14-104194161-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 104194161
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 104194161
    reference: chr 14
allele count: 1
allele frequency: 8.399832003359932e-6
allele num: 119050
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000452301
  ensembl transcript: ENST00000556610
  gene symbol: ZFYVE21
  hgvsc: ENST00000556610.1:c.139-1084G>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000216602
  ensembl transcript: ENST00000216602
  gene symbol: ZFYVE21
  hgvsc: ENST00000216602.6:c.268G>T
  hgvsp: ENSP00000216602.6:p.Val90Leu
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554630
  gene symbol: ZFYVE21
  hgvsc: ENST00000554630.1:n.279G>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000310543
  ensembl transcript: ENST00000311141
  gene symbol: ZFYVE21
  hgvsc: ENST00000311141.2:c.268G>T
  hgvsp: ENSP00000310543.2:p.Val90Leu
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000450746
  ensembl transcript: ENST00000553512
  gene symbol: ZFYVE21
  hgvsc: ENST00000553512.1:c.*173G>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000553724
  gene symbol: ZFYVE21
  hgvsc: ENST00000553724.1:n.371G>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554255
  gene symbol: ZFYVE21
  hgvsc: ENST00000554255.1:n.302G>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000555501
  gene symbol: ZFYVE21
  hgvsc: ENST00000555501.1:n.3316G>T
  variant of: http://identifiers.org/hgnc/20760
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 906
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5710
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38751
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11802
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1334
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1063
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39288
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2221
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 952
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Val90Leu
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: African
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

14-104194169-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 104194169
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 104194169
    reference: chr 14
allele count: 15
allele frequency: 1.259551599630532e-4
allele num: 119090
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554255
  gene symbol: ZFYVE21
  hgvsc: ENST00000554255.1:n.310C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000555501
  gene symbol: ZFYVE21
  hgvsc: ENST00000555501.1:n.3324C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000450746
  ensembl transcript: ENST00000553512
  gene symbol: ZFYVE21
  hgvsc: ENST00000553512.1:c.*181C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000452301
  ensembl transcript: ENST00000556610
  gene symbol: ZFYVE21
  hgvsc: ENST00000556610.1:c.139-1076C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000310543
  ensembl transcript: ENST00000311141
  gene symbol: ZFYVE21
  hgvsc: ENST00000311141.2:c.276C>T
  hgvsp: ENST00000311141.2:c.276C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554630
  gene symbol: ZFYVE21
  hgvsc: ENST00000554630.1:n.287C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000216602
  ensembl transcript: ENST00000216602
  gene symbol: ZFYVE21
  hgvsc: ENST00000216602.6:c.276C>T
  hgvsp: ENST00000216602.6:c.276C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000553724
  gene symbol: ZFYVE21
  hgvsc: ENST00000553724.1:n.379C>T
  variant of: http://identifiers.org/hgnc/20760
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38560
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11794
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1355
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5733
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7575
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 282
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1112
  bin: 9.75e1
  variant carriers: 15
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 222
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 168
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Pro92Pro
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: DP
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ

14-104194170-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 104194170
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 104194170
    reference: chr 14
allele count: 1
allele frequency: 8.396587626788473e-6
allele num: 119096
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000216602
  ensembl transcript: ENST00000216602
  gene symbol: ZFYVE21
  hgvsc: ENST00000216602.6:c.277G>A
  hgvsp: ENSP00000216602.6:p.Val93Met
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554630
  gene symbol: ZFYVE21
  hgvsc: ENST00000554630.1:n.288G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000450746
  ensembl transcript: ENST00000553512
  gene symbol: ZFYVE21
  hgvsc: ENST00000553512.1:c.*182G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000555501
  gene symbol: ZFYVE21
  hgvsc: ENST00000555501.1:n.3325G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000452301
  ensembl transcript: ENST00000556610
  gene symbol: ZFYVE21
  hgvsc: ENST00000556610.1:c.139-1075G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554255
  gene symbol: ZFYVE21
  hgvsc: ENST00000554255.1:n.311G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000310543
  ensembl transcript: ENST00000311141
  gene symbol: ZFYVE21
  hgvsc: ENST00000311141.2:c.277G>A
  hgvsp: ENSP00000310543.2:p.Val93Met
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000553724
  gene symbol: ZFYVE21
  hgvsc: ENST00000553724.1:n.380G>A
  variant of: http://identifiers.org/hgnc/20760
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38485
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11800
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5747
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1353
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 292
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 240
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 952
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 220
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Val93Met
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD

14-104194176-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 104194176
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 104194176
    reference: chr 14
allele count: 1
allele frequency: 8.388276544701125e-6
allele num: 119214
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000310543
  ensembl transcript: ENST00000311141
  gene symbol: ZFYVE21
  hgvsc: ENST00000311141.2:c.283C>T
  hgvsp: ENSP00000310543.2:p.Gln95Ter
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000553724
  gene symbol: ZFYVE21
  hgvsc: ENST00000553724.1:n.386C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000452301
  ensembl transcript: ENST00000556610
  gene symbol: ZFYVE21
  hgvsc: ENST00000556610.1:c.139-1069C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000555501
  gene symbol: ZFYVE21
  hgvsc: ENST00000555501.1:n.3331C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000216602
  ensembl transcript: ENST00000216602
  gene symbol: ZFYVE21
  hgvsc: ENST00000216602.6:c.283C>T
  hgvsp: ENSP00000216602.6:p.Gln95Ter
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000450746
  ensembl transcript: ENST00000553512
  gene symbol: ZFYVE21
  hgvsc: ENST00000553512.1:c.*188C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554255
  gene symbol: ZFYVE21
  hgvsc: ENST00000554255.1:n.317C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554630
  gene symbol: ZFYVE21
  hgvsc: ENST00000554630.1:n.294C>T
  variant of: http://identifiers.org/hgnc/20760
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1358
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5775
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38411
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11869
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2752
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 979
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3346
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 271
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 197
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Gln95Ter
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: African
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: DP

14-104194181-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 104194181
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 104194181
    reference: chr 14
allele count: 0
allele frequency: 0.0e0
allele num: 119254
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000452301
  ensembl transcript: ENST00000556610
  gene symbol: ZFYVE21
  hgvsc: ENST00000556610.1:c.139-1064C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000555501
  gene symbol: ZFYVE21
  hgvsc: ENST00000555501.1:n.3336C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554630
  gene symbol: ZFYVE21
  hgvsc: ENST00000554630.1:n.299C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554255
  gene symbol: ZFYVE21
  hgvsc: ENST00000554255.1:n.322C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000310543
  ensembl transcript: ENST00000311141
  gene symbol: ZFYVE21
  hgvsc: ENST00000311141.2:c.288C>T
  hgvsp: ENST00000311141.2:c.288C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000216602
  ensembl transcript: ENST00000216602
  gene symbol: ZFYVE21
  hgvsc: ENST00000216602.6:c.288C>T
  hgvsp: ENST00000216602.6:c.288C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000553724
  gene symbol: ZFYVE21
  hgvsc: ENST00000553724.1:n.391C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000450746
  ensembl transcript: ENST00000553512
  gene symbol: ZFYVE21
  hgvsc: ENST00000553512.1:c.*193C>T
  variant of: http://identifiers.org/hgnc/20760
canonical: true
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11834
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5789
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1367
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38385
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 313
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 942
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 955
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Cys96Cys
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD

14-104194182-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 104194182
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 104194182
    reference: chr 14
allele count: 3
allele frequency: 2.514331690636629e-5
allele num: 119316
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554255
  gene symbol: ZFYVE21
  hgvsc: ENST00000554255.1:n.323G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000450746
  ensembl transcript: ENST00000553512
  gene symbol: ZFYVE21
  hgvsc: ENST00000553512.1:c.*194G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000310543
  ensembl transcript: ENST00000311141
  gene symbol: ZFYVE21
  hgvsc: ENST00000311141.2:c.289G>A
  hgvsp: ENSP00000310543.2:p.Ala97Thr
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000452301
  ensembl transcript: ENST00000556610
  gene symbol: ZFYVE21
  hgvsc: ENST00000556610.1:c.139-1063G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000216602
  ensembl transcript: ENST00000216602
  gene symbol: ZFYVE21
  hgvsc: ENST00000216602.6:c.289G>A
  hgvsp: ENSP00000216602.6:p.Ala97Thr
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000555501
  gene symbol: ZFYVE21
  hgvsc: ENST00000555501.1:n.3337G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000553724
  gene symbol: ZFYVE21
  hgvsc: ENST00000553724.1:n.392G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554630
  gene symbol: ZFYVE21
  hgvsc: ENST00000554630.1:n.300G>A
  variant of: http://identifiers.org/hgnc/20760
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5791
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1363
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38377
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11868
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2271
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7581
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1157
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 945
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2764
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 207
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ala97Thr
num of homozygotes: 0
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff

14-104194183-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 104194183
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 104194183
    reference: chr 14
allele count: 1
allele frequency: 8.379981899239097e-6
allele num: 119332
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554255
  gene symbol: ZFYVE21
  hgvsc: ENST00000554255.1:n.324C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000450746
  ensembl transcript: ENST00000553512
  gene symbol: ZFYVE21
  hgvsc: ENST00000553512.1:c.*195C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000553724
  gene symbol: ZFYVE21
  hgvsc: ENST00000553724.1:n.393C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000555501
  gene symbol: ZFYVE21
  hgvsc: ENST00000555501.1:n.3338C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000216602
  ensembl transcript: ENST00000216602
  gene symbol: ZFYVE21
  hgvsc: ENST00000216602.6:c.290C>T
  hgvsp: ENSP00000216602.6:p.Ala97Val
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000310543
  ensembl transcript: ENST00000311141
  gene symbol: ZFYVE21
  hgvsc: ENST00000311141.2:c.290C>T
  hgvsp: ENSP00000310543.2:p.Ala97Val
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000452301
  ensembl transcript: ENST00000556610
  gene symbol: ZFYVE21
  hgvsc: ENST00000556610.1:c.139-1062C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554630
  gene symbol: ZFYVE21
  hgvsc: ENST00000554630.1:n.301C>T
  variant of: http://identifiers.org/hgnc/20760
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1364
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11865
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5803
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38382
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 958
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 287
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 915
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 945
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2770
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ala97Val
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD

14-104194184-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 104194184
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 104194184
    reference: chr 14
allele count: 1
allele frequency: 8.379139294811638e-6
allele num: 119344
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554630
  gene symbol: ZFYVE21
  hgvsc: ENST00000554630.1:n.302G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000310543
  ensembl transcript: ENST00000311141
  gene symbol: ZFYVE21
  hgvsc: ENST00000311141.2:c.291G>A
  hgvsp: ENST00000311141.2:c.291G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554255
  gene symbol: ZFYVE21
  hgvsc: ENST00000554255.1:n.325G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000216602
  ensembl transcript: ENST00000216602
  gene symbol: ZFYVE21
  hgvsc: ENST00000216602.6:c.291G>A
  hgvsp: ENST00000216602.6:c.291G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000450746
  ensembl transcript: ENST00000553512
  gene symbol: ZFYVE21
  hgvsc: ENST00000553512.1:c.*196G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000553724
  gene symbol: ZFYVE21
  hgvsc: ENST00000553724.1:n.394G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000452301
  ensembl transcript: ENST00000556610
  gene symbol: ZFYVE21
  hgvsc: ENST00000556610.1:c.139-1061G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000555501
  gene symbol: ZFYVE21
  hgvsc: ENST00000555501.1:n.3339G>A
  variant of: http://identifiers.org/hgnc/20760
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11888
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1379
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38341
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5825
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 205
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 964
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 238
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ala97Ala
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: QD

14-104194189-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 104194189
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 104194189
    reference: chr 14
allele count: 1
allele frequency: 8.373946976167747e-6
allele num: 119418
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000553724
  gene symbol: ZFYVE21
  hgvsc: ENST00000553724.1:n.399G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000450746
  ensembl transcript: ENST00000553512
  gene symbol: ZFYVE21
  hgvsc: ENST00000553512.1:c.*201G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000452301
  ensembl transcript: ENST00000556610
  gene symbol: ZFYVE21
  hgvsc: ENST00000556610.1:c.139-1056G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554255
  gene symbol: ZFYVE21
  hgvsc: ENST00000554255.1:n.330G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554630
  gene symbol: ZFYVE21
  hgvsc: ENST00000554630.1:n.307G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000310543
  ensembl transcript: ENST00000311141
  gene symbol: ZFYVE21
  hgvsc: ENST00000311141.2:c.296G>A
  hgvsp: ENSP00000310543.2:p.Cys99Tyr
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000216602
  ensembl transcript: ENST00000216602
  gene symbol: ZFYVE21
  hgvsc: ENST00000216602.6:c.296G>A
  hgvsp: ENSP00000216602.6:p.Cys99Tyr
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000555501
  gene symbol: ZFYVE21
  hgvsc: ENST00000555501.1:n.3344G>A
  variant of: http://identifiers.org/hgnc/20760
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5850
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1395
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11887
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38361
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 299
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38640
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 927
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1176
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 254
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 299
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 181
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Cys99Tyr
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

14-104194191-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 104194191
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 104194191
    reference: chr 14
allele count: 1
allele frequency: 8.37436773523599e-6
allele num: 119412
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554255
  gene symbol: ZFYVE21
  hgvsc: ENST00000554255.1:n.332G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000450746
  ensembl transcript: ENST00000553512
  gene symbol: ZFYVE21
  hgvsc: ENST00000553512.1:c.*203G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000310543
  ensembl transcript: ENST00000311141
  gene symbol: ZFYVE21
  hgvsc: ENST00000311141.2:c.298G>A
  hgvsp: ENSP00000310543.2:p.Ala100Thr
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000216602
  ensembl transcript: ENST00000216602
  gene symbol: ZFYVE21
  hgvsc: ENST00000216602.6:c.298G>A
  hgvsp: ENSP00000216602.6:p.Ala100Thr
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000553724
  gene symbol: ZFYVE21
  hgvsc: ENST00000553724.1:n.401G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000555501
  gene symbol: ZFYVE21
  hgvsc: ENST00000555501.1:n.3346G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554630
  gene symbol: ZFYVE21
  hgvsc: ENST00000554630.1:n.309G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000452301
  ensembl transcript: ENST00000556610
  gene symbol: ZFYVE21
  hgvsc: ENST00000556610.1:c.139-1054G>A
  variant of: http://identifiers.org/hgnc/20760
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5929
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38219
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1432
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11917
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 176
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 193
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 308
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 185
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 232
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ala100Thr
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: Latino
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

14-104194192-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 104194192
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 104194192
    reference: chr 14
allele count: 2
allele frequency: 1.674817444898506e-5
allele num: 119416
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000555501
  gene symbol: ZFYVE21
  hgvsc: ENST00000555501.1:n.3347C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554630
  gene symbol: ZFYVE21
  hgvsc: ENST00000554630.1:n.310C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000310543
  ensembl transcript: ENST00000311141
  gene symbol: ZFYVE21
  hgvsc: ENST00000311141.2:c.299C>T
  hgvsp: ENSP00000310543.2:p.Ala100Val
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000553724
  gene symbol: ZFYVE21
  hgvsc: ENST00000553724.1:n.402C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000216602
  ensembl transcript: ENST00000216602
  gene symbol: ZFYVE21
  hgvsc: ENST00000216602.6:c.299C>T
  hgvsp: ENSP00000216602.6:p.Ala100Val
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000450746
  ensembl transcript: ENST00000553512
  gene symbol: ZFYVE21
  hgvsc: ENST00000553512.1:c.*204C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554255
  gene symbol: ZFYVE21
  hgvsc: ENST00000554255.1:n.333C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000452301
  ensembl transcript: ENST00000556610
  gene symbol: ZFYVE21
  hgvsc: ENST00000556610.1:c.139-1053C>T
  variant of: http://identifiers.org/hgnc/20760
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1441
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11936
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38175
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5955
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 864
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 259
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 311
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 334
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 225
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ala100Val
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ

14-104194194-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 104194194
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 104194194
    reference: chr 14
allele count: 1
allele frequency: 8.371142995864656e-6
allele num: 119458
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000216602
  ensembl transcript: ENST00000216602
  gene symbol: ZFYVE21
  hgvsc: ENST00000216602.6:c.301C>T
  hgvsp: ENSP00000216602.6:p.Leu101Phe
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000450746
  ensembl transcript: ENST00000553512
  gene symbol: ZFYVE21
  hgvsc: ENST00000553512.1:c.*206C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554255
  gene symbol: ZFYVE21
  hgvsc: ENST00000554255.1:n.335C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000553724
  gene symbol: ZFYVE21
  hgvsc: ENST00000553724.1:n.404C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554630
  gene symbol: ZFYVE21
  hgvsc: ENST00000554630.1:n.312C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000310543
  ensembl transcript: ENST00000311141
  gene symbol: ZFYVE21
  hgvsc: ENST00000311141.2:c.301C>T
  hgvsp: ENSP00000310543.2:p.Leu101Phe
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000555501
  gene symbol: ZFYVE21
  hgvsc: ENST00000555501.1:n.3349C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000452301
  ensembl transcript: ENST00000556610
  gene symbol: ZFYVE21
  hgvsc: ENST00000556610.1:c.139-1051C>T
  variant of: http://identifiers.org/hgnc/20760
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11968
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1451
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38119
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5992
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2835
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 318
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Leu101Phe
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: Other
population: European (Finnish)
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ

14-104194196-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 104194196
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 104194196
    reference: chr 14
allele count: 109278
allele frequency: 9.080469321279e-1
allele num: 120344
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000553724
  gene symbol: ZFYVE21
  hgvsc: ENST00000553724.1:n.406C>G
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554630
  gene symbol: ZFYVE21
  hgvsc: ENST00000554630.1:n.314C>G
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000452301
  ensembl transcript: ENST00000556610
  gene symbol: ZFYVE21
  hgvsc: ENST00000556610.1:c.139-1049C>G
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000216602
  ensembl transcript: ENST00000216602
  gene symbol: ZFYVE21
  hgvsc: ENST00000216602.6:c.303C>G
  hgvsp: ENST00000216602.6:c.303C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554255
  gene symbol: ZFYVE21
  hgvsc: ENST00000554255.1:n.337C>G
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000450746
  ensembl transcript: ENST00000553512
  gene symbol: ZFYVE21
  hgvsc: ENST00000553512.1:c.*208C>G
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000310543
  ensembl transcript: ENST00000311141
  gene symbol: ZFYVE21
  hgvsc: ENST00000311141.2:c.303C>G
  hgvsp: ENST00000311141.2:c.303C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000555501
  gene symbol: ZFYVE21
  hgvsc: ENST00000555501.1:n.3351C>G
  variant of: http://identifiers.org/hgnc/20760
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 1.25e1
  variant carriers: 547
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 1.75e1
  variant carriers: 858
genotype depth: GenotypeDepth
  all individuals: 1587
  bin: 8.75e1
  variant carriers: 1587
genotype depth: GenotypeDepth
  all individuals: 4939
  bin: 6.25e1
  variant carriers: 4938
genotype depth: GenotypeDepth
  all individuals: 2050
  bin: 2.25e1
  variant carriers: 1449
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 7.5e0
  variant carriers: 344
genotype depth: GenotypeDepth
  all individuals: 3438
  bin: 7.25e1
  variant carriers: 3434
genotype depth: GenotypeDepth
  all individuals: 5906
  bin: 5.25e1
  variant carriers: 5902
genotype depth: GenotypeDepth
  all individuals: 2334
  bin: 2.75e1
  variant carriers: 2158
genotype depth: GenotypeDepth
  all individuals: 4185
  bin: 6.75e1
  variant carriers: 4183
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 2.5e0
  variant carriers: 67
genotype depth: GenotypeDepth
  all individuals: 5361
  bin: 4.25e1
  variant carriers: 5358
genotype depth: GenotypeDepth
  all individuals: 5430
  bin: 5.75e1
  variant carriers: 5426
genotype depth: GenotypeDepth
  all individuals: 1187
  bin: 9.25e1
  variant carriers: 1186
genotype depth: GenotypeDepth
  all individuals: 2015
  bin: 8.25e1
  variant carriers: 2014
genotype depth: GenotypeDepth
  all individuals: 2758
  bin: 7.75e1
  variant carriers: 2757
genotype depth: GenotypeDepth
  all individuals: 4522
  bin: 3.75e1
  variant carriers: 4514
genotype depth: GenotypeDepth
  all individuals: 3253
  bin: 3.25e1
  variant carriers: 3207
genotype depth: GenotypeDepth
  all individuals: 3975
  bin: 9.75e1
  variant carriers: 3973
genotype depth: GenotypeDepth
  all individuals: 5857
  bin: 4.75e1
  variant carriers: 5855
genotype quality: GenotypeQuality
  all individuals: 827
  bin: 8.25e1
  variant carriers: 824
genotype quality: GenotypeQuality
  all individuals: 53597
  bin: 9.75e1
  variant carriers: 53597
genotype quality: GenotypeQuality
  all individuals: 281
  bin: 4.75e1
  variant carriers: 276
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 4.25e1
  variant carriers: 136
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 2.25e1
  variant carriers: 141
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 2.75e1
  variant carriers: 88
genotype quality: GenotypeQuality
  all individuals: 389
  bin: 7.25e1
  variant carriers: 370
hgvs: p.Leu101Leu
num of homozygotes: 49962
population: Other
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD

14-104194200-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 104194200
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 104194200
    reference: chr 14
allele count: 1
allele frequency: 8.386869517084054e-6
allele num: 119234
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000452301
  ensembl transcript: ENST00000556610
  gene symbol: ZFYVE21
  hgvsc: ENST00000556610.1:c.139-1045T>C
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000553724
  gene symbol: ZFYVE21
  hgvsc: ENST00000553724.1:n.410T>C
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000450746
  ensembl transcript: ENST00000553512
  gene symbol: ZFYVE21
  hgvsc: ENST00000553512.1:c.*212T>C
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554630
  gene symbol: ZFYVE21
  hgvsc: ENST00000554630.1:n.318T>C
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000555501
  gene symbol: ZFYVE21
  hgvsc: ENST00000555501.1:n.3355T>C
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554255
  gene symbol: ZFYVE21
  hgvsc: ENST00000554255.1:n.341T>C
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000216602
  ensembl transcript: ENST00000216602
  gene symbol: ZFYVE21
  hgvsc: ENST00000216602.6:c.307T>C
  hgvsp: ENSP00000216602.6:p.Ser103Pro
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000310543
  ensembl transcript: ENST00000311141
  gene symbol: ZFYVE21
  hgvsc: ENST00000311141.2:c.307T>C
  hgvsp: ENSP00000310543.2:p.Ser103Pro
  variant of: http://identifiers.org/hgnc/20760
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1430
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26613
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4286
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8576
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15115
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 194
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 202
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2933
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1644
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3267
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1284
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ser103Pro
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ

14-104194211-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 104194211
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 104194211
    reference: chr 14
allele count: 2
allele frequency: 1.681350460690026e-5
allele num: 118952
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000450746
  ensembl transcript: ENST00000553512
  gene symbol: ZFYVE21
  hgvsc: ENST00000553512.1:c.*223G>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554255
  gene symbol: ZFYVE21
  hgvsc: ENST00000554255.1:n.352G>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000555501
  gene symbol: ZFYVE21
  hgvsc: ENST00000555501.1:n.3366G>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554630
  gene symbol: ZFYVE21
  hgvsc: ENST00000554630.1:n.329G>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000452301
  ensembl transcript: ENST00000556610
  gene symbol: ZFYVE21
  hgvsc: ENST00000556610.1:c.139-1034G>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000553724
  gene symbol: ZFYVE21
  hgvsc: ENST00000553724.1:n.421G>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000216602
  ensembl transcript: ENST00000216602
  gene symbol: ZFYVE21
  hgvsc: ENST00000216602.6:c.318G>T
  hgvsp: ENSP00000216602.6:p.Glu106Asp
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000310543
  ensembl transcript: ENST00000311141
  gene symbol: ZFYVE21
  hgvsc: ENST00000311141.2:c.318G>T
  hgvsp: ENSP00000310543.2:p.Glu106Asp
  variant of: http://identifiers.org/hgnc/20760
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4266
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26486
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15049
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1422
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8589
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 493
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 222
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2156
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1601
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2898
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Glu106Asp
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: Other
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: QD

14-104194212-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 104194212
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 104194212
    reference: chr 14
allele count: 1
allele frequency: 8.410004541402452e-6
allele num: 118906
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000450746
  ensembl transcript: ENST00000553512
  gene symbol: ZFYVE21
  hgvsc: ENST00000553512.1:c.*224G>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000310543
  ensembl transcript: ENST00000311141
  gene symbol: ZFYVE21
  hgvsc: ENST00000311141.2:c.319G>T
  hgvsp: ENSP00000310543.2:p.Ala107Ser
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554255
  gene symbol: ZFYVE21
  hgvsc: ENST00000554255.1:n.353G>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000553724
  gene symbol: ZFYVE21
  hgvsc: ENST00000553724.1:n.422G>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000555501
  gene symbol: ZFYVE21
  hgvsc: ENST00000555501.1:n.3367G>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000216602
  ensembl transcript: ENST00000216602
  gene symbol: ZFYVE21
  hgvsc: ENST00000216602.6:c.319G>T
  hgvsp: ENSP00000216602.6:p.Ala107Ser
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554630
  gene symbol: ZFYVE21
  hgvsc: ENST00000554630.1:n.330G>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000452301
  ensembl transcript: ENST00000556610
  gene symbol: ZFYVE21
  hgvsc: ENST00000556610.1:c.139-1033G>T
  variant of: http://identifiers.org/hgnc/20760
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15045
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1042
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1422
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26452
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8576
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1071
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4262
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1597
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 189
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3204
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10744
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 226
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ala107Ser
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD

14-104194214-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 104194214
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 104194214
    reference: chr 14
allele count: 2
allele frequency: 1.683870207284422e-5
allele num: 118774
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000310543
  ensembl transcript: ENST00000311141
  gene symbol: ZFYVE21
  hgvsc: ENST00000311141.2:c.321G>A
  hgvsp: ENST00000311141.2:c.321G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554630
  gene symbol: ZFYVE21
  hgvsc: ENST00000554630.1:n.332G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000450746
  ensembl transcript: ENST00000553512
  gene symbol: ZFYVE21
  hgvsc: ENST00000553512.1:c.*226G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000553724
  gene symbol: ZFYVE21
  hgvsc: ENST00000553724.1:n.424G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000216602
  ensembl transcript: ENST00000216602
  gene symbol: ZFYVE21
  hgvsc: ENST00000216602.6:c.321G>A
  hgvsp: ENST00000216602.6:c.321G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000555501
  gene symbol: ZFYVE21
  hgvsc: ENST00000555501.1:n.3369G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554255
  gene symbol: ZFYVE21
  hgvsc: ENST00000554255.1:n.355G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000452301
  ensembl transcript: ENST00000556610
  gene symbol: ZFYVE21
  hgvsc: ENST00000556610.1:c.139-1031G>A
  variant of: http://identifiers.org/hgnc/20760
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1094
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4254
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1418
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1227
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8470
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26365
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15008
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35965
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10675
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 264
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2150
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ala107Ala
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Other
reference allele: G
site quality: DP
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ

14-104194224-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 104194224
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 104194224
    reference: chr 14
allele count: 4
allele frequency: 3.380091262464087e-5
allele num: 118340
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000450746
  ensembl transcript: ENST00000553512
  gene symbol: ZFYVE21
  hgvsc: ENST00000553512.1:c.*236G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554630
  gene symbol: ZFYVE21
  hgvsc: ENST00000554630.1:n.342G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000553724
  gene symbol: ZFYVE21
  hgvsc: ENST00000553724.1:n.434G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000452301
  ensembl transcript: ENST00000556610
  gene symbol: ZFYVE21
  hgvsc: ENST00000556610.1:c.139-1021G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554255
  gene symbol: ZFYVE21
  hgvsc: ENST00000554255.1:n.365G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000216602
  ensembl transcript: ENST00000216602
  gene symbol: ZFYVE21
  hgvsc: ENST00000216602.6:c.331G>A
  hgvsp: ENSP00000216602.6:p.Asp111Asn
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000555501
  gene symbol: ZFYVE21
  hgvsc: ENST00000555501.1:n.3379G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000310543
  ensembl transcript: ENST00000311141
  gene symbol: ZFYVE21
  hgvsc: ENST00000311141.2:c.331G>A
  hgvsp: ENSP00000310543.2:p.Asp111Asn
  variant of: http://identifiers.org/hgnc/20760
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25927
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14780
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4224
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1257
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1823
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8307
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35418
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2818
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 239
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Asp111Asn
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum

14-104194225-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 104194225
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 104194225
    reference: chr 14
allele count: 1
allele frequency: 8.45394291897741e-6
allele num: 118288
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554630
  gene symbol: ZFYVE21
  hgvsc: ENST00000554630.1:n.343A>G
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000553724
  gene symbol: ZFYVE21
  hgvsc: ENST00000553724.1:n.435A>G
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000450746
  ensembl transcript: ENST00000553512
  gene symbol: ZFYVE21
  hgvsc: ENST00000553512.1:c.*237A>G
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000555501
  gene symbol: ZFYVE21
  hgvsc: ENST00000555501.1:n.3380A>G
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000310543
  ensembl transcript: ENST00000311141
  gene symbol: ZFYVE21
  hgvsc: ENST00000311141.2:c.332A>G
  hgvsp: ENSP00000310543.2:p.Asp111Gly
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554255
  gene symbol: ZFYVE21
  hgvsc: ENST00000554255.1:n.366A>G
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000216602
  ensembl transcript: ENST00000216602
  gene symbol: ZFYVE21
  hgvsc: ENST00000216602.6:c.332A>G
  hgvsp: ENSP00000216602.6:p.Asp111Gly
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000452301
  ensembl transcript: ENST00000556610
  gene symbol: ZFYVE21
  hgvsc: ENST00000556610.1:c.139-1020A>G
  variant of: http://identifiers.org/hgnc/20760
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1919
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14721
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8300
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25856
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1410
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1284
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4219
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10527
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2513
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 246
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1529
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Asp111Gly
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
reference allele: A
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum

14-104194226-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 104194226
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 104194226
    reference: chr 14
allele count: 1
allele frequency: 8.465250148141878e-6
allele num: 118130
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000555501
  gene symbol: ZFYVE21
  hgvsc: ENST00000555501.1:n.3381C>G
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000216602
  ensembl transcript: ENST00000216602
  gene symbol: ZFYVE21
  hgvsc: ENST00000216602.6:c.333C>G
  hgvsp: ENSP00000216602.6:p.Asp111Glu
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000553724
  gene symbol: ZFYVE21
  hgvsc: ENST00000553724.1:n.436C>G
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000310543
  ensembl transcript: ENST00000311141
  gene symbol: ZFYVE21
  hgvsc: ENST00000311141.2:c.333C>G
  hgvsp: ENSP00000310543.2:p.Asp111Glu
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000450746
  ensembl transcript: ENST00000553512
  gene symbol: ZFYVE21
  hgvsc: ENST00000553512.1:c.*238C>G
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554630
  gene symbol: ZFYVE21
  hgvsc: ENST00000554630.1:n.344C>G
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554255
  gene symbol: ZFYVE21
  hgvsc: ENST00000554255.1:n.367C>G
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000452301
  ensembl transcript: ENST00000556610
  gene symbol: ZFYVE21
  hgvsc: ENST00000556610.1:c.139-1019C>G
  variant of: http://identifiers.org/hgnc/20760
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1409
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8156
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14675
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25615
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4219
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2201
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 467
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 260
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10445
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34752
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 464
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Asp111Glu
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: Other
population: Latino
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD

14-104194228-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 104194228
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 104194228
    reference: chr 14
allele count: 1515
allele frequency: 1.283289286440333e-2
allele num: 118056
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000555501
  gene symbol: ZFYVE21
  hgvsc: ENST00000555501.1:n.3383A>G
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000452301
  ensembl transcript: ENST00000556610
  gene symbol: ZFYVE21
  hgvsc: ENST00000556610.1:c.139-1017A>G
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000216602
  ensembl transcript: ENST00000216602
  gene symbol: ZFYVE21
  hgvsc: ENST00000216602.6:c.335A>G
  hgvsp: ENSP00000216602.6:p.Lys112Arg
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554630
  gene symbol: ZFYVE21
  hgvsc: ENST00000554630.1:n.346A>G
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000310543
  ensembl transcript: ENST00000311141
  gene symbol: ZFYVE21
  hgvsc: ENST00000311141.2:c.335A>G
  hgvsp: ENSP00000310543.2:p.Lys112Arg
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554255
  gene symbol: ZFYVE21
  hgvsc: ENST00000554255.1:n.369A>G
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000450746
  ensembl transcript: ENST00000553512
  gene symbol: ZFYVE21
  hgvsc: ENST00000553512.1:c.*240A>G
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000553724
  gene symbol: ZFYVE21
  hgvsc: ENST00000553724.1:n.438A>G
  variant of: http://identifiers.org/hgnc/20760
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1369
  bin: 7.5e0
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 25432
  bin: 2.75e1
  variant carriers: 137
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 7.25e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 8162
  bin: 2.25e1
  variant carriers: 88
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 1.75e1
  variant carriers: 44
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 5.75e1
  variant carriers: 89
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 4.75e1
  variant carriers: 192
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 5.25e1
  variant carriers: 127
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 4.25e1
  variant carriers: 198
genotype depth: GenotypeDepth
  all individuals: 2397
  bin: 1.25e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 6.25e1
  variant carriers: 67
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 4192
  bin: 3.75e1
  variant carriers: 202
genotype depth: GenotypeDepth
  all individuals: 14611
  bin: 3.25e1
  variant carriers: 177
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 6.75e1
  variant carriers: 51
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.75e1
  variant carriers: 14
genotype quality: GenotypeQuality
  all individuals: 2744
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2915
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 209
  bin: 5.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 34533
  bin: 6.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 403
  bin: 8.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 255
  bin: 7.5e0
  variant carriers: 1
hgvs: p.Lys112Arg
num of homozygotes: 17
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: A
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQRankSum

http://identifiers.org/exac.variant/14-104194228-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 104194228
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 104194228
    reference: chr 14
allele count: 2
allele frequency: 1.694111269228163e-5
allele num: 118056
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000216602
  ensembl transcript: ENST00000216602
  gene symbol: ZFYVE21
  hgvsc: ENST00000216602.6:c.335A>C
  hgvsp: ENSP00000216602.6:p.Lys112Thr
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000450746
  ensembl transcript: ENST00000553512
  gene symbol: ZFYVE21
  hgvsc: ENST00000553512.1:c.*240A>C
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554630
  gene symbol: ZFYVE21
  hgvsc: ENST00000554630.1:n.346A>C
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000555501
  gene symbol: ZFYVE21
  hgvsc: ENST00000555501.1:n.3383A>C
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000310543
  ensembl transcript: ENST00000311141
  gene symbol: ZFYVE21
  hgvsc: ENST00000311141.2:c.335A>C
  hgvsp: ENSP00000310543.2:p.Lys112Thr
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000553724
  gene symbol: ZFYVE21
  hgvsc: ENST00000553724.1:n.438A>C
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000452301
  ensembl transcript: ENST00000556610
  gene symbol: ZFYVE21
  hgvsc: ENST00000556610.1:c.139-1017A>C
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554255
  gene symbol: ZFYVE21
  hgvsc: ENST00000554255.1:n.369A>C
  variant of: http://identifiers.org/hgnc/20760
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4192
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8162
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2397
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25432
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14611
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1369
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10326
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 255
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 498
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 204
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Lys112Thr
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: African
reference allele: A
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

14-104194229-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 104194229
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 104194229
    reference: chr 14
allele count: 1
allele frequency: 8.476012883539584e-6
allele num: 117980
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000310543
  ensembl transcript: ENST00000311141
  gene symbol: ZFYVE21
  hgvsc: ENST00000311141.2:c.336G>A
  hgvsp: ENST00000311141.2:c.336G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000555501
  gene symbol: ZFYVE21
  hgvsc: ENST00000555501.1:n.3384G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554255
  gene symbol: ZFYVE21
  hgvsc: ENST00000554255.1:n.370G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000216602
  ensembl transcript: ENST00000216602
  gene symbol: ZFYVE21
  hgvsc: ENST00000216602.6:c.336G>A
  hgvsp: ENST00000216602.6:c.336G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000452301
  ensembl transcript: ENST00000556610
  gene symbol: ZFYVE21
  hgvsc: ENST00000556610.1:c.139-1016G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000450746
  ensembl transcript: ENST00000553512
  gene symbol: ZFYVE21
  hgvsc: ENST00000553512.1:c.*241G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000553724
  gene symbol: ZFYVE21
  hgvsc: ENST00000553724.1:n.439G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554630
  gene symbol: ZFYVE21
  hgvsc: ENST00000554630.1:n.347G>A
  variant of: http://identifiers.org/hgnc/20760
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1403
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2444
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4051
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8324
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25990
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14748
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35613
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 273
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 516
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3018
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1416
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10583
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Lys112Lys
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: East Asian
reference allele: G
site quality: MQ
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum

14-104194235-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 104194235
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 104194235
    reference: chr 14
allele count: 1
allele frequency: 8.510348583877996e-6
allele num: 117504
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000450746
  ensembl transcript: ENST00000553512
  gene symbol: ZFYVE21
  hgvsc: ENST00000553512.1:c.*247C>G
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000216602
  ensembl transcript: ENST00000216602
  gene symbol: ZFYVE21
  hgvsc: ENST00000216602.6:c.342C>G
  hgvsp: ENST00000216602.6:c.342C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000452301
  ensembl transcript: ENST00000556610
  gene symbol: ZFYVE21
  hgvsc: ENST00000556610.1:c.139-1010C>G
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000310543
  ensembl transcript: ENST00000311141
  gene symbol: ZFYVE21
  hgvsc: ENST00000311141.2:c.342C>G
  hgvsp: ENST00000311141.2:c.342C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554630
  gene symbol: ZFYVE21
  hgvsc: ENST00000554630.1:n.353C>G
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: coding_sequence_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000473477
  ensembl transcript: ENST00000555163
  gene symbol: ZFYVE21
  hgvsc: ENST00000555163.2:c.1C>G
  hgvsp: ENST00000555163.2:c.1C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000555501
  gene symbol: ZFYVE21
  hgvsc: ENST00000555501.1:n.3390C>G
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554255
  gene symbol: ZFYVE21
  hgvsc: ENST00000554255.1:n.376C>G
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000553724
  gene symbol: ZFYVE21
  hgvsc: ENST00000553724.1:n.445C>G
  variant of: http://identifiers.org/hgnc/20760
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4016
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1586
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25187
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7877
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3528
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14412
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1212
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2901
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 319
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Leu114Leu
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

14-104194244-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 104194244
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 104194244
    reference: chr 14
allele count: 1
allele frequency: 8.567952430728104e-6
allele num: 116714
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000473477
  ensembl transcript: ENST00000555163
  gene symbol: ZFYVE21
  hgvsc: ENST00000555163.2:c.10C>T
  hgvsp: ENST00000555163.2:c.10C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000310543
  ensembl transcript: ENST00000311141
  gene symbol: ZFYVE21
  hgvsc: ENST00000311141.2:c.351C>T
  hgvsp: ENST00000311141.2:c.351C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000452301
  ensembl transcript: ENST00000556610
  gene symbol: ZFYVE21
  hgvsc: ENST00000556610.1:c.139-1001C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000450746
  ensembl transcript: ENST00000553512
  gene symbol: ZFYVE21
  hgvsc: ENST00000553512.1:c.*256C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000553724
  gene symbol: ZFYVE21
  hgvsc: ENST00000553724.1:n.454C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000216602
  ensembl transcript: ENST00000216602
  gene symbol: ZFYVE21
  hgvsc: ENST00000216602.6:c.351C>T
  hgvsp: ENST00000216602.6:c.351C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554630
  gene symbol: ZFYVE21
  hgvsc: ENST00000554630.1:n.362C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000555501
  gene symbol: ZFYVE21
  hgvsc: ENST00000555501.1:n.3399C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554255
  gene symbol: ZFYVE21
  hgvsc: ENST00000554255.1:n.385C>T
  variant of: http://identifiers.org/hgnc/20760
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3936
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1846
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2001
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22782
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13582
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1203
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6169
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7030
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9403
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 210
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31498
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 533
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1406
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Leu117Leu
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: African
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: QD

14-104194247-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 104194247
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 104194247
    reference: chr 14
allele count: 1
allele frequency: 8.605555746790128e-6
allele num: 116204
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000216602
  ensembl transcript: ENST00000216602
  gene symbol: ZFYVE21
  hgvsc: ENST00000216602.6:c.354G>A
  hgvsp: ENST00000216602.6:c.354G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000452301
  ensembl transcript: ENST00000556610
  gene symbol: ZFYVE21
  hgvsc: ENST00000556610.1:c.139-998G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000310543
  ensembl transcript: ENST00000311141
  gene symbol: ZFYVE21
  hgvsc: ENST00000311141.2:c.354G>A
  hgvsp: ENST00000311141.2:c.354G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000450746
  ensembl transcript: ENST00000553512
  gene symbol: ZFYVE21
  hgvsc: ENST00000553512.1:c.*259G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000555501
  gene symbol: ZFYVE21
  hgvsc: ENST00000555501.1:n.3402G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554255
  gene symbol: ZFYVE21
  hgvsc: ENST00000554255.1:n.388G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554630
  gene symbol: ZFYVE21
  hgvsc: ENST00000554630.1:n.365G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000473477
  ensembl transcript: ENST00000555163
  gene symbol: ZFYVE21
  hgvsc: ENST00000555163.2:c.13G>A
  hgvsp: ENST00000555163.2:c.13G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000553724
  gene symbol: ZFYVE21
  hgvsc: ENST00000553724.1:n.457G>A
  variant of: http://identifiers.org/hgnc/20760
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1195
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6396
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20470
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2014
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3657
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12816
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3884
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8049
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2052
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8791
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 387
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Leu118Leu
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQ

14-104194257-GA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 104194257
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 104194256
    reference: chr 14
allele count: 1
allele frequency: 8.69943453675511e-6
allele num: 114950
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000553724
  gene symbol: ZFYVE21
  hgvsc: ENST00000553724.1:n.461+7delA
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000452301
  ensembl transcript: ENST00000556610
  gene symbol: ZFYVE21
  hgvsc: ENST00000556610.1:c.139-987delA
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000555501
  gene symbol: ZFYVE21
  hgvsc: ENST00000555501.1:n.3406+7delA
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000450746
  ensembl transcript: ENST00000553512
  gene symbol: ZFYVE21
  hgvsc: ENST00000553512.1:c.*263+7delA
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000473477
  ensembl transcript: ENST00000555163
  gene symbol: ZFYVE21
  hgvsc: ENST00000555163.2:c.17+7delA
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000310543
  ensembl transcript: ENST00000311141
  gene symbol: ZFYVE21
  hgvsc: ENST00000311141.2:c.358+7delA
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000216602
  ensembl transcript: ENST00000216602
  gene symbol: ZFYVE21
  hgvsc: ENST00000216602.6:c.358+7delA
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554255
  gene symbol: ZFYVE21
  hgvsc: ENST00000554255.1:n.399delA
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554630
  gene symbol: ZFYVE21
  hgvsc: ENST00000554630.1:n.369+7delA
  variant of: http://identifiers.org/hgnc/20760
canonical: true
consequence: splice region
filter: VQSRTrancheINDEL96.00to97.00
genotype depth: GenotypeDepth
  all individuals: 15897
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2458
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1161
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10455
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3598
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10344
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6354
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8048
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1521
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 334
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22679
  bin: 6.25e1
  variant carriers: 0
hgvs: c.358+7delA
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: GA
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum

14-104194262-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 104194262
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 104194262
    reference: chr 14
allele count: 2
allele frequency: 1.753955168905883e-5
allele num: 114028
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000473477
  ensembl transcript: ENST00000555163
  gene symbol: ZFYVE21
  hgvsc: ENST00000555163.2:c.17+11G>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000553724
  gene symbol: ZFYVE21
  hgvsc: ENST00000553724.1:n.461+11G>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000555501
  gene symbol: ZFYVE21
  hgvsc: ENST00000555501.1:n.3406+11G>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000310543
  ensembl transcript: ENST00000311141
  gene symbol: ZFYVE21
  hgvsc: ENST00000311141.2:c.358+11G>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000450746
  ensembl transcript: ENST00000553512
  gene symbol: ZFYVE21
  hgvsc: ENST00000553512.1:c.*263+11G>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554255
  gene symbol: ZFYVE21
  hgvsc: ENST00000554255.1:n.403G>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000452301
  ensembl transcript: ENST00000556610
  gene symbol: ZFYVE21
  hgvsc: ENST00000556610.1:c.139-983G>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000216602
  ensembl transcript: ENST00000216602
  gene symbol: ZFYVE21
  hgvsc: ENST00000216602.6:c.358+11G>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554630
  gene symbol: ZFYVE21
  hgvsc: ENST00000554630.1:n.369+11G>T
  variant of: http://identifiers.org/hgnc/20760
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9556
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11112
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5590
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2803
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3531
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1145
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11127
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13368
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 458
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4716
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19194
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2127
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/14-104194266-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 104194266
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 104194266
    reference: chr 14
allele count: 3
allele frequency: 2.748007694421545e-5
allele num: 109170
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000473477
  ensembl transcript: ENST00000555163
  gene symbol: ZFYVE21
  hgvsc: ENST00000555163.2:c.17+15C>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000452301
  ensembl transcript: ENST00000556610
  gene symbol: ZFYVE21
  hgvsc: ENST00000556610.1:c.139-979C>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000555501
  gene symbol: ZFYVE21
  hgvsc: ENST00000555501.1:n.3406+15C>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554630
  gene symbol: ZFYVE21
  hgvsc: ENST00000554630.1:n.369+15C>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000216602
  ensembl transcript: ENST00000216602
  gene symbol: ZFYVE21
  hgvsc: ENST00000216602.6:c.358+15C>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000450746
  ensembl transcript: ENST00000553512
  gene symbol: ZFYVE21
  hgvsc: ENST00000553512.1:c.*263+15C>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554255
  gene symbol: ZFYVE21
  hgvsc: ENST00000554255.1:n.407C>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000553724
  gene symbol: ZFYVE21
  hgvsc: ENST00000553724.1:n.461+15C>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000310543
  ensembl transcript: ENST00000311141
  gene symbol: ZFYVE21
  hgvsc: ENST00000311141.2:c.358+15C>A
  variant of: http://identifiers.org/hgnc/20760
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11689
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10350
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14211
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 939
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4204
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2568
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7973
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6198
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5128
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 806
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11547
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2924
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15015
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: DP

14-104194266-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 104194266
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 104194266
    reference: chr 14
allele count: 1
allele frequency: 9.160025648071815e-6
allele num: 109170
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554255
  gene symbol: ZFYVE21
  hgvsc: ENST00000554255.1:n.407C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000452301
  ensembl transcript: ENST00000556610
  gene symbol: ZFYVE21
  hgvsc: ENST00000556610.1:c.139-979C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000450746
  ensembl transcript: ENST00000553512
  gene symbol: ZFYVE21
  hgvsc: ENST00000553512.1:c.*263+15C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554630
  gene symbol: ZFYVE21
  hgvsc: ENST00000554630.1:n.369+15C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000553724
  gene symbol: ZFYVE21
  hgvsc: ENST00000553724.1:n.461+15C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000555501
  gene symbol: ZFYVE21
  hgvsc: ENST00000555501.1:n.3406+15C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000310543
  ensembl transcript: ENST00000311141
  gene symbol: ZFYVE21
  hgvsc: ENST00000311141.2:c.358+15C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000473477
  ensembl transcript: ENST00000555163
  gene symbol: ZFYVE21
  hgvsc: ENST00000555163.2:c.17+15C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000216602
  ensembl transcript: ENST00000216602
  gene symbol: ZFYVE21
  hgvsc: ENST00000216602.6:c.358+15C>T
  variant of: http://identifiers.org/hgnc/20760
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10350
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11689
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4204
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 939
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7973
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6198
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14211
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2568
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2411
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1152
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 896
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2924
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: DP

14-104194275-TC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 104194275
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 104194274
    reference: chr 14
allele count: 1
allele frequency: 1.020491468691322e-5
allele num: 97992
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000473477
  ensembl transcript: ENST00000555163
  gene symbol: ZFYVE21
  hgvsc: ENST00000555163.2:c.17+27delC
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000450746
  ensembl transcript: ENST00000553512
  gene symbol: ZFYVE21
  hgvsc: ENST00000553512.1:c.*263+27delC
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000452301
  ensembl transcript: ENST00000556610
  gene symbol: ZFYVE21
  hgvsc: ENST00000556610.1:c.139-967delC
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000216602
  ensembl transcript: ENST00000216602
  gene symbol: ZFYVE21
  hgvsc: ENST00000216602.6:c.358+27delC
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000310543
  ensembl transcript: ENST00000311141
  gene symbol: ZFYVE21
  hgvsc: ENST00000311141.2:c.358+27delC
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554255
  gene symbol: ZFYVE21
  hgvsc: ENST00000554255.1:n.419delC
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000555501
  gene symbol: ZFYVE21
  hgvsc: ENST00000555501.1:n.3406+27delC
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554630
  gene symbol: ZFYVE21
  hgvsc: ENST00000554630.1:n.369+27delC
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000553724
  gene symbol: ZFYVE21
  hgvsc: ENST00000553724.1:n.461+27delC
  variant of: http://identifiers.org/hgnc/20760
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3784
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14378
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1620
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5423
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11069
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7321
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13350
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3724
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2895
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 392
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: TC
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

14-104194276-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 104194276
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 104194276
    reference: chr 14
allele count: 1
allele frequency: 1.019513488163448e-5
allele num: 98086
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000553724
  gene symbol: ZFYVE21
  hgvsc: ENST00000553724.1:n.461+25C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554255
  gene symbol: ZFYVE21
  hgvsc: ENST00000554255.1:n.417C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000555501
  gene symbol: ZFYVE21
  hgvsc: ENST00000555501.1:n.3406+25C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000452301
  ensembl transcript: ENST00000556610
  gene symbol: ZFYVE21
  hgvsc: ENST00000556610.1:c.139-969C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000310543
  ensembl transcript: ENST00000311141
  gene symbol: ZFYVE21
  hgvsc: ENST00000311141.2:c.358+25C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000473477
  ensembl transcript: ENST00000555163
  gene symbol: ZFYVE21
  hgvsc: ENST00000555163.2:c.17+25C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000216602
  ensembl transcript: ENST00000216602
  gene symbol: ZFYVE21
  hgvsc: ENST00000216602.6:c.358+25C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000450746
  ensembl transcript: ENST00000553512
  gene symbol: ZFYVE21
  hgvsc: ENST00000553512.1:c.*263+25C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554630
  gene symbol: ZFYVE21
  hgvsc: ENST00000554630.1:n.369+25C>T
  variant of: http://identifiers.org/hgnc/20760
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13370
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7335
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14326
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3782
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1052
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5460
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11074
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1602
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2896
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1180
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11867
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 399
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 614
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: DP

14-104194278-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 104194278
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 104194278
    reference: chr 14
allele count: 61002
allele frequency: 5.912879962779156e-1
allele num: 103168
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000473477
  ensembl transcript: ENST00000555163
  gene symbol: ZFYVE21
  hgvsc: ENST00000555163.2:c.17+27C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000553724
  gene symbol: ZFYVE21
  hgvsc: ENST00000553724.1:n.461+27C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000555501
  gene symbol: ZFYVE21
  hgvsc: ENST00000555501.1:n.3406+27C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000310543
  ensembl transcript: ENST00000311141
  gene symbol: ZFYVE21
  hgvsc: ENST00000311141.2:c.358+27C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554255
  gene symbol: ZFYVE21
  hgvsc: ENST00000554255.1:n.419C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000452301
  ensembl transcript: ENST00000556610
  gene symbol: ZFYVE21
  hgvsc: ENST00000556610.1:c.139-967C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000216602
  ensembl transcript: ENST00000216602
  gene symbol: ZFYVE21
  hgvsc: ENST00000216602.6:c.358+27C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554630
  gene symbol: ZFYVE21
  hgvsc: ENST00000554630.1:n.369+27C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000450746
  ensembl transcript: ENST00000553512
  gene symbol: ZFYVE21
  hgvsc: ENST00000553512.1:c.*263+27C>T
  variant of: http://identifiers.org/hgnc/20760
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1391
  bin: 3.75e1
  variant carriers: 1316
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.75e1
  variant carriers: 78
genotype depth: GenotypeDepth
  all individuals: 3476
  bin: 3.25e1
  variant carriers: 3208
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 5.25e1
  variant carriers: 168
genotype depth: GenotypeDepth
  all individuals: 5787
  bin: 7.5e0
  variant carriers: 3077
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 6.75e1
  variant carriers: 100
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.25e1
  variant carriers: 98
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.75e1
  variant carriers: 138
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 5.75e1
  variant carriers: 123
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 4.25e1
  variant carriers: 597
genotype depth: GenotypeDepth
  all individuals: 7004
  bin: 2.75e1
  variant carriers: 6211
genotype depth: GenotypeDepth
  all individuals: 13774
  bin: 1.25e1
  variant carriers: 8701
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 2.5e0
  variant carriers: 237
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.25e1
  variant carriers: 91
genotype depth: GenotypeDepth
  all individuals: 11109
  bin: 2.25e1
  variant carriers: 10328
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 49
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 57
genotype depth: GenotypeDepth
  all individuals: 14480
  bin: 1.75e1
  variant carriers: 12166
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 51
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 4.75e1
  variant carriers: 292
genotype quality: GenotypeQuality
  all individuals: 891
  bin: 9.25e1
  variant carriers: 875
genotype quality: GenotypeQuality
  all individuals: 747
  bin: 1.25e1
  variant carriers: 335
genotype quality: GenotypeQuality
  all individuals: 1394
  bin: 4.25e1
  variant carriers: 1142
genotype quality: GenotypeQuality
  all individuals: 2602
  bin: 3.75e1
  variant carriers: 1701
genotype quality: GenotypeQuality
  all individuals: 1363
  bin: 7.75e1
  variant carriers: 1332
num of homozygotes: 17807
population: Other
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: MQ

14-104194281-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 104194281
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 104194281
    reference: chr 14
allele count: 1
allele frequency: 1.171563803364731e-5
allele num: 85356
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000452301
  ensembl transcript: ENST00000556610
  gene symbol: ZFYVE21
  hgvsc: ENST00000556610.1:c.139-964G>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554255
  gene symbol: ZFYVE21
  hgvsc: ENST00000554255.1:n.422G>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000553724
  gene symbol: ZFYVE21
  hgvsc: ENST00000553724.1:n.461+30G>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000216602
  ensembl transcript: ENST00000216602
  gene symbol: ZFYVE21
  hgvsc: ENST00000216602.6:c.358+30G>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554630
  gene symbol: ZFYVE21
  hgvsc: ENST00000554630.1:n.369+30G>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000473477
  ensembl transcript: ENST00000555163
  gene symbol: ZFYVE21
  hgvsc: ENST00000555163.2:c.17+30G>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000310543
  ensembl transcript: ENST00000311141
  gene symbol: ZFYVE21
  hgvsc: ENST00000311141.2:c.358+30G>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000450746
  ensembl transcript: ENST00000553512
  gene symbol: ZFYVE21
  hgvsc: ENST00000553512.1:c.*263+30G>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000555501
  gene symbol: ZFYVE21
  hgvsc: ENST00000555501.1:n.3406+30G>T
  variant of: http://identifiers.org/hgnc/20760
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13204
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3314
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3229
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3872
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9333
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25001
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1820
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 461
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 199
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1240
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5134
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: South Asian
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD

14-104194282-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 104194282
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 104194282
    reference: chr 14
allele count: 0
allele frequency: 0.0e0
allele num: 84014
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554630
  gene symbol: ZFYVE21
  hgvsc: ENST00000554630.1:n.369+31C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000555501
  gene symbol: ZFYVE21
  hgvsc: ENST00000555501.1:n.3406+31C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554255
  gene symbol: ZFYVE21
  hgvsc: ENST00000554255.1:n.423C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000452301
  ensembl transcript: ENST00000556610
  gene symbol: ZFYVE21
  hgvsc: ENST00000556610.1:c.139-963C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000473477
  ensembl transcript: ENST00000555163
  gene symbol: ZFYVE21
  hgvsc: ENST00000555163.2:c.17+31C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000450746
  ensembl transcript: ENST00000553512
  gene symbol: ZFYVE21
  hgvsc: ENST00000553512.1:c.*263+31C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000310543
  ensembl transcript: ENST00000311141
  gene symbol: ZFYVE21
  hgvsc: ENST00000311141.2:c.358+31C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000553724
  gene symbol: ZFYVE21
  hgvsc: ENST00000553724.1:n.461+31C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000216602
  ensembl transcript: ENST00000216602
  gene symbol: ZFYVE21
  hgvsc: ENST00000216602.6:c.358+31C>T
  variant of: http://identifiers.org/hgnc/20760
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 3194
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9584
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24859
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3495
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3334
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13538
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 602
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 498
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4569
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum

14-104194283-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 104194283
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 104194283
    reference: chr 14
allele count: 1
allele frequency: 1.222195062331948e-5
allele num: 81820
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000450746
  ensembl transcript: ENST00000553512
  gene symbol: ZFYVE21
  hgvsc: ENST00000553512.1:c.*263+32G>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000452301
  ensembl transcript: ENST00000556610
  gene symbol: ZFYVE21
  hgvsc: ENST00000556610.1:c.139-962G>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000555501
  gene symbol: ZFYVE21
  hgvsc: ENST00000555501.1:n.3406+32G>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554255
  gene symbol: ZFYVE21
  hgvsc: ENST00000554255.1:n.424G>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554630
  gene symbol: ZFYVE21
  hgvsc: ENST00000554630.1:n.369+32G>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000310543
  ensembl transcript: ENST00000311141
  gene symbol: ZFYVE21
  hgvsc: ENST00000311141.2:c.358+32G>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000473477
  ensembl transcript: ENST00000555163
  gene symbol: ZFYVE21
  hgvsc: ENST00000555163.2:c.17+32G>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000216602
  ensembl transcript: ENST00000216602
  gene symbol: ZFYVE21
  hgvsc: ENST00000216602.6:c.358+32G>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000553724
  gene symbol: ZFYVE21
  hgvsc: ENST00000553724.1:n.461+32G>T
  variant of: http://identifiers.org/hgnc/20760
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3070
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13932
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9890
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24667
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3498
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2995
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1157
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8049
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 960
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Finnish)
reference allele: G
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD

14-104194287-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 104194287
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 104194287
    reference: chr 14
allele count: 1
allele frequency: 1.233654083395016e-5
allele num: 81060
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554630
  gene symbol: ZFYVE21
  hgvsc: ENST00000554630.1:n.369+36C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000310543
  ensembl transcript: ENST00000311141
  gene symbol: ZFYVE21
  hgvsc: ENST00000311141.2:c.358+36C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000555501
  gene symbol: ZFYVE21
  hgvsc: ENST00000555501.1:n.3406+36C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000452301
  ensembl transcript: ENST00000556610
  gene symbol: ZFYVE21
  hgvsc: ENST00000556610.1:c.139-958C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000473477
  ensembl transcript: ENST00000555163
  gene symbol: ZFYVE21
  hgvsc: ENST00000555163.2:c.17+36C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000450746
  ensembl transcript: ENST00000553512
  gene symbol: ZFYVE21
  hgvsc: ENST00000553512.1:c.*263+36C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554255
  gene symbol: ZFYVE21
  hgvsc: ENST00000554255.1:n.428C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000216602
  ensembl transcript: ENST00000216602
  gene symbol: ZFYVE21
  hgvsc: ENST00000216602.6:c.358+36C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000553724
  gene symbol: ZFYVE21
  hgvsc: ENST00000553724.1:n.461+36C>T
  variant of: http://identifiers.org/hgnc/20760
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24392
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2263
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2777
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14690
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10678
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3690
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 570
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5393
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 575
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3140
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum

14-104194288-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 104194288
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 104194288
    reference: chr 14
allele count: 38
allele frequency: 4.88030412000411e-4
allele num: 77864
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000310543
  ensembl transcript: ENST00000311141
  gene symbol: ZFYVE21
  hgvsc: ENST00000311141.2:c.358+37G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000452301
  ensembl transcript: ENST00000556610
  gene symbol: ZFYVE21
  hgvsc: ENST00000556610.1:c.139-957G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554255
  gene symbol: ZFYVE21
  hgvsc: ENST00000554255.1:n.429G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000216602
  ensembl transcript: ENST00000216602
  gene symbol: ZFYVE21
  hgvsc: ENST00000216602.6:c.358+37G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000473477
  ensembl transcript: ENST00000555163
  gene symbol: ZFYVE21
  hgvsc: ENST00000555163.2:c.17+37G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554630
  gene symbol: ZFYVE21
  hgvsc: ENST00000554630.1:n.369+37G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000450746
  ensembl transcript: ENST00000553512
  gene symbol: ZFYVE21
  hgvsc: ENST00000553512.1:c.*263+37G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000553724
  gene symbol: ZFYVE21
  hgvsc: ENST00000553724.1:n.461+37G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000555501
  gene symbol: ZFYVE21
  hgvsc: ENST00000555501.1:n.3406+37G>A
  variant of: http://identifiers.org/hgnc/20760
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24408
  bin: 1.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 14933
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2255
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3619
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10507
  bin: 1.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2817
  bin: 2.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8063
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2882
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6110
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2273
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 1
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: QD
site quality: ClippingRankSum

14-104194293-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 104194293
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 104194293
    reference: chr 14
allele count: 3
allele frequency: 3.720330365336442e-5
allele num: 80638
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000310543
  ensembl transcript: ENST00000311141
  gene symbol: ZFYVE21
  hgvsc: ENST00000311141.2:c.358+42C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554255
  gene symbol: ZFYVE21
  hgvsc: ENST00000554255.1:n.434C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000473477
  ensembl transcript: ENST00000555163
  gene symbol: ZFYVE21
  hgvsc: ENST00000555163.2:c.17+42C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000450746
  ensembl transcript: ENST00000553512
  gene symbol: ZFYVE21
  hgvsc: ENST00000553512.1:c.*263+42C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000216602
  ensembl transcript: ENST00000216602
  gene symbol: ZFYVE21
  hgvsc: ENST00000216602.6:c.358+42C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000553724
  gene symbol: ZFYVE21
  hgvsc: ENST00000553724.1:n.461+42C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554630
  gene symbol: ZFYVE21
  hgvsc: ENST00000554630.1:n.369+42C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000452301
  ensembl transcript: ENST00000556610
  gene symbol: ZFYVE21
  hgvsc: ENST00000556610.1:c.139-952C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000555501
  gene symbol: ZFYVE21
  hgvsc: ENST00000555501.1:n.3406+42C>T
  variant of: http://identifiers.org/hgnc/20760
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1691
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15962
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3353
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11030
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2844
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23919
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1725
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1700
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4383
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2704
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/14-104194294-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 104194294
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 104194294
    reference: chr 14
allele count: 1
allele frequency: 1.245143938639307e-5
allele num: 80312
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000450746
  ensembl transcript: ENST00000553512
  gene symbol: ZFYVE21
  hgvsc: ENST00000553512.1:c.*263+43C>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000473477
  ensembl transcript: ENST00000555163
  gene symbol: ZFYVE21
  hgvsc: ENST00000555163.2:c.17+43C>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554255
  gene symbol: ZFYVE21
  hgvsc: ENST00000554255.1:n.435C>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000555501
  gene symbol: ZFYVE21
  hgvsc: ENST00000555501.1:n.3406+43C>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000310543
  ensembl transcript: ENST00000311141
  gene symbol: ZFYVE21
  hgvsc: ENST00000311141.2:c.358+43C>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000216602
  ensembl transcript: ENST00000216602
  gene symbol: ZFYVE21
  hgvsc: ENST00000216602.6:c.358+43C>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000553724
  gene symbol: ZFYVE21
  hgvsc: ENST00000553724.1:n.461+43C>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000452301
  ensembl transcript: ENST00000556610
  gene symbol: ZFYVE21
  hgvsc: ENST00000556610.1:c.139-951C>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554630
  gene symbol: ZFYVE21
  hgvsc: ENST00000554630.1:n.369+43C>A
  variant of: http://identifiers.org/hgnc/20760
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16233
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1598
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2960
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3345
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23756
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10920
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6582
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 487
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8656
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum

14-104194294-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 104194294
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 104194294
    reference: chr 14
allele count: 1
allele frequency: 1.245143938639307e-5
allele num: 80312
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000216602
  ensembl transcript: ENST00000216602
  gene symbol: ZFYVE21
  hgvsc: ENST00000216602.6:c.358+43C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000555501
  gene symbol: ZFYVE21
  hgvsc: ENST00000555501.1:n.3406+43C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000450746
  ensembl transcript: ENST00000553512
  gene symbol: ZFYVE21
  hgvsc: ENST00000553512.1:c.*263+43C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000452301
  ensembl transcript: ENST00000556610
  gene symbol: ZFYVE21
  hgvsc: ENST00000556610.1:c.139-951C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554630
  gene symbol: ZFYVE21
  hgvsc: ENST00000554630.1:n.369+43C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000310543
  ensembl transcript: ENST00000311141
  gene symbol: ZFYVE21
  hgvsc: ENST00000311141.2:c.358+43C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000473477
  ensembl transcript: ENST00000555163
  gene symbol: ZFYVE21
  hgvsc: ENST00000555163.2:c.17+43C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554255
  gene symbol: ZFYVE21
  hgvsc: ENST00000554255.1:n.435C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000553724
  gene symbol: ZFYVE21
  hgvsc: ENST00000553724.1:n.461+43C>T
  variant of: http://identifiers.org/hgnc/20760
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10920
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2960
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23756
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16233
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3345
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1598
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 565
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20904
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1722
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 487
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: Other
reference allele: C
site quality: FS
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

14-104194295-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 104194295
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 104194295
    reference: chr 14
allele count: 2
allele frequency: 2.535047025122316e-5
allele num: 78894
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000473477
  ensembl transcript: ENST00000555163
  gene symbol: ZFYVE21
  hgvsc: ENST00000555163.2:c.17+44G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000450746
  ensembl transcript: ENST00000553512
  gene symbol: ZFYVE21
  hgvsc: ENST00000553512.1:c.*263+44G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000452301
  ensembl transcript: ENST00000556610
  gene symbol: ZFYVE21
  hgvsc: ENST00000556610.1:c.139-950G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554630
  gene symbol: ZFYVE21
  hgvsc: ENST00000554630.1:n.369+44G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000310543
  ensembl transcript: ENST00000311141
  gene symbol: ZFYVE21
  hgvsc: ENST00000311141.2:c.358+44G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554255
  gene symbol: ZFYVE21
  hgvsc: ENST00000554255.1:n.436G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000216602
  ensembl transcript: ENST00000216602
  gene symbol: ZFYVE21
  hgvsc: ENST00000216602.6:c.358+44G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000553724
  gene symbol: ZFYVE21
  hgvsc: ENST00000553724.1:n.461+44G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000555501
  gene symbol: ZFYVE21
  hgvsc: ENST00000555501.1:n.3406+44G>A
  variant of: http://identifiers.org/hgnc/20760
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1406
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16821
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3339
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23256
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10835
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3217
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2540
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 190
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8639
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6541
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3796
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ

14-104194296-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 104194296
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 104194296
    reference: chr 14
allele count: 2
allele frequency: 2.531709663535786e-5
allele num: 78998
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000310543
  ensembl transcript: ENST00000311141
  gene symbol: ZFYVE21
  hgvsc: ENST00000311141.2:c.358+45G>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000553724
  gene symbol: ZFYVE21
  hgvsc: ENST00000553724.1:n.461+45G>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554630
  gene symbol: ZFYVE21
  hgvsc: ENST00000554630.1:n.369+45G>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000450746
  ensembl transcript: ENST00000553512
  gene symbol: ZFYVE21
  hgvsc: ENST00000553512.1:c.*263+45G>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000555501
  gene symbol: ZFYVE21
  hgvsc: ENST00000555501.1:n.3406+45G>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000473477
  ensembl transcript: ENST00000555163
  gene symbol: ZFYVE21
  hgvsc: ENST00000555163.2:c.17+45G>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000216602
  ensembl transcript: ENST00000216602
  gene symbol: ZFYVE21
  hgvsc: ENST00000216602.6:c.358+45G>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554255
  gene symbol: ZFYVE21
  hgvsc: ENST00000554255.1:n.437G>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000452301
  ensembl transcript: ENST00000556610
  gene symbol: ZFYVE21
  hgvsc: ENST00000556610.1:c.139-949G>T
  variant of: http://identifiers.org/hgnc/20760
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1389
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23284
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16904
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10740
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3240
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3326
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 512
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1848
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6552
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20319
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 457
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff

14-104194302-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 104194302
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 104194302
    reference: chr 14
allele count: 0
allele frequency: 0.0e0
allele num: 76492
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000553724
  gene symbol: ZFYVE21
  hgvsc: ENST00000553724.1:n.461+51C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000555501
  gene symbol: ZFYVE21
  hgvsc: ENST00000555501.1:n.3406+51C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000473477
  ensembl transcript: ENST00000555163
  gene symbol: ZFYVE21
  hgvsc: ENST00000555163.2:c.17+51C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000310543
  ensembl transcript: ENST00000311141
  gene symbol: ZFYVE21
  hgvsc: ENST00000311141.2:c.358+51C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554630
  gene symbol: ZFYVE21
  hgvsc: ENST00000554630.1:n.369+51C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000452301
  ensembl transcript: ENST00000556610
  gene symbol: ZFYVE21
  hgvsc: ENST00000556610.1:c.139-943C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000216602
  ensembl transcript: ENST00000216602
  gene symbol: ZFYVE21
  hgvsc: ENST00000216602.6:c.358+51C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554255
  gene symbol: ZFYVE21
  hgvsc: ENST00000554255.1:n.443C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000450746
  ensembl transcript: ENST00000553512
  gene symbol: ZFYVE21
  hgvsc: ENST00000553512.1:c.*263+51C>T
  variant of: http://identifiers.org/hgnc/20760
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3228
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22584
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17813
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3685
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1101
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10541
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18010
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4073
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8701
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1215
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: ClippingRankSum

14-104194303-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 104194303
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 104194303
    reference: chr 14
allele count: 0
allele frequency: 0.0e0
allele num: 75856
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000452301
  ensembl transcript: ENST00000556610
  gene symbol: ZFYVE21
  hgvsc: ENST00000556610.1:c.139-942G>C
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000553724
  gene symbol: ZFYVE21
  hgvsc: ENST00000553724.1:n.461+52G>C
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554255
  gene symbol: ZFYVE21
  hgvsc: ENST00000554255.1:n.444G>C
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554630
  gene symbol: ZFYVE21
  hgvsc: ENST00000554630.1:n.369+52G>C
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000473477
  ensembl transcript: ENST00000555163
  gene symbol: ZFYVE21
  hgvsc: ENST00000555163.2:c.17+52G>C
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000310543
  ensembl transcript: ENST00000311141
  gene symbol: ZFYVE21
  hgvsc: ENST00000311141.2:c.358+52G>C
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000450746
  ensembl transcript: ENST00000553512
  gene symbol: ZFYVE21
  hgvsc: ENST00000553512.1:c.*263+52G>C
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000555501
  gene symbol: ZFYVE21
  hgvsc: ENST00000555501.1:n.3406+52G>C
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000216602
  ensembl transcript: ENST00000216602
  gene symbol: ZFYVE21
  hgvsc: ENST00000216602.6:c.358+52G>C
  variant of: http://identifiers.org/hgnc/20760
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17905
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10494
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1081
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3209
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3731
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22540
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1406
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2045
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 735
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17443
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1258
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff

14-104195194-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 104195194
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 104195194
    reference: chr 14
allele count: 2
allele frequency: 1.664696775482346e-5
allele num: 120142
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000452301
  ensembl transcript: ENST00000556610
  gene symbol: ZFYVE21
  hgvsc: ENST00000556610.1:c.139-51A>G
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000555501
  gene symbol: ZFYVE21
  hgvsc: ENST00000555501.1:n.3407-51A>G
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554630
  gene symbol: ZFYVE21
  hgvsc: ENST00000554630.1:n.370-51A>G
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000216602
  ensembl transcript: ENST00000216602
  gene symbol: ZFYVE21
  hgvsc: ENST00000216602.6:c.359-51A>G
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000556795
  gene symbol: ZFYVE21
  hgvsc: ENST00000556795.1:n.72A>G
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000450746
  ensembl transcript: ENST00000553512
  gene symbol: ZFYVE21
  hgvsc: ENST00000553512.1:c.*264-51A>G
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000310543
  ensembl transcript: ENST00000311141
  gene symbol: ZFYVE21
  hgvsc: ENST00000311141.2:c.359-51A>G
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000473477
  ensembl transcript: ENST00000555163
  gene symbol: ZFYVE21
  hgvsc: ENST00000555163.2:c.18-51A>G
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000553724
  gene symbol: ZFYVE21
  hgvsc: ENST00000553724.1:n.462-234A>G
  variant of: http://identifiers.org/hgnc/20760
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3802
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6762
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1670
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4430
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8894
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1633
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6632
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2661
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9533
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10137
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2636
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1001
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 705
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4196
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3869
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

14-104195196-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 104195196
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 104195196
    reference: chr 14
allele count: 1
allele frequency: 8.320298199487469e-6
allele num: 120188
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000450746
  ensembl transcript: ENST00000553512
  gene symbol: ZFYVE21
  hgvsc: ENST00000553512.1:c.*264-49G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000310543
  ensembl transcript: ENST00000311141
  gene symbol: ZFYVE21
  hgvsc: ENST00000311141.2:c.359-49G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000216602
  ensembl transcript: ENST00000216602
  gene symbol: ZFYVE21
  hgvsc: ENST00000216602.6:c.359-49G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000452301
  ensembl transcript: ENST00000556610
  gene symbol: ZFYVE21
  hgvsc: ENST00000556610.1:c.139-49G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554630
  gene symbol: ZFYVE21
  hgvsc: ENST00000554630.1:n.370-49G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000556795
  gene symbol: ZFYVE21
  hgvsc: ENST00000556795.1:n.74G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000473477
  ensembl transcript: ENST00000555163
  gene symbol: ZFYVE21
  hgvsc: ENST00000555163.2:c.18-49G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000555501
  gene symbol: ZFYVE21
  hgvsc: ENST00000555501.1:n.3407-49G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000553724
  gene symbol: ZFYVE21
  hgvsc: ENST00000553724.1:n.462-232G>A
  variant of: http://identifiers.org/hgnc/20760
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8891
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2661
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3550
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1632
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1670
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9521
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10174
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6988
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6636
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4430
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 603
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4228
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 664
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff

14-104195196-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 104195196
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 104195196
    reference: chr 14
allele count: 2
allele frequency: 1.664059639897494e-5
allele num: 120188
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000473477
  ensembl transcript: ENST00000555163
  gene symbol: ZFYVE21
  hgvsc: ENST00000555163.2:c.18-49G>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000555501
  gene symbol: ZFYVE21
  hgvsc: ENST00000555501.1:n.3407-49G>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554630
  gene symbol: ZFYVE21
  hgvsc: ENST00000554630.1:n.370-49G>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000556795
  gene symbol: ZFYVE21
  hgvsc: ENST00000556795.1:n.74G>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000310543
  ensembl transcript: ENST00000311141
  gene symbol: ZFYVE21
  hgvsc: ENST00000311141.2:c.359-49G>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000450746
  ensembl transcript: ENST00000553512
  gene symbol: ZFYVE21
  hgvsc: ENST00000553512.1:c.*264-49G>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000452301
  ensembl transcript: ENST00000556610
  gene symbol: ZFYVE21
  hgvsc: ENST00000556610.1:c.139-49G>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000216602
  ensembl transcript: ENST00000216602
  gene symbol: ZFYVE21
  hgvsc: ENST00000216602.6:c.359-49G>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000553724
  gene symbol: ZFYVE21
  hgvsc: ENST00000553724.1:n.462-232G>T
  variant of: http://identifiers.org/hgnc/20760
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6636
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9521
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3550
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2661
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8891
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10174
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6988
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4430
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1632
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1670
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1436
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 764
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2921
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25856
  bin: 9.75e1
  variant carriers: 2
num of homozygotes: 0
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum

14-104195200-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 104195200
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 104195200
    reference: chr 14
allele count: 1
allele frequency: 8.315455104857889e-6
allele num: 120258
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000555501
  gene symbol: ZFYVE21
  hgvsc: ENST00000555501.1:n.3407-45A>G
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000452301
  ensembl transcript: ENST00000556610
  gene symbol: ZFYVE21
  hgvsc: ENST00000556610.1:c.139-45A>G
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000216602
  ensembl transcript: ENST00000216602
  gene symbol: ZFYVE21
  hgvsc: ENST00000216602.6:c.359-45A>G
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554630
  gene symbol: ZFYVE21
  hgvsc: ENST00000554630.1:n.370-45A>G
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000556795
  gene symbol: ZFYVE21
  hgvsc: ENST00000556795.1:n.78A>G
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000473477
  ensembl transcript: ENST00000555163
  gene symbol: ZFYVE21
  hgvsc: ENST00000555163.2:c.18-45A>G
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000450746
  ensembl transcript: ENST00000553512
  gene symbol: ZFYVE21
  hgvsc: ENST00000553512.1:c.*264-45A>G
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000553724
  gene symbol: ZFYVE21
  hgvsc: ENST00000553724.1:n.462-228A>G
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000310543
  ensembl transcript: ENST00000311141
  gene symbol: ZFYVE21
  hgvsc: ENST00000311141.2:c.359-45A>G
  variant of: http://identifiers.org/hgnc/20760
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1612
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7626
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4435
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2664
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9571
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1670
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8917
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10362
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2661
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6645
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3930
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 266
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 856
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
reference allele: A
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/14-104195202-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 104195202
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 104195202
    reference: chr 14
allele count: 1813
allele frequency: 1.507466657797585e-2
allele num: 120268
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554630
  gene symbol: ZFYVE21
  hgvsc: ENST00000554630.1:n.370-43A>C
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000555501
  gene symbol: ZFYVE21
  hgvsc: ENST00000555501.1:n.3407-43A>C
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000556795
  gene symbol: ZFYVE21
  hgvsc: ENST00000556795.1:n.80A>C
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000216602
  ensembl transcript: ENST00000216602
  gene symbol: ZFYVE21
  hgvsc: ENST00000216602.6:c.359-43A>C
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000452301
  ensembl transcript: ENST00000556610
  gene symbol: ZFYVE21
  hgvsc: ENST00000556610.1:c.139-43A>C
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000473477
  ensembl transcript: ENST00000555163
  gene symbol: ZFYVE21
  hgvsc: ENST00000555163.2:c.18-43A>C
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000310543
  ensembl transcript: ENST00000311141
  gene symbol: ZFYVE21
  hgvsc: ENST00000311141.2:c.359-43A>C
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000450746
  ensembl transcript: ENST00000553512
  gene symbol: ZFYVE21
  hgvsc: ENST00000553512.1:c.*264-43A>C
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000553724
  gene symbol: ZFYVE21
  hgvsc: ENST00000553724.1:n.462-226A>C
  variant of: http://identifiers.org/hgnc/20760
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10405
  bin: 3.25e1
  variant carriers: 220
genotype depth: GenotypeDepth
  all individuals: 7968
  bin: 2.25e1
  variant carriers: 113
genotype depth: GenotypeDepth
  all individuals: 1575
  bin: 1.25e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 9.75e1
  variant carriers: 84
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 5.75e1
  variant carriers: 69
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 6.75e1
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 6661
  bin: 4.25e1
  variant carriers: 214
genotype depth: GenotypeDepth
  all individuals: 2705
  bin: 5.25e1
  variant carriers: 126
genotype depth: GenotypeDepth
  all individuals: 1125
  bin: 6.25e1
  variant carriers: 48
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 7.5e0
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 4486
  bin: 4.75e1
  variant carriers: 192
genotype depth: GenotypeDepth
  all individuals: 9535
  bin: 2.75e1
  variant carriers: 199
genotype depth: GenotypeDepth
  all individuals: 2162
  bin: 1.75e1
  variant carriers: 55
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 7.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 7.25e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 8.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 8.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 8942
  bin: 3.75e1
  variant carriers: 266
genotype quality: GenotypeQuality
  all individuals: 4294
  bin: 7.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 679
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 946
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 393
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 59
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/14-104195205-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 104195205
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 104195205
    reference: chr 14
allele count: 2
allele frequency: 1.661681621801263e-5
allele num: 120360
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000553724
  gene symbol: ZFYVE21
  hgvsc: ENST00000553724.1:n.462-223A>C
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000555501
  gene symbol: ZFYVE21
  hgvsc: ENST00000555501.1:n.3407-40A>C
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000216602
  ensembl transcript: ENST00000216602
  gene symbol: ZFYVE21
  hgvsc: ENST00000216602.6:c.359-40A>C
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000450746
  ensembl transcript: ENST00000553512
  gene symbol: ZFYVE21
  hgvsc: ENST00000553512.1:c.*264-40A>C
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554630
  gene symbol: ZFYVE21
  hgvsc: ENST00000554630.1:n.370-40A>C
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000556795
  gene symbol: ZFYVE21
  hgvsc: ENST00000556795.1:n.83A>C
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000473477
  ensembl transcript: ENST00000555163
  gene symbol: ZFYVE21
  hgvsc: ENST00000555163.2:c.18-40A>C
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000310543
  ensembl transcript: ENST00000311141
  gene symbol: ZFYVE21
  hgvsc: ENST00000311141.2:c.359-40A>C
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000452301
  ensembl transcript: ENST00000556610
  gene symbol: ZFYVE21
  hgvsc: ENST00000556610.1:c.139-40A>C
  variant of: http://identifiers.org/hgnc/20760
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10520
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9612
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8523
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6663
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1472
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1138
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1448
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4518
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8963
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1715
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2744
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 640
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 192
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2949
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 395
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ClippingRankSum

14-104195209-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 104195209
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 104195209
    reference: chr 14
allele count: 1
allele frequency: 8.304958059961797e-6
allele num: 120410
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000452301
  ensembl transcript: ENST00000556610
  gene symbol: ZFYVE21
  hgvsc: ENST00000556610.1:c.139-36A>G
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000216602
  ensembl transcript: ENST00000216602
  gene symbol: ZFYVE21
  hgvsc: ENST00000216602.6:c.359-36A>G
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000553724
  gene symbol: ZFYVE21
  hgvsc: ENST00000553724.1:n.462-219A>G
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000450746
  ensembl transcript: ENST00000553512
  gene symbol: ZFYVE21
  hgvsc: ENST00000553512.1:c.*264-36A>G
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000310543
  ensembl transcript: ENST00000311141
  gene symbol: ZFYVE21
  hgvsc: ENST00000311141.2:c.359-36A>G
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000556795
  gene symbol: ZFYVE21
  hgvsc: ENST00000556795.1:n.87A>G
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000473477
  ensembl transcript: ENST00000555163
  gene symbol: ZFYVE21
  hgvsc: ENST00000555163.2:c.18-36A>G
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554630
  gene symbol: ZFYVE21
  hgvsc: ENST00000554630.1:n.370-36A>G
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000555501
  gene symbol: ZFYVE21
  hgvsc: ENST00000555501.1:n.3407-36A>G
  variant of: http://identifiers.org/hgnc/20760
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9838
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1138
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9076
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9000
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1715
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10738
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6671
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4521
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2745
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4445
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 537
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 302
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8265
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: Other
reference allele: A
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD

14-104195213-CCT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 104195213
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 104195211
    reference: chr 14
allele count: 6
allele frequency: 4.978344202718176e-5
allele num: 120522
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000310543
  ensembl transcript: ENST00000311141
  gene symbol: ZFYVE21
  hgvsc: ENST00000311141.2:c.359-31_359-30delCT
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000556795
  gene symbol: ZFYVE21
  hgvsc: ENST00000556795.1:n.92_93delCT
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000450746
  ensembl transcript: ENST00000553512
  gene symbol: ZFYVE21
  hgvsc: ENST00000553512.1:c.*264-31_*264-30delCT
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554630
  gene symbol: ZFYVE21
  hgvsc: ENST00000554630.1:n.370-31_370-30delCT
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000553724
  gene symbol: ZFYVE21
  hgvsc: ENST00000553724.1:n.462-214_462-213delCT
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000216602
  ensembl transcript: ENST00000216602
  gene symbol: ZFYVE21
  hgvsc: ENST00000216602.6:c.359-31_359-30delCT
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000452301
  ensembl transcript: ENST00000556610
  gene symbol: ZFYVE21
  hgvsc: ENST00000556610.1:c.139-31_139-30delCT
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000473477
  ensembl transcript: ENST00000555163
  gene symbol: ZFYVE21
  hgvsc: ENST00000555163.2:c.18-31_18-30delCT
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000555501
  gene symbol: ZFYVE21
  hgvsc: ENST00000555501.1:n.3407-31_3407-30delCT
  variant of: http://identifiers.org/hgnc/20760
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9056
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10008
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1137
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9318
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1717
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10913
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4522
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2744
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6679
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 386
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 495
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 344
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26255
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 239
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
reference allele: CCT
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: BaseQRankSum

14-104195224-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 104195224
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 104195224
    reference: chr 14
allele count: 5
allele frequency: 4.134486579456563e-5
allele num: 120934
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000452301
  ensembl transcript: ENST00000556610
  gene symbol: ZFYVE21
  hgvsc: ENST00000556610.1:c.139-21G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000473477
  ensembl transcript: ENST00000555163
  gene symbol: ZFYVE21
  hgvsc: ENST00000555163.2:c.18-21G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000216602
  ensembl transcript: ENST00000216602
  gene symbol: ZFYVE21
  hgvsc: ENST00000216602.6:c.359-21G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000450746
  ensembl transcript: ENST00000553512
  gene symbol: ZFYVE21
  hgvsc: ENST00000553512.1:c.*264-21G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000310543
  ensembl transcript: ENST00000311141
  gene symbol: ZFYVE21
  hgvsc: ENST00000311141.2:c.359-21G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000555501
  gene symbol: ZFYVE21
  hgvsc: ENST00000555501.1:n.3407-21G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000556795
  gene symbol: ZFYVE21
  hgvsc: ENST00000556795.1:n.102G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000553724
  gene symbol: ZFYVE21
  hgvsc: ENST00000553724.1:n.462-204G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554630
  gene symbol: ZFYVE21
  hgvsc: ENST00000554630.1:n.370-21G>A
  variant of: http://identifiers.org/hgnc/20760
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6704
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10302
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9100
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11192
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2746
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1717
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4530
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1138
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9779
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4644
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9244
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP

14-104195236-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 104195236
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 104195236
    reference: chr 14
allele count: 1
allele frequency: 8.253140319891718e-6
allele num: 121166
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000310543
  ensembl transcript: ENST00000311141
  gene symbol: ZFYVE21
  hgvsc: ENST00000311141.2:c.359-9G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000216602
  ensembl transcript: ENST00000216602
  gene symbol: ZFYVE21
  hgvsc: ENST00000216602.6:c.359-9G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000556795
  gene symbol: ZFYVE21
  hgvsc: ENST00000556795.1:n.114G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000473477
  ensembl transcript: ENST00000555163
  gene symbol: ZFYVE21
  hgvsc: ENST00000555163.2:c.18-9G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000452301
  ensembl transcript: ENST00000556610
  gene symbol: ZFYVE21
  hgvsc: ENST00000556610.1:c.139-9G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000450746
  ensembl transcript: ENST00000553512
  gene symbol: ZFYVE21
  hgvsc: ENST00000553512.1:c.*264-9G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000553724
  gene symbol: ZFYVE21
  hgvsc: ENST00000553724.1:n.462-192G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000555501
  gene symbol: ZFYVE21
  hgvsc: ENST00000555501.1:n.3407-9G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554630
  gene symbol: ZFYVE21
  hgvsc: ENST00000554630.1:n.370-9G>A
  variant of: http://identifiers.org/hgnc/20760
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11251
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1139
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9945
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4535
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9126
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2746
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10385
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6711
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1716
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3145
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum

http://identifiers.org/exac.variant/14-104195241-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 104195241
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 104195241
    reference: chr 14
allele count: 3
allele frequency: 2.47520667975776e-5
allele num: 121202
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000555501
  gene symbol: ZFYVE21
  hgvsc: ENST00000555501.1:n.3407-4C>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554630
  gene symbol: ZFYVE21
  hgvsc: ENST00000554630.1:n.370-4C>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000450746
  ensembl transcript: ENST00000553512
  gene symbol: ZFYVE21
  hgvsc: ENST00000553512.1:c.*264-4C>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000216602
  ensembl transcript: ENST00000216602
  gene symbol: ZFYVE21
  hgvsc: ENST00000216602.6:c.359-4C>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000452301
  ensembl transcript: ENST00000556610
  gene symbol: ZFYVE21
  hgvsc: ENST00000556610.1:c.139-4C>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000556795
  gene symbol: ZFYVE21
  hgvsc: ENST00000556795.1:n.119C>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000473477
  ensembl transcript: ENST00000555163
  gene symbol: ZFYVE21
  hgvsc: ENST00000555163.2:c.18-4C>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000310543
  ensembl transcript: ENST00000311141
  gene symbol: ZFYVE21
  hgvsc: ENST00000311141.2:c.359-4C>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000553724
  gene symbol: ZFYVE21
  hgvsc: ENST00000553724.1:n.462-187C>A
  variant of: http://identifiers.org/hgnc/20760
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1139
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2747
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9924
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6715
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4537
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10413
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9132
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11275
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1717
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3159
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.75e1
  variant carriers: 0
hgvs: c.359-4C>A
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/14-104195251-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 104195251
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 104195251
    reference: chr 14
allele count: 1
allele frequency: 8.244838730954422e-6
allele num: 121288
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000553724
  gene symbol: ZFYVE21
  hgvsc: ENST00000553724.1:n.462-177C>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000452301
  ensembl transcript: ENST00000556610
  gene symbol: ZFYVE21
  hgvsc: ENST00000556610.1:c.145C>A
  hgvsp: ENSP00000452301.1:p.Pro49Thr
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000310543
  ensembl transcript: ENST00000311141
  gene symbol: ZFYVE21
  hgvsc: ENST00000311141.2:c.365C>A
  hgvsp: ENSP00000310543.2:p.Thr122Asn
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000216602
  ensembl transcript: ENST00000216602
  gene symbol: ZFYVE21
  hgvsc: ENST00000216602.6:c.365C>A
  hgvsp: ENSP00000216602.6:p.Thr122Asn
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000556795
  gene symbol: ZFYVE21
  hgvsc: ENST00000556795.1:n.129C>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554630
  gene symbol: ZFYVE21
  hgvsc: ENST00000554630.1:n.376C>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000450746
  ensembl transcript: ENST00000553512
  gene symbol: ZFYVE21
  hgvsc: ENST00000553512.1:c.*270C>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000555501
  gene symbol: ZFYVE21
  hgvsc: ENST00000555501.1:n.3413C>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000473477
  ensembl transcript: ENST00000555163
  gene symbol: ZFYVE21
  hgvsc: ENST00000555163.2:c.24C>A
  hgvsp: ENSP00000473477.1:p.Thr9Asn
  variant of: http://identifiers.org/hgnc/20760
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6720
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10438
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9949
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1717
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2746
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11290
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4538
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9137
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1140
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2841
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Thr122Asn
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
population: African
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ

14-104195255-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 104195255
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 104195255
    reference: chr 14
allele count: 3
allele frequency: 2.47320692497939e-5
allele num: 121300
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000555501
  gene symbol: ZFYVE21
  hgvsc: ENST00000555501.1:n.3417C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000310543
  ensembl transcript: ENST00000311141
  gene symbol: ZFYVE21
  hgvsc: ENST00000311141.2:c.369C>T
  hgvsp: ENST00000311141.2:c.369C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000452301
  ensembl transcript: ENST00000556610
  gene symbol: ZFYVE21
  hgvsc: ENST00000556610.1:c.149C>T
  hgvsp: ENSP00000452301.1:p.Ser50Phe
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000450746
  ensembl transcript: ENST00000553512
  gene symbol: ZFYVE21
  hgvsc: ENST00000553512.1:c.*274C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000553724
  gene symbol: ZFYVE21
  hgvsc: ENST00000553724.1:n.462-173C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554630
  gene symbol: ZFYVE21
  hgvsc: ENST00000554630.1:n.380C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000216602
  ensembl transcript: ENST00000216602
  gene symbol: ZFYVE21
  hgvsc: ENST00000216602.6:c.369C>T
  hgvsp: ENST00000216602.6:c.369C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000473477
  ensembl transcript: ENST00000555163
  gene symbol: ZFYVE21
  hgvsc: ENST00000555163.2:c.28C>T
  hgvsp: ENST00000555163.2:c.28C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000556795
  gene symbol: ZFYVE21
  hgvsc: ENST00000556795.1:n.133C>T
  variant of: http://identifiers.org/hgnc/20760
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1717
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2746
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4539
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10434
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11295
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1140
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6719
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9141
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9961
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3167
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4142
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ser50Phe
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum

14-104195258-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 104195258
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 104195258
    reference: chr 14
allele count: 1
allele frequency: 8.24347940778844e-6
allele num: 121308
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000450746
  ensembl transcript: ENST00000553512
  gene symbol: ZFYVE21
  hgvsc: ENST00000553512.1:c.*277C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000310543
  ensembl transcript: ENST00000311141
  gene symbol: ZFYVE21
  hgvsc: ENST00000311141.2:c.372C>T
  hgvsp: ENST00000311141.2:c.372C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000553724
  gene symbol: ZFYVE21
  hgvsc: ENST00000553724.1:n.462-170C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000452301
  ensembl transcript: ENST00000556610
  gene symbol: ZFYVE21
  hgvsc: ENST00000556610.1:c.152C>T
  hgvsp: ENSP00000452301.1:p.Ser51Leu
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000555501
  gene symbol: ZFYVE21
  hgvsc: ENST00000555501.1:n.3420C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000473477
  ensembl transcript: ENST00000555163
  gene symbol: ZFYVE21
  hgvsc: ENST00000555163.2:c.31C>T
  hgvsp: ENST00000555163.2:c.31C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000216602
  ensembl transcript: ENST00000216602
  gene symbol: ZFYVE21
  hgvsc: ENST00000216602.6:c.372C>T
  hgvsp: ENST00000216602.6:c.372C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554630
  gene symbol: ZFYVE21
  hgvsc: ENST00000554630.1:n.383C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000556795
  gene symbol: ZFYVE21
  hgvsc: ENST00000556795.1:n.136C>T
  variant of: http://identifiers.org/hgnc/20760
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10438
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11297
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9961
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6719
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4542
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1718
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2746
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9140
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4796
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ser51Leu
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum

14-104195263-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 104195263
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 104195263
    reference: chr 14
allele count: 3
allele frequency: 2.472758444470088e-5
allele num: 121322
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000553724
  gene symbol: ZFYVE21
  hgvsc: ENST00000553724.1:n.462-165C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000452301
  ensembl transcript: ENST00000556610
  gene symbol: ZFYVE21
  hgvsc: ENST00000556610.1:c.157C>T
  hgvsp: ENSP00000452301.1:p.Arg53Cys
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000556795
  gene symbol: ZFYVE21
  hgvsc: ENST00000556795.1:n.141C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000555501
  gene symbol: ZFYVE21
  hgvsc: ENST00000555501.1:n.3425C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000310543
  ensembl transcript: ENST00000311141
  gene symbol: ZFYVE21
  hgvsc: ENST00000311141.2:c.377C>T
  hgvsp: ENSP00000310543.2:p.Thr126Met
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000216602
  ensembl transcript: ENST00000216602
  gene symbol: ZFYVE21
  hgvsc: ENST00000216602.6:c.377C>T
  hgvsp: ENSP00000216602.6:p.Thr126Met
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554630
  gene symbol: ZFYVE21
  hgvsc: ENST00000554630.1:n.388C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000473477
  ensembl transcript: ENST00000555163
  gene symbol: ZFYVE21
  hgvsc: ENST00000555163.2:c.36C>T
  hgvsp: ENSP00000473477.1:p.Thr13Met
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000450746
  ensembl transcript: ENST00000553512
  gene symbol: ZFYVE21
  hgvsc: ENST00000553512.1:c.*282C>T
  variant of: http://identifiers.org/hgnc/20760
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9139
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10441
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9962
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11299
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1718
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6721
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2746
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4541
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5008
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2843
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Thr126Met
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD

14-104195264-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 104195264
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 104195264
    reference: chr 14
allele count: 6
allele frequency: 4.945435363159804e-5
allele num: 121324
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000450746
  ensembl transcript: ENST00000553512
  gene symbol: ZFYVE21
  hgvsc: ENST00000553512.1:c.*283G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000556795
  gene symbol: ZFYVE21
  hgvsc: ENST00000556795.1:n.142G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000473477
  ensembl transcript: ENST00000555163
  gene symbol: ZFYVE21
  hgvsc: ENST00000555163.2:c.37G>A
  hgvsp: ENST00000555163.2:c.37G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000452301
  ensembl transcript: ENST00000556610
  gene symbol: ZFYVE21
  hgvsc: ENST00000556610.1:c.158G>A
  hgvsp: ENSP00000452301.1:p.Arg53His
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000310543
  ensembl transcript: ENST00000311141
  gene symbol: ZFYVE21
  hgvsc: ENST00000311141.2:c.378G>A
  hgvsp: ENST00000311141.2:c.378G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000555501
  gene symbol: ZFYVE21
  hgvsc: ENST00000555501.1:n.3426G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000216602
  ensembl transcript: ENST00000216602
  gene symbol: ZFYVE21
  hgvsc: ENST00000216602.6:c.378G>A
  hgvsp: ENST00000216602.6:c.378G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554630
  gene symbol: ZFYVE21
  hgvsc: ENST00000554630.1:n.389G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000553724
  gene symbol: ZFYVE21
  hgvsc: ENST00000553724.1:n.462-164G>A
  variant of: http://identifiers.org/hgnc/20760
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9960
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11298
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2746
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10442
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1718
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4541
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6721
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9139
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Arg53His
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff

14-104195280-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 104195280
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 104195280
    reference: chr 14
allele count: 1
allele frequency: 8.241033755274261e-6
allele num: 121344
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000216602
  ensembl transcript: ENST00000216602
  gene symbol: ZFYVE21
  hgvsc: ENST00000216602.6:c.394A>G
  hgvsp: ENSP00000216602.6:p.Lys132Glu
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000555501
  gene symbol: ZFYVE21
  hgvsc: ENST00000555501.1:n.3442A>G
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000553724
  gene symbol: ZFYVE21
  hgvsc: ENST00000553724.1:n.462-148A>G
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000473477
  ensembl transcript: ENST00000555163
  gene symbol: ZFYVE21
  hgvsc: ENST00000555163.2:c.53A>G
  hgvsp: ENSP00000473477.1:p.Lys19Glu
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000452301
  ensembl transcript: ENST00000556610
  gene symbol: ZFYVE21
  hgvsc: ENST00000556610.1:c.174A>G
  hgvsp: ENST00000556610.1:c.174A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554630
  gene symbol: ZFYVE21
  hgvsc: ENST00000554630.1:n.405A>G
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000450746
  ensembl transcript: ENST00000553512
  gene symbol: ZFYVE21
  hgvsc: ENST00000553512.1:c.*299A>G
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000310543
  ensembl transcript: ENST00000311141
  gene symbol: ZFYVE21
  hgvsc: ENST00000311141.2:c.394A>G
  hgvsp: ENSP00000310543.2:p.Lys132Glu
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000556795
  gene symbol: ZFYVE21
  hgvsc: ENST00000556795.1:n.158A>G
  variant of: http://identifiers.org/hgnc/20760
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6721
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11298
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10453
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2746
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9143
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4540
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1719
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9967
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5006
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2842
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Lys132Glu
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: QD

14-104195301-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 104195301
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 104195301
    reference: chr 14
allele count: 74
allele frequency: 6.098264466896313e-4
allele num: 121346
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554630
  gene symbol: ZFYVE21
  hgvsc: ENST00000554630.1:n.426C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000553724
  gene symbol: ZFYVE21
  hgvsc: ENST00000553724.1:n.462-127C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000556795
  gene symbol: ZFYVE21
  hgvsc: ENST00000556795.1:n.179C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000452301
  ensembl transcript: ENST00000556610
  gene symbol: ZFYVE21
  hgvsc: ENST00000556610.1:c.*6C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000450746
  ensembl transcript: ENST00000553512
  gene symbol: ZFYVE21
  hgvsc: ENST00000553512.1:c.*320C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000473477
  ensembl transcript: ENST00000555163
  gene symbol: ZFYVE21
  hgvsc: ENST00000555163.2:c.74C>T
  hgvsp: ENSP00000473477.1:p.Arg26Cys
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000216602
  ensembl transcript: ENST00000216602
  gene symbol: ZFYVE21
  hgvsc: ENST00000216602.6:c.415C>T
  hgvsp: ENSP00000216602.6:p.Arg139Cys
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000310543
  ensembl transcript: ENST00000311141
  gene symbol: ZFYVE21
  hgvsc: ENST00000311141.2:c.415C>T
  hgvsp: ENSP00000310543.2:p.Arg139Cys
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000555501
  gene symbol: ZFYVE21
  hgvsc: ENST00000555501.1:n.3463C>T
  variant of: http://identifiers.org/hgnc/20760
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4538
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10444
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6713
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9939
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9135
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 7.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2743
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 9.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11290
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1719
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 8.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 9.75e1
  variant carriers: 39
genotype quality: GenotypeQuality
  all individuals: 4676
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg139Cys
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
population: African
population: East Asian
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

14-104195303-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 104195303
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 104195303
    reference: chr 14
allele count: 6
allele frequency: 4.944538756942956e-5
allele num: 121346
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000216602
  ensembl transcript: ENST00000216602
  gene symbol: ZFYVE21
  hgvsc: ENST00000216602.6:c.417T>C
  hgvsp: ENST00000216602.6:c.417T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000556795
  gene symbol: ZFYVE21
  hgvsc: ENST00000556795.1:n.181T>C
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000473477
  ensembl transcript: ENST00000555163
  gene symbol: ZFYVE21
  hgvsc: ENST00000555163.2:c.76T>C
  hgvsp: ENST00000555163.2:c.76T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000310543
  ensembl transcript: ENST00000311141
  gene symbol: ZFYVE21
  hgvsc: ENST00000311141.2:c.417T>C
  hgvsp: ENST00000311141.2:c.417T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000553724
  gene symbol: ZFYVE21
  hgvsc: ENST00000553724.1:n.462-125T>C
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000452301
  ensembl transcript: ENST00000556610
  gene symbol: ZFYVE21
  hgvsc: ENST00000556610.1:c.*8T>C
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000450746
  ensembl transcript: ENST00000553512
  gene symbol: ZFYVE21
  hgvsc: ENST00000553512.1:c.*322T>C
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000555501
  gene symbol: ZFYVE21
  hgvsc: ENST00000555501.1:n.3465T>C
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554630
  gene symbol: ZFYVE21
  hgvsc: ENST00000554630.1:n.428T>C
  variant of: http://identifiers.org/hgnc/20760
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9135
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1145
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9931
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1720
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10446
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6715
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4542
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11288
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2741
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4797
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Arg139Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
population: African
reference allele: T
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: ClippingRankSum

14-104195304-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 104195304
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 104195304
    reference: chr 14
allele count: 8
allele frequency: 6.592827004219409e-5
allele num: 121344
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000216602
  ensembl transcript: ENST00000216602
  gene symbol: ZFYVE21
  hgvsc: ENST00000216602.6:c.418C>T
  hgvsp: ENSP00000216602.6:p.Leu140Phe
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000452301
  ensembl transcript: ENST00000556610
  gene symbol: ZFYVE21
  hgvsc: ENST00000556610.1:c.*9C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000310543
  ensembl transcript: ENST00000311141
  gene symbol: ZFYVE21
  hgvsc: ENST00000311141.2:c.418C>T
  hgvsp: ENSP00000310543.2:p.Leu140Phe
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000450746
  ensembl transcript: ENST00000553512
  gene symbol: ZFYVE21
  hgvsc: ENST00000553512.1:c.*323C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000553724
  gene symbol: ZFYVE21
  hgvsc: ENST00000553724.1:n.462-124C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000473477
  ensembl transcript: ENST00000555163
  gene symbol: ZFYVE21
  hgvsc: ENST00000555163.2:c.77C>T
  hgvsp: ENSP00000473477.1:p.Leu27Phe
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000555501
  gene symbol: ZFYVE21
  hgvsc: ENST00000555501.1:n.3466C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554630
  gene symbol: ZFYVE21
  hgvsc: ENST00000554630.1:n.429C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000556795
  gene symbol: ZFYVE21
  hgvsc: ENST00000556795.1:n.182C>T
  variant of: http://identifiers.org/hgnc/20760
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1145
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10447
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1720
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9924
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2740
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9134
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6715
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11288
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4543
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4134
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4677
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Leu140Phe
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

http://identifiers.org/exac.variant/14-104195309-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 104195309
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 104195309
    reference: chr 14
allele count: 1
allele frequency: 8.240626287597857e-6
allele num: 121350
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000452301
  ensembl transcript: ENST00000556610
  gene symbol: ZFYVE21
  hgvsc: ENST00000556610.1:c.*14C>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000553724
  gene symbol: ZFYVE21
  hgvsc: ENST00000553724.1:n.462-119C>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000216602
  ensembl transcript: ENST00000216602
  gene symbol: ZFYVE21
  hgvsc: ENST00000216602.6:c.423C>A
  hgvsp: ENST00000216602.6:c.423C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000310543
  ensembl transcript: ENST00000311141
  gene symbol: ZFYVE21
  hgvsc: ENST00000311141.2:c.423C>A
  hgvsp: ENST00000311141.2:c.423C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000450746
  ensembl transcript: ENST00000553512
  gene symbol: ZFYVE21
  hgvsc: ENST00000553512.1:c.*328C>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554630
  gene symbol: ZFYVE21
  hgvsc: ENST00000554630.1:n.434C>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000473477
  ensembl transcript: ENST00000555163
  gene symbol: ZFYVE21
  hgvsc: ENST00000555163.2:c.82C>A
  hgvsp: ENST00000555163.2:c.82C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000556795
  gene symbol: ZFYVE21
  hgvsc: ENST00000556795.1:n.187C>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000555501
  gene symbol: ZFYVE21
  hgvsc: ENST00000555501.1:n.3471C>A
  variant of: http://identifiers.org/hgnc/20760
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9918
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1145
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4543
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1719
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6715
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10448
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9136
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2742
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11291
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4798
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Ser141Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff

14-104195310-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 104195310
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 104195310
    reference: chr 14
allele count: 1
allele frequency: 8.240354664864776e-6
allele num: 121354
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000473477
  ensembl transcript: ENST00000555163
  gene symbol: ZFYVE21
  hgvsc: ENST00000555163.2:c.83A>G
  hgvsp: ENSP00000473477.1:p.Asn29Asp
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000310543
  ensembl transcript: ENST00000311141
  gene symbol: ZFYVE21
  hgvsc: ENST00000311141.2:c.424A>G
  hgvsp: ENSP00000310543.2:p.Asn142Asp
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000450746
  ensembl transcript: ENST00000553512
  gene symbol: ZFYVE21
  hgvsc: ENST00000553512.1:c.*329A>G
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000216602
  ensembl transcript: ENST00000216602
  gene symbol: ZFYVE21
  hgvsc: ENST00000216602.6:c.424A>G
  hgvsp: ENSP00000216602.6:p.Asn142Asp
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554630
  gene symbol: ZFYVE21
  hgvsc: ENST00000554630.1:n.435A>G
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000556795
  gene symbol: ZFYVE21
  hgvsc: ENST00000556795.1:n.188A>G
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000553724
  gene symbol: ZFYVE21
  hgvsc: ENST00000553724.1:n.462-118A>G
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000555501
  gene symbol: ZFYVE21
  hgvsc: ENST00000555501.1:n.3472A>G
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000452301
  ensembl transcript: ENST00000556610
  gene symbol: ZFYVE21
  hgvsc: ENST00000556610.1:c.*15A>G
  variant of: http://identifiers.org/hgnc/20760
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1145
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10450
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2742
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11291
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9916
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4543
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1719
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9136
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6713
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4798
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3171
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Asn142Asp
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: Other
reference allele: A
site quality: QD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

14-104195325-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 104195325
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 104195325
    reference: chr 14
allele count: 1
allele frequency: 8.240626287597857e-6
allele num: 121350
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000473477
  ensembl transcript: ENST00000555163
  gene symbol: ZFYVE21
  hgvsc: ENST00000555163.2:c.93+5G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000553724
  gene symbol: ZFYVE21
  hgvsc: ENST00000553724.1:n.462-103G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000555501
  gene symbol: ZFYVE21
  hgvsc: ENST00000555501.1:n.3482+5G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000216602
  ensembl transcript: ENST00000216602
  gene symbol: ZFYVE21
  hgvsc: ENST00000216602.6:c.434+5G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000452301
  ensembl transcript: ENST00000556610
  gene symbol: ZFYVE21
  hgvsc: ENST00000556610.1:c.*25+5G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000556795
  gene symbol: ZFYVE21
  hgvsc: ENST00000556795.1:n.198+5G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554630
  gene symbol: ZFYVE21
  hgvsc: ENST00000554630.1:n.445+5G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000310543
  ensembl transcript: ENST00000311141
  gene symbol: ZFYVE21
  hgvsc: ENST00000311141.2:c.434+5G>A
  variant of: http://identifiers.org/hgnc/20760
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9139
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6712
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9870
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1145
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11294
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1719
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2742
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4542
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10457
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9491
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4679
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3169
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.75e1
  variant carriers: 0
hgvs: c.434+5G>A
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQ

14-104195329-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 104195329
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 104195329
    reference: chr 14
allele count: 3
allele frequency: 2.47222863170386e-5
allele num: 121348
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000556795
  gene symbol: ZFYVE21
  hgvsc: ENST00000556795.1:n.198+9C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554630
  gene symbol: ZFYVE21
  hgvsc: ENST00000554630.1:n.445+9C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000473477
  ensembl transcript: ENST00000555163
  gene symbol: ZFYVE21
  hgvsc: ENST00000555163.2:c.93+9C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000555501
  gene symbol: ZFYVE21
  hgvsc: ENST00000555501.1:n.3482+9C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000310543
  ensembl transcript: ENST00000311141
  gene symbol: ZFYVE21
  hgvsc: ENST00000311141.2:c.434+9C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000553724
  gene symbol: ZFYVE21
  hgvsc: ENST00000553724.1:n.462-99C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000216602
  ensembl transcript: ENST00000216602
  gene symbol: ZFYVE21
  hgvsc: ENST00000216602.6:c.434+9C>T
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000452301
  ensembl transcript: ENST00000556610
  gene symbol: ZFYVE21
  hgvsc: ENST00000556610.1:c.*25+9C>T
  variant of: http://identifiers.org/hgnc/20760
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10465
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1145
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11298
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9851
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6714
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9136
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2743
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4543
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1719
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4136
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum

14-104195330-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 104195330
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 104195330
    reference: chr 14
allele count: 3
allele frequency: 2.472106399459433e-5
allele num: 121354
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000556795
  gene symbol: ZFYVE21
  hgvsc: ENST00000556795.1:n.198+10G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000452301
  ensembl transcript: ENST00000556610
  gene symbol: ZFYVE21
  hgvsc: ENST00000556610.1:c.*25+10G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000216602
  ensembl transcript: ENST00000216602
  gene symbol: ZFYVE21
  hgvsc: ENST00000216602.6:c.434+10G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000553724
  gene symbol: ZFYVE21
  hgvsc: ENST00000553724.1:n.462-98G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000555501
  gene symbol: ZFYVE21
  hgvsc: ENST00000555501.1:n.3482+10G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000473477
  ensembl transcript: ENST00000555163
  gene symbol: ZFYVE21
  hgvsc: ENST00000555163.2:c.93+10G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl transcript: ENST00000554630
  gene symbol: ZFYVE21
  hgvsc: ENST00000554630.1:n.445+10G>A
  variant of: http://identifiers.org/hgnc/20760
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100711
  ensembl protein: ENSP00000310543
  ensembl transcript: ENST00000311141
  gene symbol: ZFYVE21
  hgvsc: ENST00000311141.2:c.434+10G>A
  variant of: http://identifiers.org/hgnc/20760
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6711
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11302
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10461
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1145
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9142
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4542
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1719
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2744
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9844
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2842
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9473
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Other
reference allele: G

GenotypeQuality
all individuals: 2735
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1049
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 216
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7620
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 250
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 235
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3334
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 903
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 4.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11454
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.535579374097847e-5
allele num: 65122
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16468
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6546
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10068
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -9.555e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.04e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.449954e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.387e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -8.66e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.3e-2

QD
type: SiteQuality
SIO_000300: 6.94e0

GenotypeQuality
all individuals: 39108
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1000
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 950
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 197
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 229
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 903
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 1.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.535202186127913e-5
allele num: 65138
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 886
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6542
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11458
num of homozygotes: 0

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

East Asian
type: Population
allele count: 14
allele frequency: 1.643964302489432e-3
allele num: 8516
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16466
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.1e-3

DP
type: SiteQuality
SIO_000300: 1.452502e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.266e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.4e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.74e0

QD
type: SiteQuality
SIO_000300: 1.298e1

MQRankSum
type: SiteQuality
SIO_000300: 5.7e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.0e-2

MQ
type: SiteQuality
SIO_000300: 5.955e1

GenotypeQuality
all individuals: 104
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 230
bin: 2.75e1
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
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3335
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1110
bin: 9.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11456
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10088
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6538
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 886
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16468
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.535060788407221e-5
allele num: 65144
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8516
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.74e0

MQRankSum
type: SiteQuality
SIO_000300: 1.85e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.06e-1

DP
type: SiteQuality
SIO_000300: 1.451939e6

VQSLOD
type: SiteQuality
SIO_000300: -2.766e0

FS
type: SiteQuality
SIO_000300: 7.348e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.856e0

MQ
type: SiteQuality
SIO_000300: 5.963e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

QD
type: SiteQuality
SIO_000300: 1.48e0

GenotypeQuality
all individuals: 297
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 953
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39084
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1135
bin: 9.75e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8534
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.533460099368214e-5
allele num: 65212
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 886
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6540
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10106
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16470
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.799999999999999e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.435e0

MQRankSum
type: SiteQuality
SIO_000300: -8.799999999999999e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.001e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.8e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

QD
type: SiteQuality
SIO_000300: 5.25e0

MQ
type: SiteQuality
SIO_000300: 5.947e1

DP
type: SiteQuality
SIO_000300: 1.454191e6

GenotypeQuality
all individuals: 1149
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 295
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 914
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2753
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38797
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variant carriers: 0

GenotypeQuality
all individuals: 260
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 250
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variant carriers: 0

GenotypeQuality
all individuals: 2264
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3357
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7565
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10118
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8542
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 886
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11472
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65234
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16470
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.46e-1

DP
type: SiteQuality
SIO_000300: 1.455185e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 7.000000000000001e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 5.27e-1

MQ
type: SiteQuality
SIO_000300: 5.968e1

VQSLOD
type: SiteQuality
SIO_000300: -5.238e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.371e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

QD
type: SiteQuality
SIO_000300: 5.31e0

GenotypeQuality
all individuals: 54
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38918
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3368
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 305
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 283
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 914
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 958
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 252
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 4.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 886
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11474
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10132
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.596433167861739e-5
allele num: 65268
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8544
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6534
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16478
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.216e0

VQSLOD
type: SiteQuality
SIO_000300: 1.78e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.17e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.7e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.583e0

MQ
type: SiteQuality
SIO_000300: 5.965e1

QD
type: SiteQuality
SIO_000300: 1.42e1

DP
type: SiteQuality
SIO_000300: 1.455744e6

MQRankSum
type: SiteQuality
SIO_000300: 7.32e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

GenotypeQuality
all individuals: 240
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 61
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variant carriers: 0

GenotypeQuality
all individuals: 3381
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11474
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65270
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 886
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10140
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16478
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6538
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.170138076293003e-4
allele num: 8546
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.366e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.233e0

DP
type: SiteQuality
SIO_000300: 1.45608e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

MQRankSum
type: SiteQuality
SIO_000300: 6.04e-1

MQ
type: SiteQuality
SIO_000300: 5.891e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.73e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.0e-2

FS
type: SiteQuality
SIO_000300: 8.090999999999999e0

QD
type: SiteQuality
SIO_000300: 1.742e1

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

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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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2771
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 4.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6536
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8544
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10138
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 886
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.069434328720563e-5
allele num: 16476
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11472
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65292
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.25e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.3e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.457329e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.416e0

VQSLOD
type: SiteQuality
SIO_000300: 6.96e-1

FS
type: SiteQuality
SIO_000300: 1.851e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.64e-1

QD
type: SiteQuality
SIO_000300: 8.380000000000001e0

GenotypeQuality
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bin: 5.75e1
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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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 7618
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10148
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.530596626565035e-5
allele num: 65334
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16482
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8550
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6542
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11474
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

ClippingRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.458405e6

MQRankSum
type: SiteQuality
SIO_000300: 9.45e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.323e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -9.313e-1

QD
type: SiteQuality
SIO_000300: 1.901e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.74e-1

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 982
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GenotypeQuality
all individuals: 38234
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10146
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6538
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.530549773478634e-5
allele num: 65336
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16484
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8546
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11474
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.45e-1

FS
type: SiteQuality
SIO_000300: 6.54e-1

QD
type: SiteQuality
SIO_000300: 1.133e1

MQRankSum
type: SiteQuality
SIO_000300: -1.91e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.04e-1

MQ
type: SiteQuality
SIO_000300: 5.911e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.207e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.7e-2

DP
type: SiteQuality
SIO_000300: 1.461253e6

GenotypeQuality
all individuals: 3456
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7621
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2831
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2327
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38117
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 943
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 290
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1220
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 987
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 410
bin: 5.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6540
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8550
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16480
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10146
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11472
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.060818462856968e-5
allele num: 65342
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 886
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.901e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.08e0

MQRankSum
type: SiteQuality
SIO_000300: 2.32e-1

DP
type: SiteQuality
SIO_000300: 1.462032e6

QD
type: SiteQuality
SIO_000300: 1.104e1

FS
type: SiteQuality
SIO_000300: 1.115e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 9.53e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.72e-1

MQ
type: SiteQuality
SIO_000300: 5.933e1

GenotypeQuality
all individuals: 2328
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1240
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3470
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 286
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 331
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 218
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 954
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7637
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 866
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 995
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.529847321237341e-5
allele num: 65366
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16484
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10152
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11476
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6540
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8552
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -4.32e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.46e-1

DP
type: SiteQuality
SIO_000300: 1.463644e6

FS
type: SiteQuality
SIO_000300: 2.895e0

QD
type: SiteQuality
SIO_000300: 1.755e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.889e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.400000000000001e-2

VQSLOD
type: SiteQuality
SIO_000300: -7.37e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 33
bin: 2.5e0
variant carriers: 8

GenotypeQuality
all individuals: 39
bin: 7.5e0
variant carriers: 33

GenotypeQuality
all individuals: 47
bin: 1.25e1
variant carriers: 45

GenotypeQuality
all individuals: 160
bin: 3.25e1
variant carriers: 158

GenotypeQuality
all individuals: 1169
bin: 6.25e1
variant carriers: 464

GenotypeQuality
all individuals: 676
bin: 7.75e1
variant carriers: 664

GenotypeQuality
all individuals: 329
bin: 5.25e1
variant carriers: 325

GenotypeQuality
all individuals: 109
bin: 1.75e1
variant carriers: 108

GenotypeQuality
all individuals: 228
bin: 3.75e1
variant carriers: 221

GenotypeQuality
all individuals: 614
bin: 6.75e1
variant carriers: 532

GenotypeQuality
all individuals: 222
bin: 5.75e1
variant carriers: 218

GenotypeQuality
all individuals: 532
bin: 8.75e1
variant carriers: 531

GenotypeQuality
all individuals: 1020
bin: 9.25e1
variant carriers: 1018

Other
type: Population
allele count: 821
allele frequency: 9.122222222222223e-1
allele num: 900
num of homozygotes: 378

East Asian
type: Population
allele count: 8268
allele frequency: 9.616189811584089e-1
allele num: 8598
num of homozygotes: 3977

African
type: Population
allele count: 8902
allele frequency: 8.637686784397438e-1
allele num: 10306
num of homozygotes: 3856

European (Finnish)
type: Population
allele count: 6268
allele frequency: 9.522941355211182e-1
allele num: 6582
num of homozygotes: 2989

South Asian
type: Population
allele count: 15029
allele frequency: 9.110693501454898e-1
allele num: 16496
num of homozygotes: 6862

European (Non-Finnish)
type: Population
allele count: 61714
allele frequency: 9.354291084366568e-1
allele num: 65974
num of homozygotes: 28882

Latino
type: Population
allele count: 8276
allele frequency: 7.204038997214485e-1
allele num: 11488
num of homozygotes: 3018

MQRankSum
type: SiteQuality
SIO_000300: 8.799999999999999e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.75e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.7e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.86e-1

MQ
type: SiteQuality
SIO_000300: 5.967e1

FS
type: SiteQuality
SIO_000300: 1.137e0

DP
type: SiteQuality
SIO_000300: 3.43826e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.7e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.03e-2

QD
type: SiteQuality
SIO_000300: 3.17e1

GenotypeQuality
all individuals: 72
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 187
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 157
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10810
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variant carriers: 0

GenotypeQuality
all individuals: 36044
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variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 505
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 575
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2182
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 282
bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10172
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8562
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11468
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 884
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16426
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.532003554248246e-5
allele num: 65274
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.253e0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.76e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.079e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

DP
type: SiteQuality
SIO_000300: 1.777682e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.387e0

MQRankSum
type: SiteQuality
SIO_000300: 7.48e-1

QD
type: SiteQuality
SIO_000300: 2.945e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.44e0

MQ
type: SiteQuality
SIO_000300: 5.96e1

GenotypeQuality
all individuals: 119
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 10747
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36223
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 4.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1598
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 563
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3211
bin: 7.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65120
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.170138076293003e-4
allele num: 8546
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6402
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10166
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 880
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16380
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.96e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.5e-2

VQSLOD
type: SiteQuality
SIO_000300: -5.23e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.407e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.67e-1

MQ
type: SiteQuality
SIO_000300: 5.871e1

DP
type: SiteQuality
SIO_000300: 1.771731e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

QD
type: SiteQuality
SIO_000300: 1.236e1

GenotypeQuality
all individuals: 58
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36206
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 42
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2891
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 229
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 489
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 560
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1640
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2154
bin: 9.75e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6400
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11452
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.10798924993892e-5
allele num: 16372
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8544
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10160
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65098
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 880
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.948e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.535e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.02e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

DP
type: SiteQuality
SIO_000300: 1.770683e6

ClippingRankSum
type: SiteQuality
SIO_000300: 6.11e-1

QD
type: SiteQuality
SIO_000300: 1.093e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.19e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.38e-1

GenotypeQuality
all individuals: 116
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 251
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 484
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variant carriers: 0

GenotypeQuality
all individuals: 1791
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3172
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 551
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variant carriers: 0

GenotypeQuality
all individuals: 2870
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1580
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 4.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11444
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.116956202593589e-5
allele num: 16348
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.537846399901578e-5
allele num: 65026
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10150
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6390
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 880
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.766907e6

QD
type: SiteQuality
SIO_000300: 1.311e1

FS
type: SiteQuality
SIO_000300: 1.938e0

MQRankSum
type: SiteQuality
SIO_000300: 8.0e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 5.0e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.484e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.95e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.01e0

MQ
type: SiteQuality
SIO_000300: 5.968e1

GenotypeQuality
all individuals: 48
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10528
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 334
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 471
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3109
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 542
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GenotypeQuality
all individuals: 20
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2127
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 191
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2415
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 102
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variant carriers: 0

GenotypeQuality
all individuals: 375
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1533
bin: 8.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11424
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.176747469992939e-4
allele num: 8498
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10092
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.627915586819697e-5
allele num: 64824
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16308
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6324
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.8e-2

MQ
type: SiteQuality
SIO_000300: 5.963e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.697e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.48e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.95e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.751645e6

QD
type: SiteQuality
SIO_000300: 9.42e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 3.63e-1

GenotypeQuality
all individuals: 40
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 173
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 392
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3102
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 471
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2815
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 350
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35318
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 542
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 188
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2121
bin: 9.75e1
variant carriers: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11422
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16304
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.543400419804914e-5
allele num: 64792
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8496
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6316
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10086
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

QD
type: SiteQuality
SIO_000300: 1.095e1

FS
type: SiteQuality
SIO_000300: 1.314e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.74e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.879999999999999e-1

DP
type: SiteQuality
SIO_000300: 1.748938e6

MQRankSum
type: SiteQuality
SIO_000300: 4.14e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.56e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.1e-2

GenotypeQuality
all individuals: 199
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2759
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 257
bin: 7.5e0
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
all individuals: 1519
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.5e0
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GenotypeQuality
all individuals: 93
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
all individuals: 3087
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2798
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2113
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.545021939311538e-5
allele num: 64724
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8486
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6296
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10060
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11408
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16286
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.86e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.95e-1

DP
type: SiteQuality
SIO_000300: 1.742696e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.65e-1

MQ
type: SiteQuality
SIO_000300: 5.965e1

MQRankSum
type: SiteQuality
SIO_000300: 1.06e0

FS
type: SiteQuality
SIO_000300: 1.273e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.392e0

QD
type: SiteQuality
SIO_000300: 1.286e1

GenotypeQuality
all individuals: 183
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 78
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1491

GenotypeQuality
all individuals: 1413
bin: 8.25e1
variant carriers: 4

GenotypeQuality
all individuals: 498
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 204
bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 93
allele frequency: 8.163623595505619e-3
allele num: 11392
num of homozygotes: 2

African
type: Population
allele count: 37
allele frequency: 3.680859530441703e-3
allele num: 10052
num of homozygotes: 0

South Asian
type: Population
allele count: 18
allele frequency: 1.106058744008848e-3
allele num: 16274
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 24
allele frequency: 3.814367450731087e-3
allele num: 6292
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1333
allele frequency: 2.060532987077228e-2
allele num: 64692
num of homozygotes: 15

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

Other
type: Population
allele count: 10
allele frequency: 1.149425287356322e-2
allele num: 870
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.38e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.64e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.41e-1

FS
type: SiteQuality
SIO_000300: 1.343e0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.34e-2

QD
type: SiteQuality
SIO_000300: 1.313e1

DP
type: SiteQuality
SIO_000300: 1.738595e6

MQRankSum
type: SiteQuality
SIO_000300: 1.17e-1

GenotypeQuality
all individuals: 2744
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2838
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 403
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variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 209
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 38
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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: 1413
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2915
bin: 2.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11392
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64692
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6292
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.228954160009832e-4
allele num: 16274
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10052
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.41e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.17e-1

FS
type: SiteQuality
SIO_000300: 1.343e0

QD
type: SiteQuality
SIO_000300: 1.313e1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.738595e6

VQSLOD
type: SiteQuality
SIO_000300: 4.38e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.34e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.64e-1

GenotypeQuality
all individuals: 3035
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 404
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variant carriers: 0

GenotypeQuality
all individuals: 141
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variant carriers: 0

GenotypeQuality
all individuals: 21
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variant carriers: 0

GenotypeQuality
all individuals: 81
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variant carriers: 0

GenotypeQuality
all individuals: 182
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variant carriers: 0

GenotypeQuality
all individuals: 167
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GenotypeQuality
all individuals: 49
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GenotypeQuality
all individuals: 2798
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 92
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variant carriers: 0

GenotypeQuality
all individuals: 432
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variant carriers: 0

GenotypeQuality
all individuals: 1380
bin: 9.75e1
variant carriers: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.547460617127294e-5
allele num: 64622
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6286
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10050
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16274
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11394
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.851e1

QD
type: SiteQuality
SIO_000300: 1.586e1

FS
type: SiteQuality
SIO_000300: 2.165e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.494e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.51e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.198e0

DP
type: SiteQuality
SIO_000300: 1.714782e6

MQRankSum
type: SiteQuality
SIO_000300: -3.38e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.1e-1

GenotypeQuality
all individuals: 291
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 732
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 438
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variant carriers: 0

GenotypeQuality
all individuals: 10193
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 102
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variant carriers: 0

GenotypeQuality
all individuals: 1353
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34440
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variant carriers: 0

GenotypeQuality
all individuals: 1357
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variant carriers: 1

GenotypeQuality
all individuals: 4038
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GenotypeQuality
all individuals: 657
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variant carriers: 0

GenotypeQuality
all individuals: 304
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variant carriers: 0

GenotypeQuality
all individuals: 246
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GenotypeQuality
all individuals: 2698
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variant carriers: 0

GenotypeQuality
all individuals: 391
bin: 8.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16228
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11358
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.000400160064026e-4
allele num: 9996
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64366
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6236
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.97e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.87e-1

FS
type: SiteQuality
SIO_000300: 2.27e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

QD
type: SiteQuality
SIO_000300: 1.346e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.205e0

VQSLOD
type: SiteQuality
SIO_000300: 1.81e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.860000000000001e-1

DP
type: SiteQuality
SIO_000300: 1.690219e6

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

GenotypeQuality
all individuals: 212
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
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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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1346
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2782
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 170
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 425
bin: 9.25e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6174
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63926
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.838607035531201e-5
allele num: 11314
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16154
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8356
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9926
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.1e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.397e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.4e-2

FS
type: SiteQuality
SIO_000300: 1.09e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.0e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

DP
type: SiteQuality
SIO_000300: 1.630217e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.07e0

MQ
type: SiteQuality
SIO_000300: 5.959e1

QD
type: SiteQuality
SIO_000300: 8.550000000000001e0

GenotypeQuality
all individuals: 234
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2696
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 226
bin: 4.25e1
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GenotypeQuality
all individuals: 538
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GenotypeQuality
all individuals: 415
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GenotypeQuality
all individuals: 2065
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1334
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 118
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1248
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 534
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9866
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11256
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16110
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6130
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63706
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.208021261174197e-4
allele num: 8278
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.735e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.24e-1

QD
type: SiteQuality
SIO_000300: 1.104e1

MQRankSum
type: SiteQuality
SIO_000300: -3.83e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.493e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 1.2841e1

DP
type: SiteQuality
SIO_000300: 1.579086e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.62e-1

MQ
type: SiteQuality
SIO_000300: 5.901e1

GenotypeQuality
all individuals: 3603
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1162
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
all individuals: 7186
bin: 6.75e1
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GenotypeQuality
all individuals: 397
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GenotypeQuality
all individuals: 171
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1319
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 413
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 321
bin: 4.75e1
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GenotypeQuality
all individuals: 360
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variant carriers: 0

GenotypeQuality
all individuals: 2154
bin: 7.25e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5998
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11150
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8100
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16040
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.179245283018868e-3
allele num: 848
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63054
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.470502e6

BaseQRankSum
type: SiteQuality
SIO_000300: -6.33e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.61e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.33e-1

QD
type: SiteQuality
SIO_000300: 1.491e1

FS
type: SiteQuality
SIO_000300: 9.035e0

MQ
type: SiteQuality
SIO_000300: 5.913e1

VQSLOD
type: SiteQuality
SIO_000300: 8.89e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.65e-1

GenotypeQuality
all individuals: 254
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 8.25e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8002
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11056
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5902
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.196522183863956e-5
allele num: 62568
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9674
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 836
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15990
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -9.2e-2

VQSLOD
type: SiteQuality
SIO_000300: 9.67e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.06e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.981e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.419951e6

QD
type: SiteQuality
SIO_000300: 1.277e1

FS
type: SiteQuality
SIO_000300: 3.148e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.8e-2

GenotypeQuality
all individuals: 665
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
all individuals: 896
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59896
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10686
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7754
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5362
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.927525057825752e-4
allele num: 15564
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.02e0

VQSLOD
type: SiteQuality
SIO_000300: 1.71e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.12e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.9e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 2.7e-2

QD
type: SiteQuality
SIO_000300: 1.073e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.925e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.826e0

DP
type: SiteQuality
SIO_000300: 1.292117e6

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
all individuals: 1931
bin: 4.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7754
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5362
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59896
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.097213078779899e-4
allele num: 9114
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15564
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10686
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.826e0

MQ
type: SiteQuality
SIO_000300: 5.925e1

QD
type: SiteQuality
SIO_000300: 1.073e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.7e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.12e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.9e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.02e0

VQSLOD
type: SiteQuality
SIO_000300: 1.71e-1

DP
type: SiteQuality
SIO_000300: 1.292117e6

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
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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: 286
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.457301078402798e-4
allele num: 6862
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9912
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7784
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4190
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14806
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 53764
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 674
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.29e0

MQ
type: SiteQuality
SIO_000300: 6.115e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.194198e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.2e-3

MQRankSum
type: SiteQuality
SIO_000300: 6.51e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.1e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.94e-1

QD
type: SiteQuality
SIO_000300: 6.59e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.12e0

GenotypeQuality
all individuals: 3537
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 7039
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GenotypeQuality
all individuals: 462
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7786
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4190
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6918
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9964
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 53764
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.758583400919168e-5
allele num: 14796
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 668
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.502e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.6e-1

QD
type: SiteQuality
SIO_000300: 1.128e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.21e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.55e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -6.0e-2

DP
type: SiteQuality
SIO_000300: 1.192787e6

GenotypeQuality
all individuals: 2855
bin: 3.25e1
variant carriers: 1366

GenotypeQuality
all individuals: 1306
bin: 5.75e1
variant carriers: 1237

GenotypeQuality
all individuals: 4816
bin: 2.25e1
variant carriers: 870

GenotypeQuality
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variant carriers: 1878

GenotypeQuality
all individuals: 2256
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variant carriers: 2026

GenotypeQuality
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variant carriers: 639

GenotypeQuality
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variant carriers: 1775

GenotypeQuality
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variant carriers: 25809

GenotypeQuality
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bin: 7.5e0
variant carriers: 262

GenotypeQuality
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bin: 1.75e1
variant carriers: 615

GenotypeQuality
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bin: 8.25e1
variant carriers: 1167

GenotypeQuality
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bin: 2.5e0
variant carriers: 159

GenotypeQuality
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bin: 5.25e1
variant carriers: 2139

GenotypeQuality
all individuals: 1097
bin: 7.25e1
variant carriers: 1056

GenotypeQuality
all individuals: 709
bin: 8.75e1
variant carriers: 703

Other
type: Population
allele count: 453
allele frequency: 6.239669421487604e-1
allele num: 726
num of homozygotes: 138

South Asian
type: Population
allele count: 10697
allele frequency: 6.97418177076542e-1
allele num: 15338
num of homozygotes: 3707

Latino
type: Population
allele count: 4161
allele frequency: 4.17184680168438e-1
allele num: 9974
num of homozygotes: 826

African
type: Population
allele count: 5092
allele frequency: 5.965323336457357e-1
allele num: 8536
num of homozygotes: 1420

European (Finnish)
type: Population
allele count: 2661
allele frequency: 5.58329836340747e-1
allele num: 4766
num of homozygotes: 684

European (Non-Finnish)
type: Population
allele count: 35365
allele frequency: 6.212451252503249e-1
allele num: 56926
num of homozygotes: 10634

East Asian
type: Population
allele count: 2573
allele frequency: 3.727904955085483e-1
allele num: 6902
num of homozygotes: 398

QD
type: SiteQuality
SIO_000300: 2.207e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.16e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.17e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.78e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.28e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.31e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 4.1e-2

DP
type: SiteQuality
SIO_000300: 1.171606e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 452
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 935
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
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GenotypeQuality
all individuals: 53
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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6808
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46794
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3456
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 602
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8808
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.706535141800247e-5
allele num: 12976
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5912
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.55e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -1.664e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.92e-1

MQ
type: SiteQuality
SIO_000300: 5.939e1

DP
type: SiteQuality
SIO_000300: 8.37511e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.34e0

QD
type: SiteQuality
SIO_000300: 1.018e1

VQSLOD
type: SiteQuality
SIO_000300: -8.462e-1

GenotypeQuality
all individuals: 5213
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 5020
bin: 6.25e1
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GenotypeQuality
all individuals: 684
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12800
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6704
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3370
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8698
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5820
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 590
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46032
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.222e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.16e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 5.72e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.6e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 8.25976e5

VQSLOD
type: SiteQuality
SIO_000300: 4.37e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.07e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.91e-1

GenotypeQuality
all individuals: 6146
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 152
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GenotypeQuality
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GenotypeQuality
all individuals: 177
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GenotypeQuality
all individuals: 600
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GenotypeQuality
all individuals: 5172
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GenotypeQuality
all individuals: 2929
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GenotypeQuality
all individuals: 935
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GenotypeQuality
all individuals: 2244
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20004
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GenotypeQuality
all individuals: 268
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GenotypeQuality
all individuals: 4158
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1402
bin: 4.25e1
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GenotypeQuality
all individuals: 83
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GenotypeQuality
all individuals: 616
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44828
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 584
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5612
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12668
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.553760099440646e-4
allele num: 6436
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3196
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 8.12022e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -5.145e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.28e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.25e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.21e0

FS
type: SiteQuality
SIO_000300: 6.805e0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.1e-2

MQRankSum
type: SiteQuality
SIO_000300: 9.1e-2

QD
type: SiteQuality
SIO_000300: 7.21e0

GenotypeQuality
all individuals: 1301
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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variant carriers: 0

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
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3330
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.834189288334556e-4
allele num: 5452
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 596
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8324
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6450
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44544
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12364
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 7.98702e5

ClippingRankSum
type: SiteQuality
SIO_000300: 7.27e-1

VQSLOD
type: SiteQuality
SIO_000300: -7.255e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.8e-1

QD
type: SiteQuality
SIO_000300: 1.868e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.27e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.35e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

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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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 36

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: 5978
num of homozygotes: 0

South Asian
type: Population
allele count: 35
allele frequency: 2.886836027713626e-3
allele num: 12124
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.670060243777145e-5
allele num: 42826
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 566
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8042
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 3.270111183780249e-4
allele num: 3058
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5270
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.491e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.97e-2

VQSLOD
type: SiteQuality
SIO_000300: 6.37e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.95e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.8e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 7.95566e5

FS
type: SiteQuality
SIO_000300: 1.326e0

QD
type: SiteQuality
SIO_000300: 1.232e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.12e-1

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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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
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 512
bin: 5.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 3
allele frequency: 2.518891687657431e-4
allele num: 11910
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 598
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5402
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3594
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44418
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.208e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.63e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.11e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.08e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.63e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.659999999999999e-1

DP
type: SiteQuality
SIO_000300: 7.90602e5

QD
type: SiteQuality
SIO_000300: 6.76e0

GenotypeQuality
all individuals: 4381
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
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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GenotypeQuality
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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: 2634
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GenotypeQuality
all individuals: 565
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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5350
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11856
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3578
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8142
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.25998915205207e-5
allele num: 44248
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6542
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 596
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.49e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.62e-1

DP
type: SiteQuality
SIO_000300: 7.88279e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 2.14e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.14e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

QD
type: SiteQuality
SIO_000300: 1.972e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.71e-1

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2634
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11856
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44248
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3578
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6542
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5350
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.228199459592238e-4
allele num: 8142
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 596
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.972e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.62e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.14e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.49e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.71e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.14e0

DP
type: SiteQuality
SIO_000300: 7.88279e5

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
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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
all individuals: 959
bin: 9.75e1
variant carriers: 2

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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GenotypeQuality
all individuals: 20008
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 461
bin: 6.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3522
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8014
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6438
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5228
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11676
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 590
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.605535854096624e-5
allele num: 43426
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 9.29e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.239e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.01e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.772e0

DP
type: SiteQuality
SIO_000300: 7.83758e5

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.468e0

QD
type: SiteQuality
SIO_000300: 1.325e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.18e-2

MQ
type: SiteQuality
SIO_000300: 5.82e1

GenotypeQuality
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bin: 3.75e1
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
all individuals: 959
bin: 9.75e1
variant carriers: 2

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3498
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.600027600165601e-5
allele num: 43478
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6446
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5238
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 590
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.01e-1

ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 7.79e0

VQSLOD
type: SiteQuality
SIO_000300: -3.239e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.369e0

MQRankSum
type: SiteQuality
SIO_000300: 6.6e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 7.82975e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.17e-2

GenotypeQuality
all individuals: 433
bin: 6.75e1
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
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GenotypeQuality
all individuals: 958
bin: 9.75e1
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GenotypeQuality
all individuals: 6475
bin: 2.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6274
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4990
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 42148
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11292
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3416
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.56e-1

VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 7.36e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.45e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.27e-2

QD
type: SiteQuality
SIO_000300: 7.46e0

DP
type: SiteQuality
SIO_000300: 7.78278e5

ClippingRankSum
type: SiteQuality
SIO_000300: -7.36e-1

GenotypeQuality
all individuals: 169
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 435
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2652
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 425
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 171
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7722
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4998
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11172
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3382
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6286
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 41724
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.047e0

DP
type: SiteQuality
SIO_000300: 7.78038e5

MQRankSum
type: SiteQuality
SIO_000300: 1.24e0

VQSLOD
type: SiteQuality
SIO_000300: -2.196e0

QD
type: SiteQuality
SIO_000300: 1.161e1

MQ
type: SiteQuality
SIO_000300: 5.895e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.2e-1

FS
type: SiteQuality
SIO_000300: 1.2128e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.2e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.27e-2

GenotypeQuality
all individuals: 4356
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1075
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4400
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8446
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11494
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66016
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16398
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.941370607649e-4
allele num: 10302
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6590
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.1e-3

MQRankSum
type: SiteQuality
SIO_000300: 2.05e-1

FS
type: SiteQuality
SIO_000300: 9.861000000000001e0

QD
type: SiteQuality
SIO_000300: 1.537e1

MQ
type: SiteQuality
SIO_000300: 5.744e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.15e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.2e-2

VQSLOD
type: SiteQuality
SIO_000300: -3.948e-1

DP
type: SiteQuality
SIO_000300: 2.174018e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.99e-1

GenotypeQuality
all individuals: 764
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4486
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
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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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4367
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2921
bin: 7.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6590
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8446
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10316
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11498
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.51437138443832e-5
allele num: 66034
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16404
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 5.7e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.89e-1

QD
type: SiteQuality
SIO_000300: 1.398e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 5.72e0

DP
type: SiteQuality
SIO_000300: 2.175297e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.52e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.007e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.86e-2

GenotypeQuality
all individuals: 2642
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4367
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1519
bin: 5.25e1
variant carriers: 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: 11498
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10316
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.028742768876639e-5
allele num: 66034
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16404
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8446
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6590
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.52e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.86e-2

DP
type: SiteQuality
SIO_000300: 2.175297e6

VQSLOD
type: SiteQuality
SIO_000300: 5.72e0

QD
type: SiteQuality
SIO_000300: 1.398e1

MQRankSum
type: SiteQuality
SIO_000300: 5.7e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.89e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.007e0

GenotypeQuality
all individuals: 643
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.5e0
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GenotypeQuality
all individuals: 933
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 625
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 4542
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variant carriers: 0

GenotypeQuality
all individuals: 1187
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10326
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11514
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66064
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8436
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.089392278650591e-5
allele num: 16422
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.884e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.47e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.8e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.5e0

DP
type: SiteQuality
SIO_000300: 2.182129e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.51e0

QD
type: SiteQuality
SIO_000300: 1.246e1

VQSLOD
type: SiteQuality
SIO_000300: -6.069e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.2e0

GenotypeQuality
all individuals: 45
bin: 7.5e0
variant carriers: 2

GenotypeQuality
all individuals: 23
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 861
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 5

GenotypeQuality
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bin: 9.25e1
variant carriers: 2

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 2

GenotypeQuality
all individuals: 2587
bin: 8.75e1
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GenotypeQuality
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bin: 6.25e1
variant carriers: 1

GenotypeQuality
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variant carriers: 2

GenotypeQuality
all individuals: 4220
bin: 8.25e1
variant carriers: 3

GenotypeQuality
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variant carriers: 2

GenotypeQuality
all individuals: 2889
bin: 7.25e1
variant carriers: 4

GenotypeQuality
all individuals: 26739
bin: 9.75e1
variant carriers: 1734

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

East Asian
type: Population
allele count: 519
allele frequency: 6.15366374199668e-2
allele num: 8434
num of homozygotes: 11

European (Non-Finnish)
type: Population
allele count: 73
allele frequency: 1.104922201368287e-3
allele num: 66068
num of homozygotes: 0

Latino
type: Population
allele count: 212
allele frequency: 1.841556636553162e-2
allele num: 11512
num of homozygotes: 3

Other
type: Population
allele count: 6
allele frequency: 6.666666666666667e-3
allele num: 900
num of homozygotes: 0

African
type: Population
allele count: 964
allele frequency: 9.330236159504453e-2
allele num: 10332
num of homozygotes: 45

South Asian
type: Population
allele count: 39
allele frequency: 2.37457379444715e-3
allele num: 16424
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.22e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.15e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.61e-1

QD
type: SiteQuality
SIO_000300: 1.594e1

DP
type: SiteQuality
SIO_000300: 2.192627e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.2e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.96e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.41e0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10340
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.512996641147457e-5
allele num: 66094
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: 1
allele frequency: 6.084945843981989e-5
allele num: 16434
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-3

MQRankSum
type: SiteQuality
SIO_000300: 9.379999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.51e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.61e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.652e0

VQSLOD
type: SiteQuality
SIO_000300: 6.08e-1

QD
type: SiteQuality
SIO_000300: 1.294e1

DP
type: SiteQuality
SIO_000300: 2.197511e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.022e0

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
all individuals: 238
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16434
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.512172992590352e-5
allele num: 66130
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11530
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10338
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 1.31e1

DP
type: SiteQuality
SIO_000300: 2.20857e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.33e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 4.548e0

MQRankSum
type: SiteQuality
SIO_000300: -7.45e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.8e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.75e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.371e0

VQSLOD
type: SiteQuality
SIO_000300: 5.13e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 10
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GenotypeQuality
all individuals: 142
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GenotypeQuality
all individuals: 18
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GenotypeQuality
all individuals: 169
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GenotypeQuality
all individuals: 4776
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GenotypeQuality
all individuals: 4620
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 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

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
allele num: 11540
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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East Asian
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allele frequency: 7.062146892655367e-4
allele num: 8496
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ClippingRankSum
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SIO_000300: 2.76e-1

ReadPosRankSum
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InbreedingCoeff
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VQSLOD
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QD
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MQRankSum
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MQ
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SIO_000300: 5.981e1

FS
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DP
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SIO_000300: 2.217707e6

BaseQRankSum
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SIO_000300: -7.51e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

African
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allele count: 1
allele frequency: 9.648784253184099e-5
allele num: 10364
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11556
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8588
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

European (Non-Finnish)
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allele count: 4
allele frequency: 6.019925954910755e-5
allele num: 66446
num of homozygotes: 0

MQ
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BaseQRankSum
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FS
type: SiteQuality
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ClippingRankSum
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VQSLOD
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InbreedingCoeff
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MQRankSum
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QD
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ReadPosRankSum
type: SiteQuality
SIO_000300: 8.94e-1

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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Latino
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allele frequency: 0.0e0
allele num: 11558
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8628
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10376
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.501817198810561e-5
allele num: 66586
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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BaseQRankSum
type: SiteQuality
SIO_000300: -3.957e0

FS
type: SiteQuality
SIO_000300: 2.436e0

QD
type: SiteQuality
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ClippingRankSum
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SIO_000300: -1.632e0

VQSLOD
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DP
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ReadPosRankSum
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MQ
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InbreedingCoeff
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 7.24e-1

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8632
num of homozygotes: 0

South Asian
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allele count: 3
allele frequency: 1.817080557238038e-4
allele num: 16510
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10376
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11562
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: 906
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66602
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.240699e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.55e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.179999999999999e-1

FS
type: SiteQuality
SIO_000300: 1.064e1

VQSLOD
type: SiteQuality
SIO_000300: -6.828e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.181e1

MQRankSum
type: SiteQuality
SIO_000300: 5.35e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.28e-1

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

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66660
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

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

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

African
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allele count: 0
allele frequency: 0.0e0
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ClippingRankSum
type: SiteQuality
SIO_000300: 5.23e-1

ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
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DP
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MQRankSum
type: SiteQuality
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FS
type: SiteQuality
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QD
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 1.72e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.11e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

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

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

East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.500060002400096e-5
allele num: 66664
num of homozygotes: 0

South Asian
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allele frequency: 1.211240310077519e-4
allele num: 16512
num of homozygotes: 0

InbreedingCoeff
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DP
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ClippingRankSum
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QD
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MQRankSum
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FS
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MQ
type: SiteQuality
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ReadPosRankSum
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VQSLOD
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 0.0e0
allele num: 10384
num of homozygotes: 0

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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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.499880009599232e-5
allele num: 66672
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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MQRankSum
type: SiteQuality
SIO_000300: -1.141e0

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

Latino
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num of homozygotes: 0

European (Non-Finnish)
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allele num: 66682
num of homozygotes: 0

African
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allele frequency: 9.63020030816641e-5
allele num: 10384
num of homozygotes: 0

East Asian
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European (Finnish)
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num of homozygotes: 0

South Asian
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Other
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InbreedingCoeff
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MQRankSum
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VQSLOD
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MQ
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FS
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DP
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ReadPosRankSum
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ClippingRankSum
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BaseQRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
type: Population
allele count: 0
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East Asian
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allele frequency: 0.0e0
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Other
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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 frequency: 7.498275396658768e-5
allele num: 66682
num of homozygotes: 0

African
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allele frequency: 9.628345850182938e-5
allele num: 10386
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European (Finnish)
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allele frequency: 0.0e0
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ReadPosRankSum
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QD
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MQ
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VQSLOD
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DP
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FS
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
allele num: 16512
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

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

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

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

European (Non-Finnish)
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allele frequency: 1.49934029027228e-5
allele num: 66696
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FS
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MQRankSum
type: SiteQuality
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ClippingRankSum
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ReadPosRankSum
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InbreedingCoeff
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BaseQRankSum
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VQSLOD
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MQ
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DP
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Latino
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allele frequency: 5.183137525915688e-4
allele num: 11576
num of homozygotes: 0

European (Non-Finnish)
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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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num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Other
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allele frequency: 1.103752759381898e-3
allele num: 906
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African
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allele count: 67
allele frequency: 6.447267128560431e-3
allele num: 10392
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East Asian
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allele frequency: 0.0e0
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FS
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VQSLOD
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DP
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BaseQRankSum
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MQ
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QD
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

East Asian
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allele frequency: 0.0e0
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South Asian
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Other
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allele count: 0
allele frequency: 0.0e0
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African
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allele frequency: 5.773672055427252e-4
allele num: 10392
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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ReadPosRankSum
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FS
type: SiteQuality
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MQRankSum
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QD
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MQ
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DP
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ClippingRankSum
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SIO_000300: -5.15e-1

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

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

Other
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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East Asian
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South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 8
allele frequency: 1.199544173214179e-4
allele num: 66692
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VQSLOD
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InbreedingCoeff
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MQRankSum
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FS
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MQ
type: SiteQuality
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ReadPosRankSum
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DP
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BaseQRankSum
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QD
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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num of homozygotes: 0

African
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South Asian
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Latino
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European (Finnish)
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Other
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East Asian
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BaseQRankSum
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QD
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ClippingRankSum
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MQRankSum
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VQSLOD
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FS
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ReadPosRankSum
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DP
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MQ
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

Other
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European (Non-Finnish)
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East Asian
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South Asian
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African
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European (Finnish)
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BaseQRankSum
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InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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QD
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ClippingRankSum
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FS
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VQSLOD
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DP
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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European (Finnish)
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African
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Latino
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East Asian
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South Asian
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ReadPosRankSum
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BaseQRankSum
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VQSLOD
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DP
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QD
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MQ
type: SiteQuality
SIO_000300: 5.977e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 5.19e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.72e-1

GenotypeQuality
all individuals: 4802
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26419
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 15
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 29
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4679
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4135
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3165
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5003
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10394
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.155802126675913e-4
allele num: 8652
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0