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MQRankSum
type: SiteQuality
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BaseQRankSum
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QD
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MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -6.54e-1

ReadPosRankSum
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498441620714457e-5
allele num: 66736
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

East Asian
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allele count: 0
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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African
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allele frequency: 0.0e0
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South Asian
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MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
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InbreedingCoeff
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QD
type: SiteQuality
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FS
type: SiteQuality
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BaseQRankSum
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ClippingRankSum
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DP
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VQSLOD
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ReadPosRankSum
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GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

Latino
type: Population
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allele frequency: 8.641548565502938e-5
allele num: 11572
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 16512
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

East Asian
type: Population
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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: 900
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 5.033397e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -2.76e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

FS
type: SiteQuality
SIO_000300: 3.855e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.35e0

VQSLOD
type: SiteQuality
SIO_000300: 2.67e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.0e0

QD
type: SiteQuality
SIO_000300: 1.521e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.8e-1

GenotypeQuality
all individuals: 269
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58264
bin: 9.75e1
variant carriers: 2

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

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.996883241428914e-5
allele num: 66736
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.97e0

DP
type: SiteQuality
SIO_000300: 5.033327e6

VQSLOD
type: SiteQuality
SIO_000300: 3.87e-1

FS
type: SiteQuality
SIO_000300: 5.2e-1

MQ
type: SiteQuality
SIO_000300: 5.947e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.01e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.34e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.1e-1

QD
type: SiteQuality
SIO_000300: 1.23e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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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GenotypeQuality
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variant carriers: 0

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 5.2e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.97e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.34e-1

MQ
type: SiteQuality
SIO_000300: 5.947e1

QD
type: SiteQuality
SIO_000300: 1.23e1

VQSLOD
type: SiteQuality
SIO_000300: 3.87e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.1e-1

DP
type: SiteQuality
SIO_000300: 5.033327e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 3.01e-1

GenotypeQuality
all individuals: 1
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 269
bin: 8.75e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498441620714457e-5
allele num: 66736
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.8e-1

QD
type: SiteQuality
SIO_000300: 1.106e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.38e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.054e0

VQSLOD
type: SiteQuality
SIO_000300: -3.183e-1

DP
type: SiteQuality
SIO_000300: 5.033317e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.608e0

MQ
type: SiteQuality
SIO_000300: 5.942e1

GenotypeQuality
all individuals: 6
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 243
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.75e1
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GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 269
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.996793431028799e-5
allele num: 66738
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.67e-1

MQ
type: SiteQuality
SIO_000300: 5.974e1

VQSLOD
type: SiteQuality
SIO_000300: 5.79e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.14e0

QD
type: SiteQuality
SIO_000300: 1.47e1

FS
type: SiteQuality
SIO_000300: 5.590000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.62e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

DP
type: SiteQuality
SIO_000300: 5.033305e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.45e0

GenotypeQuality
all individuals: 244
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498441620714457e-5
allele num: 66736
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 8.69e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.452e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.1e0

QD
type: SiteQuality
SIO_000300: 1.092e1

DP
type: SiteQuality
SIO_000300: 5.033282e6

MQ
type: SiteQuality
SIO_000300: 5.922e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.034e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.781e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.912e0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 244
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
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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bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.159285879897983e-4
allele num: 8626
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

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

BaseQRankSum
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SIO_000300: -1.096e0

DP
type: SiteQuality
SIO_000300: 5.033086e6

ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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VQSLOD
type: SiteQuality
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QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 5.0e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -3.03e-1

MQ
type: SiteQuality
SIO_000300: 5.567e1

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 2.25e1
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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: 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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variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.159285879897983e-4
allele num: 8626
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66738
num of homozygotes: 0

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

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

Other
type: Population
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ClippingRankSum
type: SiteQuality
SIO_000300: 3.86e-1

VQSLOD
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DP
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BaseQRankSum
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SIO_000300: -2.001e0

MQRankSum
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InbreedingCoeff
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QD
type: SiteQuality
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MQ
type: SiteQuality
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FS
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SIO_000300: 2.391e0

ReadPosRankSum
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SIO_000300: 1.07e0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498441620714457e-5
allele num: 66736
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
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allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -5.98e-1

DP
type: SiteQuality
SIO_000300: 5.033063e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.79e-1

FS
type: SiteQuality
SIO_000300: 1.597e0

VQSLOD
type: SiteQuality
SIO_000300: 1.09e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.26e-1

MQ
type: SiteQuality
SIO_000300: 5.91e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.97e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

QD
type: SiteQuality
SIO_000300: 1.22e1

GenotypeQuality
all individuals: 9
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 248
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 268
bin: 8.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 403
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 314
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 235
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 155
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58276
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 12
bin: 4.75e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 1.020199959192002e-4
allele num: 9802
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.81e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.45e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.63e-1

FS
type: SiteQuality
SIO_000300: 1.665e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.28e-1

MQ
type: SiteQuality
SIO_000300: 5.954e1

DP
type: SiteQuality
SIO_000300: 5.033027e6

QD
type: SiteQuality
SIO_000300: 1.21e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.704e0

GenotypeQuality
all individuals: 2
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59469
bin: 9.75e1
variant carriers: 1

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

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

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

GenotypeQuality
all individuals: 3
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 101
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 6.75e1
variant carriers: 0

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

Other
type: Population
allele count: 1
allele frequency: 1.111111111111111e-3
allele num: 900
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9798
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66728
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 3.213e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.06e-2

MQ
type: SiteQuality
SIO_000300: 5.97e1

MQRankSum
type: SiteQuality
SIO_000300: 9.4e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.53e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.06e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.96e0

DP
type: SiteQuality
SIO_000300: 5.991483e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.37e-1

GenotypeQuality
all individuals: 7
bin: 2.75e1
variant carriers: 3

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

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

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

GenotypeQuality
all individuals: 8
bin: 1.25e1
variant carriers: 5

GenotypeQuality
all individuals: 59
bin: 8.75e1
variant carriers: 23

GenotypeQuality
all individuals: 12
bin: 5.75e1
variant carriers: 8

GenotypeQuality
all individuals: 3
bin: 2.25e1
variant carriers: 2

GenotypeQuality
all individuals: 18
bin: 7.5e0
variant carriers: 10

GenotypeQuality
all individuals: 10
bin: 5.25e1
variant carriers: 8

GenotypeQuality
all individuals: 134
bin: 9.25e1
variant carriers: 66

GenotypeQuality
all individuals: 96
bin: 7.75e1
variant carriers: 31

GenotypeQuality
all individuals: 59469
bin: 9.75e1
variant carriers: 58643

GenotypeQuality
all individuals: 10
bin: 4.75e1
variant carriers: 8

GenotypeQuality
all individuals: 6
bin: 1.75e1
variant carriers: 4

GenotypeQuality
all individuals: 124
bin: 6.75e1
variant carriers: 19

GenotypeQuality
all individuals: 264
bin: 6.25e1
variant carriers: 13

East Asian
type: Population
allele count: 6659
allele frequency: 7.728644382544104e-1
allele num: 8616
num of homozygotes: 2581

African
type: Population
allele count: 6946
allele frequency: 7.089201877934272e-1
allele num: 9798
num of homozygotes: 2443

South Asian
type: Population
allele count: 15630
allele frequency: 9.465843023255814e-1
allele num: 16512
num of homozygotes: 7418

European (Non-Finnish)
type: Population
allele count: 57691
allele frequency: 8.64569595971706e-1
allele num: 66728
num of homozygotes: 24929

Latino
type: Population
allele count: 9660
allele frequency: 8.350622406639004e-1
allele num: 11568
num of homozygotes: 4035

European (Finnish)
type: Population
allele count: 5813
allele frequency: 8.791591046581972e-1
allele num: 6612
num of homozygotes: 2561

Other
type: Population
allele count: 806
allele frequency: 8.955555555555555e-1
allele num: 900
num of homozygotes: 360

BaseQRankSum
type: SiteQuality
SIO_000300: 3.53e0

MQRankSum
type: SiteQuality
SIO_000300: 9.4e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.06e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.06e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.96e0

DP
type: SiteQuality
SIO_000300: 5.991483e6

QD
type: SiteQuality
SIO_000300: 3.213e1

MQ
type: SiteQuality
SIO_000300: 5.97e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.37e-1

GenotypeQuality
all individuals: 4030
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1525
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2788
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10577
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2807
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34172
bin: 9.75e1
variant carriers: 2

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9800
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.996973057212216e-5
allele num: 66734
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

East 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: 6614
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.173e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.09e-1